Factors Influencing Treatment Adherence Among Drug-Sensitive Tuberculosis (DS-TB) Patients in Armenia: A Qualitative Study by Grigoryan Z, McPherson R, Harutyunyan T, Truzyan N, Sahakyan S

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Managing uncertainty : administrative theory and practice in education / by 298630 McPherson, R. Bruce, Crowson, Robert L., Pitner, Nancy J.

An unbalanced maternal diet in pregnancy associates with offspring epigenetic changes in genes controlling glucocorticoid action and foetal growth. by Drake, A, McPherson, R, Godfrey, K, Cooper, C, Lillycrop, K, Hanson, M, Meehan, R, Seckl, JR, Reynolds, R

ENPP1 processes protein ADP-ribosylation in vitro. by Palazzo, L, Daniels, C, Nettleship, J, Rahman, N, McPherson, R, Ong, S, Kato, K, Nureki, O, Leung, A, Ahel, I

Meta-analysis of gene-level tests for rare variant association. by Liu, D, Peloso, G, Zhan, X, Holmen, O, Zawistowski, M, Feng, S, Nikpay, M, Auer, P, Goel, A, Zhang, H, Peters, U, Farrall, M, Orho-Melander, M, Kooperberg, C, McPherson, R, Watkins, H, Willer, C, Hveem, K, Melander, O, Kathiresan, S, Abecasis, G

Evidence for a shared genetic determination of Ischemic Stroke And Coronary Artery Disease - a genome-wide analysis by Dichgans, M, Malik, R, Koenig, I, Rosand, J, Clarke, R, Gretarsdottir, S, Mitchell, B, Erdmann, J, Kathiresan, S, McPherson, R, Sudlow, C, Reilly, M, Thompson, JR, Sharma, P, Chambers, J, Watkins, H, Rothwell, P, Roberts, R, Markus, H, Samani, N, Farrall, M, Schunkert, H

Communications Biophysics by Poussart, D. J. M., Demko, P., Jr., Weiss, Thomas F., Zimmerman, R. R., Mulroy, M. J., Goldmark, G. M., Altmann, D. W., Brown, Robert M., Durlach, Nathaniel I., Domnitz, Robert H., Hild, J. D., Mpagazehe, C., Grundfest, S. F., Yu, J., Ladd, G. R., McPherson, R. A.

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DNA sequence variation in ACVR1C encoding the activin receptor-like kinase 7 influences body fat distribution and protects against type 2 diabetes by Emdin, C, Khera, A, Aragam, K, Haas, M, Chaffin, M, Klarin, D, Natarajan, P, Bick, A, Zekavat, S, Nomura, A, Ardissino, D, Wilson, J, Schunkert, H, McPherson, R, Watkins, H, Elosua, R, Bown, M, Samani, N, Baber, U, Erdmann, J, Gupta, N, Danesh, J, Saleheen, D, Gabriel, S, Kathiresan, S

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. by Dichgans, M, Malik, R, König, I, Rosand, J, Clarke, R, Gretarsdottir, S, Thorleifsson, G, Mitchell, B, Assimes, T, Levi, C, O'Donnell, C, Fornage, M, Thorsteinsdottir, U, Psaty, B, Hengstenberg, C, Seshadri, S, Erdmann, J, Bis, J, Peters, A, Boncoraglio, G, März, W, Meschia, J, Kathiresan, S, Ikram, M, McPherson, R

Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia. by Stitziel, N, Fouchier, S, Sjouke, B, Peloso, G, Moscoso, A, Auer, P, Goel, A, Gigante, B, Barnes, T, Melander, O, Orho-Melander, M, Duga, S, Sivapalaratnam, S, Nikpay, M, Martinelli, N, Girelli, D, Jackson, R, Kooperberg, C, Lange, L, Ardissino, D, McPherson, R, Farrall, M, Watkins, H, Reilly, M, Rader, D

Heterozygous ABCG5 gene deficiency and risk of coronary artery disease by Nomura, A, Emdin, CA, Won, HH, Peloso, GM, Natarajan, P, Ardissino, D, Danesh, J, Schunkert, H, Correa, A, Bown, MJ, Samani, NJ, Erdmann, J, McPherson, R, Watkins, H, Saleheen, D, Elosua, R, Kawashiri, M-A, Tada, H, Gupta, N, Shah, SH, Rader, DJ, Gabriel, S, Khera, AV, Kathiresan, S

Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia by Stitziel, N, Fouchier, S, Sjouke, B, Peloso, G, Moscoso, A, Auer, P, Goel, A, Gigante, B, Barnes, T, Melander, O, Orho-Melander, M, Duga, S, Sivapalaratnam, S, Nikpay, M, Martinelli, N, Girelli, D, Jackson, R, Kooperberg, C, Lange, L, Ardissino, D, McPherson, R, Farrall, M, Watkins, H, Reilly, M, Rader, D

Meta-analysis and imputation refines the association of 15q25 with smoking quantity. by Liu, J, Tozzi, F, Waterworth, D, Pillai, S, Muglia, P, Middleton, L, Berrettini, W, Knouff, C, Yuan, X, Waeber, G, Vollenweider, P, Preisig, M, Wareham, N, Zhao, J, Loos, R, Barroso, I, Khaw, K, Grundy, S, Barter, P, Mahley, R, Kesaniemi, A, McPherson, R, Vincent, J, Strauss, J, Kennedy, J

Phenotypic consequences of a genetic predisposition to enhanced nitric oxide signaling by Emdin, C, Khera, A, Klarin, D, Natarajan, P, Zekavat, S, Nomura, A, Haas, M, Aragam, K, Ardissino, D, Wilson, J, Schunkert, H, McPherson, R, Watkins, H, Elosua, R, Bown, M, Samani, N, Baber, U, Erdmann, J, Gormley, P, Palotie, A, Stitziel, N, Gupta, N, Danesh, J, Saleheen, D, Gabriel, S, Kathiresan, S

Rare protein-truncating variants in APOB, lower low-density lipoprotein cholesterol, and protection against coronary heart disease by Peloso, G, Nomura, A, Khera, A, Chaffin, M, Won, H, Ardissino, D, Danesh, J, Schunkert, H, Wilson, J, Samani, N, Erdmann, J, McPherson, R, Watkins, H, Saleheen, D, McCarthy, S, Teslovich, T, Leader, J, Kirchner, H, Marrugat, J, Nohara, A, Kawashiri, M, Tada, H, Dewey, F, Carey, D, Baras, A, Kathiresan, S

Effects of n-3 fatty acid supplements in diabetes mellitus by Ascend Study Collaborative Group, Bowman, L, Mafham, M, Wallendszus, K, Stevens, W, Buck, G, Barton, J, Murphy, K, Aung, T, Haynes, R, Cox, J, Murawska, A, Young, A, Lay, M, Chen, F, Sammons, E, Waters, E, Adler, A, Bodansky, J, Farmer, A, McPherson, R, Neil, A, Simpson, D, Peto, R, Baigent, C, Collins, R, Parish, S, Armitage, J

Phenotypic characterization of genetically lowered human lipoprotein(a) levels by Emdin, C, Khera, A, Natarajan, P, Klarin, D, Won, H, Peloso, G, Stitziel, N, Nomura, A, Zekavat, S, Bick, A, Gupta, N, Asselta, R, Duga, S, Merlini, P, Correa, A, Kessler, T, Wilson, J, Bown, M, Hall, A, Braund, P, Samani, N, Schunkert, H, Marrugat, J, Elosua, R, McPherson, R, Farrall, M, Watkins, H, Willer, C, Abecasis, G, Felix, J, Vasan, R, Lander, E, Rader, D, Danesh, J, Ardissino, D, Gabriel, S, Saleheen, D, Kathiresan, S, CHARGE–Heart Failure Consortium, CARDIoGRAM Exome Consortium

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease by Emdin, C, Khera, A, Chaffin, M, Klarin, D, Natarajan, P, Aragam, K, Haas, M, Bick, A, Zekavat, S, Nomura, A, Ardissino, D, Wilson, J, Schunkert, H, McPherson, R, Watkins, H, Elosua, R, Bown, M, Samani, N, Baber, U, Erdmann, J, Gupta, N, Danesh, J, Chasman, D, Ridker, P, Denny, J, Bastarache, L, Lichtman, J, D'Onofrio, G, Mattera, J, Spertus, J, Sheu, W, Taylor, K, Psaty, B, Rich, S, Post, W, Rotter, J, Chen, Y, Krumholz, H, Saleheen, D, Gabriel, S, Kathiresan, S

Distribution and medical impact of loss-of-function variants in the Finnish founder population by Lim, E, Würtz, P, Havulinna, A, Palta, P, Tukiainen, T, Rehnström, K, Esko, T, Mägi, R, Inouye, M, Lappalainen, T, Chan, Y, Salem, R, Lek, M, Flannick, J, Sim, X, Manning, A, Ladenvall, C, Bumpstead, S, Hämäläinen, E, Aalto, K, Maksimow, M, Salmi, M, Blankenberg, S, Ardissino, D, Shah, S, Horne, B, McPherson, R, Hovingh, G, Reilly, M, Watkins, H, Goel, A, Farrall, M, Girelli, D, Reiner, A, Stitziel, N, Kathiresan, S, Gabriel, S, Barrett, J, Lehtimäki, T, Laakso, M, Groop, L, Kaprio, J, Perola, M, McCarthy, M, Boehnke, M, Altshuler, D, Lindgren, C, Hirschhorn, J, Metspalu, A, Freimer, N, Zeller, T, Jalkanen, S, Koskinen, S, Raitakari, O, Durbin, R, Macarthur, D, Salomaa, V, Ripatti, S, Daly, M, Palotie, A

Association analyses based on false discovery rate implicate new loci for coronary artery disease by Nelson, CP, Goel, A, Butterworth, AS, Kanoni, S, Webb, TR, Marouli, E, Zeng, L, Ntalla, I, Lai, FY, Hopewell, JC, Giannakopoulou, O, Jiang, T, Hamby, SE, Di Angelantonio, E, Assimes, TL, Bottinger, EP, Chambers, JC, Clarke, R, Palmer, CNA, Cubbon, RM, Ellinor, P, Ermel, R, Evangelou, E, Franks, PW, Grace, C, Gu, D, Hingorani, AD, Howson, JMM, Ingelsson, E, Kastrati, A, Kessler, T, Kyriakou, T, Lehtimäki, T, Lu, X, Lu, Y, März, W, McPherson, R, Metspalu, A, Pujades-Rodriguez, M, Ruusalepp, A, Schadt, EE, Schmidt, AF, Sweeting, MJ, Zalloua, PA, AlGhalayini, K, Keavney, BD, Kooner, JS, Loos, RJF, Patel, RS, Rutter, MK, Tomaszewski, M, Tzoulaki, I, Zeggini, E, Erdmann, J, Dedoussis, G, Björkegren, JLM, EPIC-CVD Consortium, CARDIoGRAMplusC4D, UK Biobank CardioMetabolic Consortium CHD working group, Schunkert, H, Farrall, M, Danesh, J, Samani, NJ, Watkins, H, Deloukas, P