WDR12 c.1195-225A>G

Variant ID: 2-203745885-T-C

NM_018256.3(WDR12):c.1195-225A>G

This variant was identified in 94 publications

View GRCh38 version.




Publications:


Comparison of Genetic Susceptibility to Coronary Heart Disease in the Hungarian Populations: Risk Prediction Models for Coronary Heart Disease.

Genes
Nasr, Nayla N; Soltész, Beáta B; Sándor, János J; Ádány, Róza R; Fiatal, Szilvia S
Publication Date: 2023-04-30

Variant appearance in text: rs6725887
PubMed Link: 37239393
Variant Present in the following documents:
  • Main text
  • genes-14-01033.pdf
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Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.

Ophthalmology Science
Tomasoni, Mattia M; Beyeler, Michael Johannes MJ; Vela, Sofia Ortin SO; Mounier, Ninon N; Porcu, Eleonora E; Corre, Tanguy T; Krefl, Daniel D; Button, Alexander Luke AL; Abouzeid, Hana H; Lazaros, Konstantinidis K; Bochud, Murielle M; Schlingemann, Reinier R; Bergin, Ciara C; Bergmann, Sven S
Publication Date: 2023-09

Variant appearance in text: rs6725887
PubMed Link: 37131961
Variant Present in the following documents:
  • Main text
  • main.pdf
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Genetic Predictors of the Development of Complications after Coronary Stenting.

Journal Of Personalized Medicine
Taizhanova, Dana D; Kalimbetova, Akerke A; Bodaubay, Roza R; Toleuova, Aliya A; Toiynbekova, Rakhima R; Beysenbekova, Zhazira Z; Visternichan, Olga O; Tauesheva, Zauresh Z; Kadyrova, Irina I; Babenko, Dmitriy D; Akhmaltdinova, Lyudmila L; Kolesnichenko, Svetlana S; Kolesnikova, Yevgeniya Y; Avdienko, Olga V OV; Akilzhanova, Ainur A; Gerotziafas, Grigorios T GT
Publication Date: 2022-12-22

Variant appearance in text: rs6725887
PubMed Link: 36675675
Variant Present in the following documents:
  • jpm-13-00014.pdf
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Genetic Factors for Coronary Heart Disease and Their Mechanisms: A Meta-Analysis and Comprehensive Review of Common Variants from Genome-Wide Association Studies.

Diagnostics (Basel, Switzerland)
Zarkasi, Khairul Anwar KA; Abdullah, Noraidatulakma N; Abdul Murad, Nor Azian NA; Ahmad, Norfazilah N; Jamal, Rahman R
Publication Date: 2022-10-21

Variant appearance in text: rs6725887
PubMed Link: 36292250
Variant Present in the following documents:
  • diagnostics-12-02561.pdf
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Gene-diet interactions and cardiovascular diseases: a systematic review of observational and clinical trials.

Bmc Cardiovascular Disorders
Roa-Díaz, Zayne M ZM; Teuscher, Julian J; Gamba, Magda M; Bundo, Marvin M; Grisotto, Giorgia G; Wehrli, Faina F; Gamboa, Edna E; Rojas, Lyda Z LZ; Gómez-Ochoa, Sergio A SA; Verhoog, Sanne S; Vargas, Manuel Frias MF; Minder, Beatrice B; Franco, Oscar H OH; Dehghan, Abbas A; Pazoki, Raha R; Marques-Vidal, Pedro P; Muka, Taulant T
Publication Date: 2022-08-20

Variant appearance in text: rs6725887
PubMed Link: 35987633
Variant Present in the following documents:
  • Main text
  • 12872_2022_Article_2808.pdf
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Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad.

Bmc Cardiovascular Disorders
Gorre, Manjula M; Rayabarapu, Pranavchand P; Battini, Sriteja Reddy SR; Irgam, Kumuda K; Battini, Mohan Reddy MR
Publication Date: 2022-04-05

Variant appearance in text: rs6725887
PubMed Link: 35379196
Variant Present in the following documents:
  • Main text
  • 12872_2022_Article_2562.pdf
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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
Publication Date: 2021

Variant appearance in text: rs6725887
PubMed Link: 35069183
Variant Present in the following documents:
  • Main text
  • fphar-12-679857.pdf
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Polygenic risk for coronary artery disease in the Scottish and English population.

Bmc Cardiovascular Disorders
Yang, Chuhua C; Starnecker, Fabian F; Pang, Shichao S; Chen, Zhifen Z; Güldener, Ulrich U; Li, Ling L; Heinig, Matthias M; Schunkert, Heribert H
Publication Date: 2021-12-07

Variant appearance in text: rs6725887
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
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Polygenic risk scores predict diabetes complications and their response to intensive blood pressure and glucose control.

Diabetologia
Tremblay, Johanne J; Haloui, Mounsif M; Attaoua, Redha R; Tahir, Ramzan R; Hishmih, Camil C; Harvey, François F; Marois-Blanchet, François-Christophe FC; Long, Carole C; Simon, Paul P; Santucci, Lara L; Hizel, Candan C; Chalmers, John J; Marre, Michel M; Harrap, Stephen S; Cífková, Renata R; Krajčoviechová, Alena A; Matthews, David R DR; Williams, Bryan B; Poulter, Neil N; Zoungas, Sophia S; Colagiuri, Stephen S; Mancia, Giuseppe G; Grobbee, Diederick E DE; Rodgers, Anthony A; Liu, Liusheng L; Agbessi, Mawussé M; Bruat, Vanessa V; Favé, Marie-Julie MJ; Harwood, Michelle P MP; Awadalla, Philip P; Woodward, Mark M; Hussin, Julie G JG; Hamet, Pavel P
Publication Date: 2021-09

Variant appearance in text: rs6725887
PubMed Link: 34226943
Variant Present in the following documents:
  • 125_2021_5491_MOESM1_ESM.pdf
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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
Publication Date: 2021-01-12

Variant appearance in text: rs6725887
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.pdf
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Genetic Risk Score for Coronary Heart Disease: Review.

Journal Of Personalized Medicine
Semaev, Sergey S; Shakhtshneider, Elena E
Publication Date: 2020-11-20

Variant appearance in text: rs6725887
PubMed Link: 33233501
Variant Present in the following documents:
  • Main text
  • jpm-10-00239.pdf
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NBEAL1 controls SREBP2 processing and cholesterol metabolism and is a susceptibility locus for coronary artery disease.

Scientific Reports
Bindesbøll, Christian C; Aas, Aleksander A; Ogmundsdottir, Margret Helga MH; Pankiv, Serhiy S; Reine, Trine T; Zoncu, Roberto R; Simonsen, Anne A
Publication Date: 2020-03-11

Variant appearance in text: rs6725887
PubMed Link: 32161285
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_61352.pdf
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Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

Korean Circulation Journal
Spiller, Wes W; Jung, Keum Ji KJ; Lee, Ji Young JY; Jee, Sun Ha SH
Publication Date: 2020-02

Variant appearance in text: rs6725887
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
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Metabolic and genetic profiling of young adults with and without a family history of premature coronary heart disease (MAGNETIC). Study design and methodology.

Archives Of Medical Science : Ams
Osadnik, Tadeusz T; Osadnik, Kamila K; Pawlas, Natalia N; Strzelczyk, Joanna J; Kasperczyk, Janusz J; Poloński, Lech L; Gąsior, Mariusz M
Publication Date: 2019-05

Variant appearance in text: rs6725887
PubMed Link: 31110523
Variant Present in the following documents:
  • Main text
  • AMS-15-32834.pdf
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Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

Diabetologia
Fall, Tove T; Gustafsson, Stefan S; Orho-Melander, Marju M; Ingelsson, Erik E
Publication Date: 2018-10

Variant appearance in text: rs6725887
PubMed Link: 30003307
Variant Present in the following documents:
  • 125_2018_4686_MOESM1_ESM.pdf
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Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence.

Circulation. Genomic And Precision Medicine
Hindy, George G; Wiberg, Frans F; Almgren, Peter P; Melander, Olle O; Orho-Melander, Marju M
Publication Date: 2018-01

Variant appearance in text: rs6725887
PubMed Link: 29874179
Variant Present in the following documents:
  • hcg-11-e001856-s001.pdf
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Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia.

Scientific Reports
Han, Yi Y; Dorajoo, Rajkumar R; Chang, Xuling X; Wang, Ling L; Khor, Chiea-Chuen CC; Sim, Xueling X; Cheng, Ching-Yu CY; Shi, Yuan Y; Tham, Yih Chung YC; Zhao, Wanting W; Chee, Miao Ling ML; Sabanayagam, Charumathi C; Chee, Miao Li ML; Tan, Nicholas N; Wong, Tien Yin TY; Tai, E-Shyong ES; Liu, Jianjun J; Goh, Daniel Y T DYT; Yuan, Jian-Min JM; Koh, Woon-Puay WP; van Dam, Rob M RM; Low, Adrian F AF; Chan, Mark Yan-Yee MY; Friedlander, Yechiel Y; Heng, Chew-Kiat CK
Publication Date: 2017-12-20

Variant appearance in text: rs6725887
PubMed Link: 29263402
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_18214.pdf
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Proficiency of data interpretation: identification of signaling SNPs/specific loci for coronary artery disease.

Database : The Journal Of Biological Databases And Curation
Cheema, Asma N AN; Rosenthal, Samantha L SL; Ilyas Kamboh, M M
Publication Date: 2017-01-01

Variant appearance in text: rs6725887
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
View BVdb publication page



A clinical-genetic approach to assessing cardiovascular risk in patients with CKD.

Clinical Kidney Journal
Rodrigo, Emilio E; Pich, Sara S; Subirana, Isaac I; Fernandez-Fresnedo, Gema G; Barreda, Paloma P; Ferrer-Costa, Carles C; M de Francisco, Ángel Luis ÁL; Salas, Eduardo E; Elosua, Roberto R; Arias, Manuel M
Publication Date: 2017-10

Variant appearance in text: rs6725887
PubMed Link: 28979779
Variant Present in the following documents:
  • Main text
  • sfx039.pdf
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Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.

Frontiers In Cardiovascular Medicine
Knowles, Joshua W JW; Zarafshar, Shirin S; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Tsai, Sandra S; Li, Jin J; McConnell, Michael V MV; Absher, Devin D; Ashley, Euan A EA; Kiernan, Michaela M; Ioannidis, John P A JPA; Assimes, Themistocles L TL
Publication Date: 2017

Variant appearance in text: rs6725887
PubMed Link: 28856136
Variant Present in the following documents:
  • Main text
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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
Publication Date: 2017-07-14

Variant appearance in text: rs6725887
PubMed Link: 28710368
Variant Present in the following documents:
  • Main text
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Coronary artery disease-associated genetic variants and biomarkers of inflammation.

Plos One
Christiansen, Morten Krogh MK; Larsen, Sanne Bøjet SB; Nyegaard, Mette M; Neergaard-Petersen, Søs S; Ajjan, Ramzi R; Würtz, Morten M; Grove, Erik Lerkevang EL; Hvas, Anne-Mette AM; Jensen, Henrik Kjærulf HK; Kristensen, Steen Dalby SD
Publication Date: 2017

Variant appearance in text: rs6725887
PubMed Link: 28686695
Variant Present in the following documents:
  • Main text
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Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.

Plos Genetics
Byars, Sean G SG; Huang, Qin Qin QQ; Gray, Lesley-Ann LA; Bakshi, Andrew A; Ripatti, Samuli S; Abraham, Gad G; Stearns, Stephen C SC; Inouye, Michael M
Publication Date: 2017-06

Variant appearance in text: rs6725887
PubMed Link: 28640878
Variant Present in the following documents:
  • pgen.1006328.s006.pdf
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Transcriptional networks specifying homeostatic and inflammatory programs of gene expression in human aortic endothelial cells.

Elife
Hogan, Nicholas T NT; Whalen, Michael B MB; Stolze, Lindsey K LK; Hadeli, Nizar K NK; Lam, Michael T MT; Springstead, James R JR; Glass, Christopher K CK; Romanoski, Casey E CE
Publication Date: 2017-06-06

Variant appearance in text: rs6725887
PubMed Link: 28585919
Variant Present in the following documents:
  • Main text
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Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

Journal Of The American College Of Cardiology
Webb, Thomas R TR; Erdmann, Jeanette J; Stirrups, Kathleen E KE; Stitziel, Nathan O NO; Masca, Nicholas G D NG; Jansen, Henning H; Kanoni, Stavroula S; Nelson, Christopher P CP; Ferrario, Paola G PG; König, Inke R IR; Eicher, John D JD; Johnson, Andrew D AD; Hamby, Stephen E SE; Betsholtz, Christer C; Ruusalepp, Arno A; Franzén, Oscar O; Schadt, Eric E EE; Björkegren, Johan L M JL; Weeke, Peter E PE; Auer, Paul L PL; Schick, Ursula M UM; Lu, Yingchang Y; Zhang, He H; Dube, Marie-Pierre MP; Goel, Anuj A; Farrall, Martin M; Peloso, Gina M GM; Won, Hong-Hee HH; Do, Ron R; van Iperen, Erik E; Kruppa, Jochen J; Mahajan, Anubha A; Scott, Robert A RA; Willenborg, Christina C; Braund, Peter S PS; van Capelleveen, Julian C JC; Doney, Alex S F AS; Donnelly, Louise A LA; Asselta, Rosanna R; Merlini, Pier A PA; Duga, Stefano S; Marziliano, Nicola N; Denny, Josh C JC; Shaffer, Christian C; El-Mokhtari, Nour Eddine NE; Franke, Andre A; Heilmann, Stefanie S; Hengstenberg, Christian C; Hoffmann, Per P; Holmen, Oddgeir L OL; Hveem, Kristian K; Jansson, Jan-Håkan JH; Jöckel, Karl-Heinz KH; Kessler, Thorsten T; Kriebel, Jennifer J; Laugwitz, Karl L KL; Marouli, Eirini E; Martinelli, Nicola N; McCarthy, Mark I MI; Van Zuydam, Natalie R NR; Meisinger, Christa C; Esko, Tõnu T; Mihailov, Evelin E; Escher, Stefan A SA; Alver, Maris M; Moebus, Susanne S; Morris, Andrew D AD; Virtamo, Jarma J; Nikpay, Majid M; Olivieri, Oliviero O; Provost, Sylvie S; AlQarawi, Alaa A; Robertson, Neil R NR; Akinsansya, Karen O KO; Reilly, Dermot F DF; Vogt, Thomas F TF; Yin, Wu W; Asselbergs, Folkert W FW; Kooperberg, Charles C; Jackson, Rebecca D RD; Stahl, Eli E; Müller-Nurasyid, Martina M; Strauch, Konstantin K; Varga, Tibor V TV; Waldenberger, Melanie M; , ; Zeng, Lingyao L; Chowdhury, Rajiv R; Salomaa, Veikko V; Ford, Ian I; Jukema, J Wouter JW; Amouyel, Philippe P; Kontto, Jukka J; , ; Nordestgaard, Børge G BG; Ferrières, Jean J; Saleheen, Danish D; Sattar, Naveed N; Surendran, Praveen P; Wagner, Aline A; Young, Robin R; Howson, Joanna M M JM; Butterworth, Adam S AS; Danesh, John J; Ardissino, Diego D; Bottinger, Erwin P EP; Erbel, Raimund R; Franks, Paul W PW; Girelli, Domenico D; Hall, Alistair S AS; Hovingh, G Kees GK; Kastrati, Adnan A; Lieb, Wolfgang W; Meitinger, Thomas T; Kraus, William E WE; Shah, Svati H SH; McPherson, Ruth R; Orho-Melander, Marju M; Melander, Olle O; Metspalu, Andres A; Palmer, Colin N A CN; Peters, Annette A; Rader, Daniel J DJ; Reilly, Muredach P MP; Loos, Ruth J F RJ; Reiner, Alex P AP; Roden, Dan M DM; Tardif, Jean-Claude JC; Thompson, John R JR; Wareham, Nicholas J NJ; Watkins, Hugh H; Willer, Cristen J CJ; Samani, Nilesh J NJ; Schunkert, Heribert H; Deloukas, Panos P; Kathiresan, Sekar S; ,
Publication Date: 2017-02-21

Variant appearance in text: rs6725887
PubMed Link: 28209224
Variant Present in the following documents:
  • Main text
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Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.

Circulation
Benjamin, Emelia J EJ; Blaha, Michael J MJ; Chiuve, Stephanie E SE; Cushman, Mary M; Das, Sandeep R SR; Deo, Rajat R; de Ferranti, Sarah D SD; Floyd, James J; Fornage, Myriam M; Gillespie, Cathleen C; Isasi, Carmen R CR; Jiménez, Monik C MC; Jordan, Lori Chaffin LC; Judd, Suzanne E SE; Lackland, Daniel D; Lichtman, Judith H JH; Lisabeth, Lynda L; Liu, Simin S; Longenecker, Chris T CT; Mackey, Rachel H RH; Matsushita, Kunihiro K; Mozaffarian, Dariush D; Mussolino, Michael E ME; Nasir, Khurram K; Neumar, Robert W RW; Palaniappan, Latha L; Pandey, Dilip K DK; Thiagarajan, Ravi R RR; Reeves, Mathew J MJ; Ritchey, Matthew M; Rodriguez, Carlos J CJ; Roth, Gregory A GA; Rosamond, Wayne D WD; Sasson, Comilla C; Towfighi, Amytis A; Tsao, Connie W CW; Turner, Melanie B MB; Virani, Salim S SS; Voeks, Jenifer H JH; Willey, Joshua Z JZ; Wilkins, John T JT; Wu, Jason Hy JH; Alger, Heather M HM; Wong, Sally S SS; Muntner, Paul P; ,
Publication Date: 2017-03-07

Variant appearance in text: rs6725887
PubMed Link: 28122885
Variant Present in the following documents:
  • Main text
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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
Publication Date: 2017-01-25

Variant appearance in text: rs6725887
PubMed Link: 28122634
Variant Present in the following documents:
  • Main text
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Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis.

Scientific Reports
López-Mejías, Raquel R; Corrales, Alfonso A; Vicente, Esther E; Robustillo-Villarino, Montserrat M; González-Juanatey, Carlos C; Llorca, Javier J; Genre, Fernanda F; Remuzgo-Martínez, Sara S; Dierssen-Sotos, Trinidad T; Miranda-Filloy, José A JA; Huaranga, Marco A Ramírez MA; Pina, Trinitario T; Blanco, Ricardo R; Alegre-Sancho, Juan J JJ; Raya, Enrique E; Mijares, Verónica V; Ubilla, Begoña B; Ferraz-Amaro, Iván I; Gómez-Vaquero, Carmen C; Balsa, Alejandro A; López-Longo, Francisco J FJ; Carreira, Patricia P; González-Álvaro, Isidoro I; Ocejo-Vinyals, J Gonzalo JG; Rodríguez-Rodríguez, Luis L; Fernández-Gutiérrez, Benjamín B; Castañeda, Santos S; Martín, Javier J; González-Gay, Miguel A MA
Publication Date: 2017-01-06

Variant appearance in text: rs6725887
PubMed Link: 28059143
Variant Present in the following documents:
  • Main text
  • srep40303.pdf
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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
Publication Date: 2017-03

Variant appearance in text: rs6725887
PubMed Link: 27696788
Variant Present in the following documents:
  • Main text
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Implications of Personal Genomic Testing for Health Behaviors: The Case of Smoking.

Nicotine & Tobacco Research : Official Journal Of The Society For Research On Nicotine And Tobacco
Olfson, Emily E; Hartz, Sarah S; Carere, Deanna Alexis DA; Green, Robert C RC; Roberts, J Scott JS; Bierut, Laura J LJ; ,
Publication Date: 2016-12

Variant appearance in text: rs6725887
PubMed Link: 27613923
Variant Present in the following documents:
  • Main text
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Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.

Journal Of Postgraduate Medicine
Pranavchand, R R; Reddy, B M BM
Publication Date: 2016

Variant appearance in text: rs6725887
PubMed Link: 27424552
Variant Present in the following documents:
  • Main text
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The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

Embo Molecular Medicine
Kessler, Thorsten T; Vilne, Baiba B; Schunkert, Heribert H
Publication Date: 2016-07

Variant appearance in text: rs6725887
PubMed Link: 27189168
Variant Present in the following documents:
  • Main text
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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
Publication Date: 2016-06

Variant appearance in text: rs6725887
PubMed Link: 26958643
Variant Present in the following documents:
  • Main text
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Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

Plos One
Dehghan, Abbas A; Bis, Joshua C JC; White, Charles C CC; Smith, Albert Vernon AV; Morrison, Alanna C AC; Cupples, L Adrienne LA; Trompet, Stella S; Chasman, Daniel I DI; Lumley, Thomas T; Völker, Uwe U; Buckley, Brendan M BM; Ding, Jingzhong J; Jensen, Majken K MK; Folsom, Aaron R AR; Kritchevsky, Stephen B SB; Girman, Cynthia J CJ; Ford, Ian I; Dörr, Marcus M; Salomaa, Veikko V; Uitterlinden, André G AG; Eiriksdottir, Gudny G; Vasan, Ramachandran S RS; Franceschini, Nora N; Carty, Cara L CL; Virtamo, Jarmo J; Demissie, Serkalem S; Amouyel, Philippe P; Arveiler, Dominique D; Heckbert, Susan R SR; Ferrières, Jean J; Ducimetière, Pierre P; Smith, Nicholas L NL; Wang, Ying A YA; Siscovick, David S DS; Rice, Kenneth M KM; Wiklund, Per-Gunnar PG; Taylor, Kent D KD; Evans, Alun A; Kee, Frank F; Rotter, Jerome I JI; Karvanen, Juha J; Kuulasmaa, Kari K; Heiss, Gerardo G; Kraft, Peter P; Launer, Lenore J LJ; Hofman, Albert A; Markus, Marcello R P MR; Rose, Lynda M LM; Silander, Kaisa K; Wagner, Peter P; Benjamin, Emelia J EJ; Lohman, Kurt K; Stott, David J DJ; Rivadeneira, Fernando F; Harris, Tamara B TB; Levy, Daniel D; Liu, Yongmei Y; Rimm, Eric B EB; Jukema, J Wouter JW; Völzke, Henry H; Ridker, Paul M PM; Blankenberg, Stefan S; Franco, Oscar H OH; Gudnason, Vilmundur V; Psaty, Bruce M BM; Boerwinkle, Eric E; O'Donnell, Christopher J CJ
Publication Date: 2016

Variant appearance in text: rs6725887
PubMed Link: 26950853
Variant Present in the following documents:
  • Main text
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From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

Circulation Research
Nurnberg, Sylvia T ST; Zhang, Hanrui H; Hand, Nicholas J NJ; Bauer, Robert C RC; Saleheen, Danish D; Reilly, Muredach P MP; Rader, Daniel J DJ
Publication Date: 2016-02-19

Variant appearance in text: rs6725887
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
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Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

Cardiovascular Drugs And Therapy
Guo, Yanhong Y; Garcia-Barrio, Minerva T MT; Wang, Laiyuan L; Chen, Y Eugene YE
Publication Date: 2016-02

Variant appearance in text: rs6725887
PubMed Link: 26847647
Variant Present in the following documents:
  • Main text
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Analysis of rs6725887 in the WD Repeat Protein 12 in Association with Coronary Artery Disease in Iranian Patients.

International Journal Of Molecular And Cellular Medicine
Piryaei, Mohammad M; Ghaderian, Sayyed Mohammad Hossein SM; Vakili, Hossein H; Zaimkohan, Hooshang H; Mohammadi Ghahhari, Nastaran N; Mafi Golchin, Maryam M
Publication Date: 2015

Variant appearance in text: rs6725887
PubMed Link: 26629484
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CPAG: software for leveraging pleiotropy in GWAS to reveal similarity between human traits links plasma fatty acids and intestinal inflammation.

Genome Biology
Wang, Liuyang L; Oehlers, Stefan H SH; Espenschied, Scott T ST; Rawls, John F JF; Tobin, David M DM; Ko, Dennis C DC
Publication Date: 2015-09-15

Variant appearance in text: rs6725887
PubMed Link: 26374098
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WDR12, a Member of Nucleolar PeBoW-Complex, Is Up-Regulated in Failing Hearts and Causes Deterioration of Cardiac Function.

Plos One
Moilanen, Anne-Mari AM; Rysä, Jaana J; Kaikkonen, Leena L; Karvonen, Teemu T; Mustonen, Erja E; Serpi, Raisa R; Szabó, Zoltán Z; Tenhunen, Olli O; Bagyura, Zsolt Z; Näpänkangas, Juha J; Ohukainen, Pauli P; Tavi, Pasi P; Kerkelä, Risto R; Leósdóttir, Margrét M; Wahlstrand, Björn B; Hedner, Thomas T; Melander, Olle O; Ruskoaho, Heikki H
Publication Date: 2015

Variant appearance in text: rs6725887
PubMed Link: 25915632
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Genome-wide association studies of late-onset cardiovascular disease.

Journal Of Molecular And Cellular Cardiology
Smith, J Gustav JG; Newton-Cheh, Christopher C
Publication Date: 2015-06

Variant appearance in text: rs6725887
PubMed Link: 25870159
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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
Publication Date: 2015-06-06

Variant appearance in text: rs6725887
PubMed Link: 25748612
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Basic concepts and potential applications of genetics and genomics for cardiovascular and stroke clinicians: a scientific statement from the American Heart Association.

Circulation. Cardiovascular Genetics
Musunuru, Kiran K; Hickey, Kathleen T KT; Al-Khatib, Sana M SM; Delles, Christian C; Fornage, Myriam M; Fox, Caroline S CS; Frazier, Lorraine L; Gelb, Bruce D BD; Herrington, David M DM; Lanfear, David E DE; Rosand, Jonathan J; ,
Publication Date: 2015-02

Variant appearance in text: rs6725887
PubMed Link: 25561044
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Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

Plos One
Franceschini, Nora N; Hu, Yijuan Y; Reiner, Alex P AP; Buyske, Steven S; Nalls, Mike M; Yanek, Lisa R LR; Li, Yun Y; Hindorff, Lucia A LA; Cole, Shelley A SA; Howard, Barbara V BV; Stafford, Jeanette M JM; Carty, Cara L CL; Sethupathy, Praveen P; Martin, Lisa W LW; Lin, Dan-Yu DY; Johnson, Karen C KC; Becker, Lewis C LC; North, Kari E KE; Dehghan, Abbas A; Bis, Joshua C JC; Liu, Yongmei Y; Greenland, Philip P; Manson, JoAnn E JE; Maeda, Nobuyo N; Garcia, Melissa M; Harris, Tamara B TB; Becker, Diane M DM; O'Donnell, Christopher C; Heiss, Gerardo G; Kooperberg, Charles C; Boerwinkle, Eric E
Publication Date: 2014

Variant appearance in text: rs6725887
PubMed Link: 25542012
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  • Main text
  • pone.0113203.pdf
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Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.

Biomedical Reports
Tokoro, Fumitaka F; Matsuoka, Reiko R; Abe, Shintaro S; Arai, Masazumi M; Noda, Toshiyuki T; Watanabe, Sachiro S; Horibe, Hideki H; Fujimaki, Tetsuo T; Oguri, Mitsutoshi M; Kato, Kimihiko K; Minatoguchi, Shinya S; Yamada, Yoshiji Y
Publication Date: 2015-01

Variant appearance in text: rs6725887
PubMed Link: 25469254
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Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.

Bmc Genomics
Zhang, Xiaoling X; Gierman, Hinco J HJ; Levy, Daniel D; Plump, Andrew A; Dobrin, Radu R; Goring, Harald H H HH; Curran, Joanne E JE; Johnson, Matthew P MP; Blangero, John J; Kim, Stuart K SK; O'Donnell, Christopher J CJ; Emilsson, Valur V; Johnson, Andrew D AD
Publication Date: 2014-06-27

Variant appearance in text: rs6725887
PubMed Link: 24973796
Variant Present in the following documents:
  • Main text
  • 12864_2013_Article_6258.pdf
  • 12864_2013_6258_MOESM17_ESM.xlsx, sheet 1
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Genetics of coronary artery disease: an update.

Methodist Debakey Cardiovascular Journal
Roberts, Robert R
Publication Date: 2014

Variant appearance in text: rs6725887
PubMed Link: 24932356
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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
Publication Date: 2015-03

Variant appearance in text: rs6725887
PubMed Link: 24916650
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Current Insights into the Joint Genetic Basis of Type 2 Diabetes and Coronary Heart Disease.

Current Cardiovascular Risk Reports
Dauriz, Marco M; Meigs, James B JB
Publication Date: 2014-01-01

Variant appearance in text: rs6725887
PubMed Link: 24729826
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Additive influence of genetic predisposition and conventional risk factors in the incidence of coronary heart disease: a population-based study in Greece.

Bmj Open
Yiannakouris, Nikos N; Katsoulis, Michail M; Trichopoulou, Antonia A; Ordovas, Jose M JM; Trichopoulos, Dimitrios D
Publication Date: 2014-02-05

Variant appearance in text: rs6725887
PubMed Link: 24500614
Variant Present in the following documents:
  • Main text
  • bmjopen-2013-004387.draft_revisions.pdf
  • bmjopen-2013-004387.pdf
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Heart disease and stroke statistics--2014 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; Blaha, Michael J MJ; 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; Judd, Suzanne E SE; Kissela, Brett M BM; Kittner, Steven J SJ; Lackland, Daniel T DT; Lichtman, Judith H JH; Lisabeth, Lynda D LD; Mackey, Rachel H RH; Magid, David J DJ; 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; Neumar, Robert W RW; Nichol, Graham G; Pandey, Dilip K DK; Paynter, Nina P NP; Reeves, Matthew J MJ; Sorlie, Paul D PD; Stein, Joel J; Towfighi, Amytis A; Turan, Tanya N TN; Virani, Salim S SS; Wong, Nathan D ND; Woo, Daniel D; Turner, Melanie B MB; ,
Publication Date: 2014-01-21

Variant appearance in text: rs6725887
PubMed Link: 24352519
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Common genetic variants do not associate with CAD in familial hypercholesterolemia.

European Journal Of Human Genetics : Ejhg
van Iperen, Erik P A EP; Sivapalaratnam, Suthesh S; Boekholdt, S Matthijs SM; Hovingh, G Kees GK; Maiwald, Stephanie S; Tanck, Michael W MW; Soranzo, Nicole N; Stephens, Jonathan C JC; Sambrook, Jennifer G JG; Levi, Marcel M; Ouwehand, Willem H WH; Kastelein, John Jp JJ; Trip, Mieke D MD; Zwinderman, Aeilko H AH
Publication Date: 2014-06

Variant appearance in text: rs6725887
PubMed Link: 24219970
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Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.

Human Molecular Genetics
Zhang, Xiaoling X; Johnson, Andrew D AD; Hendricks, Audrey E AE; Hwang, Shih-Jen SJ; Tanriverdi, Kahraman K; Ganesh, Santhi K SK; Smith, Nicholas L NL; Peyser, Patricia A PA; Freedman, Jane E JE; O'Donnell, Christopher J CJ
Publication Date: 2014-02-01

Variant appearance in text: rs6725887
PubMed Link: 24057673
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  • Main text
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Genetics of coronary artery disease.

Circulation
Lieb, Wolfgang W; Vasan, Ramachandran S RS
Publication Date: 2013-09-03

Variant appearance in text: rs6725887
PubMed Link: 24002717
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  • Main text
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Genetic risk prediction and a 2-stage risk screening strategy for coronary heart disease.

Arteriosclerosis, Thrombosis, And Vascular Biology
Tikkanen, Emmi E; Havulinna, Aki S AS; Palotie, Aarno A; Salomaa, Veikko V; Ripatti, Samuli S
Publication Date: 2013-09

Variant appearance in text: rs6725887
PubMed Link: 23599444
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  • Main text
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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; ,
Publication Date: 2013-06

Variant appearance in text: rs6725887
PubMed Link: 23474010
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  • Main text
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Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.

Plos One
Bolton, Jennifer L JL; Stewart, Marlene C W MC; Wilson, James F JF; Anderson, Niall N; Price, Jackie F JF
Publication Date: 2013

Variant appearance in text: rs6725887
PubMed Link: 23468967
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Current genomics in cardiovascular medicine.

Current Genomics
Sawhney, Vinit V; Brouilette, Scott S; Abrams, Dominic D; Schilling, Richard R; O'Brien, Benjamin B
Publication Date: 2012-09

Variant appearance in text: rs6725887
PubMed Link: 23450299
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  • Main text
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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; ,
Publication Date: 2013-01-01

Variant appearance in text: rs6725887
PubMed Link: 23239837
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  • Main text
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Large-scale association analysis identifies new risk loci for coronary artery disease.

Nature Genetics
, ; Deloukas, Panos P; Kanoni, Stavroula S; Willenborg, Christina C; Farrall, Martin M; Assimes, Themistocles L TL; Thompson, John R JR; Ingelsson, Erik E; Saleheen, Danish D; Erdmann, Jeanette J; Goldstein, Benjamin A BA; Stirrups, Kathleen K; König, Inke R IR; Cazier, Jean-Baptiste JB; Johansson, Asa A; Hall, Alistair S AS; Lee, Jong-Young JY; Willer, Cristen J CJ; Chambers, John C JC; Esko, Tõnu T; Folkersen, Lasse L; Goel, Anuj A; Grundberg, Elin E; Havulinna, Aki S AS; Ho, Weang K WK; Hopewell, Jemma C JC; Eriksson, Niclas N; Kleber, Marcus E ME; Kristiansson, Kati K; Lundmark, Per P; Lyytikäinen, Leo-Pekka LP; Rafelt, Suzanne S; Shungin, Dmitry D; Strawbridge, Rona J RJ; Thorleifsson, Gudmar G; Tikkanen, Emmi E; Van Zuydam, Natalie N; Voight, Benjamin F BF; Waite, Lindsay L LL; Zhang, Weihua W; Ziegler, Andreas A; Absher, Devin D; Altshuler, David D; Balmforth, Anthony J AJ; Barroso, Inês I; Braund, Peter S PS; Burgdorf, Christof C; Claudi-Boehm, Simone S; Cox, David D; Dimitriou, Maria M; Do, Ron R; , ; , ; Doney, Alex S F AS; El Mokhtari, NourEddine N; Eriksson, Per P; Fischer, Krista K; Fontanillas, Pierre P; Franco-Cereceda, Anders A; Gigante, Bruna B; Groop, Leif L; Gustafsson, Stefan S; Hager, Jörg J; Hallmans, Göran G; Han, Bok-Ghee BG; Hunt, Sarah E SE; Kang, Hyun M HM; Illig, Thomas T; Kessler, Thorsten T; Knowles, Joshua W JW; Kolovou, Genovefa G; Kuusisto, Johanna J; Langenberg, Claudia C; Langford, Cordelia C; Leander, Karin K; Lokki, Marja-Liisa ML; Lundmark, Anders A; McCarthy, Mark I MI; Meisinger, Christa C; Melander, Olle O; Mihailov, Evelin E; Maouche, Seraya S; Morris, Andrew D AD; Müller-Nurasyid, Martina M; , ; Nikus, Kjell K; Peden, John F JF; Rayner, N William NW; Rasheed, Asif A; Rosinger, Silke S; Rubin, Diana D; Rumpf, Moritz P MP; Schäfer, Arne A; Sivananthan, Mohan M; Song, Ci C; Stewart, Alexandre F R AF; Tan, Sian-Tsung ST; Thorgeirsson, Gudmundur G; van der Schoot, C Ellen CE; Wagner, Peter J PJ; , ; Wells, George A GA; Wild, Philipp S PS; Yang, Tsun-Po TP; Amouyel, Philippe P; Arveiler, Dominique D; Basart, Hanneke H; Boehnke, Michael M; Boerwinkle, Eric E; Brambilla, Paolo P; Cambien, Francois F; Cupples, Adrienne L AL; de Faire, Ulf U; Dehghan, Abbas A; Diemert, Patrick P; Epstein, Stephen E SE; Evans, Alun A; Ferrario, Marco M MM; Ferrières, Jean J; Gauguier, Dominique D; Go, Alan S AS; Goodall, Alison H AH; Gudnason, Villi V; Hazen, Stanley L SL; Holm, Hilma H; Iribarren, Carlos C; Jang, Yangsoo Y; Kähönen, Mika M; Kee, Frank F; Kim, Hyo-Soo HS; Klopp, Norman N; Koenig, Wolfgang W; Kratzer, Wolfgang W; Kuulasmaa, Kari K; Laakso, Markku M; Laaksonen, Reijo R; Lee, Ji-Young JY; Lind, Lars L; Ouwehand, Willem H WH; Parish, Sarah S; Park, Jeong E JE; Pedersen, Nancy L NL; Peters, Annette A; Quertermous, Thomas T; Rader, Daniel J DJ; Salomaa, Veikko V; Schadt, Eric E; Shah, Svati H SH; Sinisalo, Juha J; Stark, Klaus K; Stefansson, Kari K; Trégouët, David-Alexandre DA; Virtamo, Jarmo J; Wallentin, Lars L; Wareham, Nicholas N; Zimmermann, Martina E ME; Nieminen, Markku S MS; Hengstenberg, Christian C; Sandhu, Manjinder S MS; Pastinen, Tomi T; Syvänen, Ann-Christine AC; Hovingh, G Kees GK; Dedoussis, George G; Franks, Paul W PW; Lehtimäki, Terho T; Metspalu, Andres A; Zalloua, Pierre A PA; Siegbahn, Agneta A; Schreiber, Stefan S; Ripatti, Samuli S; Blankenberg, Stefan S SS; Perola, Markus M; Clarke, Robert R; Boehm, Bernhard O BO; O'Donnell, Christopher C; Reilly, Muredach P MP; März, Winfried W; Collins, Rory R; Kathiresan, Sekar S; Hamsten, Anders A; Kooner, Jaspal S JS; Thorsteinsdottir, Unnur U; Danesh, John J; Palmer, Colin N A CN; Roberts, Robert R; Watkins, Hugh H; Schunkert, Heribert H; Samani, Nilesh J NJ
Publication Date: 2013-01

Variant appearance in text: rs6725887
PubMed Link: 23202125
Variant Present in the following documents:
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Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

European Journal Of Neurology
Heckman, M G MG; Soto-Ortolaza, A I AI; Diehl, N N NN; Rayaprolu, S S; Brott, T G TG; Wszolek, Z K ZK; Meschia, J F JF; Ross, O A OA
Publication Date: 2013-02

Variant appearance in text: rs6725887
PubMed Link: 22882272
Variant Present in the following documents:
  • Main text
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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
Publication Date: 2012

Variant appearance in text: rs6725887
PubMed Link: 22876292
Variant Present in the following documents:
  • pone.0041730.s001.pdf
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Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

Plos One
Hughes, Maria F MF; Saarela, Olli O; Stritzke, Jan J; Kee, Frank F; Silander, Kaisa K; Klopp, Norman N; Kontto, Jukka J; Karvanen, Juha J; Willenborg, Christina C; Salomaa, Veikko V; Virtamo, Jarmo J; Amouyel, Phillippe P; Arveiler, Dominique D; Ferrières, Jean J; Wiklund, Per-Gunner PG; Baumert, Jens J; Thorand, Barbara B; Diemert, Patrick P; Trégouët, David-Alexandre DA; Hengstenberg, Christian C; Peters, Annette A; Evans, Alun A; Koenig, Wolfgang W; Erdmann, Jeanette J; Samani, Nilesh J NJ; Kuulasmaa, Kari K; Schunkert, Heribert H
Publication Date: 2012

Variant appearance in text: rs6725887
PubMed Link: 22848412
Variant Present in the following documents:
  • Main text
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A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies.

Atherosclerosis
Brautbar, Ariel A; Pompeii, Lisa A LA; Dehghan, Abbas A; Ngwa, Julius S JS; Nambi, Vijay V; Virani, Salim S SS; Rivadeneira, Fernando F; Uitterlinden, André G AG; Hofman, Albert A; Witteman, Jacqueline C M JC; Pencina, Michael J MJ; Folsom, Aaron R AR; Cupples, L Adrienne LA; Ballantyne, Christie M CM; Boerwinkle, Eric E
Publication Date: 2012-08

Variant appearance in text: rs6725887
PubMed Link: 22789513
Variant Present in the following documents:
  • Main text
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Association of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography.

Circulation. Cardiovascular Genetics
Patel, Riyaz S RS; Sun, Yan V YV; Hartiala, Jaana J; Veledar, Emir E; Su, Shaoyong S; Sher, Salman S; Liu, Ying X YX; Rahman, Ayaz A; Patel, Ronak R; Rab, S Tanveer ST; Vaccarino, Viola V; Zafari, A Maziar AM; Samady, Habib H; Tang, W H Wilson WH; Allayee, Hooman H; Hazen, Stanley L SL; Quyyumi, Arshed A AA
Publication Date: 2012-08-01

Variant appearance in text: rs6725887
PubMed Link: 22767652
Variant Present in the following documents:
  • Main text
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Randomized trial of personal genomics for preventive cardiology: design and challenges.

Circulation. Cardiovascular Genetics
Knowles, Joshua W JW; Assimes, Themistocles L TL; Kiernan, Michaela M; Pavlovic, Aleksandra A; Goldstein, Benjamin A BA; Yank, Veronica V; McConnell, Michael V MV; Absher, Devin D; Bustamante, Carlos C; Ashley, Euan A EA; Ioannidis, John P A JP
Publication Date: 2012-06

Variant appearance in text: rs6725887
PubMed Link: 22715281
Variant Present in the following documents:
  • Main text
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Circulating, imaging, and genetic biomarkers in cardiovascular risk prediction.

Trends In Cardiovascular Medicine
Ge, Yin Y; Wang, Thomas J TJ
Publication Date: 2011-05

Variant appearance in text: rs6725887
PubMed Link: 22681965
Variant Present in the following documents:
  • Main text
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Genetics of coronary artery disease in the 21st century.

Clinical Cardiology
Roberts, Robert R; Stewart, Alexandre F R AF
Publication Date: 2012-09

Variant appearance in text: rs6725887
PubMed Link: 22588700
Variant Present in the following documents:
  • Main text
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Assessment of the value of a genetic risk score in improving the estimation of coronary risk.

Atherosclerosis
Lluis-Ganella, Carla C; Subirana, Isaac I; Lucas, Gavin G; Tomás, Marta M; Muñoz, Daniel D; Sentí, Mariano M; Salas, Eduardo E; Sala, Joan J; Ramos, Rafel R; Ordovas, Jose M JM; Marrugat, Jaume J; Elosua, Roberto R
Publication Date: 2012-06

Variant appearance in text: rs6725887
PubMed Link: 22521901
Variant Present in the following documents:
  • Main text
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Atherosclerosis, inflammation, genetics, and stem cells: 2012 update.

Current Atherosclerosis Reports
Goldschmidt-Clermont, Pascal J PJ; Dong, Chunming C; Seo, David M DM; Velazquez, Omaida C OC
Publication Date: 2012-06

Variant appearance in text: rs6725887
PubMed Link: 22476914
Variant Present in the following documents:
  • Main text
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Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece.

Atherosclerosis
Yiannakouris, N N; Katsoulis, M M; Dilis, V V; Parnell, L D LD; Trichopoulos, D D; Ordovas, J M JM; Trichopoulou, A A
Publication Date: 2012-05

Variant appearance in text: rs6725887
PubMed Link: 22429504
Variant Present in the following documents:
  • Main text
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Genetics of human cardiovascular disease.

Cell
Kathiresan, Sekar S; Srivastava, Deepak D
Publication Date: 2012-03-16

Variant appearance in text: rs6725887
PubMed Link: 22424232
Variant Present in the following documents:
  • Main text
View BVdb publication page