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Number of items: 39.


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 363 more authors) (2018) Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder. COMMUNICATIONS BIOLOGY, 1.


Pulit, Sara L, Weng, Lu-Chen, McArdle, Patrick F, Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D, Rosand, Jonathan, de Bakker, Paul IW, Benjamin, Emelia J, Ellinor, Patrick T
et al (show 353 more authors) (2018) Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes. NEUROLOGY-GENETICS, 4 (6).


Fehringer, Gordon, Kraft, Peter, Pharoah, Paul D, Eeles, Rosalind A, Chatterjee, Nilanjan, Schumacher, Fredrick R, Schildkraut, Joellen M, Lindstrom, Sara, Brennan, Paul, Bickeboller, Heike
et al (show 128 more authors) (2016) Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. CANCER RESEARCH, 76 (17). 5103 - 5114.


van der Laan, Sander W, Fall, Tove, Soumare, Aicha, Teumer, Alexander, Sedaghat, Sanaz, Baumert, Jens, Zabaneh, Delilah, van Setten, Jessica, Isgum, Ivana, Galesloot, Tessel E
et al (show 62 more authors) (2016) Cystatin C and Cardiovascular Disease A Mendelian Randomization Study. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 68 (9). 934 - 945.


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). 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 364 more authors) (2019) Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium. PSYCHOLOGICAL MEDICINE, 49 (7). 1218 - 1226.


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. 1412 - 1425.


Satizabal, Claudia L, Adams, Hieab HH, Hibar, Derrek P, White, Charles C, Knol, Maria J, Stein, Jason L, Scholz, Markus, Sargurupremraj, Muralidharan, Jahanshad, Neda, Roshchupkin, Gennady V
et al (show 279 more authors) (2019) Genetic architecture of subcortical brain structures in 38,851 individuals. NATURE GENETICS, 51 (11). 1624 - +.


Nolte, Ilja M, Munoz, M Loretto, Tragante, Vinicius, Amare, Azmeraw T, Jansen, Rick, Vaez, Ahmad, von der Heyde, Benedikt, Avery, Christy L, Bis, Joshua C, Dierckx, Bram
et al (show 154 more authors) (2017) Genetic loci associated with heart rate variability and their effects on cardiac disease risk. NATURE COMMUNICATIONS, 8.


Amin, Najaf, Allebrandt, Karla V, van der Spek, Ashley, Mueller-Myhsok, Bertram, 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 RBFOX3 are associated with sleep latency. EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (10). 1488 - 1495.


Ligthart, Symen, Vaez, Ahmad, Vosa, Urmo, Stathopoulou, Maria G, de Vries, Paul S, Prins, Bram P, Van der Most, Peter J, Tanaka, Toshiko, Naderi, Elnaz, Rose, Lynda M
et al (show 278 more authors) (2018) Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (5). 691 - 706.


Bolton, Jennifer L, Hayward, Caroline, Direk, Nese, Lewis, John G, Hammond, Geoffrey L, Hill, Lesley A, Anderson, Anna, Huffman, Jennifer, Wilson, James F, Campbell, Harry
et al (show 46 more authors) (2014) Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. PLoS Genetics, 10 (7). e1004474 - ?.


van Rooij, Frank JA, Qayyum, Rehan, Smith, Albert V, Zhou, Yi, Trompet, Stella, Tanaka, Toshiko, Keller, Margaux F, Chang, Li-Ching, Schmidt, Helena, Yang, Min-Lee
et al (show 91 more authors) (2017) Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. AMERICAN JOURNAL OF HUMAN GENETICS, 100 (1). 51 - 63.


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). 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).


Teumer, Alexander, Li, Yong, Ghasemi, Sahar, Prins, Bram P, Wuttke, Matthias, Hermle, Tobias, Giri, Ayush, Sieber, Karsten B, Qiu, Chengxiang, Kirsten, Holger
et al (show 176 more authors) (2019) Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. NATURE COMMUNICATIONS, 10.


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 197 more authors) (2019) Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. TRANSLATIONAL PSYCHIATRY, 9.


Coffee and Caffeine Genetics Consortium, , Cornelis, Marilyn C, Byrne, Enda M ORCID: 0000-0002-9491-7797, Esko, Tõnu ORCID: 0000-0003-1982-6569, Nalls, Michael A, Ganna, Andrea ORCID: 0000-0002-8147-240X, Paynter, Nina, Monda, Keri L, Amin, Najaf ORCID: 0000-0002-8944-1771, Fischer, Krista
et al (show 148 more authors) (2015) Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Molecular psychiatry, 20 (5). 647 - 656.


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.


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). 234 - 244.


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). 378 - 385.


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 220 more authors) (2019) Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. NATURE COMMUNICATIONS, 10.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. NATURE COMMUNICATIONS, 8.


Zillikens, M Carola, Demissie, Serkalem, Hsu, Yi-Hsiang, Yerges-Armstrong, Laura M, Chou, Wen-Chi, Stolk, Lisette, Livshits, Gregory, Broer, Linda, Johnson, Toby, Koller, Daniel L
et al (show 183 more authors) (2017) Large meta-analysis of genome-wide association studies identifies five loci for lean body mass (vol 8, 80, 2017). NATURE COMMUNICATIONS, 8.


Wild, Philipp S, Felix, Janine F, Schillert, Arne, Teumer, Alexander, Chen, Ming-Huei, Leening, Maarten JG, Voelker, Uwe, Grossmann, Vera, Brody, Jennifer A, Irvin, Marguerite R
et al (show 116 more authors) (2017) Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). 1798 - 1812.


Warrington, Nicole M, Beaumont, Robin N, Horikoshi, Momoko, Day, Felix R, Helgeland, Oyvind, Laurin, Charles, Bacelis, Jonas, Peng, Shouneng, Hao, Ke, Feenstra, Bjarke
et al (show 199 more authors) (2019) Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. NATURE GENETICS, 51 (5). 804 - +.


Liu, Chunyu, Kraja, Aldi T, Smith, Jennifer A, Brody, Jennifer A, Franceschini, Nora, Bis, Joshua C, Rice, Kenneth, Morrison, Alanna C, Lu, Yingchang, Weiss, Stefan
et al (show 91 more authors) (2016) Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. NATURE GENETICS, 48 (10). 1162 - 1170.


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 295 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. 1225 - 1233.


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 239 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 - +.


Hibar, Derrek P, Adams, Hieab HH, Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L, Hofer, Edith, Renteria, Miguel E, Bis, Joshua C, Arias-Vasquez, Alejandro, Ikram, M Kamran
et al (show 322 more authors) (2017) Novel genetic loci associated with hippocampal volume. NATURE COMMUNICATIONS, 8.


Kraja, Aldi T, Chasman, Daniel I, North, Kari E, Reiner, Alexander P, Yanek, Lisa R, Kilpeläinen, Tuomas O, Smith, Jennifer A, Dehghan, Abbas, Dupuis, Josée, Johnson, Andrew D
et al (show 58 more authors) (2014) Pleiotropic genes for metabolic syndrome and inflammation. Molecular Genetics and Metabolism, 112 (4). 317 - 338.


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. 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 372 more authors) (2017) Rare and low-frequency coding variants alter human adult height. NATURE, 542 (7640). 186 - 190.


May, Patrick, Girard, Simon, Harrer, Merle, Bobbili, Dheeraj R, Schubert, Julian, Wolking, Stefan, Becker, Felicitas, Lachance-Touchette, Pamela, Meloche, Caroline, Gravel, Micheline
et al (show 91 more authors) (2018) Rare coding variants in genes encoding GABA(A) receptors in genetic generalised epilepsies: an exome-based case-control study. LANCET NEUROLOGY, 17 (8). 699 - 708.


Mahajan, Anubha, Wessel, Jennifer, Willems, Sara M, Zhao, Wei, Robertson, Neil R, Chu, Audrey Y, Gan, Wei, Kitajima, Hidetoshi, Taliun, Daniel, Rayner, N William
et al (show 233 more authors) (2018) Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. NATURE GENETICS, 50 (4). 559 - 571+.


Tachmazidou, Ioanna, Suveges, Daniel, Min, Josine L, Ritchie, Graham RS, Steinberg, Julia, Walter, Klaudia, Iotchkova, Valentina, Schwartzentruber, Jeremy, Huang, Jie, Memari, Yasin
et al (show 98 more authors) (2017) Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. AMERICAN JOURNAL OF HUMAN GENETICS, 100 (6). 865 - 884.


Wuttke, Matthias, Li, Yong, Li, Man, Sieber, Karsten B, Feitosa, Mary F, Gorski, Mathias, Tin, Adrienne, Wang, Lihua, Chu, Audrey Y, Hoppmann, Anselm
et al (show 319 more authors) (2019) A catalog of genetic loci associated with kidney function from analyses of a million individuals. NATURE GENETICS, 51 (6). 957 - +.


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.

This list was generated on Thu Nov 26 12:54:31 2020 GMT.