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Number of items: 24.


de Jong, Simone, Abdalla Diniz, Mateus Jose, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L, Ota, Vanessa K, Noto, Cristiano, Curtis, Charlesg, Newhouse, Stephen J, Patel, Hamel
et al (show 362 more authors) (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1 (1). 163-.


Glanville, Kylie P, Coleman, Jonathan RI, Hanscombe, Ken B, Euesden, Jack, Choi, Shing Wan, Purves, Kirstin L, Breen, Gerome, Air, Tracy M, Andlauer, Till FM, Baune, Bernhard T
et al (show 197 more authors) (2020) Classical Human Leukocyte Antigen Alleles and C4 Haplotypes Are Not Significantly Associated With Depression. BIOLOGICAL PSYCHIATRY, 87 (5). pp. 419-430.


Gormley, Padhraig, Kurki, Mitja I, Hiekkala, Marjo Eveliina, Veerapen, Kumar, Häppölä, Paavo, Mitchell, Adele A, Lal, Dennis, Palta, Priit, Surakka, Ida, Kaunisto, Mari Anneli
et al (show 124 more authors) (2018) Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families. Neuron, 98 (4). 743-753.e4.


Foo, Jerome C, Streit, Fabian, Frank, Josef, Witt, Stephanie H, Treutlein, Jens, Baune, Bernhard T, Moebus, Susanne, Joeckel, Karl-Heinz, Forstner, Andreas J, Noethen, Markus M
et al (show 195 more authors) (2019) Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (1). pp. 35-45.


Polimanti, Renato, Peterson, Roseann E, Ong, Jue-Sheng, MacGregor, Stuart, Edwards, Alexis C, Clarke, Toni-Kim, Frank, Josef, Gerring, Zachary, Gillespie, Nathan A, Lind, Penelope A
et al (show 362 more authors) (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49 (7). pp. 1218-1226.


Huckins, Laura M, Dobbyn, Amanda, Ruderfer, Douglas M, Hoffman, Gabriel, Wang, Weiqing, Pardinas, Antonio F, Rajagopal, Veera M, Als, Thomas D, Nguyen, Hoang T, Girdhar, Kiran
et al (show 346 more authors) (2019) Gene expression imputation across multiple brain regions provides insights into schizophrenia risk. NATURE GENETICS, 51 (4). 659-+.


Zhao, Huiying, Eising, Else, de Vries, Boukje, Vijfhuizen, Lisanne S, Anttila, Verneri, Winsvold, Bendik S, Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer
et al (show 26 more authors) (2016) Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. CEPHALALGIA, 36 (7). pp. 648-657.


Power, Robert A, Tansey, Katherine E, Buttenschon, Henriette Normolle, Cohen-Woods, Sarah, Bigdeli, Tim, Hall, Lynsey S, Kutalik, Zoltn, Lee, S Hong, Ripke, Stephan, Steinberg, Stacy
et al (show 66 more authors) (2017) Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. BIOLOGICAL PSYCHIATRY, 81 (4). pp. 325-335.


Wray, Naomi R, Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M, Abdellaoui, Abdel, Adams, Mark J, Agerbo, Esben, Air, Tracy M, Andlauer, Till MF
et al (show 208 more authors) (2018) Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. NATURE GENETICS, 50 (05). pp. 668-681.


Stahl, Eli A, Breen, Gerome, Forstner, Andreas J, McQuillin, Andrew, Ripke, Stephan, Trubetskoy, Vassily, Mattheisen, Manuel, Wang, Yunpeng, Coleman, Jonathan RI, Gaspar, Helena A
et al (show 267 more authors) (2019) Genome-wide association study identifies 30 loci associated with bipolar disorder. NATURE GENETICS, 51 (5). 793-+.


Mullins, Niamh, Forstner, Andreas J, O'Connell, Kevin S, Coombes, Brandon, Coleman, Jonathan RI, Qiao, Zhen, Als, Thomas D, Bigdeli, Tim B, Borte, Sigrid, Bryois, Julien
et al (show 305 more authors) (2021) Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. NATURE GENETICS, 53 (6). 817-+.


Forstner, Andreas J, Awasthi, Swapnil, Wolf, Christiane, Maron, Eduard, Erhardt, Angelika, Czamara, Darina, Eriksson, Elias, Lavebratt, Catharina, Allgulander, Christer, Friedrich, Nina
et al (show 65 more authors) (2021) Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. MOLECULAR PSYCHIATRY, 26 (8). pp. 4179-4190.


Arnau-Soler, Aleix, Macdonald-Dunlop, Erin, Adams, Mark J, Clarke, Toni-Kim, MacIntyre, Donald J, Milburn, Keith, Navrady, Lauren, Hayward, Caroline, McIntosh, Andrew M, Thomson, Pippa A
et al (show 195 more authors) (2019) Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9 (1). 14-.


Coleman, Jonathan RI, Peyrot, Wouter J, Purves, Kirstin L, Davis, Katrina AS, Rayner, Christopher, Choi, Shing Wan, Hubel, Christopher, Gaspar, Helena A, Kan, Carol, Van der Auwera, Sandra
et al (show 215 more authors) (2020) Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. MOLECULAR PSYCHIATRY, 25 (7). pp. 1430-1446.


Ruderfer, Douglas M, Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A, Pavlides, Jennifer M Whitehead, Mullins, Niamh, Charney, Alexander W, Ori, Anil PS, Loohuis, Loes M Olde
et al (show 534 more authors) (2018) Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes. CELL, 173 (7). pp. 1705-1715.


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
et al (show 592 more authors) (2019) Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. CELL, 179 (7). 1469-+.


Heavin, Sinead B, McCormack, Mark, Wolking, Stefan, Slattery, Lisa, Walley, Nicole, Avbersek, Andreja, Novy, Jan, Sinha, Saurabh R, Radtke, Rod, Doherty, Colin
et al (show 21 more authors) (2019) Genomic and clinical predictors of lacosamide response in refractory epilepsies. EPILEPSIA OPEN, 4 (4). pp. 563-571.


Konte, Bettina, Walters, James TR, Rujescu, Dan, Legge, Sophie E, Pardinas, Antonio F, Cohen, Dan, Pirmohamed, Munir ORCID: 0000-0002-7534-7266, Tiihonen, Jari, Hartmann, Annette M, Bogers, Jan P
et al (show 17 more authors) (2021) HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestry. TRANSLATIONAL PSYCHIATRY, 11 (1). 214-.


Grove, Jakob, Ripke, Stephan, Als, Thomas D, Mattheisen, Manuel, Walters, Raymond K, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A, Anney, Richard
et al (show 266 more authors) (2019) Identification of common genetic risk variants for autism spectrum disorder. NATURE GENETICS, 51 (3). 431-+.


Czamara, Darina, Eraslan, Goekcen, Page, Christian M, Lahti, Jari, Lahti-Pulkkinen, Marius, Hamalainen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M, Reynolds, Rebecca M
et al (show 219 more authors) (2019) Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10 (1). 2548-.


Kogelman, Lisette JA, Esserlind, Ann-Louise, Christensen, Anne Francke, Awasthi, Swapnil, Ripke, Stephan, Ingason, Andres, Davidsson, Olafur B, Erikstrup, Christian, Hjalgrim, Henrik, Ullum, Henrik
et al (show 85 more authors) (2019) Migraine polygenic risk score associates with efficacy of migraine-specific drugs. Neurology Genetics, 5 (6). e364-.


Harold, Denise, Connolly, Siobhan, Riley, Brien P, Kendler, Kenneth S, McCarthy, Shane E, McCombie, William R, Richards, Alex, Owen, Michael J, O'Donovan, Michael C, Walters, James
et al (show 350 more authors) (2019) Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 180 (3). pp. 223-231.


Boothman, Isabelle, Clayton, Lisa M, Mccormack, Mark, Driscoll, Alexandra McKibben, Stevelink, Remi, Moloney, Patrick, Krause, Roland, Kunz, Wolfram S, Diehl, Sarah, O'Brien, Terence J
et al (show 17 more authors) (2023) Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin. FRONTIERS IN NEUROSCIENCE, 17. 1156362-.


Berghuis, Bianca, Stapleton, Caragh, Sonsma, Anja CM, Hulst, Janic, de Haan, Gerrit-Jan, Lindhout, Dick, Demurtas, Rita, EpiPGX Consortium, , Krause, Roland, Depondt, Chantal
et al (show 17 more authors) (2019) A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Epilepsia Open, 4 (1). pp. 102-109.

This list was generated on Sun Mar 24 23:52:18 2024 GMT.