Browse by Schools (by year)

, Vernooij, Meike W., Ikram, M. Arfan, Amin, Najaf and van Duijn, Cornelia M. 2018. Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study. Alzheimer's and Dementia 14 (7) , pp. 848-857. 10.1016/j.jalz.2018.01.005

Al-Ansari, A. and Robertson, N. P.

2018. Anti-epileptics and pregnancy: an update. Journal of Neurology 265 (11) , pp. 2749-2751. 10.1007/s00415-018-9058-6

Allardyce, Judith

, Leonenko, Ganna

, Hamshere, Marian

, Pardiñas, Antonio F., Forty, Liz, Knott, Sarah, Gordon-Smith, Katherine, Porteous, David J., Haywood, Caroline, Di Florio, Arianna

, Jones, Lisa

, McIntosh, Andrew M., Owen, Michael J.

, Walters, James T. R.

, Craddock, Nicholas

and Escott-Price, Valentina

2018. Association between schizophrenia-related polygenic liability and the occurrence and level of mood-incongruent psychotic symptoms in bipolar disorder. JAMA Psychiatry 75 (1) , pp. 28-35. 10.1001/jamapsychiatry.2017.3485

Alonso-Llamazares, Carmen, Gomez, Carlos, Garcia-Manrique, Pablo, Pardinas, Antonio F.

and Lopez, Belen 2018. Medical diagnostic methods applied to a medieval female with vitamin D deficiency from the North of Spain. International Journal of Paleopathology 22 , pp. 109-120. 10.1016/j.ijpp.2018.07.007

Alsaeed, Meshari, Harding, Katharine, Williams, O. H., Willis, Mark

, Hrastelj, James

, Tallantyre, Emma

, Joseph, Fady, Wardle, Mark, Pickersgill, T. P. and Robertson, Neil

2018. Multiple sclerosis: long-term outcomes in ethnic minorities. analysis of a UK population-based registry. European Journal of Neurology 25 (4) , pp. 701-704. 10.1111/ene.13571

Anttila, Verneri, Bulik-Sullivan, Brendan, Finucane, Hilary K., Walters, Raymond K., Bras, Jose, Duncan, Laramie, Escott-Price, Valentina

, 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

, Russo, Giancarlo, Rubinsztein, David C., Bayer, Antony

, Tsolaki, Magda, Proitsi, Petra, Fox, Nick C., Hampel, Harald, Owen, Michael J.

, Mead, Simon, Passmore, Peter, Morgan, Kevin, Nöthen, Markus M., Rossor, Martin, Lupton, Michelle K., Hoffmann, Per, Kornhuber, Johannes, Lawlor, Brian, McQuillin, Andrew,

, ,

, , ,

and

2018. Analysis of shared heritability in common disorders of the brain. Science 360 (6395) , eaap8757. 10.1126/science.aap8757

Arnau-Soler, Aleix, Adams, Mark J., Hayward, Caroline, Thomson, Pippa A., Craddock, Nick

, Owen, M J

, Tansey, Katherine and O'Donovan, Michael

2018. Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. PLoS ONE 13 (12) , e0209160. 10.1371/journal.pone.0209160

Auvin, Stéphane, Wirrell, Elaine, Donald, Kirsten A., Berl, Madison, Hartmann, Hans, Valente, Kette D., Van Bogaert, Patrick, Cross, J. Helen, Osawa, Makiko, Kanemura, Hideaki, Aihara, Masao, Guerreiro, Marilisa M., Samia, Pauline, Vinayan, Kollencheri Puthenveettil, Smith, Mary Lou, Carmant, Lionel, Kerr, Michael, Hermann, Bruce, Dunn, David and Wilmshurst, Jo M. 2018. Systematic review of the screening, diagnosis, and management of ADHD in children with epilepsy. Consensus paper of the Task Force on Comorbidities of the ILAE Pediatric Commission. Epilepsia 59 (10) , pp. 1867-1880. 10.1111/epi.14549

B

Baker, Emily, Schmidt, Karl Michael

, Sims, Rebecca

, Williams, Julie

and Escott-Price, Valentina

2018. POLARIS: polygenic LD-adjusted risk score approach for set-based analysis of GWAS data. Genetic Epidemiology 42 (4) , pp. 366-377. 10.1002/gepi.22117

Bakhsh, Ameen D., Ladas, Ioannis, Hamshere, Marian L.

, Bullock, Martyn, Kirov, George

, Zhang, Lei

, Taylor, Peter N.

, Gregory, John W.

, Scott-Coombes, David, Völzke, Henry, Teumer, Alexander, Mantripragada, Kiran

, Williams, E. Dillwyn

, Clifton-Bligh, Roderick J., Williams, Nigel M.

and Ludgate, Marian E. 2018. An InDel in Phospholipase-C-B-1 is linked with euthyroid multinodular goiter. Thyroid 28 (7) , pp. 891-901. 10.1089/thy.2017.0312

Beesley, Rebecca, Anderson, Valerie, Harding, Katharine E, Joseph, Fady, Tomassini, Valentina

, Pickersgill, Trevor P, Robertson, Neil P

and Tallantyre, Emma C

2018. Impact of the 2017 revisions to McDonald criteria on the diagnosis of Multiple Sclerosis. Multiple Sclerosis 24 (13) , pp. 1786-1787. 10.1177/1352458518778007

Beltrami, Cristina, Simpson, Kate, Jesky, Mark, Wonnacott, Alexa

, Carrington, Christopher, Holmans, Peter

, Newbury, Lucy, Jenkins, Robert

, Ashdown, Thomas, Dayan, Colin

, Satchell, Simon, Corish, Peter, Cockwell, Paul, Fraser, Donald

and Bowen, Timothy

2018. Association of elevated urinary miR-126, miR-155, and miR-29b with diabetic kidney disease. American Journal of Pathology 188 (9) , pp. 1982-1992. 10.1016/j.ajpath.2018.06.006

Ben-Ezra, Menachem, Karatzias, Thanos, Hyland, Philip, Brewine, Chris R., Cloitre, Marylene, Bisson, Jonathan

, Roberts, Neil P., Lueger-Schuster, Brigitte and Shevlin, Mark 2018. Posttraumatic Stress Disorder (PTSD) and Complex PTSD (CPTSD) as per ICD-11 Proposals: a population study in Israel. Depression and Anxiety 35 (3) , pp. 264-274. 10.1002/da.22723

Berni, Thomas, Morgan, Christopher, Berni, Ellen and Rees, Dafydd Aled

2018. Polycystic ovary syndrome is associated with adverse mental health and neurodevelopmental outcomes. Journal of Clinical Endocrinology and Metabolism 103 (6) , pp. 2116-2125. 10.1530/endoabs.50.P353

Bevan Jones, Rhys

, Rice, Frances

, Beeching, Harriet, Cichosz, Rachel, Mars, Becky, Smith, Daniel J., Merry, Sally, Stallard, Paul, Jones, Ian

, Thapar, Ajay K.

and Simpson, Sharon A. 2018. A web-based psychoeducational intervention for adolescent depression: design and development of MoodHwb. JMIR Mental Health 5 (1) , e13. 10.2196/mental.8894

Blokland, Gabriëlla A.M., del Re, Elisabetta C., Mesholam-Gately, Raquelle I., Jovicich, Jorge, Trampush, Joey W., Keshavan, Matcheri S., DeLisi, Lynn E., Walters, James

, Turner, Jessica A., Malhotra, Anil K., Lencz, Todd, Shenton, Martha E., Voineskos, Aristotle N., Rujescu, Dan, Giegling, Ina, Kahn, René S., Roffman, Joshua L., Holt, Daphne J., Ehrlich, Stefan, Kikinis, Zora, Dazzan, Paola, Murray, Robin M., Di Forti, Marta, Lee, Jimmy, Sim, Kang, Lam, Max, Wolthusen, Rick P.F., de Zwarte, Sonja M.C., Walton, Esther, Cosgrove, Donna, Kelly, Sinead, Maleki, Nasim, Osiecki, Lisa, Picchioni, Marco M., Bramon, Elvira, Russo, Manuela, David, Anthony S., Mondelli, Valeria, Reinders, Antje A.T.S., Falcone, M. Aurora, Hartmann, Annette M., Konte, Bettina, Morris, Derek W., Gill, Michael, Corvin, Aiden P., Cahn, Wiepke, Ho, New Fei, Liu, Jian Jun, Keefe, Richard S.E., Gollub, Randy L., Manoach, Dara S., Calhoun, Vince D., Schulz, S. Charles, Sponheim, Scott R., Goff, Donald C., Buka, Stephen L., Cherkerzian, Sara, Thermenos, Heidi W., Kubicki, Marek, Nestor, Paul G., Dickie, Erin W., Vassos, Evangelos, Ciufolini, Simone, Reis Marques, Tiago, Crossley, Nicolas A., Purcell, Shaun M., Smoller, Jordan W., van Haren, Neeltje E.M., Toulopoulou, Timothea, Donohoe, Gary, Goldstein, Jill M., Seidman, Larry J., McCarley, Robert W. and Petryshen, Tracey L. 2018. The genetics of endophenotypes of neurofunction to understand schizophrenia (GENUS) consortium: a collaborative cognitive and neuroimaging genetics project. Schizophrenia Research 195 , pp. 306-317. 10.1016/j.schres.2017.09.024

Boot, Erik, Butcher, Nancy J., Udow, Sean, Marras, Connie, Mok, Kin Y., Kaneko, Satoshi, Barrett, Matthew J., Prontera, Paolo, Berman, Brian D., Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M., Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M.

, Wood, Nicholas W., Booij, Jan, Lang, Anthony E. and Bassett, Anne S. 2018. Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2. Neurology 90 (23) , e2059-e2067. 10.1212/WNL.0000000000005660

Bray, Nicholas J.

and O'Donovan, Michael C.

2018. The genetics of neuropsychiatric disorders. Brain and Neuroscience Advances 2 , pp. 1-6. 10.1177/2398212818799271

Brieva, Jorge, Lepore, Natasha, Romero, Eduardo, Cunningham, Adam C., Goodrich-Hunsaker, Naomi J., Simon, Tony J., Schmitt, Eric, Gur, Raquel E., Roalf, David, Ruparel, Kosha, McDonald-McGinn, Donna, Emanuel, Beverly, Craig, Michael, Murphy, Declan, Murphy, Clodaph, Gudbrandsen, Maria, Daly, Eileen, Kates, Wendy R., Bakker, Geor, van Amelsvoort, Therese, Jonas, Rachel, Hansen, Laura, Lin, Amy, Nir, Talia, Sun, Daqiang V., Kothapalli, Deydeep, Ching, Christopher R., Thompson, Paul M., Bearden, Carrie E., Jahanshad, Neda, Moss, Hayley, Owen, Michael

, Linden, David E., Van Den Bree, Marianne

, Doherty, Joanne, Durdle, Courtney A., McCabe, Kathryn L., Campbell, Linda E., Fremont, Wanda, Antshel, Kevin M., Jalbrzikowski, Maria, Vajdi, Ariana V., Kushan, Leila V., Forsyth, Jennifer K. and Villalón-Reina, Julio 2018. Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome. Presented at: 14th International Symposium on Medical Information Processing and Analysis,, Mazatlán, Mexico, 24-26 October 2018. Published in: Romero, Eduardo, Lepore, Natasha and Brieva, Jorge eds. 14th International Symposium on Medical Information Processing and Analysis. Proceedings of SPIE , vol.10975 Bellingham, Washington: SPIE, p. 51. 10.1117/12.2513788

Brikell, Isabell, Larsson, Henrik, Lu, Yi, Pettersson, Erik, Chen, Qi, Kuja-Halkola, Ralf, Karlsson, Robert, Lahey, Benjamin B, Lichtenstein, Paul and Martin, Joanna

2018. The contribution of common genetic risk variants for ADHD to a general factor of childhood psychopathology. Molecular Psychiatry 10.1038/s41380-018-0109-2

Brophy, Sinead, Kennedy, Jonathan, Fernandez-Gutierrez, Fabiola, John, Ann, Potter, Robert, Linehan, Christine and Kerr, Michael 2018. Characteristics of children prescribed antipsychotics: analysis of routinely collected data. Journal of Child and Adolescent Psychopharmacology 28 (3) , pp. 180-191. 10.1089/cap.2017.0003

C

Carboni, Lucia, Marchetti, Luca, Lauria, Mario, Gass, Peter, Vollmayr, Barbara, Redfern, Amanda, Jones, Lesley

, Razzoli, Maria, Malki, Karim, Begni, Veronica, Riva, Marco A., Domenici, Enrico, Caberlotto, Laura and Mathé, Aleksander A. 2018. Cross-species evidence from human and rat brain transcriptome for growth factor signaling pathway dysregulation in major depression. Neuropsychopharmacology 43 , pp. 2134-2145. 10.1038/s41386-018-0117-6

Castle, Daniel and Robertson, Neil P.

2018. Monoclonal antibodies for migraine: an update. Journal of Neurology 265 (6) , pp. 1491-1492. 10.1007/s00415-018-8886-8

Chao, Michael J., Kim, Kyung-Hee, Shin, Jun Wan, Lucente, Diane, Wheeler, Vanessa C., Li, Hong, Roach, Jared C., Hood, Leroy, Wexler, Nancy S., Jardim, Laura B., Holmans, Peter

, Jones, Lesley

, Orth, Michael, Kwak, Seung, MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2018. Population-specific genetic modification of Huntington's disease in Venezuela. PLoS Genetics 14 (5) , e1007274. 10.1371/journal.pgen.1007274

Chawner, Samuel J.R.A., Niarchou, Maria

, Doherty, Joanne L., Moss, Hayley, Owen, Michael J.

and Van Den Bree, Marianne

2018. The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome. Journal of Psychiatric Research 109 , pp. 10-17. 10.1016/j.jpsychires.2018.11.002

Chen, Chia-Yen, Lee, Phil H., Castro, Victor M., Minnier, Jessica, Charney, Alexander W., Stahl, Eli A., Ruderfer, Douglas M., Murphy, Shawn N., Gainer, Vivian, Cai, Tianxi, Jones, Ian

, Pato, Carlos N., Pato, Michele T., Landén, Mikael, Sklar, Pamela, Perlis, Roy H. and Smoller, Jordan W. 2018. Genetic validation of bipolar disorder identified by automated phenotyping using electronic health records. Translational Psychiatry 8 , 86. 10.1038/s41398-018-0133-7

Clifton, Nicholas

, Thomas, Kerrie

and Hall, Jeremy

2018. The effect of ketamine on the consolidation and extinction of contextual fear memory. Journal of Psychopharmacology 32 (2) , pp. 156-162. 10.1177/0269881117748903

Cloitre, M., Shevlin, M., Brewin, C. R., Bisson, Jonathan I.

, Roberts, Neil P., Maercker, A., Karatzias, T. and Hyland, P. 2018. The International Trauma Questionnaire: development of a self-report measure of ICD-11 PTSD and complex PTSD. Acta Psychiatrica Scandinavica 138 (6) , pp. 536-546. 10.1111/acps.12956

Connolly, Katherine D.

, Wadey, Rebecca M., Mathew, Donna, Johnson, Errin, Rees, D. Aled

and James, Philip E.. 2018. Evidence for adipocyte-derived extracellular vesicles in the human circulation. Endocrinology 159 (9) , pp. 3259-3267. 10.1210/en.2018-00266

Cooper, Miriam

, Hammerton, Gemma, Collishaw, Stephan

, Langley, Kate

, Thapar, Ajay

, Dalsgaard, Soren, Stergiakouli, Evie, Tilling, Kate, Davey Smith, George, Maughan, Barbara, O'Donovan, Michael

and Riglin, Lucy 2018. Investigating late-onset ADHD: a population cohort investigation. Journal of Child Psychology and Psychiatry 59 (10) , pp. 1105-1113. 10.1111/jcpp.12911

Corbin, L, Tan, V, Wade, K, Paul, D, Tansey, Katherine E., Butcher, F, Dudbridge, F, Howson, J, Jallow, M, John, C, Kingston, N, Lindgren, C, O' Donavan, Michael, O’Rahilly, S, Owen, Michael

, Palmer, C, Pearson, E, Scott, R, van Heel, D, Whittaker, J, Frayling, T, Tobin, M, Wain, L, Smith, G, Evans, D, Karpe, F, McCarthy, M, Danesh, J, Franks, P and Timpson, N 2018. Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference. Nature Communications 9 , 711. 10.1038/s41467-018-03109-y

Cosgrove, Donna, Mothersill, David O., Whitton, Laura, Harold, Denise, Kelly, Sinead, Holleran, Laurena, Holland, Jessica, Anney, Richard

, Richards, Alexander, Mantripragada, Kiran

, Owen, Michael

, O'Donovan, Michael

, 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

Creeth, H. D. J., McNamara, G. I., Tunster, S. J., Boque Sastre, R.

, Allen, B., Sumption, L.

, Eddy, J. B., Isles, A. R.

and John, R. M.

2018. Maternal care boosted by paternal imprinting in mammals. PLoS Biology 16 (7) , e2006599. 10.1371/journal.pbio.2006599

Cunningham, Adam C., Delport, Sue

, Cumines, Wendy, Busse, Monica, Linden, David E. J.

, Hall, Jeremy

and van den Bree, Marianne

2018. Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome. British Journal of Psychiatry 212 (1) , pp. 27-33. 10.1192/bjp.2017.6

Curtin, Paul, Austin, Christine, Curtin, Austen, Gennings, Chris, Arora, Manish, Tammimies, Kristiina, Willfors, Charlotte, Berggren, Steve, Siper, Paige, Rai, Dheeraj, Meyering, Kristin, Kolevzon, Alexander, Mollon, Josephine, David, Anthony S., Lewis, Glyn, Zammit, Stanley

, Heilbrun, Lynne, Palmer, Raymond F., Wright, Robert O., Bölte, Sven and Reichenberg, Abraham 2018. Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder. Science Advances 4 (5) , eaat1293. 10.1126/sciadv.aat1293

D

Dahoun, Tarik, Pardinas, Antonio F.

, Veronese, Mattia, Bloomfield, Michael A. P., Jauhar, Sameer, Bonoldi, Ilaria, Froudist-Walsh, Sean, Nosarti, Chiara, Korth, Carsten, Hennah, William, Walters, James

, Prata, Diana and Howes, Oliver D. 2018. The effect of the DISC1 Ser704Cys polymorphism on striatal dopamine synthesis capacity: an [18F]-DOPA PET study. Human Molecular Genetics 27 (20) , pp. 3498-3506. 10.1093/hmg/ddy242

Dantchev, Slava, Zammit, Stanley

and Wolke, Dieter 2018. Sibling bullying in middle childhood and psychotic disorder at 18 years: a prospective cohort study. Psychological Medicine 48 (14) , pp. 2321-2328. 10.1017/S0033291717003841

Darlay, Rebecca, Ayers, Kristin L., Mells, George F., Hall, Lynsey S., Liu, Jimmy Z., Almarri, Mohamed A., Alexander, Graeme J., Jones, David E., Sandford, Richard N., Anderson, Carl A. and Cordell, Heather J. 2018. Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis. PLoS Genetics 14 (12) , e1007833. 10.1371/journal.pgen.1007833

Davies, William

2018. Sulfation pathways: The steroid sulfate axis and its relationship to maternal behaviour and mental health. Journal of Molecular Endocrinology 61 , T199-T210. 10.1530/JME-17-0219

Davies, Jonathan, Sullivan, Sarah and Zammit, Stanley

2018. Adverse life outcomes associated with adolescent psychotic experiences and depressive symptoms. Social Psychiatry and Psychiatric Epidemiology 53 (5) , pp. 497-507. 10.1007/s00127-018-1496-z

Davis, Katrina A. S., Coleman, Jonathan R. I., Adams, Mark, Allen, Naomi, Breen, Gerome, Cullen, Breda, Dickens, Chris, Fox, Elaine, Graham, Nick, Holliday, Jo, Howard, Louise M., John, Ann, Lee, William, McCabe, Rose, McIntosh, Andrew, Pearsall, Robert, Sudlow, Cathie, Ward, Joey, Zammit, Stan

and Hotopf, Matthew 2018. Mental health in UK Biobank: development, implementation and results from an online questionnaire completed by 157 366 participants [RETRACTED]. Bjpsych Open 4 (03) , pp. 83-90. 10.1192/bjo.2018.12

Dazzan, Paola, Fusté, Montserrat and Davies, William

2018. Do defective immune system-mediated myelination processes increase postpartum psychosis risk? Trends in Molecular Medicine 24 (11) , pp. 942-949. 10.1016/j.molmed.2018.09.002

DeMichele-Sweet, M. A. A., Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R.

, Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J.

, Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B. and Sweet, R. A. 2018. Genetic risk for schizophrenia and psychosis in Alzheimer disease. Molecular Psychiatry 23 , pp. 963-972. 10.1038/mp.2017.81

Demontis, Ditte, Walters, Raymond K., Martin, Joanna

, 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., Martin, Nicholas G., 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

, 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

, 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

2018. 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

Dent, Claire L., Humby, Trevor

, Lewis, Katie, Ward, Andrew, Fischer-Colbrie, Reiner, Wilkinson, Lawrence S.

, Wilkins, Jon F. and Isles, Anthony R.

2018. Impulsive choice in mice lacking paternal expression of Grb10 suggests intragenomic conflict in behavior. Genetics 209 (1) , pp. 233-239. 10.1534/genetics.118.300898

Di Florio, Arianna

, Alexander, Danny, Schmidt, Peter J. and Rubinow, David R. 2018. Progesterone and plasma metabolites in women with and in those without premenstrual dysphoric disorder. Depression and Anxiety 35 (12) , pp. 1168-1177. 10.1002/da.22827

Dimitriadis, Stavros

and Liparas, D. 2018. How random is the random forest? Random forest algorithm on the service of structural imaging biomarkers for Alzheimer's disease: from Alzheimer's disease neuroimaging initiative (ADNI) database. Neural Regeneration Research 13 (6) , pp. 962-970. 10.4103/1673-5374.233433

Dimitriadis, Stavros

, Liparas, D and Tsolaki, Magda N 2018. Random forest feature selection, fusion and ensemble strategy: combining multiple morphological MRI measures to discriminate among healthy elderly, MCI, cMCI and Alzheimer's disease patients: from the Alzheimer's disease neuroimaging initiative (ADNI) database. Journal of Neuroscience Methods 302 , pp. 14-23. 10.1016/j.jneumeth.2017.12.010

Dimitriadis, Stavros

, Salis, Christos and Linden, David

2018. A novel, fast and efficient single-sensor automatic sleep-stage classification based on complementary cross-frequency coupling estimates. Clinical Neurophysiology 129 (4) , pp. 815-828. 10.1016/j.clinph.2017.12.039

Dimitriadis, Stavros

, Simos, Panagiotis G., Fletcher, Jack M and Papanicolaou, Andrew C. 2018. Aberrant resting-state functional brain networks in dyslexia: Symbolic mutual information analysis of neuromagnetic signals. International Journal of Psychophysiology 126 , pp. 20-29. 10.1016/j.ijpsycho.2018.02.008

Doherty, Joanne, Cooper, Miriam

and Thapar, Anita

2018. Advances in our understanding of the genetics of childhood neurodevelopmental disorders. Evidence-Based Mental Health 21 (4) , pp. 171-172. 10.1136/ebmental-2018-300067

Donohoe, G., Holland, J., Mothersill, D., McCarthy-Jones, S., Cosgrove, D., Harold, D., Richards, A., Mantripragada, K.

, Owen, M. J.

, O'Donovan, M. C.

, Gill, M., Corvin, A. and Morris, D. W. 2018. Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine 48 (10) , pp. 1608-1615. 10.1017/S0033291717002987

Duncan, L. E., Ratanatharathorn, A., Aiello, A. E., Almli, L. M., Amstadter, A. B., Ashley-Koch, A. E., Baker, D. G., Beckham, J. C., Bierut, L. J., Bisson, J.

, Bradley, B., Chen, C-Y, Dalvie, S., Farrer, L. A., Galea, S., Garrett, M. E., Gelernter, J. E ., Guffanti, G., Hauser, M. A., Johnson, E. O., Kessler, R. C., Kimbrel, N. A., King, A., Koen, N., Kranzler, H. R., Logue, M. W., Maihofer, A. X., Martin, A. R., Miller, M. W., Morey, R. A., Nugent, N. R., Rice, J. P., Ripke, S., Roberts, A. L., Saccone, N. L., Smoller, J. W., Stein, D. J., Sumner, J. A., Uddin, M., Ursano, R. J., Wildman, D. E., Yehuda, Zhao, H., Daly, M. J., Liberzon, I., Ressler, K. J., Nievergelt, C. M. and Koenen, K. C. 2018. Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability. Molecular Psychiatry 23 , pp. 666-673. 10.1038/mp.2017.77

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Eddowes, Lucy A., Al-Hourani, Kinda, Ramamurthy, Narayan, Frankish, Jamie, Baddock, Hannah T, Sandor, Cynthia

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