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Number of items: 46.


Direk, Nese, Williams, Stephanie, Smith, Jennifer A, Ripke, Stephan, Air, Tracy, Amare, Azmeraw T, Amin, Najaf, Baune, Bernhard T, Bennett, David A, Blackwood, Douglas HR
et al (show 92 more authors) (2017) An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. BIOLOGICAL PSYCHIATRY, 82 (5). pp. 322-329.


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.


Flannick, Jason, Fuchsberger, Christian, Mahajan, Anubha, Teslovich, Tanya M, Agarwala, Vineeta, Gaulton, Kyle J, Caulkins, Lizz, Koesterer, Ryan, Ma, Clement, Moutsianas, Loukas
et al (show 291 more authors) (2017) Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. SCIENTIFIC DATA, 4 (1). 170179-.


Surendran, Praveen, Feofanova, Elena V, Lahrouchi, Najim, Ntalla, Ioanna, Karthikeyan, Savita, Cook, James, Chen, Lingyan, Mifsud, Borbala, Yao, Chen, Kraja, Aldi T
et al (show 271 more authors) (2020) Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. NATURE GENETICS, 52 (12). pp. 1314-1332.


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-+.


Scott, Robert A, Scott, Laura J, Maegi, Reedik, Marullo, Letizia, Gaulton, Kyle J, Kaakinen, Marika, Pervjakova, Natalia, Pers, Tune H, Johnson, Andrew D, Eicher, John D
et al (show 165 more authors) (2017) An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. DIABETES, 66 (11). pp. 2888-2902.


Walton, E, Hibar, D, Yilmaz, Z, Jahanshad, N, Cheung, J, Batury, V-L, Seitz, J, Bulik, CM, Thompson, PM, Ehrlich, Stefan
et al (show 500 more authors) (2019) Exploration of Shared Genetic Architecture Between Subcortical Brain Volumes and Anorexia Nervosa. MOLECULAR NEUROBIOLOGY, 56 (7). pp. 5146-5156.


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-+.


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.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tonu, van Mill, Josine G, Mbarek, Hamdi
et al (show 64 more authors) (2016) Genetic variants in <i>RBFOX3</i> are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). pp. 1488-1495.


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.


Shah, Sonia, Henry, Albert, Roselli, Carolina, Lin, Honghuang, Sveinbjornsson, Gardar, Fatemifar, Ghazaleh, Hedman, Asa K, Wilk, Jemma B, Morley, Michael P, Chaffin, Mark D
et al (show 194 more authors) (2020) Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications, 11 (1). 163-.


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-+.


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.


Justice, Anne E, Winkler, Thomas W, Feitosa, Mary F, Graff, Misa, Fisher, Virginia A, Young, Kristin, Barata, Llilda, Deng, Xuan, Czajkowski, Jacek, Hadley, David
et al (show 307 more authors) (2017) Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. NATURE COMMUNICATIONS, 8 (1). 14977-.


Mahajan, Anubha, Go, Min Jin, Zhang, Weihua, Below, Jennifer E, Gaulton, Kyle J, Ferreira, Teresa, Horikoshi, Momoko, Johnson, Andrew D, Ng, Maggie CY, Prokopenko, Inga
et al (show 322 more authors) (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nature Genetics, 46 (3). pp. 234-244.


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.


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-+.


Mitt, Mario, Kals, Mart, Parn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tonu
et al (show 2 more authors) (2016) Improved Imputation Accuracy of Rare and Low-Frequency Genetic Variants Using Population-Specific High-Coverage Whole-Genome Sequencing Data Based Imputation Reference Panel. HUMAN HEREDITY, 81 (4). p. 235.


Mitt, Mario, Kals, Mart, Parn, Kalle, Gabriel, Stacey B, Lander, Eric S, Palotie, Aarno, Ripatti, Samuli, Morris, Andrew P, Metspalu, Andres, Esko, Tonu
et al (show 2 more authors) (2017) Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. EUROPEAN JOURNAL OF HUMAN GENETICS, 25 (7). pp. 869-876.


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-.


Tsoi, Lam C, Stuart, Philip E, Tian, Chao, Gudjonsson, Johann E, Das, Sayantan, Zawistowski, Matthew, Ellinghaus, Eva, Barker, Jonathan N, Chandran, Vinod, Dand, Nick
et al (show 27 more authors) (2017) Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. NATURE COMMUNICATIONS, 8 (1). 15382-.


Sung, Yun J, Winkler, Thomas W, de las Fuentes, Lisa, Bentley, Amy R, Brown, Michael R, Kraja, Aldi T, Schwander, Karen, Ntalla, Ioanna, Guo, Xiuqing, Franceschini, Nora
et al (show 287 more authors) (2018) A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. AMERICAN JOURNAL OF HUMAN GENETICS, 102 (3). pp. 375-400.


Manning, Alisa, Highland, Heather M, Gasser, Jessica, Sim, Xueling, Tukiainen, Taru, Fontanillas, Pierre, Grarup, Niels, Rivas, Manuel A, Mahajan, Anubha, Locke, Adam E
et al (show 253 more authors) (2017) A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. DIABETES, 66 (7). pp. 2019-2032.


Niemi, Mari EK, Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja
et al (show 3481 more authors) (2021) Mapping the human genetic architecture of COVID-19. NATURE, 600 (7889). 472-+.


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-.


Bentley, Amy R, Sung, Yun J, Brown, Michael R, Winkler, Thomas W, Kraja, Aldi T, Ntalla, Ioanna, Schwander, Karen, Chasman, Daniel I, Lim, Elise, Deng, Xuan
et al (show 291 more authors) (2019) Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. NATURE GENETICS, 51 (4). 636-+.


Roselli, Carolina, Chaffin, Mark D, Weng, Lu-Chen, Aeschbacher, Stefanie, Ahlberg, Gustav, Albert, Christine M, Almgren, Peter, Alonso, Alvaro, Anderson, Christopher D, Aragam, Krishna G
et al (show 208 more authors) (2018) Multi-ethnic genome-wide association study for atrial fibrillation. Nature Genetics, 50 (9). pp. 1225-1233.


Kraja, Aldi T, Cook, James P, Warren, Helen R, Surendran, Praveen, Liu, Chunyu, Evangelou, Evangelos, Manning, Alisa K, Grarup, Niels, Drenos, Fotios, Sim, Xueling
et al (show 132 more authors) (2017) New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475000 Individuals. CIRCULATION-CARDIOVASCULAR GENETICS, 10 (5). e001778-.


Loley, Christina, Alver, Maris, Assimes, Themistocles L, Bjonnes, Andrew, Goel, Anuj, Gustafsson, Stefan, Hernesniemi, Jussi, Hopewell, Jemma C, Kanoni, Stavroula, Kleber, Marcus E
et al (show 68 more authors) (2016) No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis. SCIENTIFIC REPORTS, 6 (1). 35278-.


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-+.


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.


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.


Flannick, Jason, Fuchsberger, Christian, Mahajan, Anubha, Teslovich, Tanya M, Agarwala, Vineeta, Gaulton, Kyle J, Caulkins, Lizz, Koesterer, Ryan, Ma, Clement, Moutsianas, Loukas
et al (show 291 more authors) (2018) Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (vol 4, 170179, 2017). SCIENTIFIC DATA, 5 (1). 180002-.


Blokland, Gabriella AM, Grove, Jakob, Chen, Chia-Yen, Cotsapas, Chris, Tobet, Stuart, Handa, Robert, St Clair, David, Lencz, Todd, Mowry, Bryan J, Periyasamy, Sathish
et al (show 119 more authors) (2022) Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. BIOLOGICAL PSYCHIATRY, 91 (1). pp. 102-117.


Munn-Chernoff, Melissa A, Johnson, Emma C, Chou, Yi-Ling, Coleman, Jonathan RI, Thornton, Laura M, Walters, Raymond K, Yilmaz, Zeynep, Baker, Jessica H, Hubel, Christopher, Gordon, Scott
et al (show 342 more authors) (2021) Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. ADDICTION BIOLOGY, 26 (1). e12880-.


Surendran, Praveen, Drenos, Fotios, Young, Robin, Warren, Helen, Cook, James P, Manning, Alisa K, Grarup, Niels, Sim, Xueling, Barnes, Daniel R, Witkowska, Kate
et al (show 200 more authors) (2016) Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. NATURE GENETICS, 48 (10). pp. 1151-1161.


Fuchsberger, Christian, Flannick, Jason, Teslovich, Tanya M, Mahajan, Anubha, Agarwala, Vineeta, Gaulton, Kyle J, Ma, Clement, Fontanillas, Pierre, Moutsianas, Loukas, McCarthy, Davis J
et al (show 291 more authors) (2016) The genetic architecture of type 2 diabetes. NATURE, 536 (7614). 41-+.


Ried, Janina S, Jeff, Janina M, Chu, Audrey Y, Bragg-Gresham, Jennifer L, van Dongen, Jenny, Huffman, Jennifer E, Ahluwalia, Tarunveer S, Cadby, Gemma, Eklund, Niina, Eriksson, Joel
et al (show 266 more authors) (2016) A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. NATURE COMMUNICATIONS, 7 (1). 13357-.

This list was generated on Sat Mar 23 20:20:12 2024 GMT.