LIPA c.229+2506G>A

Variant ID: 10-91002927-C-T

NM_000235.2(LIPA):c.229+2506G>A

This variant was identified in 51 publications

View GRCh38 version.




Publications:


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: rs1412444
PubMed Link: 36292250
Variant Present in the following documents:
  • diagnostics-12-02561.pdf
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Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?

Life (Basel, Switzerland)
Butnariu, Lăcrămioara Ionela LI; Florea, Laura L; Badescu, Minerva Codruta MC; Țarcă, Elena E; Costache, Irina-Iuliana II; Gorduza, Eusebiu Vlad EV
Publication Date: 2022-06-09

Variant appearance in text: rs1412444
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
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Interpreting coronary artery disease GWAS results: A functional genomics approach assessing biological significance.

Plos One
Hartmann, Katherine K; Seweryn, Michał M; Sadee, Wolfgang W
Publication Date: 2022

Variant appearance in text: rs1412444
PubMed Link: 35192625
Variant Present in the following documents:
  • Main text
  • pone.0244904.s010.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: rs1412444
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_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: rs1412444
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.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: rs1412444
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
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Functional Characterization of LIPA (Lysosomal Acid Lipase) Variants Associated With Coronary Artery Disease.

Arteriosclerosis, Thrombosis, And Vascular Biology
Evans, Trent D TD; Zhang, Xiangyu X; Clark, Reece E RE; Alisio, Arturo A; Song, Eric E; Zhang, Hanrui H; Reilly, Muredach P MP; Stitziel, Nathan O NO; Razani, Babak B
Publication Date: 2019-12

Variant appearance in text: rs1412444
PubMed Link: 31645127
Variant Present in the following documents:
  • Main text
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Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction.

Scientific Reports
Zhao, Juan J; Feng, QiPing Q; Wu, Patrick P; Lupu, Roxana A RA; Wilke, Russell A RA; Wells, Quinn S QS; Denny, Joshua C JC; Wei, Wei-Qi WQ
Publication Date: 2019-01-24

Variant appearance in text: rs1412444
PubMed Link: 30679510
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_36745.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: rs1412444
PubMed Link: 30003307
Variant Present in the following documents:
  • 125_2018_4686_MOESM1_ESM.pdf
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Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation.

Nature Genetics
Gamazon, Eric R ER; Segrè, Ayellet V AV; van de Bunt, Martijn M; Wen, Xiaoquan X; Xi, Hualin S HS; Hormozdiari, Farhad F; Ongen, Halit H; Konkashbaev, Anuar A; Derks, Eske M EM; Aguet, François F; Quan, Jie J; , ; Nicolae, Dan L DL; Eskin, Eleazar E; Kellis, Manolis M; Getz, Gad G; McCarthy, Mark I MI; Dermitzakis, Emmanouil T ET; Cox, Nancy J NJ; Ardlie, Kristin G KG
Publication Date: 2018-07

Variant appearance in text: rs1412444
PubMed Link: 29955180
Variant Present in the following documents:
  • Main text
  • emss-77665.pdf
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Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.

Nature Communications
Barbeira, Alvaro N AN; Dickinson, Scott P SP; Bonazzola, Rodrigo R; Zheng, Jiamao J; Wheeler, Heather E HE; Torres, Jason M JM; Torstenson, Eric S ES; Shah, Kaanan P KP; Garcia, Tzintzuni T; Edwards, Todd L TL; Stahl, Eli A EA; Huckins, Laura M LM; , ; Nicolae, Dan L DL; Cox, Nancy J NJ; Im, Hae Kyung HK
Publication Date: 2018-05-08

Variant appearance in text: rs1412444
PubMed Link: 29739930
Variant Present in the following documents:
  • 41467_2018_3621_MOESM1_ESM.pdf
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Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

Cardiovascular Diabetology
Charmet, Romain R; Duffy, Seamus S; Keshavarzi, Sareh S; Gyorgy, Beata B; Marre, Michel M; Rossing, Peter P; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; Ahluwalia, Tarun Veer Singh TVS; Paterson, Andrew D AD; Trégouët, David-Alexandre DA; Hadjadj, Samy S
Publication Date: 2018-04-25

Variant appearance in text: rs1412444
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
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Lysosomal acid lipase and lipid metabolism: new mechanisms, new questions, and new therapies.

Current Opinion In Lipidology
Zhang, Hanrui H
Publication Date: 2018-06

Variant appearance in text: rs1412444
PubMed Link: 29547398
Variant Present in the following documents:
  • Main text
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Prospective association of a genetic risk score with major adverse cardiovascular events in patients with coronary artery disease.

Medicine
Zhao, Chen C; Zhu, Pin P; Shen, Qile Q; Jin, Li L
Publication Date: 2017-12

Variant appearance in text: rs1412444
PubMed Link: 29390587
Variant Present in the following documents:
  • medi-96-e9473.pdf
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Bioinformatic Analysis of Coronary Disease Associated SNPs and Genes to Identify Proteins Potentially Involved in the Pathogenesis of Atherosclerosis.

Journal Of Proteomics And Genomics Research
Mao, Chunhong C; Howard, Timothy D TD; Sullivan, Dan D; Fu, Zongming Z; Yu, Guoqiang G; Parker, Sarah J SJ; Will, Rebecca R; Vander Heide, Richard S RS; Wang, Yue Y; Hixson, James J; Van Eyk, Jennifer J; Herrington, David M DM
Publication Date: 2017

Variant appearance in text: rs1412444
PubMed Link: 29367937
Variant Present in the following documents:
  • Main text
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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: rs1412444
PubMed Link: 29220472
Variant Present in the following documents:
  • Main text
  • bax078.pdf
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Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

Circulation Research
van der Harst, Pim P; Verweij, Niek N
Publication Date: 2018-02-02

Variant appearance in text: rs1412444
PubMed Link: 29212778
Variant Present in the following documents:
  • res-122-433-s002.xlsx, sheet 10
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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: rs1412444
PubMed Link: 28686695
Variant Present in the following documents:
  • Main text
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A comparison of Cox and logistic regression for use in genome-wide association studies of cohort and case-cohort design.

European Journal Of Human Genetics : Ejhg
Staley, James R JR; Jones, Edmund E; Kaptoge, Stephen S; Butterworth, Adam S AS; Sweeting, Michael J MJ; Wood, Angela M AM; Howson, Joanna M M JMM
Publication Date: 2017-06

Variant appearance in text: rs1412444
PubMed Link: 28594416
Variant Present in the following documents:
  • Main text
  • ejhg201778x1.pdf
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Identification of 15 novel risk loci for coronary artery disease and genetic risk of recurrent events, atrial fibrillation and heart failure.

Scientific Reports
Verweij, Niek N; Eppinga, Ruben N RN; Hagemeijer, Yanick Y; van der Harst, Pim P
Publication Date: 2017-06-05

Variant appearance in text: rs1412444
PubMed Link: 28584231
Variant Present in the following documents:
  • 41598_2017_3062_MOESM2_ESM.xls, sheet 4
View BVdb publication page



Genetic determinants of inherited susceptibility to hypercholesterolemia - a comprehensive literature review.

Lipids In Health And Disease
Paththinige, C S CS; Sirisena, N D ND; Dissanayake, Vhw V
Publication Date: 2017-06-02

Variant appearance in text: rs1412444
PubMed Link: 28577571
Variant Present in the following documents:
  • Main text
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A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death.

Plos One
Svensson, Thomas T; Kitlinski, Mariusz M; Engström, Gunnar G; Melander, Olle O
Publication Date: 2017

Variant appearance in text: rs1412444
PubMed Link: 28426714
Variant Present in the following documents:
  • Main text
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The Genetic Architecture of Coronary Artery Disease: Current Knowledge and Future Opportunities.

Current Atherosclerosis Reports
Hartiala, Jaana J; Schwartzman, William S WS; Gabbay, Julian J; Ghazalpour, Anatole A; Bennett, Brian J BJ; Allayee, Hooman H
Publication Date: 2017-02

Variant appearance in text: rs1412444
PubMed Link: 28130654
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: rs1412444
PubMed Link: 28122634
Variant Present in the following documents:
  • 13059_2016_1142_MOESM1_ESM.pdf
View BVdb publication page



Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.

Scientific Reports
Lin, Eugene E; Kuo, Po-Hsiu PH; Liu, Yu-Li YL; Yang, Albert C AC; Kao, Chung-Feng CF; Tsai, Shih-Jen SJ
Publication Date: 2016-11-09

Variant appearance in text: rs1412444
PubMed Link: 27827461
Variant Present in the following documents:
  • Main text
  • srep36830.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: rs1412444
PubMed Link: 27696788
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: rs1412444
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: rs1412444
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: rs1412444
PubMed Link: 26958643
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs1412444
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: rs1412444
PubMed Link: 26847647
Variant Present in the following documents:
  • Main text
  • 10557_2016_Article_6644.pdf
View BVdb publication page



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: rs1412444
PubMed Link: 25542012
Variant Present in the following documents:
  • Main text
  • pone.0113203.pdf
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Integromic analysis of genetic variation and gene expression identifies networks for cardiovascular disease phenotypes.

Circulation
Yao, Chen C; Chen, Brian H BH; Joehanes, Roby R; Otlu, Burcak B; Zhang, Xiaoling X; Liu, Chunyu C; Huan, Tianxiao T; Tastan, Oznur O; Cupples, L Adrienne LA; Meigs, James B JB; Fox, Caroline S CS; Freedman, Jane E JE; Courchesne, Paul P; O'Donnell, Christopher J CJ; Munson, Peter J PJ; Keles, Sunduz S; Levy, Daniel D
Publication Date: 2015-02-10

Variant appearance in text: rs1412444
PubMed Link: 25533967
Variant Present in the following documents:
  • Main text
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Association of common genetic variants with lipid traits in the Indian population.

Plos One
Walia, Gagandeep Kaur GK; Gupta, Vipin V; Aggarwal, Aastha A; Asghar, Mohammad M; Dudbridge, Frank F; Timpson, Nicholas N; Singh, Nongmaithem Suraj NS; Kumar, M Ravi MR; Kinra, Sanjay S; Prabhakaran, Dorairaj D; Reddy, K Srinath KS; Chandak, Giriraj Ratan GR; Smith, George Davey GD; Ebrahim, Shah S
Publication Date: 2014

Variant appearance in text: rs1412444
PubMed Link: 24991929
Variant Present in the following documents:
  • Main text
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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: rs1412444
PubMed Link: 24932356
Variant Present in the following documents:
  • Main text
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Heritability and genomics of gene expression in peripheral blood.

Nature Genetics
Wright, Fred A FA; Sullivan, Patrick F PF; Brooks, Andrew I AI; Zou, Fei F; Sun, Wei W; Xia, Kai K; Madar, Vered V; Jansen, Rick R; Chung, Wonil W; Zhou, Yi-Hui YH; Abdellaoui, Abdel A; Batista, Sandra S; Butler, Casey C; Chen, Guanhua G; Chen, Ting-Huei TH; D'Ambrosio, David D; Gallins, Paul P; Ha, Min Jin MJ; Hottenga, Jouke Jan JJ; Huang, Shunping S; Kattenberg, Mathijs M; Kochar, Jaspreet J; Middeldorp, Christel M CM; Qu, Ani A; Shabalin, Andrey A; Tischfield, Jay J; Todd, Laura L; Tzeng, Jung-Ying JY; van Grootheest, Gerard G; Vink, Jacqueline M JM; Wang, Qi Q; Wang, Wei W; Wang, Weibo W; Willemsen, Gonneke G; Smit, Johannes H JH; de Geus, Eco J EJ; Yin, Zhaoyu Z; Penninx, Brenda W J H BW; Boomsma, Dorret I DI
Publication Date: 2014-05

Variant appearance in text: rs1412444
PubMed Link: 24728292
Variant Present in the following documents:
  • NIHMS576016-supplement-1.pdf
View BVdb publication page



Genetic variants associated with myocardial infarction and the risk factors in Chinese population.

Plos One
Wang, Yongqin Y; Wang, Lefeng L; Liu, Xin X; Zhang, Yongzhi Y; Yu, Liping L; Zhang, Fan F; Liu, Lisheng L; Cai, Jun J; Yang, Xinchun X; Wang, Xingyu X
Publication Date: 2014

Variant appearance in text: rs1412444
PubMed Link: 24475106
Variant Present in the following documents:
  • Main text
  • pone.0086332.pdf
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Single nucleotide polymorphisms within LIPA (Lysosomal Acid Lipase A) gene are associated with susceptibility to premature coronary artery disease. a replication in the genetic of atherosclerotic disease (GEA) Mexican study.

Plos One
Vargas-Alarcón, Gilberto G; Posadas-Romero, Carlos C; Villarreal-Molina, Teresa T; Alvarez-León, Edith E; Angeles, Javier J; Vallejo, Maite M; Posadas-Sánchez, Rosalinda R; Cardoso, Guillermo G; Medina-Urrutia, Aida A; Kimura-Hayama, Eric E
Publication Date: 2013

Variant appearance in text: rs1412444
PubMed Link: 24069331
Variant Present in the following documents:
  • 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: rs1412444
PubMed Link: 24002717
Variant Present in the following documents:
  • Main text
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Positive correlation between variants of lipid metabolism‑related genes and coronary heart disease.

Molecular Medicine Reports
Zhang, Li-Na LN; Liu, Pan-Pan PP; Zhou, Jianqing J; Huang, R Stephanie RS; Yuan, Fang F; Fei, Li-Juan LJ; Huang, Yi Y; Xu, Limin L; Hao, Ling-Mei LM; Qiu, Xu-Jun XJ; Le, Yanping Y; Yang, Xi X; Xu, Weifeng W; Huang, Xiaoyan X; Ye, Meng M; Lian, Jiangfang J; Duan, Shiwei S
Publication Date: 2013-07

Variant appearance in text: rs1412444
PubMed Link: 23653095
Variant Present in the following documents:
  • 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: rs1412444
PubMed Link: 23468967
Variant Present in the following documents:
  • Main text
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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: rs1412444
PubMed Link: 23450299
Variant Present in the following documents:
  • 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: rs1412444
PubMed Link: 23202125
Variant Present in the following documents:
  • Main text
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Association of cardiovascular and metabolic disease genes with psoriasis.

The Journal Of Investigative Dermatology
Lu, Yingchang Y; Chen, Haoyan H; Nikamo, Pernilla P; Qi Low, Hui H; Helms, Cynthia C; Seielstad, Mark M; Liu, Jianjun J; Bowcock, Anne M AM; Stahle, Mona M; Liao, Wilson W
Publication Date: 2013-03

Variant appearance in text: rs1412444
PubMed Link: 23190900
Variant Present in the following documents:
  • NIHMS404713-supplement-01.pdf
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Adaptive linear rank tests for eQTL studies.

Statistics In Medicine
Szymczak, Silke S; Scheinhardt, Markus O MO; Zeller, Tanja T; Wild, Philipp S PS; Blankenberg, Stefan S; Ziegler, Andreas A
Publication Date: 2013-02-10

Variant appearance in text: rs1412444
PubMed Link: 22933317
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  • 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: rs1412444
PubMed Link: 22588700
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  • 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: rs1412444
PubMed Link: 22476914
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: rs1412444
PubMed Link: 22424232
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  • Main text
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Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

Human Molecular Genetics
Peden, John F JF; Farrall, Martin M
Publication Date: 2011-10-15

Variant appearance in text: rs1412444
PubMed Link: 21875899
Variant Present in the following documents:
  • Main text
  • ddr384.pdf
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A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease.

Circulation. Cardiovascular Genetics
Mehta, Nehal N NN
Publication Date: 2011-08-01

Variant appearance in text: rs1412444
PubMed Link: 21846871
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A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.

Circulation. Cardiovascular Genetics
Wild, Philipp S PS; Zeller, Tanja T; Schillert, Arne A; Szymczak, Silke S; Sinning, Christoph R CR; Deiseroth, Arne A; Schnabel, Renate B RB; Lubos, Edith E; Keller, Till T; Eleftheriadis, Medea S MS; Bickel, Christoph C; Rupprecht, Hans J HJ; Wilde, Sandra S; Rossmann, Heidi H; Diemert, Patrick P; Cupples, L Adrienne LA; Perret, Claire C; Erdmann, Jeanette J; Stark, Klaus K; Kleber, Marcus E ME; Epstein, Stephen E SE; Voight, Benjamin F BF; Kuulasmaa, Kari K; Li, Mingyao M; Schäfer, Arne S AS; Klopp, Norman N; Braund, Peter S PS; Sager, Hendrik B HB; Demissie, Serkalem S; Proust, Carole C; König, Inke R IR; Wichmann, Heinz-Erich HE; Reinhard, Wibke W; Hoffmann, Michael M MM; Virtamo, Jarmo J; Burnett, Mary Susan MS; Siscovick, David D; Wiklund, Per Gunnar PG; Qu, Liming L; El Mokthari, Nour Eddine NE; Thompson, John R JR; Peters, Annette A; Smith, Albert V AV; Yon, Emmanuelle E; Baumert, Jens J; Hengstenberg, Christian C; März, Winfried W; Amouyel, Philippe P; Devaney, Joseph J; Schwartz, Stephen M SM; Saarela, Olli O; Mehta, Nehal N NN; Rubin, Diana D; Silander, Kaisa K; Hall, Alistair S AS; Ferrieres, Jean J; Harris, Tamara B TB; Melander, Olle O; Kee, Frank F; Hakonarson, Hakon H; Schrezenmeir, Juergen J; Gudnason, Vilmundur V; Elosua, Roberto R; Arveiler, Dominique D; Evans, Alun A; Rader, Daniel J DJ; Illig, Thomas T; Schreiber, Stefan S; Bis, Joshua C JC; Altshuler, David D; Kavousi, Maryam M; Witteman, Jaqueline C M JC; Uitterlinden, Andre G AG; Hofman, Albert A; Folsom, Aaron R AR; Barbalic, Maja M; Boerwinkle, Eric E; Kathiresan, Sekar S; Reilly, Muredach P MP; O'Donnell, Christopher J CJ; Samani, Nilesh J NJ; Schunkert, Heribert H; Cambien, Francois F; Lackner, Karl J KJ; Tiret, Laurence L; Salomaa, Veikko V; Munzel, Thomas T; Ziegler, Andreas A; Blankenberg, Stefan S
Publication Date: 2011-08-01

Variant appearance in text: rs1412444
PubMed Link: 21606135
Variant Present in the following documents:
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