Zurück zum Zitat G.M. Peloso, P.L. Auer, J.C. Bis, A. Voorman, A.C. Morrison, N.O. Stitziel, J.A. Brody, S.A. Khetarpal, J.R. Crosby, M. Fornage, A. Isaacs, J. Jakobsdottir, M.F. Feitosa, G. Davies, J.E. Huffman, A. Manichaikul, B. Davis, K. Lohman, A.Y. Joon, A.V. Smith, M.L. Grove, P. Zanoni, V. Redon, S. Demissie, K. Lawson, U. Peters, C. Carlson, R.D. Jackson, K.K. Ryckman, R.H. Mackey, J.G. Robinson, D.S. Siscovick, P.J. Schreiner, J.C. Mychaleckyj, J.S. Pankow, A. Hofman, A.G. Uitterlinden, T.B. Harris, K.D. Taylor, J.M. Stafford, L.M. Reynolds, R.E. Marioni, A. Dehghan, O.H. Franco, A.P. Patel, Y. Lu, G. Hindy, O. Gottesman, E.P. Bottinger, O. Melander, M. Orho-Melander, R.J.F. Loos, S. Duga, P.A. Merlini, M. Farrall, A. Goel, R. Asselta, D. Girelli, N. Martinelli, S.H. Shah, W.E. Kraus, M. Li, D.J. Rader, M.P. Reilly, R. McPherson, H. Watkins, D. Ardissino, NHLBI GO Exome Sequencing Project, Q. Zhang, J. Wang, M.Y. Tsai, H.A. Taylor, A. Correa, M.E. Griswold, L.A. Lange, J.M. Starr, I. Rudan, G. Eiriksdottir, L.J. Launer, J.M. Ordovas, D. Levy, Y.D.I. Chen, A.P. Reiner, C. Hayward, O. Polasek, I.J. Deary, I.B. Borecki, Y. Liu, V. Gudnason, J.G. Wilson, C.M. van Duijn, C. Kooperberg, S.S. Rich, B.M. Psaty, J.I. Rotter, C.J. O’Donnell, K. Rice, E. Boerwinkle, S. Kathiresan, L.A. Cupples, Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. Am. J. Hum. Genet. 94, 223–232 (2014)CrossRefPubMedPubMedCentral
G.M. Peloso, P.L. Auer, J.C. Bis, A. Voorman, A.C. Morrison, N.O. Stitziel, J.A. Brody, S.A. Khetarpal, J.R. Crosby, M. Fornage, A. Isaacs, J. Jakobsdottir, M.F. Feitosa, G. Davies, J.E. Huffman, A. Manichaikul, B. Davis, K. Lohman, A.Y. Joon, A.V. Smith, M.L. Grove, P. Zanoni, V. Redon, S. Demissie, K. Lawson, U. Peters, C. Carlson, R.D. Jackson, K.K. Ryckman, R.H. Mackey, J.G. Robinson, D.S. Siscovick, P.J. Schreiner, J.C. Mychaleckyj, J.S. Pankow, A. Hofman, A.G. Uitterlinden, T.B. Harris, K.D. Taylor, J.M. Stafford, L.M. Reynolds, R.E. Marioni, A. Dehghan, O.H. Franco, A.P. Patel, Y. Lu, G. Hindy, O. Gottesman, E.P. Bottinger, O. Melander, M. Orho-Melander, R.J.F. Loos, S. Duga, P.A. Merlini, M. Farrall, A. Goel, R. Asselta, D. Girelli, N. Martinelli, S.H. Shah, W.E. Kraus, M. Li, D.J. Rader, M.P. Reilly, R. McPherson, H. Watkins, D. Ardissino, NHLBI GO Exome Sequencing Project, Q. Zhang, J. Wang, M.Y. Tsai, H.A. Taylor, A. Correa, M.E. Griswold, L.A. Lange, J.M. Starr, I. Rudan, G. Eiriksdottir, L.J. Launer, J.M. Ordovas, D. Levy, Y.D.I. Chen, A.P. Reiner, C. Hayward, O. Polasek, I.J. Deary, I.B. Borecki, Y. Liu, V. Gudnason, J.G. Wilson, C.M. van Duijn, C. Kooperberg, S.S. Rich, B.M. Psaty, J.I. Rotter, C.J. O’Donnell, K. Rice, E. Boerwinkle, S. Kathiresan, L.A. Cupples, Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. Am. J. Hum. Genet.
94, 223–232 (2014)
CrossRefPubMedPubMedCentral