Dan Chasman

Biography

Publications

• Genetic Insights Into Protective Effects of GLP-1 Receptor Agonists on Stroke and Alzheimer Disease Across Ancestries.

  Caro-Châtelier I, Sargurupremraj M, Yang C, Akinleye C, Trégouët DA, Akinyemi RO, Shigemizu D, Coker M, Akinyemi JO, Tiwari HK, Chasman DI, Ovbiagele B, Chabriat H, Mooser V, Couffinhal T, Mishra A, Cruchaga C, Reitz C, Kunkle B, Kamatani Y, Owolabi MO, Mohammedi K, Debette S. Neurol Genet 2026

  PMID: 42812740

• Genetic associations with pulmonary embolism among those with a deep vein thrombosis: the International Network Against Venous Thrombosis Consortium.

  Lozano-Esparza S, Shakt GE, Brody JA, Martinez-Perez A, Conomos MP, Germain M, Clapham KR, Teder-Laving M, van Hylckama Vlieg A, Kauko A, Thibord F, Bezerra OCL, Nadkarni GN, Munsch G, Nøst TH, Goode EL, Ji Y, Chasman DI, Reiner AP, Turman C, Wiggins KL, Sitlani CM, Souto JC, Lutsey PL, Bellomo T, Biobank E, Program MV, Li-Gao R, Winstén AK, Chen MH, Do R, Gourhant L, Hveem K, Armasu SM, Saut N, Pankratz N, Giulianini F, Haessler J, Song M, Olaso R, Boerwinkle E, Dochtermann D, Soria JM, Rich SS, Smadja D, Koyama S, Rosendaal FR, Niiranen T, Gagnon F, Vy HMT, Zakai N, Lemarie C, Skogholt AH, Deleuze JF, Pankow JS, Ridker PM, Liu Y, Rice KM, Pyarajan S, Cushman M, Emmerich J, Psaty BM, Natarajan P, Johnson AD, Rodger MA, Suchon P, Couturaud F, Morange PE, Tang W, Kooperberg C, Kabrhel C, Sabater-Lleal M, Trégouët DA, Wolberg AS, Damrauer SM, Smith NL. J Thromb Haemost 2026 Jul 27

  PMID: 42508647

• Co-occurring clonal hematopoiesis exhibits strong selection and high leukemia risk.

  Barnao KM, Hubbard AK, Chan ICC, Zhou W, Jakubek YA, Genovese G, Wong WSW, Kelly RL, Young CD, Brown DW, Huang WY, Freedman ND, Jones K, Hutchinson A, Hicks B, Tran D, Arnett D, Barnes KC, Bis JC, Boerwinkle E, Brody JA, Carson AP, Chasman DI, Cho MH, Desai P, Doyle MF, Fornage M, Guo X, Heard-Costa N, Irvin MR, Johnson AD, Kardia SLR, Kooperberg C, Levy D, Lewis JP, Li Y, Loos RJF, Mack TM, Mathias RA, Mitchell BD, North KE, Pankratz N, Peyser PA, Preuss MH, Psaty BM, Raffield LM, Redline S, Rich SS, Rotter JI, Silverman EK, Smith AV, Smith JA, Stilp A, Cao Y, Scheet P, Reiner AP, Bick AG, Chanock SJ, Auer PL, Bolton KL, Machiela MJ. Nat Commun 2026 May 21

  PMID: 42168198

• Rare coding variant architecture and gene discovery from 130,000 sequenced cases of atrial fibrillation.

  Jurgens SJ, Enzan N, Dinsmore IR, Choi SH, Luo J, Lipov A, Hartle C, Wang X, Marston NA, Weng LC, Melloni GE, Chalazan B, Gray MP, Pirruccello JP, Diaz A, Chaffin MD, Ornelas-Loredo A, Tang O, Darbar FA, Kany S, Chen Y, von Falkenhausen AS, Morrison AC, Natale A, Tveit A, Geelhoed B, Cade B, Van Wagoner DR, Haase D, Soliman EZ, Davogustto GE, Calkins H, Anderson JL, Brody JA, Barnard J, Hokanson JE, Smith JD, Bis JC, Young K, Johnson LS, Long L, Risch L, Gula LJ, Kwee LC, Kühne M, Preuss M, Gupta N, Nafissi NA, Smith NL, Nilsson PM, van der Harst P, Wells QS, Judy RL, Schnabel RB, Johnson R, Smit RA, Gabriel S, Knight S, Furukawa T, Min YI, Yoneda ZT, Laksman ZW, Alonso A, Psaty BM, Albert CM, Arking DE, Roden DM, Chasman DI, Rader DJ, Conen D, McManus DD, Fatkin D, Boerwinkle E, Marcus GM, Christophersen IE, Smith JG, Roberts JD, Raffield LM, Shoemaker MB, Cho MH, Cutler MJ, Chung MK, Olesen MS, Sinner MF, Sotoodehnia N, Kirchhof P, Loos RJ, Nazarian S, Mohanty S, Damrauer SM, Kaab S, Heckbert SR, Redline S, Shah SH, Tanaka T, Ebana Y, Lubitz SA, Lunetta KL, Benjamin EJ, Rienstra M, Figtree GA, Darbar D, Bezzina CR, Ruff CT, Sabatine MS, Mirshahi T, Ellinor PT. Res Sq 2026 May 04

  PMID: 42147184

• Genomic analyses implicate hormonal and metabolic dysregulation in polycystic ovary syndrome.

  Moolhuijsen LME, Zhu J, Mullin BH, Pujol-Gualdo N, Actkins KV, Mack JA, Rao H, Trivedi B, Kentistou KA, Zhao Y, Westergaard D, Tyrmi JS, Thorleifsson G, Zhang Y, Wittemans L, DeVries A, Brewer K, Sisk R, Danning R, Preuss MH, Jones MR, Ruth KS, Andersen M, Azziz R, Banasik K, Boehnke M, Broer L, Brunak S, Chan YM, Chasman DI, Daly M, Ehrmann DA, Fauser BC, Fritsche LG, Hayes MG, He C, Huang H, Kowalska I, Kraft P, Legro RS, Lin N, Loos RJ, Louwers YV, Magi R, McCarthy MI, Morin-Papunen L, Morrison JV, Morton C, Nadkarni GN, Neale BM, Nielsen HS, Nyegaard M, Ostrowski SR, Pedersen OBV, Sørensen E, Mikkelsen C, Erikstrup C, Kaspersen KA, Bruun MT, Aagaard B, Ullum H, Obermayer-Pietsch B, Palotie A, Reeve MP, Salumets A, Saxena R, Spector TD, Stuckey BGA, Thorsteinsdottir U, Uitterlinden AG, Urbanek M, Zöllner S, van Heel DA, Hirschhorn JN, Stefansson K, Perry JRB, Styrkarsdottir U, Wilson SG, Piltonen T, Laisk T, Jarvelin MR, Burns K, Justice AE, Laivuori H, Ong KK, Goodarzi MO, Davis LK, Dunaif A, Lindgren CM, Laven JSE, Franks S, Visser JA, Welt CK, Karaderi T, Day FR. Nat Genet 2026

  PMID: 42026183