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Number of items: 122.

Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Simmonds, Emily, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Legge, Sophie E., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Harrison, Neil A. ORCID: https://orcid.org/0000-0002-9584-3769, O’Donovan, Michael C. and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2024. Common risk alleles for schizophrenia within the major histocompatibility complex predict white matter microstructure. Translational Psychiatry 14 , 194. 10.1038/s41398-024-02910-2
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Guintivano, Jerry, Byrne, Enda M., Kiewa, Jacqueline, Yao, Shuyang, Bauer, Anna E., Aberg, Karolina A., Adams, Mark J., Campbell, Archie, Campbell, Megan L., Choi, Karmel W., Corfield, Elizabeth C., Havdahl, Alexandra, Hucks, Donald, Koen, Nastassja, Lu, Yi, Mægbæk, Merete L., Mullaert, Jimmy, Peterson, Roseann E., Raffield, Laura M., Sallis, Hannah M., Sealock, Julia M., Walker, Alicia, Watson, Hunna J., Xiong, Ying, Yang, Jessica M.K. ORCID: https://orcid.org/0000-0002-3685-4126, Anney, Richard J.L. ORCID: https://orcid.org/0000-0002-6083-407X, Gordon-Smith, Katherine, Hubbard, Leon, Jones, Lisa A., Mihaescu, Raluca, Nyegaard, Mette, Pardiñas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Perry, Amy, Saquib, Nazmus, Shadyab, Aladdin H., Viktorin, Alexander, Andreassen, Ole A., Bigdeli, Tim B., Davis, Lea K., Dennis, Cindy-Lee, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Dubertret, Caroline, Feng, Yen-Chen A., Frey, Benicio N., Grigoriadis, Sophie, Gloaguen, Emilie, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Kennedy, James L., Krohn, Holly, Kunovac Kallak, Theodora, Li, Yun, Martin, Nicholas G., McIntosh, Andrew M., Milgrom, Jeannette, Munk-Olsen, Trine, Oberlander, Tim, Olsen, Catherine M., Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Robertson Blackmore, Emma, Rubinow, David, Skalkidou, Alkistis, Smoller, Jordan W., Stein, Dan J., Stowe, Zachary N., Taylor, Valerie, Tebeka, Sarah, Tesli, Martin, Van Lieshout, Ryan J., van den Oord, Edwin J.C.G., Vigod, Simone N., Werge, Thomas, Westlye, Lars T., Whiteman, David C., Zar, Heather J., Wray, Naomi, Meltzer-Brody, Samantha and Sullivan, Patrick 2023. Meta-analyses of genome-wide association studies for postpartum depression. The American Journal of Psychiatry 180 (12) , pp. 884-895. 10.1176/appi.ajp.20230053
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Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891, Legge, Sophie, Bracher-Smith, Matthew, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950 2023. Copy Number Variants increasing risk for schizophrenia: shared and distinct effects on brain morphometry and cognitive performance. Biological Psychiatry: Global Open Science 3 (4) , pp. 902-911. 10.1016/j.bpsgos.2022.10.006
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Weavers, Bryony ORCID: https://orcid.org/0000-0001-9654-3939, Riglin, Lucy, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Collishaw, Stephan ORCID: https://orcid.org/0000-0002-4296-820X, Heron, Jon, Thapar, Ajay ORCID: https://orcid.org/0000-0002-4589-8833, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729 2023. Characterising depression trajectories in young people at high familial risk of depression. Journal of Affective Disorders 337 , pp. 66-74. 10.1016/j.jad.2023.05.063
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Lewis, Katie, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Gregory, Alice M., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657 2023. Sleep disturbances in ADHD: Investigating the contribution of polygenic liability for ADHD and sleep-related phenotypes. European Child and Adolescent Psychiatry 32 , pp. 1253-1261. 10.1007/s00787-021-01931-2
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Rolland, Thomas, Cliquet, Freddy, Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Moreau, Clara, Traut, Nicolas, Mathieu, Alexandre, Huguet, Guillaume, Duan, Jinjie, Warrier, Varun, Portalier, Swan, Dry, Louise, Leblond, Claire S., Douard, Elise, Amsellem, Frédérique, Malesys, Simon, Maruani, Anna, Toro, Roberto, Børglum, Anders D., Grove, Jakob, Baron-Cohen, Simon, Packer, Alan, Chung, Wendy K., Jacquemont, Sébastien, Delorme, Richard and Bourgeron, Thomas 2023. Phenotypic effects of genetic variants associated with autism. Nature Medicine 29 (7) , pp. 1671-1680. 10.1038/s41591-023-02408-2
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Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Knott, Sarah, Underwood, Jack F. G. ORCID: https://orcid.org/0000-0003-1731-6039, Hubbard, Leon, Agha, Sharifah S. ORCID: https://orcid.org/0000-0001-9541-6786, Bisson, Jonathan I. ORCID: https://orcid.org/0000-0001-5170-1243, van den Bree, Marianne B. M. ORCID: https://orcid.org/0000-0002-4426-3254, Chawner, Samuel J. R. A., Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Jones, Ian R. ORCID: https://orcid.org/0000-0001-5821-5889, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Roberts, Neil P., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2023. DRAGON-Data: A platform and protocol for integrating genomic and phenotypic data across large psychiatric cohorts. BJPsych Open 9 (2) , e32. 10.1192/bjo.2022.636
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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Wray, Matthew, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Lewis, Katie J. S., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657 2023. Investigating direct and indirect genetic effects in attention-deficit/hyperactivity disorder using parent-offspring trios. Biological Psychiatry 93 (1) , pp. 37-44. 10.1016/j.biopsych.2022.06.008
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Pat, Narun, Yue, Wang, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Riglin, Lucy, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Argyris, Stringaris 2022. Longitudinally stable, brain-based predictive models mediate the relationships between childhood cognition and socio-demographic, psychological and genetic factors. Human Brain Mapping 43 (18) , pp. 5520-5542. 10.1002/hbm.26027
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Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Files, Christian, Davies, William ORCID: https://orcid.org/0000-0002-7714-2440 and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2022. Embedding genomic research into teaching practice: the rewards and potential pitfalls. Genetics Society News 87 , pp. 30-31.

Pat, Narun, Riglin, Lucy, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Wang, Yue, Barch, Deanna, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Stringaris, Argyris 2022. Motivation and cognitive abilities as mediators between polygenic scores and psychopathology in children. Journal of the American Academy of Child and Adolescent Psychiatry 61 (6) , pp. 782-795. 10.1016/j.jaac.2021.08.019
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Chambers, Tom, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Legge, Sophie, Baker, Emily, Singh, Krish ORCID: https://orcid.org/0000-0002-3094-2475, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891 and Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X 2022. Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Molecular Psychiatry 27 , pp. 2282-2290. 10.1038/s41380-022-01443-8
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Weavers, Bryony ORCID: https://orcid.org/0000-0001-9654-3939, Heron, Jon, Thapar, Ajay ORCID: https://orcid.org/0000-0002-3689-737X, Stephens, Alice, Lennon, Jessica, Bevan-Jones, Rhys ORCID: https://orcid.org/0000-0001-8976-9825, Eyre, Olga, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Collishaw, Stephan ORCID: https://orcid.org/0000-0002-4296-820X, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729 2021. The antecedents and outcomes of persistent and remitting adolescent depressive symptom trajectories: a longitudinal, population-based English study. The Lancet Psychiatry 8 (12) , pp. 1053-1061. 10.1016/S2215-0366(21)00281-9
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Hall, Lynsey S., Pain, Oliver, O’Brien, Heath E., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Bray, Nicholas J. ORCID: https://orcid.org/0000-0002-4357-574X 2021. Cis-effects on gene expression in the human prenatal brain associated with genetic risk for neuropsychiatric disorders. Molecular Psychiatry 26 , pp. 2082-2088. 10.1038/s41380-020-0743-3
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Powell, Victoria, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729 and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2021. Investigating regions of shared genetic variation in attention deficit/hyperactivity disorder and major depressive disorder: a GWAS meta-analysis. Scientific Reports 11 , 7353. 10.1038/s41598-021-86802-1
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Chambers, Tom, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Taylor, Peter N. ORCID: https://orcid.org/0000-0002-3436-422X, Teumer, Alexander, Peeters, Robin P., Medici, Marco, Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891 and Rees, D. Aled ORCID: https://orcid.org/0000-0002-1165-9092 2021. Effects of thyroid status on regional brain volumes: a diagnostic and genetic imaging study in UK Biobank. Journal of Clinical Endocrinology and Metabolism 106 (3) , pp. 688-696. 10.1210/clinem/dgaa903
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Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Cormand, Bru, Hougaard, David M., Neale, Benjamin M., Franke, Barbara, Faraone, Stephen V., Børglum, Anders D., ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479 2021. Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Nature Communications 12 (1) , 576. 10.1038/s41467-020-20443-2
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Chawner, Samuel, Doherty, Joanne L., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Antshel, Kevin M., Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Koche, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., MihaljevicMihaljevic, Marina Mihaljevic, Miller, Judith S., Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and van den Bree, Marianne B.M. ORCID: https://orcid.org/0000-0002-4426-3254 2021. A genetics-first approach to dissecting the heterogeneity of autism: phenotypic comparison of autism risk copy number variants. American Journal of Psychiatry 178 (1) , pp. 77-86. 10.1176/appi.ajp.2020.20010015
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Powell, Victoria, Riglin, Lucy, Hammerton, Gemma, Eyre, Olga, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729 2020. What explains the link between childhood ADHD and adolescent depression? Investigating the role of peer relationships and academic attainment. European Child and Adolescent Psychiatry 29 , pp. 1581-1591. 10.1007/s00787-019-01463-w
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Grama, Steluta, Willcocks, Isabella ORCID: https://orcid.org/0000-0002-3568-5236, Hubert, John, Pardiñas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie, Bracher-Smith, Matthew, Menzies, Georgina ORCID: https://orcid.org/0000-0002-6600-6507, Hall, Lynsey, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bray, Nicholas ORCID: https://orcid.org/0000-0002-4357-574X, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 and Caseras, Xavier ORCID: https://orcid.org/0000-0002-8490-6891 2020. Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Translational Psychiatry 10 , 309. 10.1038/s41398-020-00940-0
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Riglin, Lucy, Thapar, Ajay ORCID: https://orcid.org/0000-0002-4589-8833, Leppert, Beate, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Richards, Alexander, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Davey Smith, George, Tilling, Kate, Stegiakouli, Evie, Lahey, Benjamin, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Collishaw, Stephan ORCID: https://orcid.org/0000-0002-4296-820X and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2020. Using genetics to examine a general liability to childhood psychopathology. Behavior Genetics 50 , pp. 213-220. 10.1007/s10519-019-09985-4
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Lee, Phil H., Anttila, Verneri, Won, Hyejung, Feng, Yen-Chen A., Rosenthal, Jacob, Zhu, Zhaozhong, Tucker-Drob, Elliot M., Nivard, Michel G., Grotzinger, Andrew D., Posthuma, Danielle, Wang, Meg M.-J., Yu, Dongmei, Stahl, Eli A., Walters, Raymond K. ORCID: https://orcid.org/0000-0002-6980-4053, Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Duncan, Laramie E., Ge, Tian, Adolfsson, Rolf, Banaschewski, Tobias, Belangero, Sintia, Cook, Edwin H., Coppola, Giovanni, Derks, Eske M., Hoekstra, Pieter J., Kaprio, Jaakko, Keski-Rahkonen, Anna, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Kranzler, Henry R., Luykx, Jurjen J., Rohde, Luis A., Zai, Clement C., Agerbo, Esben, Arranz, M.J., Asherson, Philip, Bækvad-Hansen, Marie, Baldursson, Gísli, Bellgrove, Mark, Belliveau, Richard A., Buitelaar, Jan, Burton, Christie L., Bybjerg-Grauholm, Jonas, Casas, Miquel, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Cormand, Bru, Crosbie, Jennifer, Dalsgaard, Søren, Demontis, Ditte, Doyle, Alysa E., Dumont, Ashley, Elia, Josephine, Grove, Jakob, Gudmundsson, Olafur O., Haavik, Jan, Hakonarson, Hakon, Hansen, Christine S., Hartman, Catharina A., Hawi, Ziarih, Hervás, Amaia, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Kuntsi, Jonna, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Lesch, Klaus-Peter, Leung, Patrick W.L., Loo, Sandra K., Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, McGough, James J., Medland, Sarah E., Moran, Jennifer L., Mors, Ole, Mortensen, Preben B., Oades, Robert D., Palmer, Duncan S., Pedersen, Carsten B., Pedersen, Marianne G., Peters, Triinu, Poterba, Timothy, Poulsen, Jesper B., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Ribasés, Marta, Rothenberger, Aribert, Rovira, Paula, Sánchez-Mora, Cristina, Satterstrom, F. Kyle, Schachar, Russell, Artigas, Maria Soler, Steinberg, Stacy, Stefansson, Hreinn, Turley, Patrick, Walters, G. Bragi ORCID: https://orcid.org/0000-0002-6980-4053, Werge, Thomas, Zayats, Tetyana, Arking, Dan E., Bettella, Francesco, Buxbaum, Joseph D., Christensen, Jane H., Collins, Ryan L., Coon, Hilary, De Rubeis, Silvia, Delorme, Richard, Grice, Dorothy E., Hansen, Thomas F., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hope, Sigrun, Hultman, Christina M., Klei, Lambertus, Ladd-Acosta, Christine, Magnusson, Pall, Nærland, Terje, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Roeder, Kathryn, Rouleau, Guy A., Saemundsen, Evald, Sanders, Stephan J., Sandin, Sven, St Pourcain, Beate, Stefansson, Kari, Sutcliffe, James S., Talkowski, Michael E., Weiss, Lauren A., Willsey, A. Jeremy, Agartz, Ingrid, Akil, Huda, Albani, Diego, Alda, Martin, Als, Thomas D., Anjorin, Adebayo, Backlund, Lena, Bass, Nicholas, Bauer, Michael, Baune, Bernhard T., Bellivier, Frank, Bergen, Sarah E., Berrettini, Wade H., Biernacka, Joanna M., Blackwood, Douglas H.R., Bøen, Erlend, Budde, Monika, Bunney, William, Burmeister, Margit, Byerley, William, Byrne, Enda M., Cichon, Sven, Clarke, Toni-Kim, Coleman, Jonathan R.I., Craddock, Nicholas ORCID: https://orcid.org/0000-0003-2171-0610, Curtis, David, Czerski, Piotr M., Dale, Anders M., Dalkner, Nina, Dannlowski, Udo, Degenhardt, Franziska, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Elvsåshagen, Torbjørn, Etain, Bruno, Fischer, Sascha B., Forstner, Andreas J., Forty, Liz, Frank, Josef, Frye, Mark, Fullerton, Janice M., Gade, Katrin, Gaspar, Héléna A., Gershon, Elliot S., Gill, Michael, Goes, Fernando S., Gordon, Scott D., Gordon-Smith, Katherine, Green, Melissa J., Greenwood, Tiffany A., Grigoroiu-Serbanescu, Maria, Guzman-Parra, José, Hauser, Joanna, Hautzinger, Martin, Heilbronner, Urs, Herms, Stefan, Hoffmann, Per, Holland, Dominic, Jamain, Stéphane, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Jones, Lisa A. ORCID: https://orcid.org/0000-0001-5821-5889, Kandaswamy, Radhika, Kelsoe, John R., Kennedy, James L., Joachim, Oedegaard Ketil, Kittel-Schneider, Sarah, Kogevinas, Manolis, Koller, Anna C., Lavebratt, Catharina, Lewis, Cathryn M., Li, Qingqin S., Lissowska, Jolanta, Loohuis, Loes M.O., Lucae, Susanne, Maaser, Anna, Malt, Ulrik F., Martin, Nicholas G. ORCID: https://orcid.org/0000-0002-8911-3479, Martinsson, Lina, McElroy, Susan L., McMahon, Francis J., McQuillin, Andrew, Melle, Ingrid, Metspalu, Andres, Millischer, Vincent, Mitchell, Philip B., Montgomery, Grant W., Morken, Gunnar, Morris, Derek W., Müller-Myhsok, Bertram, Mullins, Niamh, Myers, Richard M., Nievergelt, Caroline M., Nordentoft, Merete, Adolfsson, Annelie Nordin, Nöthen, Markus M., Ophoff, Roel A., Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Paciga, Sara A., Pato, Carlos N., Pato, Michele T., Perlis, Roy H., Perry, Amy, Potash, James B., Reinbold, Céline S., Rietschel, Marcella, Rivera, Margarita, Roberson, Mary, Schalling, Martin, Schofield, Peter R., Schulze, Thomas G., Scott, Laura J., Serretti, Alessandro, Sigurdsson, Engilbert, Smeland, Olav B., Stordal, Eystein, Streit, Fabian, Strohmaier, Jana, Thorgeirsson, Thorgeir E., Treutlein, Jens, Turecki, Gustavo, Vaaler, Arne E., Vieta, Eduard, Vincent, John B., Wang, Yunpeng, Witt, Stephanie H., Zandi, Peter, Adan, Roger A.H., Alfredsson, Lars, Ando, Tetsuya, Aschauer, Harald, Baker, Jessica H., Bencko, Vladimir, Bergen, Andrew W., Birgegård, Andreas, Perica, Vesna Boraska, Brandt, Harry, Burghardt, Roland, Carlberg, Laura, Cassina, Matteo, Clementi, Maurizio, Courtet, Philippe, Crawford, Steven, Crow, Scott, Crowley, James J., Danner, Unna N., Davis, Oliver S.P., Degortes, Daniela, DeSocio, Janiece E., Dick, Danielle M., Dina, Christian, Docampo, Elisa, Egberts, Karin, Ehrlich, Stefan, Espeseth, Thomas, Fernández-Aranda, Fernando, Fichter, Manfred M., Foretova, Lenka, Forzan, Monica, Gambaro, Giovanni, Giegling, Ina, Gonidakis, Fragiskos, Gorwood, Philip, Mayora, Monica Gratacos, Guo, Yiran, Halmi, Katherine A., Hatzikotoulas, Konstantinos, Hebebrand, Johannes, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Hinney, Anke, Imgart, Hartmut, Jiménez-Murcia, Susana, Johnson, Craig, Jordan, Jennifer, Julià, Antonio, Kaminská, Deborah, Karhunen, Leila, Karwautz, Andreas, Kas, Martien J.H., Kaye, Walter H., Kennedy, Martin A., Kim, Youl-Ri, Klareskog, Lars, Klump, Kelly L., Knudsen, Gun Peggy S., Landén, Mikael, Le Hellard, Stephanie, Levitan, Robert D., Li, Dong, Lichtenstein, Paul, Maj, Mario, Marsal, Sara, McDevitt, Sara, Mitchell, James, Monteleone, Palmiero, Monteleone, Alessio Maria, Munn-Chernoff, Melissa A., Nacmias, Benedetta, Navratilova, Marie, O'Toole, Julie K., Padyukov, Leonid, Pantel, Jacques, Papezova, Hana, Rabionet, Raquel, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ricca, Valdo, Roberts, Marion, Rujescu, Dan, Rybakowski, Filip, Scherag, André, Schmidt, Ulrike, Seitz, Jochen, Slachtova, Lenka, Slof-Opt Landt, Margarita C.T., Slopien, Agnieszka, Sorbi, Sandro, Southam, Lorraine, Strober, Michael, Tortorella, Alfonso, Tozzi, Federica, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., Wade, Tracey D., Wagner, Gudrun, Walton, Esther, Watson, Hunna J., Wichmann, H-Erich, Woodside, D. 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Anthony, Oh, Sang-Yun, Palotie, Aarno, Pantelis, Christos, Pulver, Ann E., Petryshen, Tracey L., Quested, Digby J., Riley, Brien, Sanders, Alan R., Schall, Ulrich, Schwab, Sibylle G., Scott, Rodney J., Sham, Pak C., Silverman, Jeremy M., Sim, Kang, Steixner, Agnes A., Tooney, Paul A., van Os, Jim, Vawter, Marquis P., Walsh, Dermot, Weiser, Mark, Wildenauer, Dieter B., Williams, Nigel M., Wormley, Brandon K., Zhang, Fuquan, Androutsos, Christos, Arnold, Paul D., Barr, Cathy L., Barta, Csaba, Bey, Katharina, Bienvenu, O. Joseph, Black, Donald W., Brown, Lawrence W., Budman, Cathy, Cath, Danielle, Cheon, Keun-Ah, Ciullo, Valentina, Coffey, Barbara J., Cusi, Daniele, Davis, Lea K., Denys, Damiaan, Depienne, Christel, Dietrich, Andrea, Eapen, Valsamma, Falkai, Peter, Fernandez, Thomas V., Garcia-Delgar, Blanca, Geller, Daniel A., Gilbert, Donald L., Grados, Marco A., Greenberg, Erica, Grünblatt, Edna, Hagstrøm, Julie, Hanna, Gregory L., Hartmann, Andreas, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hong, Hyun Ju, Huang, Alden, Huyser, Chaim, Ibanez-Gomez, Laura, Khramtsova, Ekaterina A., Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Konstantinidis, Anastasios, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett L., Lochner, Christine, Ludolph, Andrea G., Madruga-Garrido, Marcos, Malaty, Irene, Maras, Athanasios, McCracken, James T., Meijer, Inge A., Mir, Pablo, Morer, Astrid, Müller-Vahl, Kirsten R., Münchau, Alexander, Murphy, Tara L., Naarden, Allan, Nagy, Peter, Nestadt, Gerald, Nestadt, Paul S., Nicolini, Humberto, Nurmi, Erika L., Okun, Michael S., Paschou, Peristera, Piras, Fabrizio, Piras, Federica, Pittenger, Christopher, Plessen, Kerstin J., Richter, Margaret A., Rizzo, Renata, Robertson, Mary, Roessner, Veit, Ruhrmann, Stephan, Samuels, Jack F., Sandor, Paul, Schlögelhofer, Monika, Shin, Eun-Young, Singer, Harvey, Song, Dong-Ho, Song, Jungeun, Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Stuhrmann, Manfred, Tarnok, Zsanett, Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Vulink, Nienke, Wagner, Michael, Walitza, Susanne, Wanderer, Sina, Woods, Martin, Worbe, Yulia, Zai, Gwyneth, Zinner, Samuel H., Sullivan, Patrick F., Franke, Barbara, Daly, Mark J., Bulik, Cynthia M., Lewis, Cathryn M., McIntosh, Andrew M., O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Zheutlin, Amanda, Andreassen, Ole A., Børglum, Anders D., Breen, Gerome, Edenberg, Howard J., Fanous, Ayman H., Faraone, Stephen V., Gelernter, Joel, Mathews, Carol A., Mattheisen, Manuel, Mitchell, Karen S., Neale, Michael C., Nurnberger, John I., Ripke, Stephan, Santangelo, Susan L., Scharf, Jeremiah M., Stein, Murray B., Thornton, Laura M., Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Wray, Naomi R., Geschwind, Daniel H., Neale, Benjamin M., Kendler, Kenneth S. and Smoller, Jordan W. 2019. Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders. Cell 179 (7) , 1469-1482.e11. 10.1016/j.cell.2019.11.020
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Underwood, Jack ORCID: https://orcid.org/0000-0003-1731-6039, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Berrett, Jennifer, Lewis, Catrin ORCID: https://orcid.org/0000-0002-3818-9377, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Van den Bree, Marianne ORCID: https://orcid.org/0000-0002-4426-3254 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2019. Autism spectrum disorder diagnosis in adults: phenotype and genotype findings from a clinically derived cohort. British Journal of Psychiatry 215 (5) , pp. 647-653. 10.1192/bjp.2019.30
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Connolly, Siobhan, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gallagher, Louise and Heron, Elizabeth 2019. Evidence of assortative mating in autism spectrum disorder. Biological Psychiatry 86 (4) , pp. 286-293. 10.1016/j.biopsych.2019.04.014
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Pain, Oliver, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Holmans, Peter A. ORCID: https://orcid.org/0000-0003-0870-9412, Bray, Nichloas J. ORCID: https://orcid.org/0000-0002-4357-574X, O'Brian, Heath E., Hall, Lynsey S., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2019. Novel insight into the etiology of autism spectrum disorder gained by integrating expression data with genome-wide association statistics. Biological Psychiatry 86 (4) , pp. 265-273. 10.1016/j.biopsych.2019.04.034
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Underwood, Jack ORCID: https://orcid.org/0000-0003-1731-6039, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Berrett, Jennifer, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bree, Marianne Van Den and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2019. SA20COPY Number variants and polygenic risk scores in adults with autism spectrum disorder (ASD): results from the NCMH adult ASD cohort. European Neuropsychopharmacology 29 (S4) , S1198-S1199. 10.1016/j.euroneuro.2018.08.242

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Campbell, Talks, Kate, Tan, Yvonne, Thachil, Jecko, Thaventhiran, James, Thomas, Ellen, Thomas, Moira, Thompson, Dorothy, Thrasher, Adrian, Tischkowitz, Marc, Titterton, Catherine, Toh, Cheng-Hock, Toshner, Mark, Treacy, Carmen, Trembath, Richard, Tuna, Salih, Turek, Wojciech, Turro, Ernest, Van Geet, Chris, Veltman, Marijke, Vogt, Julie, von Ziegenweldt, Julie, Vonk Noordegraaf, Anton, Wakeling, Emma, Wanjiku, Ivy, Warner, Timothy Q., Wassmer, Evangeline, Watkins, Hugh, Webster, Andrew, Welch, Steve, Westbury, Sarah, Wharton, John, Whitehorn, Deborah, Wilkins, Martin, Willcocks, Lisa, Williamson, Catherine, Woods, Geoffrey, Wort, John, Yeatman, Nigel, Yong, Patrick, Young, Tim and Yu, Ping 2019. Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia. American Journal of Human Genetics 104 (5) , pp. 948-956. 10.1016/j.ajhg.2019.03.005
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Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Riglin, Lucy, Thapar, Ajay K. ORCID: https://orcid.org/0000-0002-3689-737X, Heron, Jon, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2019. Characterizing developmental trajectories and the role of neuropsychiatric genetic risk variants in early-onset depression. JAMA Psychiatry 76 (3) , pp. 306-313. 10.1001/jamapsychiatry.2018.3338
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Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Baekved-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, Moran, Jennifer L., Nyegaard, Mette, Naerland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, St Pourcain, Beate, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Smith, George Davey ORCID: https://orcid.org/0000-0003-1069-5347, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine, Sullivan, Patrick F, Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J. and Borglum, Anders D. 2019. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics 51 , pp. 431-444. 10.1038/s41588-019-0344-8
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O'Brien, Heath ORCID: https://orcid.org/0000-0003-2309-8736, Hannon, Eilis ORCID: https://orcid.org/0000-0001-6840-072X, Jeffries, Aaron R., Davies, William ORCID: https://orcid.org/0000-0002-7714-2440, Hill, Matthew J. ORCID: https://orcid.org/0000-0001-6776-8709, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Mill, Jonathan and Bray, Nicholas ORCID: https://orcid.org/0000-0002-4357-574X 2019. Sex differences in gene expression in the human fetal brain. [Online]. bioRxiv. Available at: https://doi.org/10.1101/483636
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Demontis, Ditte, Walters, Raymond K., Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Mattheisen, Manuel, Als, Thomas Damm, Agerbo, Esben, Baldursson, Gísli, Belliveau, Rich, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Eriksson, Nicholas, Gandal, Michael, Goldstein, Jacqueline, Grasby, Katrina L., Grove, Jakob, Gudmundsson, Olafur O., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, Martin, Nicholas G. ORCID: https://orcid.org/0000-0002-8911-3479, Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Bøcker Pedersen, Carsten, Giørtz Pedersen, Marianne, Poterba, Timothy, Buchhave Poulsen, Jesper, Ripke, Stephan, Robinson, Elise B., Satterstrom, F. Kyle, Stefansson, Hreinn, Stevens, Christine, Turley, Patrick, Walters, G. Bragi, Won, Hyejung, Wright, Margaret J., Andreassen, Ole A., Asherson, Philip, Burton, Christie, Boomsma, Dorret I., Cormand, Bru, Dalsgaard, Soren, Franke, Barbara, Gelernter, Joel, Geschwind, Daniel, Hakonarson, Hakon, Haavik, Jan, Kranzler, Henry, Kuntsi, Jonna, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Lesch, Klaus-Peter, Middeldorp, Christel, Reif, Andreas, Rohde, Luis Augusto, Roussos, Panos, Schacha, Russell, Sklar, Pamela, Sonuga-Barke, Edmund J. S., Sullivan, Patrick F., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Tung, Joyce Y., Waldman, Irwin ., Medland, Sarah E., Stefansson, Kari, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Bo Mortensen, Preben, Daly, Mark J., Faraone, Stephen V., Børglum, Anders D., Neale, Benjamin M. and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2019. Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder. Nature Genetics 51 , pp. 63-75. 10.1038/s41588-018-0269-7
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Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K., Walters, Raymond K., Bras, Jose, Duncan, Laramie, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Falcone, Guido J., Gormley, Padhraig, Malik, Rainer, Patsopoulos, Nikolaos A., Ripke, Stephan, Wei, Zhi, Yu, Dongmei, Lee, Phil H., Turley, Patrick, Grenier-Boley, Benjamin, Chouraki, Vincent, Kamatani, Yoichiro, Berr, Claudine, Letenneur, Luc, Hannequin, Didier, Amouyel, Philippe, Boland, Anne, Deleuze, Jean-François, Duron, Emmanuelle, Vardarajan, Badri N., Reitz, Christiane, Goate, Alison M., Huentelman, Matthew J., Kamboh, M. Ilyas, Larson, Eric B., Rogaeva, Ekaterina, St George-Hyslop, Peter, Hakonarson, Hakon, Kukull, Walter A., Farrer, Lindsay A., Barnes, Lisa L., Beach, Thomas G., Demirci, F. Yesim, Head, Elizabeth, Hulette, Christine M., Jicha, Gregory A., Kauwe, John S.K., Kaye, Jeffrey A., Leverenz, James B., Levey, Allan I., Lieberman, Andrew P., Pankratz, Vernon S., Poon, Wayne W., Quinn, Joseph F., Saykin, Andrew J., Schneider, Lon S., Smith, Amanda G., Sonnen, Joshua A., Stern, Robert A., Van Deerlin, Vivianna M., Van Eldik, Linda J., Harold, Denise ORCID: https://orcid.org/0000-0001-5195-0143, Russo, Giancarlo, Rubinsztein, David C., Bayer, Antony ORCID: https://orcid.org/0000-0002-7514-248X, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C., Hampel, Harald, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M., Rossor, Martin, Lupton, Michelle K., Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew, ORCID: https://orcid.org/0000-0002-8905-1052, ORCID: https://orcid.org/0000-0001-8063-7674, ORCID: https://orcid.org/0000-0002-3491-4519, , ORCID: https://orcid.org/0000-0003-1177-6931, ORCID: https://orcid.org/0000-0002-2033-2657, ORCID: https://orcid.org/0000-0003-2171-0610, ORCID: https://orcid.org/0000-0002-1682-9134, , , ORCID: https://orcid.org/0000-0002-6980-4053, ORCID: https://orcid.org/0000-0003-0870-9412, ORCID: https://orcid.org/0000-0002-4069-0259 and ORCID: https://orcid.org/0000-0002-6083-407X 2018. Analysis of shared heritability in common disorders of the brain. Science 360 (6395) , eaap8757. 10.1126/science.aap8757
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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Walters, Raymond K., Demontis, Ditte, Mattheisen, Manuel, Lee, S. Hong, Robinson, Elise, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Eriksson, Nicholas, Werge, Thomas, Mortensen, Preben Bo, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Wray, Naomi R., Franke, Barbara, Faraone, Stephen V., O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Børglum, Anders D., Neale, Benjamin M., Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hinds, David A., Hromatka, Bethann S., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Northover, Carrie A.M., Pitts, Steven J., Sathirapongsasuti, J. Fah, Sazonova, Olga V., Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y., Vacic, Vladimir, Wilson, Catherine H., Albayrak, Özgür, Anney, Richard J. L. ORCID: https://orcid.org/0000-0002-6083-407X, Vasquez, Alejandro Arias, Arranz, Maria Jesús, Asherson, Philip, Banaschewski, Tobias, Banaschewski, Tobias J., Bau, Claiton, Biederman, Joseph, Buitelaar, Jan K., Casas, Miguel, Charach, Alice, Cormand, Bru, Crosbie, Jennifer, Dalsgaard, Soeren, Daly, Mark J., Dempfle, Astrid, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Föcker, Manuel, Freitag, Christine, Gelernter, Joel, Gill, Michael, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hebebrand, Johannes, Herpertz-Dahlmann, Beate, Hervas, Amaia, Hinney, Anke, Hohmann, Sarah, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Hutz, Mara, Ickowitz, Abel, Johansson, Stefan, Kent, Lindsey, Kittel-Schneider, Sarah, Kranzler, Henry, Kuntsi, Jonna, Lambregts-Rommelse, Nanda, Langley, Kate, Lehmkuhl, Gerd, Lesch, Klaus-Peter, Loo, Sandra K., McGough, James J., Medland, Sarah E., Meyer, Jobst, Mick, Eric, Middletion, Frank, Miranda, Ana, Mulas, Fernando, Mulligan, Aisling, Nelson, Stan F., Nguyen, T. Trang, Oades, Robert D., Palmason, Haukur, Ramos-Quiroga, Josep Antoni, Reif, Andreas, Renner, Tobias J., Rhode, Luis, Ribasés, Marta, Rietschel, Marcella, Ripke, Stephan, Rivero, Olga, Sánchez-Mora, Cristina, Schachar, Russell, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Sinzig, Judith, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Thompsom, Margaret, Todorov, Alexandre, Waldman, Irwin, Walitza, Susanne, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Zayats, Tetyana, Zhang-James, Yanli, Agerbo, Esben, Damm Als, Thomas, Bækved-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Hansen, Christine S., Engel Hauberg, Mads, Hollegaard, Mads V., Howrigan, Daniel P., Huang, Hailiang, Maller, Julian, Martin, Alicia R. ORCID: https://orcid.org/0000-0002-8911-3479, Moran, Jennifer, Pallesen, Jonatan, Palmer, Duncan S., Pedersen, Carsten Bøcker, Poterba, Timothy, Poulson, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine and Turley, Patrick 2018. A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder. Biological Psychiatry 83 (12) , pp. 1044-1053. 10.1016/j.biopsych.2017.11.026
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Cosgrove, Donna, Mothersill, David O., Whitton, Laura, Harold, Denise, Kelly, Sinead, Holleran, Laurena, Holland, Jessica, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Richards, Alexander, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379, Gill, Michael, Corvin, Aiden, Morris, Derek W. and Donohoe, Gary 2018. Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 (3) , pp. 369-376. 10.1002/ajmg.b.32620
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Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S., Zhang, Xiaochang, D'Gama, Alissa M., Kim, Sonia N., Hill, Robert Sean, Goldberg, Arthur P., Poultney, Christopher, Minshew, Nancy J., Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J., Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M., Weiss, Lauren A., Fromer, Menachem, Chiocchetti, Andreas G., Freitag, Christine M., Church, George M., Scherer, Stephen W., Buxbaum, Joseph D., Walsh, Christopher A. and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2017. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nature Neuroscience 20 (9) , pp. 1217-1224. 10.1038/nn.4598
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Weiner, Daniel J., Wigdor, Emilie M., Ripke, Stephan, Walters, Raymond K., Kosmicki, Jack A., Grove, Jakob, Samocha, Kaitlin E., Goldstein, Jacqueline I., Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M., Taylor, Jacob, Bækvad-Hansen, Marie, Dumont, Ashley, Hansen, Christine, Hansen, Thomas F., Howrigan, Daniel, Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Nordentoft, Merete, Nørgaard-Pedersen, Bent, Poterba, Timothy, Poulsen, Jesper, Stevens, Christine, Anttila, Verneri, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Huang, Hailiang, Klei, Lambertus, Lee, Phil H., Medland, Sarah E., Neale, Benjamin, Weiss, Lauren A., Zwaigenbaum, Lonnie, Yu, Timothy W., Wittemeyer, Kerstin, Willsey, A. Jeremy, Wijsman, Ellen M., Wassink, Thomas H., Waltes, Regina, Walsh, Christopher A., Wallace, Simon, Vorstman, Jacob A. S., Vieland, Veronica J., Vicente, Astrid M., van Engeland, Herman, Tsang, Kathryn, Thompson, Ann P., Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W., Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W., Schellenberg, Gerard D., Sandin, Sven, Saemundsen, Evald, Rouleau, Guy A., Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S., Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A., Pejovic-Milovancevic, Milica, Pedersen, Marianne G., Pedersen, Carsten B., Paterson, Andrew D., Parr, Jeremy R., Pagnamenta, Alistair T., Oliveira, Guiomar, Nurnberger, John I., Nordentoft, Merete, Murtha, Michael T., Mouga, Susana, Mors, Ole, Morrow, Eric M., De Luca, Daniel Moreno, Monaco, Anthony P., Minshew, Nancy, Merikangas, Alison, McMahon, William M., McGrew, Susan G., Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M., Mane, Shrikant M., Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K., Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H., Leboyer, Marion, Le Couteur, Ann S., Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M., Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M., Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine S., Haines, Jonathan L., Guter, Stephen J., Grice, Dorothy E., Green, Jonathan M., Green, Andrew, Goldberg, Arthur P., Gillberg, Christopher, Gilbert, John, Gallagher, Louise, Freitag, Christine M., Fombonne, Eric, Folstein, Susan E., Fernandez, Bridget, Fallin, M. Daniele, Ercan-Sencicek, A. Gulhan, Ennis, Sean, Duque, Frederico, Duketis, Eftichia, Delorme, Richard, De Rubeis, Silvia, De Jonge, Maretha V., Dawson, Geraldine, Cuccaro, Michael L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Celestino-Soper, Patrícia B. S., Casey, Jillian, Cantor, Rita M., Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bölte, Sven, Bolshakova, Nadia, Betancur, Catalina, Bernier, Raphael, Beaudet, Arthur L., Battaglia, Agatino, Bal, Vanessa H., Baird, Gillian, Bailey, Anthony J., Bækvad-Hansen, Marie, Bader, Joel S., Bacchelli, Elena, Anagnostou, Evdokia, Amaral, David, Almeida, Joana, Buxbaum, Joseph D., Chakravarti, Aravinda, Cook, Edwin H., Coon, Hilary, Geschwind, Daniel H., Gill, Michael, Hakonarson, Hakon, Hallmayer, Joachim, Palotie, Aarno, Santangelo, Susan, Sutcliffe, James S., Arking, Dan E., Skuse, David, Devlin, Bernie, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Sanders, Stephan J., Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D., Smith, George Davey, Daly, Mark J. and Robinson, Elise B. 2017. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics 49 (7) , pp. 978-985. 10.1038/ng.3863
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Merikangas, Alison K., Segurado, Ricardo, Cormican, Paul, Heron, Elizabeth A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Moore, Susan, Kelleher, Eric, Hargreaves, April, Anderson-Schmidt, Heike, Gill, Michael, Gallagher, Louise and Corvin, Aiden 2014. The phenotypic manifestations of rare CNVs in schizophrenia. Schizophrenia Research 158 (1-3) , pp. 255-260. 10.1016/j.schres.2014.06.016

Kenny, E. M., Cormican, P., Furlong, S., Heron, E., Kenny, G., Fahey, C., Kelleher, E., Ennis, S., Tropea, D., Anney, R. ORCID: https://orcid.org/0000-0002-6083-407X, Corvin, P., Donohoe, G., Gallagher, L., Gill, M. and Morris, D. W. 2014. Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders. Molecular Psychiatry 19 (8) , pp. 872-879. 10.1038/mp.2013.127

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Avbersek, A., Balding, D., Baum, L., Becker, F., Berkovic, S. F., Bradfield, J. P., Brody, L. C., Buono, R. J., Catarino, C. B., Cavalleri, G. L., Cherny, S. S., Chinthapalli, K., Coffey, A. J., Compston, A., Cossette, P., de Haan, G-J., De Jonghe, P., de Kovel, C. G. F., Delanty, N., Depondt, C., Dlugos, D. J., Doherty, C. P., Elger, C. E., Ferraro, T. N., Feucht, M., Franke, A., French, J., Gaus, V., Goldstein, D. B., Gui, H., Guo, Y., Hakonarson, H., Hallman, K., Heinzen, E. L., Helbig, I., Hjalgrim, H., Jackson, M., Jamnadas-Khoda, J., Janz, D., Johnson, M. R., Kalviainen, R., Kantanen, A-M., Kasperaviciute, D., Kasteleijn-Nolst Trenite, D., Koeleman, B. P. C., Kunz, W. S., Kwan, P., Lung Lau, Y., Lehesjoki, A-E., Lerche, H., Leu, C., Lieb, W., Lindhout, D., Lo, W., Lowenstein, D. H., Malovini, A., Marson, A. G., McCormack, M., Mills, J. M., Moerzinger, M., Moller, R. S., Molloy, A. M., Muhle, H., Newton, M., Ng, P-W., Nothen, M. M., Nurnberg, P., O'Brien, T. J., Oliver, K. L., Palotie, A., Pangilinan, F., Pernhorst, K., Petrovski, S., Privitera, M., Radtke, R., Reif, P. S., Rosenow, F., Ruppert, A-K., Sander, T., Scattergood, T., Schachter, S., Schankin, C., Scheffer, I. E., Schmitz, B., Schoch, S., Sham, P. C., Sisodiya, S., Smith, D. F., Smith, Philip E. M. ORCID: https://orcid.org/0000-0003-4250-2562, Speed, D., Sperling, M. R., Steffens, M., Stephanie, U., Striano, P., Stroink, H., Surges, R., Tan, K. M., The KORA Study Group, Thomas, G. N., Todaro, M., Tostevin, A., Tozzi, R., Trucks, H., Visscher, F., von Spiczak, S., Walley, N. M., Weber, Y. G., Wei, Z., Whelan, C., Yang, W., Zara, F. and Zimprich, F. 2014. Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. The Lancet Neurology 13 (9) , pp. 893-903. 10.1016/S1474-4422(14)70171-1

Nicodemus, Kristin K., Hargreaves, April, Morris, Derek, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, Michael, Corvin, Aiden and Donohoe, Gary 2014. Variability in working memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. JAMA Psychiatry 71 (7) , pp. 778-785. 10.1001/jamapsychiatry.2014.528

Hargreaves, A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, O'Dushlaine, C., Nicodemus, K. K., Gill, M., Corvin, A., Morris, D. and Donohoe, Gary 2014. The one and the many: effects of the cell adhesion molecule pathway on neuropsychological function in psychosis. Psychological Medicine 44 (10) , pp. 2177-2187. 10.1017/S0033291713002663

Nicodemus, Kristin K., Hargreaves, April, Morris, Derek, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, Michael, Corvin, Aiden and Donohoe, Gary 2014. Variability inworking memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway. JAMA Psychiatry 71 (7) , pp. 778-785. 10.1001/jamapsychiatry.2014.528

Waltes, Regina, Duketis, Eftichia, Knapp, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Huguet, Guillaume, Schlitt, Sabine, Jarczok, Tomasz A., Sachse, Michael, Kaempfer, Laura M., Kleinboeck, Tina, Poustka, Fritz, Boelte, Sven, Schmoetzer, Gabriele, Voran, Anette, Huy, Ellen, Meyer, Jobst, Bourgeron, Thomas, Klauck, Sabine M., Freitag, Christine M. and Chiocchetti, Andreas G. 2014. Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics 133 (6) , pp. 781-792. 10.1007/s00439-013-1416-y

Buxbaum, Joseph D., Bolshakova, Nadia, Brownfeld, Jessica M., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bender, Patrick, Bernier, Raphael, Cook, Edwin H., Coon, Hilary, Cuccaro, Michael, Freitag, Christine M., Hallmayer, Joachim, Geschwind, Daniel, Klauck, Sabine M., Nurnberger, John I., Oliveira, Guiomar, Pinto, Dalila, Poustka, Fritz, Scherer, Stephen W., Shih, Andy, Sutcliffe, James S., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica and Gallagher, Louise 2014. The autism simplex collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses. Molecular Autism 5 , p. 34. 10.1186/2040-2392-5-34

Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Wang, Zhuozhi, Vorstman, Jacob A. S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Barbara, Marshall, Christian R., Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Griswold, Anthony J., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., De Jonge, Maretha V., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceicao, Ines C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bolshakova, Nadia, Bacchelli, Elena, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gallinger, Steven, Cotterchio, Michelle, Casey, Graham, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, Wallace, Simon, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Soorya, Latha, Roge, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Gonzalez, Patricia Jimenez, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Fernandez, Bridget A., Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Cafe, Catia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Boelte, Sven, Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Anagnostou, Evdokia, Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina and Scherer, Stephen W. 2014. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. American Journal of Human Genetics 94 (5) , pp. 677-694. 10.1016/j.ajhg.2014.03.018

Hart, A. B., Gamazon, E. R., Engelhardt, B. E., Sklar, P., Kahler, A. K., Hultman, C. M., Sullivan, P. F., Neale, B. M., Faraone, S. V., de Wit, H., Cox, N. J., Palmer, A. A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Asherson, P., Banaschewski, T., Bayes, M., Biederman, J., Buitelaar, J. K., Casas, M., Cormand, B., Crosbie, J., Doyle, A. E., Elia, J., Faraone, S. V., Franke, B., Kent, L., Kuntsi, J., Lesch, K.-P., Loo, S. K., McGough, J. J., Medland, S. E., Neale, B., Nelson, S. F., Oades, R. D., Ramos-Quiroga, J. A., Reif, A., Ribases, M., Rothenberger, A., Schachar, R., Smalley, S. L., Sonuga-Barke, E., Steinhausen, H.-C., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931 2014. Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder. Proceedings of the National Academy of Sciences 111 (16) , pp. 5968-5973. 10.1073/pnas.1318810111

Lee, S., Ripke, S., Neale, B., Faraone, S., Purcell, S., Perlis, R., Mowry, B., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Goddard, M., Witte, J., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O., Anjorin, A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Anttila, V., Arking, D., Asherson, P., Azevedo, M., Backlund, L., Badner, J., Bailey, A., Banaschewski, T., Barchas, J., Barnes, M., Barrett, T., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E., Black, D., Blackwood, D., Bloss, C., Boehnke, M., Boomsma, D., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N., Buitelaar, J., Bunney, W., Buxbaum, J., Byerley, W., Byrne, E., Caesar, S., Cahn, W., Cantor, R., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C., Collier, D., Cook, E., Coon, H., Cormand, B., Corvin, A., Coryell, W., Craig, D., Craig, I., Crosbie, J., Cuccaro, M., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De Geus, E., Degenhardt, F., Djurovic, S., Donohoe, G., Doyle, A., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R., Edenberg, H., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A., Ferrier, I., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, Christine, Freedman, R., Freimer, N., Freitag, C., Friedl, M., Frisén, L., Gallagher, L., Gejman, P., Georgieva, Lyudmila, Gershon, E., Geschwind, D., Giegling, I., Gill, M., Gordon, S., Gordon-Smith, K., Green, E., Greenwood, T., Grice, D., Gross, M., Grozeva, Detelina ORCID: https://orcid.org/0000-0003-3239-8415, Guan, W., Gurling, H., De Haan, L., Haines, J., Hakonarson, H., Hallmayer, J., Hamilton, S., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Hansen, T., Hartmann, A., Hautzinger, M., Heath, A., Henders, A., Herms, S., Hickie, I., Hipolito, M., Hoefels, S., Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Holsboer, F., Hoogendijk, W., Hottenga, J., Hultman, C., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E., Jones, Ian Richard ORCID: https://orcid.org/0000-0001-5821-5889, Jones, L., Tzeng, J., Kähler, A., Kahn, R., Kandaswamy, R., Keller, M., Kennedy, J., Kenny, E., Kent, L., Kim, Y., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Klauck, S., Klei, L., Knowles, J., Kohli, M., Koller, D., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W., Leboyer, M., Ledbetter, D., Lee, P., Lencz, T., Lesch, K., Levinson, D., Lewis, C., Li, J., Lichtenstein, P., Lieberman, J., Lin, D., Linszen, D., Liu, C., Lohoff, F., Loo, S., Lord, C., Lowe, J., Lucae, S., MacIntyre, D., Madden, P., Maestrini, E., Magnusson, P., Mahon, P., Maier, W., Malhotra, A., Mane, S., Martin, C., Martin, N., Mattheisen, M., Matthews, K., Mattingsdal, M., McCarroll, S., McGhee, K., McGough, J., McGrath, P., McGuffin, P., McInnis, M., McIntosh, A., McKinney, R., McLean, A., McMahon, F., McMahon, W., McQuillin, A., Medeiros, H., Medland, S., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C., Middleton, L., Milanova, V., Miranda, A., Monaco, A., Montgomery, G., Moran, J., Moreno-De-Luca, D., Morken, G., Morris, D., Morrow, E., Moskvina, V., Muglia, P., Mühleisen, T., Muir, W., Müller-Myhsok, B., Murtha, M., Myers, R., Myin-Germeys, I., Neale, M., Nelson, S., Nievergelt, C., Nikolov, I., Nimgaonkar, V., Nolen, W., Nöthen, M., Nurnberger, J., Nwulia, E., Nyholt, D., O'Dushlaine, C., Oades, R., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R., Osby, U., Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Palotie, A., Parr, J., Paterson, A., Pato, C., Pato, M., Penninx, B., Pergadia, M., Pericak-Vance, M., Pickard, B., Pimm, J., Piven, J., Posthuma, D., Potash, J., Poustka, F., Propping, P., Puri, V., Quested, D., Quinn, E., Ramos-Quiroga, J., Rasmussen, H., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A., Sanders, S., Santangelo, S., Sergeant, J., Schachar, R., Schalling, M., Schatzberg, A., Scheftner, W., Schellenberg, G., Scherer, S., Schork, N., Schulze, T., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L., Shi, J., Shilling, P., Shyn, S., Silverman, J., Slager, S., Smalley, S., Smit, J., Smith, E., Sonuga-Barke, E., St. Clair, D., State, M., Steffens, M., Steinhausen, H., Strauss, J., Strohmaier, J., Stroup, T., Sutcliffe, J., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R., Todorov, A., Tozzi, F., Treutlein, J., Uhr, M., van den Oord, E., Van Grootheest, G., Van Os, J., Vicente, A., Vieland, V., Vincent, J., Visscher, P., Walsh, C., Wassink, T., Watson, S., Weissman, M., Werge, T., Wienker, T., Wijsman, E., Willemsen, G., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Willsey, A., Witt, S., Xu, W., Young, A., Yu, T., Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Zandi, P., Zhang, P., Zitman, F., Zöllner, S., Devlin, B., Kelsoe, J., Sklar, P., Daly, M., O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Sullivan, P., Smoller, J., Kendler, K., Wray, N. and Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483 2013. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 45 (9) , pp. 984-994. 10.1038/ng.2711

Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Stergiakouli, Evangelia, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Buitelaar, Jan, Faraone, Stephen V., Lesch, Klaus-Peter, Neale, Benjamin M., Franke, Barbara, Sonuga-Barke, Edmund, Asherson, Philip, Merwood, Andrew, Kuntsi, Jonna, Medland, Sarah E., Ripke, Stephan, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Roeyers, Herbert, Biederman, Joseph, Doyle, Alysa E., Hakonarson, Hakon, Rothenberger, Aribert, Banaschewski, Tobias, Oades, Robert D., McGough, James J., Kent, Lindsey, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2013. High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry 170 (8) , pp. 909-916. 10.1176/appi.ajp.2013.12081129

Merikangas, Alison, Heron, Elizabeth, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Corvin, Aiden and Gallagher, Louise 2013. Risk factors and clinical correlates of CNVs associated with autism spectrum disorders: evidence for joint contribution of genetic and environmental risk factors [Conference Abstract]. European Child & Adolescent Psychiatry 22 (Suppl2) , S188-S188. 10.1007/s00787-013-0423-9

Smoller, Jordan W., Kendler, Kenneth, Craddock, Nicholas John ORCID: https://orcid.org/0000-0003-2171-0610, Lee, Phil Hyoun, Neale, Benjamin M., Nurnberger, John I., Ripke, Stephan, Santangelo, Susan, Sullivan, Patrick F., Purcell, Shaun, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Buitelaar, Jan, Fanous, Ayman, Faraone,, Stephen V., Hoogendijk, Witte, Lesch, Klaus-Peter, Levinson, Douglas F., Perlis, Roy H., Rietschel, Marcella, Riley, Brien, Sonuga-Barke, Edmund, Schachar, Russell, Schulze, Thomas G., Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Neale, Michael, Bender, Patrick, Cichon, Sven, Daly, Mark J., Kelsoe, John, Lehner, Thomas, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Gejman, Pablo, Sebat, Jonathan and Sklar, Pamela 2013. Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. The Lancet 381 (9875) , pp. 1371-1379. 10.1016/S0140-6736(12)62129-1

Quinn, Emma M., Cormican, Paul, Kenny, Elaine M., Hill, Matthew, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, Michael, Corvin, Aiden P. and Morris, Derek W. 2013. Development of strategies for SNP detection in RNA-seq data: application to lymphoblastoid cell lines and evaluation using 1000 genomes data. PLoS ONE 8 (3) , e58815. 10.1371/journal.pone.0058815
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Mulligan, A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Butler, L., O'Regan, M., Richardson, T., Tulewicz, E. M., Fitzgerald, M. and Gill, M. 2013. Home environment: association with hyperactivity/impulsivity in children with ADHD and their non-ADHD siblings. Child Care Health and Development 39 (2) , pp. 202-212. 10.1111/j.1365-2214.2011.01345.x

Vorstman, Jacob A. S., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Derks, Eske M., Gallagher, Louise, Gill, Michael, de Jonge, Maretha V., van Engeland, Herman, Kahn, Rene S. and Ophoff, Roel A. 2013. No evidence that common genetic risk variation is shared between schizophrenia and autism. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162B (1) , pp. 55-60. 10.1002/ajmg.b.32121

Holt, Richard, Sykes, Nuala H., Conceicao, Ines C., Cazier, Jean-Baptiste, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Oliveira, Guiomar, Gallagher, Louise, Vicente, Astrid, Monaco, Anthony P. and Pagnamenta, Alistair T. 2012. CNVs leading to fusion transcripts in individuals with autism spectrum disorder. European Journal of Human Genetics 20 (11) , pp. 1141-1147. 10.1038/ejhg.2012.73

Quinn, E. M., Hill, M., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, M., Corvin, A. P. and Morris, D. W. 2012. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression [Erratum]. Bipolar Disorders 14 (7) , p. 792. 10.1111/bdi.12020

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Klei, Lambertus, Pinto, Dalila, Almeida, Joana, Bacchelli, Elena, Baird, Gillian, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Casey, Jillian, Conroy, Judith, Correia, Catarina, Corsello, Christina, Crawford, Emily L., de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Green, Andrew, Green, Jonathan, Guter, Stephen J., Heron, Elizabeth A., Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Jacob, Suma, Kenny, Graham P., Kim, Cecilia, Kolevzon, Alexander, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Law-Smith, Miriam, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Liu, Xiao-Qing, Lombard, Frances, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Magalhaes, Tiago R., Mantoulan, Carine, McDougle, Christopher J., Melhem, Nadine M., Merikangas, Alison, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Noakes, Carolyn, Nygren, Gudrun, Papanikolaou, Katerina, Pagnamenta, Alistair T., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Posey, David J., Poustka, Fritz, Ragoussis, Jiannis, Regan, Regina, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Schlitt, Sabine, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stoppioni, Vera, Sykes, Nuala, Tancredi, Raffaella, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Vorstman, J. A. S., Wallace, Simon, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Bailey, Anthony J., Battaglia, Agatino, Cantor, Rita M., Coon, Hilary, Cuccaro, Michael L., Dawson, Geraldine, Ennis, Sean, Freitag, Christine M., Geschwind, Daniel H., Haines, Jonathan L., Klauck, Sabine M., McMahon, William M., Maestrini, Elena, Miller, Judith, Monaco, Anthony P., Nelson, Stanley F., Nurnberger, John I., Oliveira, Guiomar, Parr, Jeremy R., Pericak-Vance, Margaret A., Piven, Joseph, Schellenberg, Gerard D., Scherer, StephenW., Vicente, Astrid M., Wassink, Thomas H., Wijsman, Ellen M., Betancur, Catalina, Buxbaum, Joseph D., Cook, Edwin H., Gallagher, Louise, Gill, Michael, Hallmayer, Joachim, Paterson, Andrew D., Sutcliffe, James S., Szatmari, Peter, Vieland, Veronica J., Hakonarson, Hakon and Devlin, Bernie 2012. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics 21 (21) , pp. 4781-4792. 10.1093/hmg/dds301

Casey, Jillian P., Magalhaes, Tiago, Conroy, Judith M., Regan, Regina, Shah, Naisha, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Shields, Denis C., Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Cali, Phil, Correia, Catarina, Corsello, Christina, Coutanche, Marc, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Foley, Suzanne, Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Holt, Richard, Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Lamb, Janine A., Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Lund, Sabata C., Maestrini, Elena, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Miller, Judith, Minopoli, Fiorella, Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Nygren, Gudrun, Oliveira, Guiomar, Pagnamenta, Alistair T., Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Pickles, Andrew, Pinto, Dalila, Piven, Joseph, Posey, David J., Poustka, Annemarie, Poustka, Fritz, Ragoussis, Jiannis, Roge, Bernadette, Rutter, Michael L., Sequeira, Ana F., Soorya, Latha, Sousa, Ines, Sykes, Nuala, Stoppioni, Vera, Tancredi, Raffaella, Tauber, Maite, Thompson, Ann P., Thomson, Susanne, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Vorstman, Jacob A. S., Wallace, Simon, Wang, Kai, Wassink, Thomas H., White, Kathy, Wing, Kirsty, Wittemeyer, Kerstin, Yaspan, Brian L., Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Geschwind, Daniel H., Haines, Jonathan L., Hallmayer, Joachim, Monaco, Anthony P., Nurnberger, John I., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter, Vieland, Veronica J., Wijsman, Ellen M., Green, Andrew, Gill, Michael, Gallagher, Louise, Vicente, Astrid and Ennis, Sean 2012. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human Genetics 131 (4) , pp. 565-579. 10.1007/s00439-011-1094-6

Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Franke, Barbara, Mick, Eric, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Freitag, Christine M., Gill, Michael, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter and Faraone, Stephen V. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169 (2) , pp. 195-204. 10.1176/appi.ajp.2011.11060822
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Elia, Josephine, Glessner, Joseph T., Wang, Kai, Takahashi, Nagahide, Shtir, Corina J., Hadley, Dexter, Sleiman, Patrick M. A., Zhang, Haitao, Kim, Cecilia E., Robison, Reid, Lyon, Gholson J., Flory, James H., Bradfield, Jonathan P., Imielinski, Marcin, Hou, Cuiping, Frackelton, Edward C., Chiavacci, Rosetta M., Sakurai, Takeshi, Rabin, Cara, Middleton, Frank A., Thomas, Kelly A., Garris, Maria, Mentch, Frank, Freitag, Christine M., Steinhausen, Hans-Christoph, Todorov, Alexandre A., Reif, Andreas, Rothenberger, Aribert, Franke, Barbara, Mick, Eric O., Roeyers, Herbert, Buitelaar, Jan, Lesch, Klaus-Peter, Banaschewski, Tobias, Ebstein, Richard P., Mulas, Fernando, Oades, Robert D., Sergeant, Joseph, Sonuga-Barke, Edmund, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Meyer, Jobst, Pálmason, Haukur, Seitz, Christiane, Loo, Sandra K., Smalley, Susan L., Biederman, Joseph, Kent, Lindsey, Asherson, Philip, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gaynor, J. William, Shaw, Philip, Devoto, Marcella, White, Peter S., Grant, Struan F. A., Buxbaum, Joseph D., Rapoport, Judith L., Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Nelson, Stanley F., Faraone, Stephen V. and Hakonarson, Hakon 2012. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder. Nature Genetics 44 (1) , pp. 78-84. 10.1038/ng.1013

Hill, Matthew James, Kenny, Elaine, Roche, Siobhan, Morris, Derek W., Corvin, Aiden, Hawi, Ziarih, Gill, Michael and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2011. Allelic expression imbalance of the schizophrenia susceptibility gene CHI3L1: evidence of cis-acting variation and tissue specific regulation. Psychiatric Genetics 21 (6) , pp. 281-286. 10.1097/YPG.0b013e328348045b

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Kenny, Elaine M., O'Dushlaine, Colm, Yaspan, Brian L., Parkhomenka, Elena, Buxbaum, Joseph D., Sutcliffe, James, Gill, Michael and Gallagher, Louise 2011. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. European Journal of Human Genetics 19 (10) , pp. 1082-1089. 10.1038/ejhg.2011.75

Sonuga-Barke, Edmund J. S., Kumsta, Robert, Schlotz, Wolff, Lasky-Su, Jessica, Marco, Rafaela, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Banaschewski, Tobias, Mueller, Ueli, Andreou, Penny, Christiansen, Hanna, Gabriels, Isabel, Uebel, Henrik, Kuntsi, Jonna, Franke, Barbara, Buitelaar, Jan, Ebstein, Richard, Gill, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Asherson, Philip and Faraone, Stephen V. 2011. A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings. Biological psychiatry 70 (3) , pp. 230-236. 10.1016/j.biopsych.2011.01.040

Tansey, Katherine E., Hill, Matthew J., Cochrane, Lynne E., Gill, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X and Gallagher, Louise 2011. Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism. Molecular Autism 2 (1) , p. 3. 10.1186/2040-2392-2-3

Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, Van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J., Evans, David M., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans Christoph, Taylor, Eric, Faraone, Stephen V., Franke, Barbara and Posthuma, Danielle 2011. The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156B (2) , pp. 145-157. 10.1002/ajmg.b.31149

Cochrane, Lynne E., Tansey, Katherine E., Gill, Michael, Gallagher, Louise and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2010. Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample. Autism Research 3 (6) , pp. 342-344. 10.1002/aur.157

Merikangas, Alison K., Heron, Elizabeth A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Corvin, Aiden P. and Gallagher, Louise 2010. Investigating the association between rare copy number variation and developmental anomalies in autism spectrum disorders [Conference Abstract]. Genetic Epidemiology 34 (8) , p. 929. 10.1002/gepi.20553

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Klei, Lambertus, Pinto, Dalila, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Correia, Catarina, Abrahams, Brett S., Sykes, Nuala, Pagnamenta, Alistair T., Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Carson, Andrew R., Casallo, Guillermo, Casey, Jillian, Chu, Su H., Cochrane, Lynne, Corsello, Christina, Crawford, Emily L., Crossett, Andrew, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Goldberg, Jeremy, Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Heron, Elizabeth A., Hill, Matthew, Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lionel, Anath C., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Melhem, Nadine M., Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Piven, Joseph, osey, David J., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Ragoussis, Jiannis, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stoppioni, Vera, Strawbridge, Christina, Tancredi, Raffaella, Tansey, Katherine E., Thiruvahindrapduram, Bhooma, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Yaspan, Brian L., Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Miller, Judith, Monaco, Anthony P., Nurnberger, John I., Paterson, Andrew D., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Wijsman, Ellen M., Devlin, Bernie, Ennis, Sean and Hallmayer, Joachim 2010. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics 19 (20) , pp. 4072-4082. 10.1093/hmg/ddq307

Hill, M., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, M. and Hawi, Z. 2010. Functional analysis of intron 8 and 3 ' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants. Pharmacogenomics Journal 10 (5) , pp. 442-447. 10.1038/tpj.2009.66

Sobanski, Esther, Banaschewski, Tobias, Asherson, Philip, Buitelaar, Jan, Chen, Wai, Franke, Barbara, Holtmann, Martin, Krumm, Bertram, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Stringaris, Argyris, Taylor, Eric, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Ebstein, Richard P., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Steinhausen, Hans-Christoph and Faraone, Stephen V. 2010. Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence. Journal of Child Psychology and Psychiatry 51 (8) , pp. 915-923. 10.1111/j.1469-7610.2010.02217.x

Pinto, Dalila, Pagnamenta, Alistair T., Klei, Lambertus, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Merico, Daniele, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Correia, Catarina, Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bader, Gary D., Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Bryson, Susan E., Carson, Andrew R., Casallo, Guillermo, Casey, Jillian, Chung, Brian H. Y., Cochrane, Lynne, Corsello, Christina, Crawford, Emily L., Crossett, Andrew, Cytrynbaum, Cheryl, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Goldberg, Jeremy, Green, Andrew, Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Heron, Elizabeth A., Hill, Matthew, Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lionel, Anath C., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Pilorge, Marion, Piven, Joseph, Ponting, Chris P., Posey, David J., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Ragoussis, Jiannis, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Sequeira, Ana F., Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stein, Olaf, Sykes, Nuala, Stoppioni, Vera, Strawbridge, Christina, Tancredi, Raffaella, Tansey, Katherine E., Thiruvahindrapduram, Bhooma, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Weksberg, Rosanna, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Wu, Jing, Yaspan, Brian L., Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Devlin, Bernie, Ennis, Sean, Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Hallmayer, Joachim, Miller, Judith, Monaco, Anthony P., Nurnberger, John I., Paterson, Andrew D., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Wijsman, Ellen M., Scherer, Stephen W., Sutcliffe, James S. and Betancur, Catalina 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466 (7304) , pp. 368-372. 10.1038/nature09146

Nijmeijer, Judith S., Arias-Vasquez, Alejandro, Rommelse, Nanda N. J., Altink, Marieke E., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Asherson, Philip, Banaschewski, Tobias, Buschgens, Cathelijne J. M., Fliers, Ellen A., Gill, Michael, Minderaa, Ruud B., Poustka, Luise, Sergeant, Joseph A., Buitelaar, Jan K., Franke, Barbara, Ebstein, Richard P., Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sonuga-Barke, Edmund J. S., Steinhausen, Hans-Christoph, Faraone, Stephen. V., Hartman, Catharina A. and Hoekstra, Pieter J. 2010. Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach. Journal of the American Academy of Child & Adolescent Psychiatry 49 (7) , pp. 675-685. 10.1016/j.jaac.2010.03.015

Quinn, Emma M., Hill, Matthew, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Gill, Michael, Corvin, Aiden P. and Morris, Derek W. 2010. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression. Bipolar Disorders 12 (4) , pp. 440-445. 10.1111/j.1399-5618.2010.00817.x

Tansey, Katherine E., Brookes, Keeley J., Hill, Matthew J., Cochrane, Lynne E., Gill, Michael, Skuse, David, Correia, Catarina, Vicente, Astrid, Kent, Lindsey, Gallagher, Louise and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2010. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studies. Neuroscience Letters 474 (3) , pp. 163-167. 10.1016/j.neulet.2010.03.035

Lasky-Su, Jessica, Won, Sungho, Mick, Eric, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Franke, Barbara, Neale, Benjamin, Biederman, Joseph, Smalley, Susan L., Loo, Sandra K., Todorov, Alexandre, Faraone, Stephen V., Weiss, Scott T. and Lange, Christoph 2010. On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls. American Journal of Human Genetics 86 (4) , pp. 573-580. 10.1016/j.ajhg.2010.02.019

Olsson, C. A., Foley, D. L., Parkinson-Bates, M., Byrnes, G., McKenzie, M., Patton, G. C., Morley, R., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Craig, J. M. and Saffery, R. 2010. Prospects for epigenetic research within cohort studies of psychological disorder: A pilot investigation of a peripheral cell marker of epigenetic risk for depression. Biological Psychology 83 (2) , pp. 159-165. 10.1016/j.biopsycho.2009.12.003

Hawi, Z., Kent, L., Hill, M., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Brookes, K. J., Barry, E., Franke, B., Banaschewski, T., Buitelaar, J., Ebstein, R., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Faraone, S. V., Asherson, P. and Gill, M. 2010. ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (1) , pp. 97-102. 10.1002/ajmg.b.30960

Neale, Benjamin M., Medland, Sarah, Ripke, Stephan, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Asherson, Philip, Buitelaar, Jan, Franke, Barbara, Gill, Michael, Kent, Lindsey, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Middleton, Frank, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Lesch, Klaus-Peter, Daly, Mark, Nguyen, Thuy Trang, Schäfer, Helmut, Steinhausen, Hans-Christoph, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Freitag, Christine, Meyer, Jobst, Palmason, Haukur, Rothenberger, Aribert, Hawi, Ziarih, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric and Biederman, Joseph 2010. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 906-920. 10.1016/j.jaac.2010.06.007

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Sonuga-Barke, Edmund J. S., Oades, Robert D., Psychogiou, Lamprini, Chen, Wai, Franke, Barbara, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard P., Gil, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Miranda, Ana, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Asherson, Philip and Faraone, Stephen V. 2009. Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry 50 (9) , pp. 1052-1063. 10.1111/j.1469-7610.2009.02095.x

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X and Lasky-Su, J. 2009. S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations [Conference abstract]. European Neuropsychopharmacology 19 , S203-S203. 10.1016/S0924-977X(09)70264-0

Conroy, Judith, Cochrane, Lynne, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Sutcliffe, James S., Carthy, Paula, Dunlop, Adam, Mullarkey, Marice, O'hlci, Bronagh, Green, Andrew J., Ennis, Sean, Gill, Michael and Gallagher, Louise 2009. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (4) , pp. 535-544. 10.1002/ajmg.b.30854

Mulligan, Aisling, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, O'Regan, Myra, Chen, Wai, Butler, Louise, Fitzgerald, Michael, Buitelaar, Jan, Steinhausen, Hans-Christoph, Rothenberger, Aribert, Minderaa, Ruud, Nijmeijer, Judith, Hoekstra, Pieter J., Oades, Robert D., Roeyers, Herbert, Buschgens, Cathelijne, Christiansen, Hanna, Franke, Barbara, Gabriels, Isabel, Hartman, Catharina, Kuntsi, Jonna, Marco, Rafaela, Meidad, Sheera, Mueller, Ueli, Psychogiou, Lamprini, Rommelse, Nanda, Thompson, Margaret, Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Eisenberg, Jacques, Manor, Iris, Miranda, Ana, Mulas, Fernando, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Asherson, Phil, Faraone, Stephen V. and Gill, Michael 2009. Autism symptoms in attention-deficit/hyperactivity disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders. Journal of Autism and Developmental Disorders 39 (2) , pp. 197-209. 10.1007/s10803-008-0621-3

Lasky-Su, Jessica, Neale, Benjamin M., Franke, Barbara, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Chen, Wai, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans Christoph, Taylor, Eric, Daly, Mark, Laird, Nan, Lange, Christoph and Faraone, Stephen V. 2008. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1345-1354. 10.1002/ajmg.b.30867

Brookes, K. J., Xu, X., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Franke, B., Zhou, K., Chen, Wai, Banaschewski, T., Buitelaar, J., Ebstein, R., Eisenberg, J., Gill, M., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2008. Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1519-1523. 10.1002/ajmg.b.30782

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Lasky-Su, Jessica, O'Dushlaine, Colm, Kenny, Elaine, Neale, Benjamin M., Mulligan, Aisling, Franke, Barbara, Zhou, Kaixin, Chen, Wai, Christiansen, Hanna, Arias-Vasquez, Alejandro, Banaschewski, Tobias, Buitelaar, Jan, Ebstein, Richard, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans, Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1369-1378. 10.1002/ajmg.b.30871

Neale, Benjamin M., Lasky-Su, Jessica, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Franke, Barbara, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Asherson, Philip, Chen, Wai, Banasehewski, Tobias, Buitelaar, Jan, Ebstein, Richard, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Sonuga-Barke, Edmund J. S., Mulas, Fernando, Taylor, Eric, Laird, Nan, Lange, Christoph, Daly, Mark and Faraone, Stephen V. 2008. Genome-wide association scan of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1337-1344. 10.1002/ajmg.b.30866

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Hawi, Ziarih, Sheehan, Karen, Mulligan, Aisling, Pinto, Carlos, Brookes, Keeley J., Xu, Xiaohui, Zhou, Kaixin, Franke, Barbara, Buitelaar, Jan, Vermeulen, Sita H., Banaschewski, Tobias, Sonuga-Barke, Edmund J. S., Ebstein, Richard, Manor, Iris, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rommelse, Nanda, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans-Christoph, Taylor, Eric, Thompson, Margaret, Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Parent of Origin Effects in Attention/Deficit Hyperactivity Disorder (ADHD): Analysis of Data From the International Multicenter ADHD Genetics (IMAGE) Program. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1495-1500. 10.1002/ajmg.b.30659

Xu, X., Hawi, Z., Brookes, K. J., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bellgrove, M., Franke, B., Barry, E., Chen, W., Kuntsi, J., Banaschewski, T., Buitelaar, J., Ebstein, R., Fitzgerald, M., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Faraone, S. V., Gill, M. and Asherson, P. 2008. Replication of a Rare Protective Allele in the Noradrenaline Transporter Gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1564-1567. 10.1002/ajmg.b.30872

Sonuga-Barke, Edmund J. S., Lasky-Su, Jessica, Neale, Benjamin M., Oades, Robert, Chen, Wai, Franke, Barbara, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Miranda, Ana, Mulas, Fernando, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Asherson, Philip and Faraone, Stephen V. 2008. Does Parental Expressed Emotion Moderate Genetic Effects in ADHD? An Exploration Using a Genome Wide Association Scan. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1359-1368. 10.1002/ajmg.b.30860

Lasky-Su, Jessica, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Neale, Benjamin M., Franke, Barbara, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Chen, Wai, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans Christoph, Taylor, Eric, Daly, Mark, Laird, Nan, Lange, Christoph and Faraone, Stephen V. 2008. Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1355-1358. 10.1002/ajmg.b.30869

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Kenny, Elaine, O'Dushlaine, Colm T., Lasky-Su, Jessica, Franke, Barbara, Morris, Derek W., Neale, Benjamin M., Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1379-1386. 10.1002/ajmg.b.30836

Oades, Robert D., Lasky-Su, Jessica, Christiansen, Hanna, Faraone, Stephen V., Sonuga-Barke, Edmund J. S., Banaschewski, Tobias, Chen, Wai, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Buitelaar, Jan K., Ebstein, Richard P., Franke, Barbara, Gill, Michael, Miranda, Ana, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph A., Steinhausen, Hans-Christoph, Taylor, Eric A., Thompson, Margaret and Asherson, Philip 2008. The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis. Behavioral and Brain Functions : BBF 4 , p. 48. 10.1186/1744-9081-4-48

Xu, X., Aysimi, E., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Brookes, K., Franke, B., Zhou, K., Buschgens, C., Chen, W., Christiansen, H., Eisenberg, J., Gabriels, I., Manor, I., Marco, R., Muller, U. C., Mulligan, A., Rommelse, N., Thompson, M., Uebel, H., Banaschewski, T., Buitelaar, J., Ebstein, R., Gill, M., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2008. No association between two polymorphisms of the Serotonin Transporter Gene and combined type Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics. Part B 147B (7) , pp. 1306-1309. 10.1002/ajmg.b.30737

Zhou, Kaixin, Asherson, Philip, Sham, Pak, Franke, Barbara, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Buitelaar, Jan, Ebstein, Richard, Gill, Michael, Brookes, Keeley, Buschgens, Cathelijne, Campbell, Desmond, Chen, Wai, Christiansen, Hanna, Fliers, Ellen, Gabris, Isabel, Johansson, Lena, Marco, Rafaela, Mulas, Fernando, Mueller, Ueli, Mulligan, Aisling, Neale, Benjamin M., Rijsdijk, Fruhling, Rommelse, Nanda, Uebel, Henrik, Psychogiou, Lamprini, Xu, Xiaohui, Banaschewski, Tobias, Sonuga-Barke, Edmund J. S., Eisenberg, Jacques, Manor, Iris, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans-Christoph, Taylor, Eric, Thompson, Margaret and Faraone, Stephen V. 2008. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological psychiatry 64 (7) , pp. 571-576. 10.1016/j.biopsych.2008.02.024

Altink, Marieke E., Arias-Vasquez, Alejandro, Franke, Barbara, Slaats-Willemse, Dorine I. E., Buschgens, Cathelijne J. M., Rommelse, Nanda N. J., Fliers, Ellen A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Brookes, Keeley-Joanne, Chen, Wai, Gill, Michael, Mulligan, Aisling, Sonuga-Barke, Edmund J. S., Thompson, Margaret, Sergeant, Joseph A., Faraone, Stephen V., Asherson, Philip and Buitelaar, Jan K. 2008. The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction. Journal of Child Psychology and Psychiatry 49 (10) , pp. 1053-1060. 10.1111/j.1469-7610.2008.01998.x

Sonuga-Barke, Edmund J. S., Brookes, Keeley-Joanne, Buitelaar, Jan, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bitsakou, Paraskevi, Baeyens, Dieter, Buschgens, Cathelijne, Chen, Wai, Christiansen, Hanna, Eisenberg, Jacques, Kuntsi, Jonna, Manor, Iris, Melia, Amanda, Mulligan, Aisling, Rommelse, Nanda, Mueller, Ueli C., Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Franke, Barbara, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Taylor, Eric, Asherson, Philip and Faraone, Stephen V. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder [Erratum]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (5) , p. 670. 10.1002/ajmg.b.30820

Asherson, P., Zhou, K., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Franke, B., Buitelaar, J., Ebstein, R., Gill, M., Altink, M., Arnold, R., Boer, F., Brookes, K., Buschgens, C., Butler, L., Cambell, D., Chen, W., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabrieels, I., Johansson, L., Lubetzki, I., Marco, R., Medad, S., Minderaa, R., Mulas, F., Mueller, U., Mulligan, A., Neale, B., Rijsdijk, F., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Xu, X., Banaschewski, T., Sonuga-Barke, E. J. S., Eisenberg, J., Manor, I., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C, Taylor, E., Thompson, M. and Faraone, S. V. 2008. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry 13 (5) , pp. 514-521. 10.1038/sj.mp.4002140

Sonuga-Barke, Edmund J. S., Brookes, Keeley-Joanne, Buitelaar, Jan, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Bitsakou, Paraskevi, Baeyens, Dieter, Buschgens, Cathelijne, Chen, Wai, Christiansen, Hanna, Eisenberg, Jacques, Kuntsi, Jonna, Manor, Iris, Melia, Amanda, Mulligan, Aisling, Rommelse, Nanda, Mueller, Ueli C., Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Franke, Barbara, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Taylor, Eric, Asherson, Philip and Faraone, Stephen V. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder. American Journal of Medical Genetics. Part B 147B (3) , pp. 316-319. 10.1002/ajmg.b.30596

Olsson, C. A., Byrnes, G. B., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Collins, V., Hemphill, S. A., Williamson, R. and Patton, G. C. 2007. COMT Val(158)Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study. Genes Brain and Behavior 6 (7) , pp. 647-652. 10.1111/j.1601-183X.2007.00313.x

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Lotfi-Miri, Mehrnoush, Olsson, Craig A., Reid, Sophie C., Hemphill, Sheryl A. and Patton, George C. 2007. Variation in the gene coding for the M5 Muscarinic receptor (CHRM5) influences cigarette dose but is not associated with dependence to drugs of addiction: evidence from a prospective population based cohort study of young adults. BMC Genetics 8 , p. 46. 10.1186/1471-2156-8-46

Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Franke, B., Gill, M., Ebstein, R., Buitelaar, J., Sham, P., Campbell, D., Knight, J., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C., Butler, L., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriels, I., Korn-Lubetzki, I., Johansson, L., Marco, R., Medad, S., Minderaa, R., Mulas, F., Mueller, U., Mulligan, A., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Craig, I., Banaschewski, T., Sonuga-Barke, E. J. S., Eisenberg, J., Kuntsi, J., Manor, I., McGuffin, P., Miranda, A., D Oades, R., Plomin, R., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C, Taylor, E., Thompson, M., Faraone, S. V. and Asherson, P. 2006. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry 11 (12) , pp. 934-953. 10.1038/sj.mp.4001869

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Hawi, Ziarah, Sheehan, Karen, Brookes, Keeley, Zhou, Kaixin, Banaschewski, Tobias, Buitelaar, Jan, Ebstein, Richard. P., Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S. and Steinhausen, Hans-Christoph 2006. Epigenetic effects in ADHD: Parent-of-origin effects in image sample [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 736-737. 10.1002/ajmg.b.30408

Mulligan, A., Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Chen, W., Butler, L., Fitzgerald, M. and Gill, M. 2006. Autistic symptoms in ADHD- A report from the International Multi-Center ADHD Gene Project (IMAGE) [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , p. 687. 10.1002/ajmg.b.30408

Olsson, CA, Byrnes, GB, Lotfi-Miri, M, Collins, V, Williamson, R, Patton, C and Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X 2005. Association between 5-HTTLPR genotypes and persisting patterns of anxiety and alcohol use: results from a 10-year longitudinal study of adolescent mental health. Molecular Psychiatry 10 (9) , pp. 868-876. 10.1038/sj.mp.4001677

Olsson, CA, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Lotfi-Miri, M, Byrnes, GB, Williamson, R and Patton, GC 2005. Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health. Psychiatric Genetics 15 (2) , pp. 109-115.

Staddon, Susan, Arranz, Maria J., Mancama, Dalu, Perez-Nievas, Fernando, Arrizabalaga, Iñaki, Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Buckland, Paul Robert, Elkin, Amanda, Osborne, Sarah, Munro, Janet, Mata, Ignacio and Kerwin, Robert W. 2005. Association between dopamine D3 receptor gene polymorphisms and schizophrenia in an isolate population. Schizophrenia Research 73 (1) , pp. 49-54. 10.1016/j.schres.2004.06.011

Anney, Richard ORCID: https://orcid.org/0000-0002-6083-407X, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville ORCID: https://orcid.org/0000-0003-1177-6931, Norton, Nadine ORCID: https://orcid.org/0000-0002-3848-4288, Williams, Hywel John ORCID: https://orcid.org/0000-0001-7758-0312, Cardno, Alastair George, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Jones, S., Jones, G., Hoogendoorn, Bastiaan ORCID: https://orcid.org/0000-0001-9753-169X, Smith, K. J., Hamshere, Marian Lindsay ORCID: https://orcid.org/0000-0002-8990-0958, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862 and Buckland, Paul Robert 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7 (5) , pp. 493-502. 10.1038/sj.mp.4001003

This list was generated on Sun Jul 21 13:05:26 2024 BST.