CPT1A methylation is associated with plasma adiponectin von Aslibekyan, S, Do, A.N, Xu, H, Li, S, Irvin, M.R, Zhi, D, Tiwari, H.K, Absher, D.M, Shuldiner, A.R, Zhang, T, Chen, W, Tanner, K, Hong, C, Mitchell, B.D, Berenson, G, Arnett, D.K

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Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network von Aslibekyan, S, An, P, Frazier-Wood, A.C, Kabagambe, E.K, Irvin, M.R, Straka, R.J, Tiwari, H.K, Tsai, M.Y, Hopkins, P.N, Borecki, I.B, Ordovas, J.M, Arnett, D.K

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Genetic risk factors for type 2 diabetes with pharmacologic intervention in African-American patients with schizophrenia or schizoaffective disorder von Irvin, M.R, Wiener, H.W, Perry, R.P, Savage, R.M, Go, R.C.P

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Hemostasis biomarkers and risk of sepsis: the REGARDS cohort von Moore, J.X., Zakai, N.A., Mahalingam, M., Griffin, R.L., Irvin, M.R., Safford, M.M., Baddley, J.W., Wang, H.E.

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The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study von Do, A N, Lynch, A I, Claas, S A, Boerwinkle, E, Davis, B R, Ford, C E, Eckfeldt, J H, Tiwari, H K, Arnett, D K, Irvin, M R

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RYR3 gene polymorphisms and cardiovascular disease outcomes in the context of antihypertensive treatment von Lynch, A I, Irvin, M R, Boerwinkle, E, Davis, B R, Vaughan, L K, Ford, C E, Aissani, B, Eckfeldt, J H, Arnett, D K, Shrestha, S

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Supplementary Material for: APOL1 Risk Variants Associated with Serum Albumin in a Population-Based Cohort Study von N.S., Chaudhary, H.K., Tiwari, B.A., Hidalgo, N.A., Limdi, R.J., Reynolds, M., Cushman, N.A., Zakai, L., Lange, S.E., Judd, C.A., Winkler, J.B., Kopp, O.M., Gutiérrez, M.R., Irvin

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DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation von Richard, M.A., Huan, T.X., Ligthart, S., Gondalia, R., Jhun, M.A., Brody, J.A., Irvin, M.R., Marioni, R., Shen, J.C., Tsai, P.C., Montasser, M.E., Jia, Y.C., Syme, C., Salfati, E.L., Boerwinkle, E., Guan, W.H., Mosley, T.H., Bressler, J., Morrison, A.C., Liu, C.Y., Mendelson, M.M., Uitterlinden, A.G., Meurs, J.B. van, Franco, O.H., Zhang, G.S., Li, Y., Stewart, J.D., Bis, J.C., Psaty, B.M., Chen, Y.D.I., Kardia, S.L.R., Zhao, W., Turner, S.T., Absher, D., Aslibekyan, S., Starr, J.M., Mcrae, A.F., Hou, L.F., Just, A.C., Schwartz, J.D., Vokonas, P.S., Menni, C., Spector, T.D., Shuldiner, A., Damcott, C.M., Rotter, J.I., Palmas, W., Liu, Y.M., Paus, T., Horvath, S., O'Connell, J.R., Guo, X.Q., Pausova, Z., Assimes, T.L., Sotoodehnia, N., Smith, J.A., Arnett, D.K., Deary, I.J., Baccarelli, A.A., Bell, J.T., Whitsel, E., Dehghan, A., Levy, D., Fornage, M.

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes von Chauhan, G., Traylor, M., Sargurupremraj, M., Okada, Y., Rutten-Jacobs, L., Laan, S.W. van der, Anderson, C.D., Chong, M., Adams, H.H.H., Ago, T., Amouyel, P., Ay, H., Boncoraglio, G.B., Brown, R.D., Carrera, C., Carty, C.L., Chasman, D.I., Chen, W.M., Cole, J.W., Danesh, J., Duan, Q., Engelter, S.T., Gudnason, V., Gustafsson, S., Haessler, J., Havulinna, A.S., Howard, G., Hyacinth, H.I., Ikram, M.A., Jian, X.Q., Johnson, J.A., Kanai, M., Keene, K.L., Kissela, B.M., Kleindorfer, D.O., Kooperberg, C., Kubo, M., Lange, L.A., Launer, L.J., Leys, D., Lindgren, A.G., Lorentzen, E., Magnusson, P.K., Maguire, J., Meschia, J.F., Mosley, T.H., Nalls, M.A., Ninomiya, T., O'Donnell, M.J., Pulit, S.L., Rannikmae, K., Rexrode, K.M., Ridker, P.M., Rost, N.S., Rundek, T., Sacco, R.L., Sakaue, S., Sale, M.M., Schmidt, R., Schminke, U., Slowik, A., Sudlow, C.L.M., Tanislav, C., Thorsteinsdottir, U., Tzourio, C., Duijn, C.M. van, Walters, M., Wareham, N.J., Wiggins, K.L., Yang, Q., Yusuf, S., Ruusalepp, A., Schadt, E.E., Koplev, S., Smith, N.L., Lubitz, S.A., Ellinor, P.T., Tai, E.S., He, J., Harst, P. van der, Elliott, P., Chambers, J.C., Takeuchi, F., Sanghera, D.K., Jern, C., Strbian, D., Longstreth, W.T., Hata, J., Woo, D., Rosand, J., Pare, G., Hopewell, J.C., Saleheen, D., Stefansson, K., Kittner, S.J., Fornage, M., Markus, H.S., Howson, J.M.M., Kamatani, Y., Dichgans, M.

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RYR3 gene polymorphisms and cardiovascular disease outcomes in the context of antihypertensive treatment von Lynch, A.I, Irvin, M.R, Boerwinkle, E, Davis, B.R, Vaughan, L.K, Ford, C.E, Aissani, B, Eckfeldt, J.H, Arnett, D.K, Shrestha, S

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Evaluating the Need and Potential Benefits of Testing for Plasma Homocyst(e)ine, an Independent Risk Factor for Atherosclerotic Disease von Irvin‐Jones, Andrea, Barton Duell, P., Malinow, M.R.

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