Kyong-Mi Chang, MD

Cindi Z, Cardone KM, Bradford Y, Hall MA, Kim H, Daar ES, Gulick R, Riddler SA, Vujkovic M, Chang KM, Tsao PS, Sinxadi P, Haas DW, Ritchie MD; VA Million Veteran Program. Polygenic risk score and risk of drug-induced liver injury after initiating antiretroviral therapy in people living with HIV , Pharmacogenomics: 2026

Alkhairo H, Koyama S, Iyer K, Hilliard AT, Kho PF, Clarke S, Abdulwahab FM, Assimes TL, Lynch JA, Ramsay M; Human Heredity and Health in Africa (H3Africa); VA Million Veteran Program (MVP); Chang KM, Tsao PS, Alkuraya FS, Ito K, Risch N, Tcheandjieu C. Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in Africans , Am J Hum Genet: 2026

Zhou JJ, Jensen A, Samuels DC, Markianos K, Zhou H, Zhang H, Vujkovic M, Lynch JA, Dinatale T, Joseph J, Liu C, Hung A, Sun YV, Pyarajan S, Tsao PS, Chang KM, Hulgan T, Reaven P; VA Million Veteran Program. A large-scale multi-ancestry mitochondrial variant association analysis for cardiometabolic traits , Nat Commun: 2026

Koyama S, Yu Z, Choi SH, Jurgens SJ, Selvaraj MS, Klarin D, Huffman JE, Clarke SL, Zhang SK, Trinh MN, Ravi A, Dron JS, Spinks C, Surakka I, Bhatnagar A, Lannery K, Hornsby W, Damrauer SM, Chang KM, Lynch JA, Assimes TL, Tsao PS, Rader DJ, Cho K, Peloso GM, Ellinor PT, Sun YV, Wilson PWF, VA Million Veteran Program, Natarajan P Exome-wide association study of blood lipids in 1,158,017 individuals from diverse populations , Nature Genetics, 58(6): 2026

Sinnott-Armstrong N, Strausz S, Urpa L, Abner E, Johnson JP, Valliere J, Palumaa T, FinnGen, Estonian Biobank Research Team, VA Million Veteran Program, Palta P, Dashti HS, Chang KM, Vujkovic M, Daly M, Pritchard JK, Saxena R, Jones SE, Ollila HM Genetic variants affect diurnal glucose levels throughout the day , Nature Communications, 17(1): 2026

Wendland ZD, Teerlink CC, Pridgen KM, Lo S, Sayed C, van Straalen KR, Tcheandjieu C, Tsao PS, Chang KM, Li Y, Mohlke KL, Sun Q, Lynch JA, Goldfarb N. A genome-wide association study of hidradenitis suppurativa from the VA's Million Veteran Program , Dermatology: 2026

Bermudez F, Shakt G, Bowles A, Alba P, Dinatale T, Chang KM, Tsao PS, Lynch J, Dochtermann D, Pyarajan S, Small A, Levin MG, Damrauer SM. Multipopulation Genome-Wide Association Study Identifies Novel Loci for Bicuspid Aortic Valve and Reveals Shared Genetic Architecture With Aortopathies , Circ Genom Precis Med: 2026

Sideris K, Nelson TJ, Brinker L, Gao A, Tcheandjieu C, Kyriakopoulos CP, Berlowitz D, Hull L, Ferraro JP, Agiri FY, Pridgen KM, Roblin S, Joseph J, Damrauer SM, Chang KM, Teerlink CC, Stehlik J, Carter S, Lynch JA. Systemic Manifestations and Mortality Risk in Transthyretin V142I Variant Carriers: A Million Veteran Program Analysis , JACC CardioOncol: 2026

Mureddu M, Pelusi S, Jamialahmadi O, Vujkovic M, Miano L, Eidgah Torghabehei H, Ronzoni L, Malvestiti F, Saracino M, Periti G, Moretti V, Teerlink CC, Lynch JA, Tsao PS, Johnson JP, La Mura V, Dilena R, Alqahtani SA, Cherubini A, Russo FP, D'Ambrosio R, Fraquelli M, Petta S, Miele L, Vespasiani-Gentilucci U, Bugianesi E, Mancina RM, Parini P, Prati D, Chang KM, Schneider CV, Romeo S, Valenti LV. Carriage of rare APOB variants predisposes to severe steatotic liver disease and hepatocellular carcinoma , J Clin Invest: 2026

Sideris K, Nelson TJ, Brinker L, Gao A, Tcheandjieu C, Kyriakopoulos CP, Berlowitz D, Hull L, Ferraro JP, Agiri FY, Pridgen KM, Roblin S, Joseph J, Levin MG, Damrauer SM, Chang KM, Teerlink CC, Stehlik J, Carter S, Lynch JA. Risk of Systemic Manifestations in Homozygous Carriers of the Transthyretin V142I Variant: A Million Veteran Program Analysis , J Am Heart Assoc, 14: 2025,e044923