The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.
Frontiers In Pharmacology
Trompet, Stella S; Postmus, Iris I; Warren, Helen R HR; Noordam, Raymond R; Smit, Roelof A J RAJ; Theusch, Elizabeth E; Li, Xiaohui X; Arsenault, Benoit B; Chasman, Daniel I DI; Hitman, Graham A GA; Munroe, Patricia B PB; Rotter, Jerome I JI; Psaty, Bruce M BM; Caulfield, Mark J MJ; Krauss, Ron M RM; Cupples, Adrienne L AL; Jukema, Wouter J WJ
Coronary Heart Disease in Type 2 Diabetes Mellitus: Genetic Factors and Their Mechanisms, Gene-Gene, and Gene-Environment Interactions in the Asian Populations.
International Journal Of Environmental Research And Public Health
Zarkasi, Khairul Anwar KA; Abdul Murad, Nor Azian NA; Ahmad, Norfazilah N; Jamal, Rahman R; Abdullah, Noraidatulakma N
Coronary Heart Disease in Type 2 Diabetes Mellitus: Genetic Factors and Their Mechanisms, Gene-Gene, and Gene-Environment Interactions in the Asian Populations.
International Journal Of Environmental Research And Public Health
Zarkasi, Khairul Anwar KA; Abdul Murad, Nor Azian NA; Ahmad, Norfazilah N; Jamal, Rahman R; Abdullah, Noraidatulakma N
Cardiovascular risk factor mediation of the effects of education and Genetic Risk Score on cardiovascular disease: a prospective observational cohort study of the Framingham Heart Study.
Bmj Open
Powell, Katie L KL; Stephens, Sebastien R SR; Stephens, Alexandre S AS
Glucose-dependent insulinotropic peptide and risk of cardiovascular events and mortality: a prospective study.
Diabetologia
Jujić, Amra A; Atabaki-Pasdar, Naeimeh N; Nilsson, Peter M PM; Almgren, Peter P; Hakaste, Liisa L; Tuomi, Tiinamaija T; Berglund, Lisa M LM; Franks, Paul W PW; Holst, Jens J JJ; Prasad, Rashmi B RB; Torekov, Signe S SS; Ravassa, Susana S; Díez, Javier J; Persson, Margaretha M; Melander, Olle O; Gomez, Maria F MF; Groop, Leif L; Ahlqvist, Emma E; Magnusson, Martin M
Genetic Variability of the Glucose-Dependent Insulinotropic Peptide Gene Is Involved in the Premature Coronary Artery Disease in a Chinese Population with Type 2 Diabetes.
Journal Of Diabetes Research
Ma, Xiaowei X; Huang, Jia J; Lu, Difei D; Gu, Nan N; Lu, Ran R; Zhang, Jianwei J; Zhang, Hong H; Li, Jianping J; Zhang, Junqing J; Guo, Xiaohui X
Genetic variation associated with cardiovascular risk in autoimmune diseases.
Plos One
Perrotti, Pedro P PP; Aterido, Adrià A; Fernández-Nebro, Antonio A; Cañete, Juan D JD; Ferrándiz, Carlos C; Tornero, Jesús J; Gisbert, Javier P JP; Domènech, Eugeni E; Fernández-Gutiérrez, Benjamín B; Gomollón, Fernando F; García-Planella, Esther E; Fernández, Emilia E; Sanmartí, Raimon R; Gratacós, Jordi J; Martínez-Taboada, Víctor Manuel VM; Rodríguez-Rodríguez, Luís L; Palau, Núria N; Tortosa, Raül R; Corbeto, Mireia L ML; Lasanta, María L ML; Marsal, Sara S; Julià, Antonio A; ,
Rs46522 in the Ubiquitin-Conjugating Enzyme E2Z Gene Is Associated with the Risk of Coronary Artery Disease in Individuals of Chinese Han Population with Type 2 Diabetes.
Journal Of Diabetes Research
Lu, Difei D; Huang, Jia J; Ma, Xiaowei X; Gu, Nan N; Zhang, Junqing J; Zhang, Hong H; Guo, Xiaohui X
Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.
Scientific Reports
Guo, Yang Y; Wang, Fan F; Li, Lin L; Gao, Hanxiang H; Arckacki, Stephen S; Wang, Isabel Z IZ; Barnard, John J; Ellis, Stephen S; Hubbard, Carlos C; Topol, Eric J EJ; Chen, Qiuyun Q; Wang, Qing K QK
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Diabetes
Scott, Robert A RA; Scott, Laura J LJ; Mägi, Reedik R; Marullo, Letizia L; Gaulton, Kyle J KJ; Kaakinen, Marika M; Pervjakova, Natalia N; Pers, Tune H TH; Johnson, Andrew D AD; Eicher, John D JD; Jackson, Anne U AU; Ferreira, Teresa T; Lee, Yeji Y; Ma, Clement C; Steinthorsdottir, Valgerdur V; Thorleifsson, Gudmar G; Qi, Lu L; Van Zuydam, Natalie R NR; Mahajan, Anubha A; Chen, Han H; Almgren, Peter P; Voight, Ben F BF; Grallert, Harald H; Müller-Nurasyid, Martina M; Ried, Janina S JS; Rayner, Nigel W NW; Robertson, Neil N; Karssen, Lennart C LC; van Leeuwen, Elisabeth M EM; Willems, Sara M SM; Fuchsberger, Christian C; Kwan, Phoenix P; Teslovich, Tanya M TM; Chanda, Pritam P; Li, Man M; Lu, Yingchang Y; Dina, Christian C; Thuillier, Dorothee D; Yengo, Loic L; Jiang, Longda L; Sparso, Thomas T; Kestler, Hans A HA; Chheda, Himanshu H; Eisele, Lewin L; Gustafsson, Stefan S; Frånberg, Mattias M; Strawbridge, Rona J RJ; Benediktsson, Rafn R; Hreidarsson, Astradur B AB; Kong, Augustine A; Sigurðsson, Gunnar G; Kerrison, Nicola D ND; Luan, Jian'an J; Liang, Liming L; Meitinger, Thomas T; Roden, Michael M; Thorand, Barbara B; Esko, Tõnu T; Mihailov, Evelin E; Fox, Caroline C; Liu, Ching-Ti CT; Rybin, Denis D; Isomaa, Bo B; Lyssenko, Valeriya V; Tuomi, Tiinamaija T; Couper, David J DJ; Pankow, James S JS; Grarup, Niels N; Have, Christian T CT; Jørgensen, Marit E ME; Jørgensen, Torben T; Linneberg, Allan A; Cornelis, Marilyn C MC; van Dam, Rob M RM; Hunter, David J DJ; Kraft, Peter P; Sun, Qi Q; Edkins, Sarah S; Owen, Katharine R KR; Perry, John R B JRB; Wood, Andrew R AR; Zeggini, Eleftheria E; Tajes-Fernandes, Juan J; Abecasis, Goncalo R GR; Bonnycastle, Lori L LL; Chines, Peter S PS; Stringham, Heather M HM; Koistinen, Heikki A HA; Kinnunen, Leena L; Sennblad, Bengt B; Mühleisen, Thomas W TW; Nöthen, Markus M MM; Pechlivanis, Sonali S; Baldassarre, Damiano D; Gertow, Karl K; Humphries, Steve E SE; Tremoli, Elena E; Klopp, Norman N; Meyer, Julia J; Steinbach, Gerald G; Wennauer, Roman R; Eriksson, Johan G JG; Mӓnnistö, Satu S; Peltonen, Leena L; Tikkanen, Emmi E; Charpentier, Guillaume G; Eury, Elodie E; Lobbens, Stéphane S; Gigante, Bruna B; Leander, Karin K; McLeod, Olga O; Bottinger, Erwin P EP; Gottesman, Omri O; Ruderfer, Douglas D; Blüher, Matthias M; Kovacs, Peter P; Tonjes, Anke A; Maruthur, Nisa M NM; Scapoli, Chiara C; Erbel, Raimund R; Jöckel, Karl-Heinz KH; Moebus, Susanne S; de Faire, Ulf U; Hamsten, Anders A; Stumvoll, Michael M; Deloukas, Panagiotis P; Donnelly, Peter J PJ; Frayling, Timothy M TM; Hattersley, Andrew T AT; Ripatti, Samuli S; Salomaa, Veikko V; Pedersen, Nancy L NL; Boehm, Bernhard O BO; Bergman, Richard N RN; Collins, Francis S FS; Mohlke, Karen L KL; Tuomilehto, Jaakko J; Hansen, Torben T; Pedersen, Oluf O; Barroso, Inês I; Lannfelt, Lars L; Ingelsson, Erik E; Lind, Lars L; Lindgren, Cecilia M CM; Cauchi, Stephane S; Froguel, Philippe P; Loos, Ruth J F RJF; Balkau, Beverley B; Boeing, Heiner H; Franks, Paul W PW; Barricarte Gurrea, Aurelio A; Palli, Domenico D; van der Schouw, Yvonne T YT; Altshuler, David D; Groop, Leif C LC; Langenberg, Claudia C; Wareham, Nicholas J NJ; Sijbrands, Eric E; van Duijn, Cornelia M CM; Florez, Jose C JC; Meigs, James B JB; Boerwinkle, Eric E; Gieger, Christian C; Strauch, Konstantin K; Metspalu, Andres A; Morris, Andrew D AD; Palmer, Colin N A CNA; Hu, Frank B FB; Thorsteinsdottir, Unnur U; Stefansson, Kari K; Dupuis, Josée J; Morris, Andrew P AP; Boehnke, Michael M; McCarthy, Mark I MI; Prokopenko, Inga I; ,
Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.
Genome Biology
Joehanes, Roby R; Zhang, Xiaoling X; Huan, Tianxiao T; Yao, Chen C; Ying, Sai-Xia SX; Nguyen, Quang Tri QT; Demirkale, Cumhur Yusuf CY; Feolo, Michael L ML; Sharopova, Nataliya R NR; Sturcke, Anne A; Schäffer, Alejandro A AA; Heard-Costa, Nancy N; Chen, Han H; Liu, Po-Ching PC; Wang, Richard R; Woodhouse, Kimberly A KA; Tanriverdi, Kahraman K; Freedman, Jane E JE; Raghavachari, Nalini N; Dupuis, Josée J; Johnson, Andrew D AD; O'Donnell, Christopher J CJ; Levy, Daniel D; Munson, Peter J PJ
Coronary Artery Calcification and Rheumatoid Arthritis: Lack of Relationship to Risk Alleles for Coronary Artery Disease in the General Population.
Arthritis & Rheumatology (Hoboken, N.J.)
Ferraz-Amaro, Iván I; Winchester, Robert R; Gregersen, Peter K PK; Reynolds, Richard J RJ; Wasko, Mary Chester MC; Oeser, Anette A; Chung, Cecilia P CP; Stein, C Michael CM; Giles, Jon T JT; Bathon, Joan M JM
Genetic analysis for a shared biological basis between migraine and coronary artery disease.
Neurology. Genetics
Winsvold, Bendik S BS; Nelson, Christopher P CP; Malik, Rainer R; Gormley, Padhraig P; Anttila, Verneri V; Vander Heiden, Jason J; Elliott, Katherine S KS; Jacobsen, Line M LM; Palta, Priit P; Amin, Najaf N; de Vries, Boukje B; Hämäläinen, Eija E; Freilinger, Tobias T; Ikram, M Arfan MA; Kessler, Thorsten T; Koiranen, Markku M; Ligthart, Lannie L; McMahon, George G; Pedersen, Linda M LM; Willenborg, Christina C; Won, Hong-Hee HH; Olesen, Jes J; Artto, Ville V; Assimes, Themistocles L TL; Blankenberg, Stefan S; Boomsma, Dorret I DI; Cherkas, Lynn L; Davey Smith, George G; Epstein, Stephen E SE; Erdmann, Jeanette J; Ferrari, Michel D MD; Göbel, Hartmut H; Hall, Alistair S AS; Jarvelin, Marjo-Riitta MR; Kallela, Mikko M; Kaprio, Jaakko J; Kathiresan, Sekar S; Lehtimäki, Terho T; McPherson, Ruth R; März, Winfried W; Nyholt, Dale R DR; O'Donnell, Christopher J CJ; Quaye, Lydia L; Rader, Daniel J DJ; Raitakari, Olli O; Roberts, Robert R; Schunkert, Heribert H; Schürks, Markus M; Stewart, Alexandre F R AF; Terwindt, Gisela M GM; Thorsteinsdottir, Unnur U; van den Maagdenberg, Arn M J M AM; van Duijn, Cornelia C; Wessman, Maija M; Kurth, Tobias T; Kubisch, Christian C; Dichgans, Martin M; Chasman, Daniel I DI; Cotsapas, Chris C; Zwart, John-Anker JA; Samani, Nilesh J NJ; Palotie, Aarno A; ,
Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.
Data In Brief
Vargas, Jose D JD; Manichaikul, Ani A; Wang, Xin-Qun XQ; Rich, Stephen S SS; Rotter, Jerome I JI; Post, Wendy S WS; Polak, Joseph F JF; Budoff, Matthew J MJ; Bluemke, David A DA
Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
Lancet (London, England)
Mega, J L JL; Stitziel, N O NO; Smith, J G JG; Chasman, D I DI; Caulfield, M M; Devlin, J J JJ; Nordio, F F; Hyde, C C; Cannon, C P CP; Sacks, F F; Poulter, N N; Sever, P P; Ridker, P M PM; Braunwald, E E; Melander, O O; Kathiresan, S S; Sabatine, M S MS
Two novel type 2 diabetes loci revealed through integration of TCF7L2 DNA occupancy and SNP association data.
Bmj Open Diabetes Research & Care
Johnson, Matthew E ME; Zhao, Jianhua J; Schug, Jonathan J; Deliard, Sandra S; Xia, Qianghua Q; Guy, Vanessa C VC; Sainz, Jesus J; Kaestner, Klaus H KH; Wells, Andrew D AD; Grant, Struan F A SF
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.
European Journal Of Human Genetics : Ejhg
Versmissen, Jorie J; Oosterveer, Daniëlla M DM; Yazdanpanah, Mojgan M; Dehghan, Abbas A; Hólm, Hilma H; Erdman, Jeanette J; Aulchenko, Yurii S YS; Thorleifsson, Gudmar G; Schunkert, Heribert H; Huijgen, Roeland R; Vongpromek, Ranitha R; Uitterlinden, André G AG; Defesche, Joep C JC; van Duijn, Cornelia M CM; Mulder, Monique M; Dadd, Tony T; Karlsson, Hróbjartur D HD; Ordovas, Jose J; Kindt, Iris I; Jarman, Amelia A; Hofman, Albert A; van Vark-van der Zee, Leonie L; Blommesteijn-Touw, Adriana C AC; Kwekkeboom, Jaap J; Liem, Anho H AH; van der Ouderaa, Frans J FJ; Calandra, Sebastiano S; Bertolini, Stefano S; Averna, Maurizio M; Langslet, Gisle G; Ose, Leiv L; Ros, Emilio E; Almagro, Fátima F; de Leeuw, Peter W PW; Civeira, Fernando F; Masana, Luis L; Pintó, Xavier X; Simoons, Maarten L ML; Schinkel, Arend F L AF; Green, Martin R MR; Zwinderman, Aeilko H AH; Johnson, Keith J KJ; Schaefer, Arne A; Neil, Andrew A; Witteman, Jacqueline C M JC; Humphries, Steve E SE; Kastelein, John J P JJ; Sijbrands, Eric J G EJ
Overlap between common genetic polymorphisms underpinning kidney traits and cardiovascular disease phenotypes: the CKDGen consortium.
American Journal Of Kidney Diseases : The Official Journal Of The National Kidney Foundation
Olden, Matthias M; Teumer, Alexander A; Bochud, Murielle M; Pattaro, Cristian C; Köttgen, Anna A; Turner, Stephen T ST; Rettig, Rainer R; Chen, Ming-Huei MH; Dehghan, Abbas A; Bastardot, Francois F; Schmidt, Reinhold R; Vollenweider, Peter P; Schunkert, Heribert H; Reilly, Muredach P MP; Fornage, Myriam M; Launer, Lenore J LJ; Verwoert, Germaine C GC; Mitchell, Gary F GF; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Cheng, Ching-Yu CY; Sim, Xueling X; Siscovick, David S DS; Coresh, Josef J; Kao, W H Linda WH; Fox, Caroline S CS; O'Seaghdha, Conall M CM; ,
Heart disease and stroke statistics--2013 update: a report from the American Heart Association.
Circulation
Go, Alan S AS; Mozaffarian, Dariush D; Roger, Véronique L VL; Benjamin, Emelia J EJ; Berry, Jarett D JD; Borden, William B WB; Bravata, Dawn M DM; Dai, Shifan S; Ford, Earl S ES; Fox, Caroline S CS; Franco, Sheila S; Fullerton, Heather J HJ; Gillespie, Cathleen C; Hailpern, Susan M SM; Heit, John A JA; Howard, Virginia J VJ; Huffman, Mark D MD; Kissela, Brett M BM; Kittner, Steven J SJ; Lackland, Daniel T DT; Lichtman, Judith H JH; Lisabeth, Lynda D LD; Magid, David D; Marcus, Gregory M GM; Marelli, Ariane A; Matchar, David B DB; McGuire, Darren K DK; Mohler, Emile R ER; Moy, Claudia S CS; Mussolino, Michael E ME; Nichol, Graham G; Paynter, Nina P NP; Schreiner, Pamela J PJ; Sorlie, Paul D PD; Stein, Joel J; Turan, Tanya N TN; Virani, Salim S SS; Wong, Nathan D ND; Woo, Daniel D; Turner, Melanie B MB; ,
Large-scale association analysis identifies new risk loci for coronary artery disease.
Nature Genetics
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Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction.
Plos One
Lucas, Gavin G; Lluís-Ganella, Carla C; Subirana, Isaac I; Musameh, Muntaser D MD; Gonzalez, Juan Ramon JR; Nelson, Christopher P CP; Sentí, Mariano M; , ; , ; Schwartz, Stephen M SM; Siscovick, David D; O'Donnell, Christopher J CJ; Melander, Olle O; Salomaa, Veikko V; Purcell, Shaun S; Altshuler, David D; Samani, Nilesh J NJ; Kathiresan, Sekar S; Elosua, Roberto R
Heart disease and stroke statistics--2012 update: a report from the American Heart Association.
Circulation
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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
Nature Genetics
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