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Number of items: 12.


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.


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-+.


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 276 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). pp. 691-706.


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-+.


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.


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 113 more authors) (2017) Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. JOURNAL OF CLINICAL INVESTIGATION, 127 (5). pp. 1798-1812.


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.


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.


Justice, Anne E, Karaderi, Tugce, Highland, Heather M, Young, Kristin L, Graff, Mariaelisa, Lu, Yingchang, Turcot, Valérie, Auer, Paul L, Fine, Rebecca S, Guo, Xiuqing
et al (show 279 more authors) (2019) Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Nature genetics, 51 (3). 452-+.


Linscheid, Nora, Logantha, Sunil Jit RJ, Poulsen, Camilla, Zhang, Shanzhuo, Schrolkamp, Maren, Egerod, Kristoffer Lihme, Thompson, Jonatan James, Kitmitto, Ashraf, Galli, Gina, Humphries, Martin J
et al (show 5 more authors) (2019) Quantitative proteomics and single-nucleus transcriptomics of the sinus node elucidates the foundation of cardiac pacemaking. Nature Communications, 10 (1). 2889-.


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 Sun Feb 11 14:30:22 2024 GMT.