Publications:

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs6589566

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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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: rs6589566

PubMed Link: 35379196

Variant Present in the following documents:

• Main text
• 12872_2022_Article_2562.pdf

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Genetic factors increase the identification efficiency of predictive models for dyslipidaemia: a prospective cohort study.

Lipids In Health And Disease

Niu, Miaomiao M; Zhang, Liying L; Wang, Yikang Y; Tu, Runqi R; Liu, Xiaotian X; Hou, Jian J; Huo, Wenqian W; Mao, Zhenxing Z; Wang, Zhenfei Z; Wang, Chongjian C

Publication Date: 2021-02-12

Variant appearance in text: rs6589566

PubMed Link: 33579296

Variant Present in the following documents:

• Main text
• 12944_2021_Article_1439.pdf

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Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.

Human Genetics

Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Alsmadi, Osama O; Elkum, Naser N; Alkayal, Fadi F; John, Sumi Elsa SE; Channanath, Arshad A; Iqbal, Rasheeba R; Pitkaniemi, Janne J; Tuomilehto, Jaakko J; Sladek, Robert R; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA

Publication Date: 2021-03

Variant appearance in text: rs6589566

PubMed Link: 32902719

Variant Present in the following documents:

• Main text

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Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels.

Journal Of Human Genetics

Carlson, Jenna C JC; Weeks, Daniel E DE; Hawley, Nicola L NL; Sun, Guangyun G; Cheng, Hong H; Naseri, Take T; Reupena, Muagututi'a Sefuiva MS; Tuitele, John J; Deka, Ranjan R; McGarvey, Stephen T ST; Minster, Ryan L RL

Publication Date: 2021-02

Variant appearance in text: rs6589566

PubMed Link: 32759990

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Plos One

Oh, Seung-Won SW; Lee, Jong-Eun JE; Shin, Eunsoon E; Kwon, Hyuktae H; Choe, Eun Kyung EK; Choi, Su-Yeon SY; Rhee, Hwanseok H; Choi, Seung Ho SH

Publication Date: 2020

Variant appearance in text: rs6589566

PubMed Link: 31910446

Variant Present in the following documents:

• Main text
• pone.0227357.pdf

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

Genes & Genomics

Li, Donghe D; Kang, Hahn H; Lee, Sanghun S; Won, Sungho S

Publication Date: 2020-04

Variant appearance in text: rs6589566

PubMed Link: 31902109

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Oxidative Medicine And Cellular Longevity

Lee, Ho-Sun HS; Leem, Sangseob S; Oh, Bermseok B; Park, Taesung T

Publication Date: 2019

Variant appearance in text: rs6589566

PubMed Link: 30931082

Variant Present in the following documents:

• Main text
• OMCL2019-9148920.pdf

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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

Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J

Publication Date: 2018-11-01

Variant appearance in text: rs6589566

PubMed Link: 30382898

Variant Present in the following documents:

• Main text

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

Journal Of Lipid Research

Geller, Andrew S AS; Polisecki, Eliana Y EY; Diffenderfer, Margaret R MR; Asztalos, Bela F BF; Karathanasis, Sotirios K SK; Hegele, Robert A RA; Schaefer, Ernst J EJ

Publication Date: 2018-12

Variant appearance in text: rs6589566

PubMed Link: 30333156

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Scientific Reports

Lee, Ho-Sun HS; Kim, Yongkang Y; Park, Taesung T

Publication Date: 2018-04-09

Variant appearance in text: rs6589566

PubMed Link: 29632305

Variant Present in the following documents:

• Main text

View BVdb publication page

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Prediction of cholesterol ratios within a Korean population.

Royal Society Open Science

Lee, Jin Sol JS; Cheong, Hyun Sub HS; Shin, Hyoung Doo HD

Publication Date: 2018-01

Variant appearance in text: rs6589566

PubMed Link: 29410832

Variant Present in the following documents:

• Main text
• rsos171204.pdf

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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

Pranavchand, Rayabarapu R; Reddy, Battini Mohan BM

Publication Date: 2017-06-13

Variant appearance in text: rs6589566

PubMed Link: 28610615

Variant Present in the following documents:

• Main text

View BVdb publication page

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Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits.

Nature Communications

Southam, Lorraine L; Gilly, Arthur A; Süveges, Dániel D; Farmaki, Aliki-Eleni AE; Schwartzentruber, Jeremy J; Tachmazidou, Ioanna I; Matchan, Angela A; Rayner, Nigel W NW; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Xue, Yali Y; Dedoussis, George G; Zeggini, Eleftheria E

Publication Date: 2017-05-26

Variant appearance in text: rs6589566

PubMed Link: 28548082

Variant Present in the following documents:

• ncomms15606-s1.pdf

View BVdb publication page

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

Human Genomics

Pranavchand, Rayabarapu R; Kumar, Arramraju Sreenivas AS; Reddy, Battini Mohan BM

Publication Date: 2017-03-04

Variant appearance in text: rs6589566

PubMed Link: 28257648

Variant Present in the following documents:

• Main text

View BVdb publication page

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Combinatorial bZIP dimers display complex DNA-binding specificity landscapes.

Elife

Rodríguez-Martínez, José A JA; Reinke, Aaron W AW; Bhimsaria, Devesh D; Keating, Amy E AE; Ansari, Aseem Z AZ

Publication Date: 2017-02-10

Variant appearance in text: rs6589566

PubMed Link: 28186491

Variant Present in the following documents:

• elife-19272.pdf

View BVdb publication page

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

Pharmacogenetics And Genomics

Verma, Anurag A; Bradford, Yuki Y; Verma, Shefali S SS; Pendergrass, Sarah A SA; Daar, Eric S ES; Venuto, Charles C; Morse, Gene D GD; Ritchie, Marylyn D MD; Haas, David W DW

Publication Date: 2017-03

Variant appearance in text: rs6589566

PubMed Link: 28099408

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Plos One

Kim, Taehyeung T; Park, Ah Yeon AY; Baek, Younghwa Y; Cha, Seongwon S

Publication Date: 2017

Variant appearance in text: rs6589566

PubMed Link: 28046027

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Guan, Fanglin F; Niu, Yu Y; Zhang, Tianxiao T; Liu, Songfang S; Ma, Lei L; Qi, Ting T; Feng, Jia J; Zuo, Hong H; Li, Guohong G; Liu, Xufeng X; Wang, Shujin S

Publication Date: 2016-07-14

Variant appearance in text: rs6589566

PubMed Link: 27411854

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Pranav Chand, Rayabarapu R; Kumar, Arramraju Sreenivas AS; Anuj, Kapadia K; Vishnupriya, Satti S; Mohan Reddy, Battini B

Publication Date: 2016

Variant appearance in text: rs6589566

PubMed Link: 27257688

Variant Present in the following documents:

• Main text
• pone.0153720.pdf

View BVdb publication page

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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

Fu, Qianxi Q; Tang, Xiaojun X; Chen, Juan J; Su, Li L; Zhang, Mingjun M; Wang, Long L; Jing, Jinjin J; Zhou, Li L

Publication Date: 2015

Variant appearance in text: rs6589566

PubMed Link: 26397108

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Plos One

Drenos, Fotios F; Grossi, Enzo E; Buscema, Massimo M; Humphries, Steve E SE

Publication Date: 2015

Variant appearance in text: rs6589566

PubMed Link: 25951190

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association study of metabolic syndrome in koreans.

Genomics & Informatics

Jeong, Seok Won SW; Chung, Myungguen M; Park, Soo-Jung SJ; Cho, Seong Beom SB; Hong, Kyung-Won KW

Publication Date: 2014-12

Variant appearance in text: rs6589566

PubMed Link: 25705157

Variant Present in the following documents:

• Main text
• gni-12-187.pdf

View BVdb publication page

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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

Lee, Young Y; Park, Suyeon S; Moon, Sanghoon S; Lee, Juyoung J; Elston, Robert C RC; Lee, Woojoo W; Won, Sungho S

Publication Date: 2014-11-28

Variant appearance in text: rs6589566

PubMed Link: 25464127

Variant Present in the following documents:

• Main text
• ijerph-11-12283.pdf

View BVdb publication page

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

Bmc Complementary And Alternative Medicine

Chung, Sun-Ku SK; Yu, Hyunjoo H; Park, Ah Yeon AY; Kim, Jong Yeol JY; Cha, Seongwon S

Publication Date: 2014-07-09

Variant appearance in text: rs6589566

PubMed Link: 25005712

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Aung, Lynn-Htet-Htet LH; Yin, Rui-Xing RX; Wu, Jin-Zhen JZ; Wu, Dong-Feng DF; Wang, Wei W; Li, Hui H

Publication Date: 2014-07-03

Variant appearance in text: rs6589566

PubMed Link: 24989072

Variant Present in the following documents:

• Main text
• srep05565.pdf

View BVdb publication page

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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

Cha, Seongwon S; Yu, Hyunjoo H; Park, Ah Yeon AY; Song, Kwang Hoon KH

Publication Date: 2014-03-12

Variant appearance in text: rs6589566

PubMed Link: 24618354

Variant Present in the following documents:

• Main text
• 1476-511X-13-45.pdf

View BVdb publication page

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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

Raffield, Laura M LM; Cox, Amanda J AJ; Hsu, Fang-Chi FC; Ng, Maggie C-Y MC; Langefeld, Carl D CD; Carr, J Jeffrey JJ; Freedman, Barry I BI; Bowden, Donald W DW

Publication Date: 2013-06-25

Variant appearance in text: rs6589566

PubMed Link: 23799899

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Coram, Marc A MA; Duan, Qing Q; Hoffmann, Thomas J TJ; Thornton, Timothy T; Knowles, Joshua W JW; Johnson, Nicholas A NA; Ochs-Balcom, Heather M HM; Donlon, Timothy A TA; Martin, Lisa W LW; Eaton, Charles B CB; Robinson, Jennifer G JG; Risch, Neil J NJ; Zhu, Xiaofeng X; Kooperberg, Charles C; Li, Yun Y; Reiner, Alex P AP; Tang, Hua H

Publication Date: 2013-06-06

Variant appearance in text: rs6589566

PubMed Link: 23726366

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Plos One

Radovica, Ilze I; Fridmanis, Davids D; Vaivade, Iveta I; Nikitina-Zake, Liene L; Klovins, Janis J

Publication Date: 2013

Variant appearance in text: rs6589566

PubMed Link: 23675527

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Povel, Cécile M CM; Boer, Jolanda M A JM; Onland-Moret, N Charlotte NC; Dollé, Martijn E T ME; Feskens, Edith J M EJ; van der Schouw, Yvonne T YT

Publication Date: 2012-10-29

Variant appearance in text: rs6589566

PubMed Link: 23101478

Variant Present in the following documents:

• Main text
• 1475-2840-11-133.pdf

View BVdb publication page

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

Lancet (London, England)

Voight, Benjamin F BF; Peloso, Gina M GM; Orho-Melander, Marju M; Frikke-Schmidt, Ruth R; Barbalic, Maja M; Jensen, Majken K MK; Hindy, George G; Hólm, Hilma H; Ding, Eric L EL; Johnson, Toby T; Schunkert, Heribert H; Samani, Nilesh J NJ; Clarke, Robert R; Hopewell, Jemma C JC; Thompson, John F JF; Li, Mingyao M; Thorleifsson, Gudmar G; Newton-Cheh, Christopher C; Musunuru, Kiran K; Pirruccello, James P JP; Saleheen, Danish D; Chen, Li L; Stewart, Alexandre F R A; Schillert, Arne A; Thorsteinsdottir, Unnur U; Thorgeirsson, Gudmundur G; Anand, Sonia S; Engert, James C JC; Morgan, Thomas T; Spertus, John J; Stoll, Monika M; Berger, Klaus K; Martinelli, Nicola N; Girelli, Domenico D; McKeown, Pascal P PP; Patterson, Christopher C CC; Epstein, Stephen E SE; Devaney, Joseph J; Burnett, Mary-Susan MS; Mooser, Vincent V; Ripatti, Samuli S; Surakka, Ida I; Nieminen, Markku S MS; Sinisalo, Juha J; Lokki, Marja-Liisa ML; Perola, Markus M; Havulinna, Aki A; de Faire, Ulf U; Gigante, Bruna B; Ingelsson, Erik E; Zeller, Tanja T; Wild, Philipp P; de Bakker, Paul I W PI; Klungel, Olaf H OH; Maitland-van der Zee, Anke-Hilse AH; Peters, Bas J M BJ; de Boer, Anthonius A; Grobbee, Diederick E DE; Kamphuisen, Pieter W PW; Deneer, Vera H M VH; Elbers, Clara C CC; Onland-Moret, N Charlotte NC; Hofker, Marten H MH; Wijmenga, Cisca C; Verschuren, W M Monique WM; Boer, Jolanda M A JM; van der Schouw, Yvonne T YT; Rasheed, Asif A; Frossard, Philippe P; Demissie, Serkalem S; Willer, Cristen C; Do, Ron R; Ordovas, Jose M JM; Abecasis, Gonçalo R GR; Boehnke, Michael M; Mohlke, Karen L KL; Daly, Mark J MJ; Guiducci, Candace C; Burtt, Noël P NP; Surti, Aarti A; Gonzalez, Elena E; Purcell, Shaun S; Gabriel, Stacey S; Marrugat, Jaume J; Peden, John J; Erdmann, Jeanette J; Diemert, Patrick P; Willenborg, Christina C; König, Inke R IR; Fischer, Marcus M; Hengstenberg, Christian C; Ziegler, Andreas A; Buysschaert, Ian I; Lambrechts, Diether D; Van de Werf, Frans F; Fox, Keith A KA; El Mokhtari, Nour Eddine NE; Rubin, Diana D; Schrezenmeir, Jürgen J; Schreiber, Stefan S; Schäfer, Arne A; Danesh, John J; Blankenberg, Stefan S; Roberts, Robert R; McPherson, Ruth R; Watkins, Hugh H; Hall, Alistair S AS; Overvad, Kim K; Rimm, Eric E; Boerwinkle, Eric E; Tybjaerg-Hansen, Anne A; Cupples, L Adrienne LA; Reilly, Muredach P MP; Melander, Olle O; Mannucci, Pier M PM; Ardissino, Diego D; Siscovick, David D; Elosua, Roberto R; Stefansson, Kari K; O'Donnell, Christopher J CJ; Salomaa, Veikko V; Rader, Daniel J DJ; Peltonen, Leena L; Schwartz, Stephen M SM; Altshuler, David D; Kathiresan, Sekar S

Publication Date: 2012-08-11

Variant appearance in text: rs6589566

PubMed Link: 22607825

Variant Present in the following documents:

• Main text

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

World Journal Of Cardiology

Jeemon, Panniyammakal P; Pettigrew, Kerry K; Sainsbury, Christopher C; Prabhakaran, Dorairaj D; Padmanabhan, Sandosh S

Publication Date: 2011-07-26

Variant appearance in text: rs6589566

PubMed Link: 21860704

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Angelakopoulou, Aspasia A; Shah, Tina T; Sofat, Reecha R; Shah, Sonia S; Berry, Diane J DJ; Cooper, Jackie J; Palmen, Jutta J; Tzoulaki, Ioanna I; Wong, Andrew A; Jefferis, Barbara J BJ; Maniatis, Nikolas N; Drenos, Fotios F; Gigante, Bruna B; Hardy, Rebecca R; Laxton, Ross C RC; Leander, Karin K; Motterle, Anna A; Simpson, Iain A IA; Smeeth, Liam L; Thomson, Andy A; Verzilli, Claudio C; Kuh, Diana D; Ireland, Helen H; Deanfield, John J; Caulfield, Mark M; Wallace, Chris C; Samani, Nilesh N; Munroe, Patricia B PB; Lathrop, Mark M; Fowkes, F Gerry R FG; Marmot, Michael M; Whincup, Peter H PH; Whittaker, John C JC; de Faire, Ulf U; Kivimaki, Mika M; Kumari, Meena M; Hypponen, Elina E; Power, Chris C; Humphries, Steve E SE; Talmud, Philippa J PJ; Price, Jackie J; Morris, Richard W RW; Ye, Shu S; Casas, Juan P JP; Hingorani, Aroon D AD

Publication Date: 2012-02

Variant appearance in text: rs6589566

PubMed Link: 21804106

Variant Present in the following documents:

• Main text
• ehr225.pdf

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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

Taylor, Kira C KC; Lange, Leslie A LA; Zabaneh, Delilah D; Lange, Ethan E; Keating, Brendan J BJ; Tang, Weihong W; Smith, Nicholas L NL; Delaney, Joseph A JA; Kumari, Meena M; Hingorani, Aroon A; North, Kari E KE; Kivimaki, Mika M; Tracy, Russell P RP; O'Donnell, Christopher J CJ; Folsom, Aaron R AR; Green, David D; Humphries, Steve E SE; Reiner, Alexander P AP

Publication Date: 2011-09-01

Variant appearance in text: rs6589566

PubMed Link: 21676895

Variant Present in the following documents:

• Main text

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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

Panagiotou, Orestis A OA; Evangelou, Evangelos E; Ioannidis, John P A JP

Publication Date: 2010-10-15

Variant appearance in text: rs6589566

PubMed Link: 20876667

Variant Present in the following documents:

• Main text

View BVdb publication page

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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets

Monda, Keri L KL; North, Kari E KE; Hunt, Steven C SC; Rao, D C DC; Province, Michael A MA; Kraja, Aldi T AT

Publication Date: 2010-06

Variant appearance in text: rs6589566

PubMed Link: 20406164

Variant Present in the following documents:

• Main text

View BVdb publication page

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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

Yoo, Yun Joo YJ; Pinnaduwage, Dushanthi D; Waggott, Daryl D; Bull, Shelley B SB; Sun, Lei L

Publication Date: 2009-12-15

Variant appearance in text: rs6589566

PubMed Link: 20017967

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Human Molecular Genetics

Hegele, Robert A RA; Ban, Matthew R MR; Hsueh, Neil N; Kennedy, Brooke A BA; Cao, Henian H; Zou, Guang Yong GY; Anand, Sonia S; Yusuf, Salim S; Huff, Murray W MW; Wang, Jian J

Publication Date: 2009-11-01

Variant appearance in text: rs6589566

PubMed Link: 19656773

Variant Present in the following documents:

• Main text

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

Human Molecular Genetics

Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD

Publication Date: 2009-06-15

Variant appearance in text: rs6589566

PubMed Link: 19336475

Variant Present in the following documents:

• Main text
• ddp159_1.pdf
• ddp159.pdf

View BVdb publication page

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

American Journal Of Human Genetics

Wallace, Chris C; Newhouse, Stephen J SJ; Braund, Peter P; Zhang, Feng F; Tobin, Martin M; Falchi, Mario M; Ahmadi, Kourosh K; Dobson, Richard J RJ; Marçano, Ana Carolina B AC; Hajat, Cother C; Burton, Paul P; Deloukas, Panagiotis P; Brown, Morris M; Connell, John M JM; Dominiczak, Anna A; Lathrop, G Mark GM; Webster, John J; Farrall, Martin M; Spector, Tim T; Samani, Nilesh J NJ; Caulfield, Mark J MJ; Munroe, Patricia B PB

Publication Date: 2008-01

Variant appearance in text: rs6589566

PubMed Link: 18179892

Variant Present in the following documents:

• Main text

View BVdb publication page

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