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Number of items: 25.

Real, Raquel, Martinez-Carrasco, Alejandro, Reynolds, Regina, Lawton, Michael, Tan, Manuela, Shoai, Maryam, Corvol, Jean-Christophe, Ryten, Mina, Bresner, Catherine, Hubbard, Leon, Brice, Alexis, Lesage, Suzanne, Faouzi, Johann, Elbaz, Alexis, Artaud, Fanny, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Hu, Michele, Ben-Shlomo, Yoav, Grosset, Donald, Hardy, John and Morris, Huw 2023. Association between the LRP1B and APOE loci in the development of Parkinson’s disease dementia. Brain 146 (5) , pp. 1873-1887. 10.1093/brain/awac414
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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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Rammos, Alexandros, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Hubbard, Leon, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2023. Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia. Molecular Psychiatry 10.1038/s41380-023-02013-2
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Kappel, Djenifer B., Legge, Sophie E., Hubbard, Leon, Willcocks, Isabella R. ORCID: https://orcid.org/0000-0002-3568-5236, O'Connell, Kevin S., Smith, Robert L., Molden, Espen, Andreassen, Ole A., King, Adrian, Jansen, John, Helthuis, Marinka, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 and Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590 2023. Genomic stratification of clozapine prescription patterns using schizophrenia polygenic scores. Biological Psychiatry 93 , pp. 149-156. 10.1016/j.biopsych.2022.07.014
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Harvey, Joshua, Smith, Adam R., Weymouth, Luke Stephen, Smith, Rebecca G., Hubbard, Leon, Bresner, Kate, Pishva, Ehsan, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Lunnon, Katie and Creese, Byron 2022. An epigenome wide association study of sub-phenotypes in Parkinson's disease. Alzheimer's & Dementia: The Journal of the Alzheimer's Association 18 (S4) , e069252. 10.1002/alz.069252

Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Millin, Stephanie, Dahl, Andrew, Schalkamp, Ann-Kathrin, Lawton, Michael, Hubbard, Leon, Rahman, Nabila, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Ben-Shlomo, Yoav, Grosset, Donald G., Hu, Michele T., Marchini, Jonathan and Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674 2022. Universal clinical Parkinson’s disease axes identify a major influence of neuroinflammation. Genome Medicine 14 , 129. 10.1186/s13073-022-01132-9
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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Agha, Sharifah Shameem ORCID: https://orcid.org/0000-0001-9541-6786, Eyre, Olga, Riglin, Lucy, Langley, Kate ORCID: https://orcid.org/0000-0002-2033-2657, Hubbard, Leon, Stergiakouli, Evie, Psychiatric Genomics Consortium ADHD Working group, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X 2021. Sex differences in anxiety and depression in children with ADHD investigating genetic liability and comorbidity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 186 (7) , pp. 412-422. 10.1002/ajmg.b.32842
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Dennison, Charlotte, Legge, Sophie, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Cardno, Alastair, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2021. Risk factors, clinical features, and polygenic risk scores in schizophrenia and schizoaffective disorder depressive-type. Schizophrenia Bulletin 47 (5) , pp. 1375-1384. 10.1093/schbul/sbab036
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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Asjadi, Kimiya, Hubbard, Leon, Kendall, Kimberley ORCID: https://orcid.org/0000-0002-6755-6121, Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Jermy, Bradley, Lewis, Cathryn M., Baune, Bernhard T., Boomsma, Dorret I., Hamilton, Steven P., Lucae, Susanne, Magnusson, Patrik K., Martin, Nicholas G., McIntosh, Andrew M., Mehta, Divya, Mors, Ole, Mullins, Niamh, Penninx, Brenda W. J. H., Preisig, Martin, Rietschel, Marcella, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Rice, Frances ORCID: https://orcid.org/0000-0002-9484-1729, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X and O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 2021. Examining sex differences in neurodevelopmental and psychiatric genetic risk in anxiety and depression. PLoS ONE 16 (9) , e0248254. 10.1371/journal.pone.0248254
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Legge, Sophie, Cardno, Alastair, Allardyce, Judith ORCID: https://orcid.org/0000-0003-4094-552X, Dennison, Charlotte, Hubbard, Leon, Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Di Florio, Arianna ORCID: https://orcid.org/0000-0003-0338-2748, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Associations between schizophrenia polygenic liability, symptom dimensions, and cognitive ability in schizophrenia. JAMA Psychiatry 78 (10) , pp. 1143-1151. 10.1001/jamapsychiatry.2021.1961
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Hubbard, Leon, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Morris, Derek W., Lynham, Amy J. ORCID: https://orcid.org/0000-0002-3189-6888, Richards, Alex L., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Legge, Sophie E., Harold, Denise, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862, Donohoe, Gary, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452 and Walters, James T.R. ORCID: https://orcid.org/0000-0002-6980-4053 2021. Rare copy number variations are associated with poorer cognition in schizophrenia. Biological Psychiatry 90 (1) , pp. 28-34. 10.1016/j.biopsych.2020.11.025
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Kia, Demis A., Zhang, David, Guelfi, Sebastian, Manzoni, Claudia, Hubbard, Leon, Reynolds, Regina H., Botía, Juan, Ryten, Mina, Ferrari, Raffaele, Lewis, Patrick A., Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Trabzuni, Daniah, Hardy, John, Wood, Nicholas W., Noyce, Alastair J., Kaiyrzhanov, Rauan, Middlehurst, Ben, Kia, Demis A., Tan, Manuela, Houlden, Henry, Morris, Huw R., Plun-Favreau, Helene, Holmans, Peter, Hardy, John, Trabzuni, Daniah, Bras, Jose, PhD, John Quinn, Mok, Kin Y., Kinghorn, Kerri J., Billingsley, Kimberley, Wood, Nicholas W., Lewis, Patrick, Schreglmann, Sebastian, Guerreiro, Rita, Lovering, Ruth, R'Bibo, Lea, Manzoni, Claudia, Rizig, Mie, Ryten, Mina, Guelfi, Sebastian, Escott-Price, Valentina, Chelban, Viorica, Foltynie, Thomas, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Brice, Alexis, Danjou, Fabrice, Lesage, Suzanne, Corvol, Jean-Christophe, Martinez, Maria, Schulte, Claudia, Brockmann, Kathrin, Simón-Sánchez, Javier, Heutink, Peter, Rizzu, Patrizia, Sharma, Manu, Gasser, Thomas, Nicolas, Aude, Cookson, Mark R., Bandres-Ciga, Sara, Blauwendraat, Cornelis, Craig, David W., Faghri, Faraz, Gibbs, J. Raphael, Hernandez, Dena G., Van Keuren-Jensen, Kendall, Shulman, Joshua M., Leonard, Hampton L., Nalls, Mike A., Robak, Laurie, Lubbe, Steven, Finkbeiner, Steven, Mencacci, Niccolo E., Lungu, Codrin, Singleton, Andrew B, Scholz, Sonja W., Reed, Xylena, Alcalay, Roy N., Gan-Or, Ziv, Rouleau, Guy A., Krohn, Lynne, van Hilten, Jacobus J., Marinus, Johan, Adarmes-Gómez, Astrid D., Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Javier Barrero, Francisco, Bergareche Yarza, Jesús A., Bernal-Bernal, Inmaculada, Blazquez, Marta, Bonilla-Toribio, Marta, Botía, Juan A., Boungiorno, María T., Buiza-Rueda, Dolores, Càmara, Ana, Carrillo, Fátima, Carrión-Claro, Mario, Cerdan, Debora, Clarimón, Jordi, Compta, Yaroslau, Diez-Fairen, Monica, Dols-Icardo, Oriol, Duarte, Jacinto, Duran, Raquel, Escamilla-Sevilla, Francisco, Ezquerra, Mario, Feliz, Cici, Fernàndez, Manel, Fernàndez-Santiago, Rubén, Garcia, Ciara, García-Ruiz, Pedro, Gómez-Garre, Pilar, Gomez Heredia, Maria J., Gonzalez-Aramburu, Isabel, Pagola, Ana G., Hoenicka, Janet, Infante, Jon, Jimenez-Escrig, Adriano, Kulisevsky, Jaime, Labrador-Espinosa, Miguel A., Lopez-Sendon, Jose Luis, Arregui, Adolfo López de Munain, Macias, Daniel, Torres, Irene Martínez, Marín, Juan, Marti, Maria Jose, Martínez-Castrillo, Juan Carlos, Mèndez-del-Barrio, Carlota, González, Manuel Menéndez, Adolfo Mínguez, Marina Mata, Mir, Pablo, Rezola, Elisabet Mondragon, Muñoz, Esteban, Pagonabarraga, Javier, Pastor, Pau, Errazquin, Francisco Perez, Perinán-Tocino, Teresa, Ruiz-Martínez, Javier, Ruz, Clara, Rodriguez, Antonio Sanchez, Sierra, María, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tartari, Juan Pablo, Tejera-Parrado, Cristina, Tolosa, Eduard, Valldeoriola, Francesc, Vargas-González, Laura, Vela, Lydia, Vives, Francisco, Zimprich, Alexander, Pihlstrom, Lasse, Toft, Mathias, Koks, Sulev, Taba, Pille, Hassin-Baer, Sharon, Weale, Michael, Ramasamy, Adaikalavan, Smith, Colin, Guelfi, Manuel Sebastian, D'sa, Karishma, Forabosco, Paola and Botiá, Juan A. 2021. Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets. JAMA Neurology 78 (4) , pp. 464-472. 10.1001/jamaneurol.2020.5257
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Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams-Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Ben-Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam and Morris, Huw R. 2021. Genome-wide association studies of cognitive and motor progression in Parkinson's disease. Movement Disorders 36 (2) , pp. 424-433. 10.1002/mds.28342
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Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Hubbard, Leon, Sandor, Cynthia ORCID: https://orcid.org/0000-0002-8905-1052, Webber, Caleb ORCID: https://orcid.org/0000-0001-8063-7674, Hendry, Hannah, Lawton, Michael, Carroll, Camille, Chaudhuri, K. Ray, Morris, Huw, Hu, Michele T., Grosset, Donald G., Kobylecki, Christopher and Silverdale, Monty 2020. Genome‐wide association study of pain in Parkinson's disease implicates TRPM8 as a risk factor. Movement Disorders 35 (4) , pp. 705-707. 10.1002/mds.28001
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Tan, Manuela M.X., Malek, Naveed, Lawton, Michael A., Hubbard, Leon, Pittman, Alan M., Joseph, Theresita, Hehir, Jason, Swallow, Diane M.A., Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Hardy, John, Wood, Nicholas, Ben-Shlomo, Yoav, Grosset, Donald G., Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931 and Morris, Huw R. 2019. Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study. Brain 142 (9) , pp. 2828-2844. 10.1093/brain/awz191
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Jones, Hannah J. ORCID: https://orcid.org/0000-0001-7297-9711, Hubbard, Leon, Mitchell, Ruth E., Jones, Simon A. ORCID: https://orcid.org/0000-0001-7297-9711, Williams, Nigel M. ORCID: https://orcid.org/0000-0003-1177-6931, Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 and Hall, Jeremy ORCID: https://orcid.org/0000-0003-2737-9009 2019. Association of genetic risk for rheumatoid arthritis with cognitive and psychiatric phenotypes across childhood and adolescence. JAMA Network Open 2 (6) , -. 10.1001/jamanetworkopen.2019.6118
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Silverdale, Monty A., Kobylecki, Christopher, Kass-Iliyya, Lewis, Martinez-Martin, Pablo, Lawton, Michael, Cotterill, Sarah, Chaudhuri, K. Ray, Morris, Huw, Baig, Fahd, Williams, Nigel ORCID: https://orcid.org/0000-0003-1177-6931, Hubbard, Leon, Hu, Michele T. and Grosset, Donald G. 2018. A detailed clinical study of pain in 1957 participants with early/moderate Parkinson's disease. Parkinsonism & Related Disorders 56 , pp. 27-32. 10.1016/j.parkreldis.2018.06.001
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Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Hubbard, Leon, Tansey, Katherine, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Legge, Sophie, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, Jones, Ian ORCID: https://orcid.org/0000-0001-5821-5889 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2018. Examining cognition across the bipolar / schizophrenia diagnostic spectrum. Journal of Psychiatry and Neuroscience 43 (3) , 170076. 10.1503/jpn.170076
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Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, GERAD Consortium, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and CRESTAR Consortium 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2
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Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. [Online]. bioRxiv. Available at: http://dx.doi.org/10.1101/068593
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Martin, Joanna ORCID: https://orcid.org/0000-0002-8911-3479, Tilling, Kate, Hubbard, Leon, Stergiakouli, Evie, Thapar, Anita ORCID: https://orcid.org/0000-0002-3689-737X, Davey Smith, George, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2016. Association of genetic risk for schizophrenia with nonparticipation over time in a population-based cohort study. American Journal of Epidemiology 183 (12) , pp. 1149-1158. 10.1093/aje/kww009
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Jones, Hannah J., Stergiakouli, Evie, Tansey, Katherine E., Hubbard, Leon, Heron, Jon, Cannon, Mary, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, Lewis, Glyn, Linden, David Edmund Johannes ORCID: https://orcid.org/0000-0002-5638-9292, Jones, Peter B., Davey Smith, George, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2016. Phenotypic manifestation of genetic risk for schizophrenia during adolescence in the general population. JAMA Psychiatry 73 (3) , pp. 221-228. 10.1001/jamapsychiatry.2015.3058

Hubbard, Leon, Tansey, Katherine E., Rai, Dheeraj, Jones, Peter, Ripke, Stephan, Chambert, Kimberly D., Moran, Jennifer L., McCarroll, Steven A., Linden, David Edmund Johannes ORCID: https://orcid.org/0000-0002-5638-9292, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James Tynan Rhys ORCID: https://orcid.org/0000-0002-6980-4053 and Zammit, Stanley ORCID: https://orcid.org/0000-0002-2647-9211 2016. Evidence of common genetic overlap between schizophrenia and cognition. Schizophrenia Bulletin 42 (3) , pp. 832-842. 10.1093/schbul/sbv168
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Akpudo, Hilary, Aleksic, Branko, Alkelai, Anna, Burton, Christie, Carillo Roa, Tania, Chen, David T.W., Cheng, Min-Chih, Cocchi, Enrico, Davis, Lea K., Giori, Isabele G., Hubbard, Leon, Merikangas, Alison, Moily, Nagaraj S., Okewole, Adeniran, Olfson, Emily, Pappa, Irene, Reitt, Markus, Singh, Ajeet B., Steinberg, Julia, Strohmaier, Jana, Ting, Te-Tien, van Hulzen, Kimm J.E., O?Shea, Anne and DeLisi, Lynn E. 2014. Summaries of oral sessions at the XXI World Congress of Psychiatric Genetics, Boston, Massachusetts, 17-21 October 2013. Psychiatric Genetics 24 (4) , pp. 125-150. 10.1097/YPG.0000000000000043

Hubbard, Leon 2014. Common and rare genetic risk factors for schizophrenia and their associations with cognition. PhD Thesis, Cardiff University.
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