Publications:

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Genome-wide association study of metabolic syndrome in Korean populations.

Plos One

SW Oh, JE Lee, E Shin, H Kwon, EK Choe, SY Choi, H Rhee, SH Choi

Publication Date: 2020

Variant appearance in text: N/A

PMID: 31910446

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Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data.

Genes & Genomics

D Li, H Kang, S Lee, S Won

Publication Date: 2020-01-04

Variant appearance in text: rs6589566

PMID: 31902109

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Effect of Interaction between Early Menarche and Genetic Polymorphisms on Triglyceride.

Oxidative Medicine And Cellular Longevity

HS Lee, S Leem, B Oh, T Park

Publication Date: 2019

Variant appearance in text: rs6589566

PMID: 30931082

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Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics

S Moon, Y Lee, S Won, J Lee

Publication Date: 2018-11-01

Variant appearance in text: rs6589566

PMID: 30382898

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Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

Journal Of Lipid Research

AS Geller, EY Polisecki, MR Diffenderfer, BF Asztalos, SK Karathanasis, RA Hegele, EJ Schaefer

Publication Date: 2018-12

Variant appearance in text: N/A

PMID: 30333156

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New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.

Scientific Reports

HS Lee, Y Kim, T Park

Publication Date: 2018-04-09

Variant appearance in text: rs6589566

PMID: 29632305

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Prediction of cholesterol ratios within a Korean population.

Royal Society Open Science

JS Lee, HS Cheong, HD Shin

Publication Date: 2018-01

Variant appearance in text: rs6589566

PMID: 29410832

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Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.

Lipids In Health And Disease

R Pranavchand, BM Reddy

Publication Date: 2017-06-13

Variant appearance in text: rs6589566

PMID: 28610615

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Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.

Human Genomics

R Pranavchand, AS Kumar, BM Reddy

Publication Date: 2017-03-04

Variant appearance in text: N/A

PMID: 28257648

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Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.

Pharmacogenetics And Genomics

A Verma, Y Bradford, SS Verma, SA Pendergrass, ES Daar, C Venuto, GD Morse, MD Ritchie, DW Haas

Publication Date: 2017-03

Variant appearance in text: rs6589566

PMID: 28099408

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Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup.

Plos One

T Kim, AY Park, Y Baek, S Cha

Publication Date: 2017

Variant appearance in text: N/A

PMID: 28046027

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Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes.

Scientific Reports

F Guan, Y Niu, T Zhang, S Liu, L Ma, T Qi, J Feng, H Zuo, G Li, X Liu, S Wang

Publication Date: 2016-07-14

Variant appearance in text: rs6589566

PMID: 27411854

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Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Plos One

R Pranav Chand, AS Kumar, K Anuj, S Vishnupriya, B Mohan Reddy

Publication Date: 2016

Variant appearance in text: rs6589566

PMID: 27257688

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Effects of Polymorphisms in APOA4-APOA5-ZNF259-BUD13 Gene Cluster on Plasma Levels of Triglycerides and Risk of Coronary Heart Disease in a Chinese Han Population.

Plos One

Q Fu, X Tang, J Chen, L Su, M Zhang, L Wang, J Jing, L Zhou

Publication Date: 2015

Variant appearance in text: rs6589566

PMID: 26397108

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Networks in Coronary Heart Disease Genetics As a Step towards Systems Epidemiology.

Plos One

F Drenos, E Grossi, M Buscema, SE Humphries

Publication Date: 2015

Variant appearance in text: rs6589566

PMID: 25951190

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Genome-wide association study of metabolic syndrome in koreans.

Genomics & Informatics

SW Jeong, M Chung, SJ Park, SB Cho, KW Hong

Publication Date: 2014-12

Variant appearance in text: rs6589566

PMID: 25705157

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On the analysis of a repeated measure design in genome-wide association analysis.

International Journal Of Environmental Research And Public Health

Y Lee, S Park, S Moon, J Lee, RC Elston, W Lee, S Won

Publication Date: 2014-11-28

Variant appearance in text: rs6589566

PMID: 25464127

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Genetic loci associated with changes in lipid levels leading to constitution-based discrepancy in Koreans.

Bmc Complementary And Alternative Medicine

SK Chung, H Yu, AY Park, JY Kim, S Cha

Publication Date: 2014-07-09

Variant appearance in text: N/A

PMID: 25005712

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Association between the MLX interacting protein-like, BUD13 homolog and zinc finger protein 259 gene polymorphisms and serum lipid levels.

Scientific Reports

LH Aung, RX Yin, JZ Wu, DF Wu, W Wang, H Li

Publication Date: 2014-07-03

Variant appearance in text: rs6589566

PMID: 24989072

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Effects of apolipoprotein A5 haplotypes on the ratio of triglyceride to high-density lipoprotein cholesterol and the risk for metabolic syndrome in Koreans.

Lipids In Health And Disease

S Cha, H Yu, AY Park, KH Song

Publication Date: 2014-03-12

Variant appearance in text: rs6589566

PMID: 24618354

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Impact of HDL genetic risk scores on coronary artery calcified plaque and mortality in individuals with type 2 diabetes from the Diabetes Heart Study.

Cardiovascular Diabetology

LM Raffield, AJ Cox, FC Hsu, MC Ng, CD Langefeld, JJ Carr, BI Freedman, DW Bowden

Publication Date: 2013-06-25

Variant appearance in text: rs6589566

PMID: 23799899

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Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.

American Journal Of Human Genetics

MA Coram, Q Duan, TJ Hoffmann, T Thornton, JW Knowles, NA Johnson, HM Ochs-Balcom, TA Donlon, LW Martin, CB Eaton, JG Robinson, NJ Risch, X Zhu, C Kooperberg, Y Li, AP Reiner, H Tang

Publication Date: 2013-06-06

Variant appearance in text: rs6589566

PMID: 23726366

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The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population.

Plos One

I Radovica, D Fridmanis, I Vaivade, L Nikitina-Zake, J Klovins

Publication Date: 2013

Variant appearance in text: rs6589566

PMID: 23675527

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Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.

Cardiovascular Diabetology

CM Povel, JM Boer, NC Onland-Moret, ME Dollé, EJ Feskens, YT van der Schouw

Publication Date: 2012-10-29

Variant appearance in text: rs6589566

PMID: 23101478

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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.

Lancet (London, England)

BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, MK Jensen, G Hindy, H Hólm, EL Ding, T Johnson, H Schunkert, NJ Samani, R Clarke, JC Hopewell, JF Thompson, M Li, G Thorleifsson, C Newton-Cheh, K Musunuru, JP Pirruccello, D Saleheen, L Chen, A Stewart, A Schillert, U Thorsteinsdottir, G Thorgeirsson, S Anand, JC Engert, T Morgan, J Spertus, M Stoll, K Berger, N Martinelli, D Girelli, PP McKeown, CC Patterson, SE Epstein, J Devaney, MS Burnett, V Mooser, S Ripatti, I Surakka, MS Nieminen, J Sinisalo, ML Lokki, M Perola, A Havulinna, U de Faire, B Gigante, E Ingelsson, T Zeller, P Wild, PI de Bakker, OH Klungel, AH Maitland-van der Zee, BJ Peters, A de Boer, DE Grobbee, PW Kamphuisen, VH Deneer, CC Elbers, NC Onland-Moret, MH Hofker, C Wijmenga, WM Verschuren, JM Boer, YT van der Schouw, A Rasheed, P Frossard, S Demissie, C Willer, R Do, JM Ordovas, GR Abecasis, M Boehnke, KL Mohlke, MJ Daly, C Guiducci, NP Burtt, A Surti, E Gonzalez, S Purcell, S Gabriel, J Marrugat, J Peden, J Erdmann, P Diemert, C Willenborg, IR König, M Fischer, C Hengstenberg, A Ziegler, I Buysschaert, D Lambrechts, F Van de Werf, KA Fox, NE El Mokhtari, D Rubin, J Schrezenmeir, S Schreiber, A Schäfer, J Danesh, S Blankenberg, R Roberts, R McPherson, H Watkins, AS Hall, K Overvad, E Rimm, E Boerwinkle, A Tybjaerg-Hansen, LA Cupples, MP Reilly, O Melander, PM Mannucci, D Ardissino, D Siscovick, R Elosua, K Stefansson, CJ O'Donnell, V Salomaa, DJ Rader, L Peltonen, SM Schwartz, D Altshuler, S Kathiresan

Publication Date: 2012-08-11

Variant appearance in text: rs6589566

PMID: 22607825

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Implications of discoveries from genome-wide association studies in current cardiovascular practice.

World Journal Of Cardiology

P Jeemon, K Pettigrew, C Sainsbury, D Prabhakaran, S Padmanabhan

Publication Date: 2011-07-26

Variant appearance in text: rs6589566

PMID: 21860704

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Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.

European Heart Journal

A Angelakopoulou, T Shah, R Sofat, S Shah, DJ Berry, J Cooper, J Palmen, I Tzoulaki, A Wong, BJ Jefferis, N Maniatis, F Drenos, B Gigante, R Hardy, RC Laxton, K Leander, A Motterle, IA Simpson, L Smeeth, A Thomson, C Verzilli, D Kuh, H Ireland, J Deanfield, M Caulfield, C Wallace, N Samani, PB Munroe, M Lathrop, FG Fowkes, M Marmot, PH Whincup, JC Whittaker, U de Faire, M Kivimaki, M Kumari, E Hypponen, C Power, SE Humphries, PJ Talmud, J Price, RW Morris, S Ye, JP Casas, AD Hingorani

Publication Date: 2012-02

Variant appearance in text: rs6589566

PMID: 21804106

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A gene-centric association scan for Coagulation Factor VII levels in European and African Americans: the Candidate Gene Association Resource (CARe) Consortium.

Human Molecular Genetics

KC Taylor, LA Lange, D Zabaneh, E Lange, BJ Keating, W Tang, NL Smith, JA Delaney, M Kumari, A Hingorani, KE North, M Kivimaki, RP Tracy, CJ O'Donnell, AR Folsom, D Green, SE Humphries, AP Reiner

Publication Date: 2011-09-01

Variant appearance in text: N/A

PMID: 21676895

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Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

American Journal Of Epidemiology

OA Panagiotou, E Evangelou, JP Ioannidis

Publication Date: 2010-10-15

Variant appearance in text: N/A

PMID: 20876667

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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets

KL Monda, KE North, SC Hunt, DC Rao, MA Province, AT Kraja

Publication Date: 2010-06

Variant appearance in text: rs6589566

PMID: 20406164

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Genome-wide association analyses of North American Rheumatoid Arthritis Consortium and Framingham Heart Study data utilizing genome-wide linkage results.

Bmc Proceedings

YJ Yoo, D Pinnaduwage, D Waggott, SB Bull, L Sun

Publication Date: 2009-12-15

Variant appearance in text: rs6589566

PMID: 20017967

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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.

Human Molecular Genetics

RA Hegele, MR Ban, N Hsueh, BA Kennedy, H Cao, GY Zou, S Anand, S Yusuf, MW Huff, J Wang

Publication Date: 2009-11-01

Variant appearance in text: rs6589566

PMID: 19656773

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Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics

F Drenos, PJ Talmud, JP Casas, L Smeeth, J Palmen, SE Humphries, AD Hingorani

Publication Date: 2009-06-15

Variant appearance in text: rs6589566

PMID: 19336475

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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.

American Journal Of Human Genetics

C Wallace, SJ Newhouse, P Braund, F Zhang, M Tobin, M Falchi, K Ahmadi, RJ Dobson, AC Marçano, C Hajat, P Burton, P Deloukas, M Brown, JM Connell, A Dominiczak, GM Lathrop, J Webster, M Farrall, T Spector, NJ Samani, MJ Caulfield, PB Munroe

Publication Date: 2008-01

Variant appearance in text: rs6589566

PMID: 18179892

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000227322.3	c.1179+451C>A	-	intron_variant	-	12/13
ENST00000429220.1	c.958+451C>A	-	intron_variant	-	10/11
ENST00000444935.1	c.1091+1212C>A	-	intron_variant	-	11/12
NM_001317086.2	c.1017+451C>A	-	intron_variant	-	11/12
NM_003904.5	c.1179+451C>A	-	intron_variant	-	12/13