The use of human genetics in drug target identification and validation by Bovijn, J

Genetic variants mimicking therapeutic inhibition of IL-6 receptor signaling and risk of COVID-19 by Bovijn, J, Lindgren, CM, Holmes, MV

Commentary: Mendelian randomization and women's health by Censin, JC, Bovijn, J, Holmes, MV, Lindgren, CM

Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins by Censin, JC, Bovijn, J, Holmes, MV, Lindgren, CM

Using human genetics to guide the repurposing of medicines by Bovijn, J, Censin, JC, Lindgren, CM, Holmes, MV

Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes by Akbari, P, Sosina, OA, Bovijn, J, Torres, J, Emberson, J, Collins, R, Rader, D

Causal relevance of obesity on the leading causes of death in women and men: A Mendelian randomization study by Censin, JC, Bovijn, J, Ferreira, T, Pulit, SL, Magi, R, Mahajan, A, Holmes, MV, Lindgren, CM

Causal relationships between obesity and the leading causes of death in women and men by Censin, JC, Peters, SAE, Bovijn, J, Ferreira, T, Pulit, SL, Mägi, R, Mahajan, A, Holmes, MV, Lindgren, CM

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics by Bovijn, J, Krebs, K, Chen, C-Y, Boxall, R, Censin, JC, Ferreira, T, Pulit, SL, Glastonbury, CA, Millwood, IY, Lin, K, Chen, Z, Walters, RG, Mägi, R, Neale, BM, Neale, BM, Lindgren, CM, Holmes, MV

Lifelong genetically lowered sclerostin and risk of cardiovascular disease by Bovijn, J, Krebs, K, Chen, C, Boxall, R, Censin, JC, Ferreira, T, Pulit, SL, Glastonbury, CA, Laber, S, Millwood, IY, Lin, K, Li, L, Chen, Z, Milani, L, Walters, RG, Magi, R, Neale, BM, Lindgren, CM, Holmes, MV

Response to comment on “Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics” by Bovijn, J, Krebs, K, Chen, C-Y, Boxall, R, Censin, JC, Ferreira, T, Pulit, SL, Glastonbury, CA, Laber, S, Millwood, IY, Lin, K, Li, L, Chen, Z, Milani, L, Smith, GD, Walters, RG, Mägi, R, Neale, BM, Lindgren, CM, Holmes, MV

GWAS identifies risk locus for erectile dysfunction and implicates hypothalamic neurobiology and diabetes in etiology by Bovijn, J, Jackson, L, Censin, J, Chen, CY, Laisk, T, Laber, S, Ferreira, T, Pulit, SL, Glastonbury, CA, Smoller, JW, Harrison, JW, Ruth, KS, Beaumont, RN, Jones, SE, Tyrrell, J, Wood, AR, Weedon, MN, Mägi, R, Neale, B, Lindgren, CM, Murray, A, Holmes, MV

Genome-wide study identifies association between HLA-B∗55:01 and self-reported penicillin allergy by Krebs, K, Bovijn, J, Zheng, N, Lepamets, M, Censin, JC, Jürgenson, T, Särg, D, Abner, E, Laisk, T, Luo, Y, Skotte, L, Geller, F, Feenstra, B, Wang, W, Auton, A, 23andMe Research Team, Raychaudhuri, S, Esko, T, Metspalu, A, Laur, S, Roden, DM, Wei, W-Q, Holmes, MV, Lindgren, CM, Phillips, EJ, Mägi, R, Milani, L, Fadista, J

A deep catalogue of protein-coding variation in 983,578 individuals by Sun, KY, Bai, X, Chen, S, Bao, S, Zhang, C, Kapoor, M, Backman, J, Joseph, T, Maxwell, E, Mitra, G, Gorovits, A, Mansfield, A, Boutkov, B, Gokhale, S, Habegger, L, Marcketta, A, Locke, AE, Ganel, L, Hawes, A, Kessler, MD, Sharma, D, Staples, J, Bovijn, J, Gelfman, S, Di Gioia, A, Rajagopal, VM, Lopez, A, Varela, JR, Alegre, J, Berumen, J, Tapia-Conyer, R, Kuri-Morales, P, Torres, J, Emberson, J, Collins, R, Regeneron Genetics Center, RGC-ME Cohort Partners, Cantor, M, Thornton, T, Kang, HM, Overton, JD, Shuldiner, AR, Cremona, ML, Nafde, M, Baras, A, Abecasis, G, Marchini, J, Reid, JG, Salerno, W, Balasubramanian, S