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Number of items: 17.


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.


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.


Liu, Dajiang J, Peloso, Gina M, Yu, Haojie, Butterworth, Adam S, Wang, Xiao, Mahajan, Anubha, Saleheen, Danish, Emdin, Connor, Alam, Dewan, Alves, Alexessander Couto
et al (show 217 more authors) (2017) Exome-wide association study of plasma lipids in >300,000 individuals. NATURE GENETICS, 49 (12). 1758-+.


Evangelou, Evangelos, Warren, Helen R, Mosen-Ansorena, David, Mifsu, Borbala, Pazoki, Raha, Gao, He, Ntritsos, Georgios, Dimou, Niki, Cabrer, Claudia P, Karaman, Ibrahim
et al (show 271 more authors) (2018) Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature Genetics, 50 (10). pp. 1412-1425.


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.


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.


Alonso, Nerea, Estrada, Karol, Albagha, Omar ME, Herrera, Lizbeth, Reppe, Sjur, Olstad, Ole K, Gautvik, Kaare M, Ryan, Niamh M, Evans, Kathryn L, Nielson, Carrie M
et al (show 51 more authors) (2018) Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density. ANNALS OF THE RHEUMATIC DISEASES, 77 (3). pp. 378-385.


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-.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 97 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome Open Research, 3. p. 4.


Jackson, Victoria E ORCID: 0000-0002-9758-9784, Latourelle, Jeanne C, Wain, Louise V ORCID: 0000-0003-4951-1867, Smith, Albert V, Grove, Megan L, Bartz, Traci M, Obeidat, Ma'en ORCID: 0000-0002-5443-2752, Province, Michael A, Gao, Wei, Qaiser, Beenish
et al (show 98 more authors) (2018) Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome open research, 3. 4-.


Wain, Louise V, Vaez, Ahmad, Jansen, Rick, Joehanes, Roby, van der Most, Peter J, Erzurumluoglu, A Mesut, O'Reilly, Paul F, Cabrera, Claudia P, Warren, Helen R, Rose, Lynda M
et al (show 236 more authors) (2017) Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. HYPERTENSION, 70 (3). E4-+.


Turcot, Valerie, Lu, Yingchang, Highland, Heather M, Schurmann, Claudia, Justice, Anne E, Fine, Rebecca S, Bradfield, Jonathan P, Esko, Tonu, Giri, Ayush, Graff, Mariaelisa
et al (show 401 more authors) (2018) Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. NATURE GENETICS, 50 (1). pp. 26-41.


Marouli, Eirini, Graff, Mariaelisa, Medina-Gomez, Carolina, Lo, Ken Sin, Wood, Andrew R, Kjaer, Troels R, Fine, Rebecca S, Lu, Yingchang, Schurmann, Claudia, Highland, Heather M
et al (show 363 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). pp. 186-190.

This list was generated on Sat Mar 23 02:35:33 2024 GMT.