Selected Publications
Yang G, Alarcon C, Chanfreau C, Lee NH, Friedman P, Nutescu E, Tuck M, O'Brien T, Gong L, Klein TE, Chang KM, Tsao PS, Meltzer DO, Lynch JA; Million Veteran Program; Tuteja S, Perera MA.: Investigation of Genomic and Transcriptomic Risk Factors of Clopidogrel Response in African Americans Clin Pharmacol Ther : 2025.
Zhang X, Chang KM, Yu J, Loomba R.: Unraveling Mechanisms of Genetic Risks in Metabolic Dysfunction-Associated Steatotic Liver Diseases: A Pathway to Precision Medicine Annu Rev Pathol 20 (1): 375-403,2025.
SJ Jurgens, JT Rämö, DR Kramarenko, LFJM Wijdeveld, J Haas, MD Chaffin, S Garnier, L Gaziano, LC Weng, A Lipov, SL Zheng, Al Henry, JE Huffman, S Challa, F Rühle, CD Verdugo, CK Juárez, S Kany, CA van Orsouw, K Biddinger, E Poel, AL Elliott, X Wang, C Francis, R Ruan, S Koyama, L Beekman, DS Zimmerman, JF Deleuze, E Villard, DA Trégouët, R Isnard, FinnGen, VA Million Veteran Program, HERMES Consortium, DI Boomsma, EJC de Geus, R Tadros, YM Pinto, AAM Wilde, JJ Hottenga, J Sinisalo, T Niiranen, R Walsh, AF Schmidt, SH Choi, KM Chang, PS Tsao, PM Matthews, JS Ware, RT Lumbers, S van der Crabben, J Laukkanen, A Palotie, AS Amin, P Charron, B Meder, PT Ellinor, M Daly, KG Aragam, CR Bezzina: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience Nature Genetics 56 (12): 1-10,2024.
Yu YH, Pridgen KM, Nelson TJ, Miller DR, Wells JM, Assimes TL, O'Donnell CJ, Tsao PS, Chang KM, Lynch JA.: Oral Health, Inflammation, and Cardiometabolic Factors in the VA Million Veteran Program JDR Clin Trans Res : 2024.
Kaplan DE, Teerlink CC, Schwantes-An TH, Norden-Krichmar TM, DuVall SL, Morgan TR, Tsao PS, Voight BF, Lynch JA, Vujković M, Chang KM: Clinical and genetic risk factors for progressive fibrosis in metabolic dysfunction-associated steatotic liver disease Hepatol Commun : 2024.
Ghouse J, Sveinbjörnsson G, Vujkovic M, Seidelin AS, Gellert-Kristensen H, Ahlberg G, Tragante V, Rand SA, Brancale J, Vilarinho S, Lundegaard PR, Sørensen E, Erikstrup C, Bruun MT, Jensen BA, Brunak S, Banasik K, Ullum H; DBDS Genomic Consortium; Verweij N, Lotta L, Baras A; Regeneron Genetics Center; Mirshahi T, Carey DJ; Geisinger-Regeneron DiscovEHR Collaboration; VA Million Veteran Program; Kaplan DE, Lynch J, Morgan T, Schwantes-An TH, Dochtermann DR, Pyarajan S, Tsao PS; Estonian Biobank Research Team; Laisk T, Mägi R, Kozlitina J, Tybjærg-Hansen A, Jones D, Knowlton KU, Nadauld L, Ferkingstad E, Björnsson ES, Ulfarsson MO, Sturluson Á, Sulem P, Pedersen OB, Ostrowski SR, Gudbjartsson DF, Stefansson K, Olesen MS, Chang KM, Holm H, Bundgaard H, Stender S.: Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis Nat Genet : 2024.
Suzuki K, Hatzikotoulas K, Southam L, Taylor HJ, Yin X, Lorenz KM, Mandla R, Huerta-Chagoya A, Melloni GEM, Kanoni S, Rayner NW, Bocher O, Arruda AL, Sonehara K, Namba S, Lee SSK, Preuss MH, Petty LE, Schroeder P, Vanderwerff B, Kals M, Bragg F, Lin K, Guo X, Zhang W, Yao J, Kim YJ, Graff M, Takeuchi F, Nano J, Lamri A, Nakatochi M, Moon S, Scott RA, Cook JP, Lee JJ, Pan I, Taliun D, Parra EJ, Chai JF, Bielak LF, Tabara Y, Hai Y, Thorleifsson G, Grarup N, Sofer T, Wuttke M, Sarnowski C, Gieger C, Nousome D, Trompet S, Kwak SH, Long J, Sun M, Tong L, Chen WM, Nongmaithem SS, Noordam R, Lim VJY, Tam CHT, Joo YY, Chen CH, Raffield LM, Prins BP, Nicolas A, Yanek LR, Chen G, Brody JA, Kabagambe E, An P, Xiang AH, Choi HS, Cade BE, Tan J, Broadaway KA, Williamson A, Kamali Z, Cui J, Thangam M, Adair LS, Adeyemo A, Aguilar-Salinas CA, Ahluwalia TS, Anand SS, Bertoni A, Bork-Jensen J, Brandslund I, Buchanan TA, Burant CF, Butterworth AS, Canouil M, Chan JCN, Chang LC, Chee ML, Chen J, Chen SH, Chen YT, Chen Z, Chuang LM, Cushman M…….. Chang KM, MI McCarthy, JB Meigs, A Mahajan, CN Spracklen, JM Mercader, M Boehnke, JI Rotter, M Vujkovic, BF Voight, AP Morris and E Zeggini: Genetic drivers of heterogeneity in type 2 diabetes pathophysiology Nature : 2024.
Smith JL, Tcheandjieu C, Dikilitas O, Iyer K, Miyazawa K, Hilliard A, Lynch J, Rotter JI, Chen YI, Sheu WH, Chang KM, Kanoni S, Tsao P, Ito K, Kosel M, Clarke SL, Schaid DJ, Assimes TL, Kullo IJ.: Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization Circ Genom Precis Med : 2024.
Scorletti E, Saiman Y, Jeon S, Schneider CV, Buyco DG, Lin C, Himes BE, Mesaros CA, Vujkovic M, Creasy KT, Furth EE, Billheimer JT, Hand NJ, Kaplan DE, Chang KM, Tsao PS, Lynch JA, Dempsey JL, Harkin J, Bayen S, Conlon D, Guerraty M, Phillips MC, Rader DJ, Carr RM.: A missense variant in human perilipin 2 (PLIN2 Ser251Pro) reduces hepatic steatosis in mice JHEP Rep 6 : 100902,2023.
Manning A, Sevilla-González M, Smith K, Wang N, Jensen A, Litkowski E, Kim H, DiCorpo D, Westerman K, Cui J, Liu CT, Yu C, McNeil J, Lacaze P, Chang KM, Tsao P, Phillips L, Goodarzi M, Sladek R, Rotter J, Dupuis J, Florez J, Merino J, Meigs J, Zhou J, Raghavan S, Udler M.: Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin Res Sq 19 : rs.3.rs-3317661,2023.
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Academic Contact Information
Corporal Michael J. Crescenz VAMC &
University of Pennsylvania Perelman School of Medicine
3900 Woodland Avenue
Philadelphia,
PA
19104
Phone: 215-823-5893