Publications:

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Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

Nature Communications

R Noordam, MM Bos, H Wang, TW Winkler, AR Bentley, TO Kilpeläinen, PS de Vries, YJ Sung, K Schwander, BE Cade, A Manning, H Aschard, MR Brown, H Chen, N Franceschini, SK Musani, M Richard, D Vojinovic, S Aslibekyan, TM Bartz, L de Las Fuentes, M Feitosa, AR Horimoto, M Ilkov, M Kho, A Kraja, C Li, E Lim, Y Liu, DO Mook-Kanamori, T Rankinen, SM Tajuddin, A van der Spek, Z Wang, J Marten, V Laville, M Alver, E Evangelou, ME Graff, M He, B Kühnel, LP Lyytikäinen, P Marques-Vidal, IM Nolte, ND Palmer, R Rauramaa, XO Shu, H Snieder, S Weiss, W Wen, LR Yanek, C Adolfo, C Ballantyne, L Bielak, NR Biermasz, E Boerwinkle, N Dimou, G Eiriksdottir, C Gao, SA Gharib, DJ Gottlieb, J Haba-Rubio, TB Harris, S Heikkinen, R Heinzer, JE Hixson, G Homuth, MA Ikram, P Komulainen, JE Krieger, J Lee, J Liu, KK Lohman, AI Luik, R Mägi, LW Martin, T Meitinger, A Metspalu, Y Milaneschi, MA Nalls, J O'Connell, A Peters, P Peyser, OT Raitakari, AP Reiner, PCN Rensen, TK Rice, SS Rich, T Roenneberg, JI Rotter, PJ Schreiner, J Shikany, SS Sidney, M Sims, CM Sitlani, T Sofer, K Strauch, MA Swertz, KD Taylor, AG Uitterlinden, CM van Duijn, H Völzke, M Waldenberger, RB Wallance, KW van Dijk, C Yu, AB Zonderman, DM Becker, P Elliott, T Esko, C Gieger, HJ Grabe, TA Lakka, T Lehtimäki, KE North, BWJH Penninx, P Vollenweider, LE Wagenknecht, T Wu, YB Xiang, W Zheng, DK Arnett, C Bouchard, MK Evans, V Gudnason, S Kardia, TN Kelly, SB Kritchevsky, RJF Loos, AC Pereira, M Province, BM Psaty, C Rotimi, X Zhu, N Amin, LA Cupples, M Fornage, EF Fox, X Guo, WJ Gauderman, K Rice, C Kooperberg, PB Munroe, CT Liu, AC Morrison, DC Rao, D van Heemst, S Redline

Publication Date: 2019-11-12

Variant appearance in text: rs10790162

PubMed Link: 31719535

Variant Present in the following documents:

• 41467_2019_12958_MOESM7_ESM.xlsx

View BVdb publication page

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Scaffold-Free Endometrial Organoids Respond to Excess Androgens Associated With Polycystic Ovarian Syndrome.

The Journal Of Clinical Endocrinology And Metabolism

T Wiwatpanit, AR Murphy, Z Lu, M Urbanek, JE Burdette, TK Woodruff, JJ Kim

Publication Date: 2020-03-01

Variant appearance in text: rs10790162

PubMed Link: 31614364

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic architecture of human plasma lipidome and its link to cardiovascular disease.

Nature Communications

R Tabassum, JT Rämö, P Ripatti, JT Koskela, M Kurki, J Karjalainen, P Palta, S Hassan, J Nunez-Fontarnau, TTJ Kiiskinen, S Söderlund, N Matikainen, MJ Gerl, MA Surma, C Klose, NO Stitziel, H Laivuori, AS Havulinna, SK Service, V Salomaa, M Pirinen, , M Jauhiainen, MJ Daly, NB Freimer, A Palotie, MR Taskinen, K Simons, S Ripatti

Publication Date: 2019-09-24

Variant appearance in text: rs10790162

PubMed Link: 31551469

Variant Present in the following documents:

• 41467_2019_11954_MOESM13_ESM.xlsx
• 41467_2019_11954_MOESM14_ESM.xlsx

View BVdb publication page

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The transferability of lipid loci across African, Asian and European cohorts.

Nature Communications

K Kuchenbaecker, N Telkar, T Reiker, RG Walters, K Lin, A Eriksson, D Gurdasani, A Gilly, L Southam, E Tsafantakis, M Karaleftheri, J Seeley, A Kamali, G Asiki, IY Millwood, M Holmes, H Du, Y Guo, M Kumari, G Dedoussis, L Li, Z Chen, MS Sandhu, E Zeggini,

Publication Date: 2019-09-24

Variant appearance in text: rs10790162

PubMed Link: 31551420

Variant Present in the following documents:

• 41467_2019_12026_MOESM2_ESM.pdf

View BVdb publication page

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Robust methods in Mendelian randomization via penalization of heterogeneous causal estimates.

Plos One

JMB Rees, AM Wood, F Dudbridge, S Burgess

Publication Date: 2019

Variant appearance in text: rs10790162

PubMed Link: 31545794

Variant Present in the following documents:

• pone.0222362.s001.pdf

View BVdb publication page

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Evolutionary history of disease-susceptibility loci identified in longitudinal exome-wide association studies.

Molecular Genetics & Genomic Medicine

Y Yasukochi, J Sakuma, I Takeuchi, K Kato, M Oguri, T Fujimaki, H Horibe, Y Yamada

Publication Date: 2019-09

Variant appearance in text: rs10790162

PubMed Link: 31402603

Variant Present in the following documents:

• MGG3-7-e925-s002.pdf

View BVdb publication page

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Association of Triglyceride-Lowering LPL Variants and LDL-C-Lowering LDLR Variants With Risk of Coronary Heart Disease.

Jama

BA Ference, JJP Kastelein, KK Ray, HN Ginsberg, MJ Chapman, CJ Packard, U Laufs, C Oliver-Williams, AM Wood, AS Butterworth, E Di Angelantonio, J Danesh, SJ Nicholls, DL Bhatt, MS Sabatine, AL Catapano

Publication Date: 2019-01-29

Variant appearance in text: rs10790162

PubMed Link: 30694319

Variant Present in the following documents:

• jama-321-364-s001.pdf

View BVdb publication page

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Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.

International Journal Of Molecular Medicine

Y Yamada, K Kato, M Oguri, H Horibe, T Fujimaki, Y Yasukochi, I Takeuchi, J Sakuma

Publication Date: 2019-01

Variant appearance in text: rs10790162

PubMed Link: 30365130

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs10790162

PubMed Link: 30333156

Variant Present in the following documents:

• Main text
• jlrM088203.pdf

View BVdb publication page

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Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics

JP Davis, JR Huyghe, AE Locke, AU Jackson, X Sim, HM Stringham, TM Teslovich, RP Welch, C Fuchsberger, N Narisu, PS Chines, AJ Kangas, P Soininen, M Ala-Korpela, J Kuusisto, FS Collins, M Laakso, M Boehnke, KL Mohlke

Publication Date: 2017-10

Variant appearance in text: rs10790162

PubMed Link: 29084231

Variant Present in the following documents:

• pgen.1007079.s010.xlsx
• pgen.1007079.s011.xlsx

View BVdb publication page

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Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.

Nature Genetics

X Lu, GM Peloso, DJ Liu, Y Wu, H Zhang, W Zhou, J Li, CS Tang, R Dorajoo, H Li, J Long, X Guo, M Xu, CN Spracklen, Y Chen, X Liu, Y Zhang, CC Khor, J Liu, L Sun, L Wang, YT Gao, Y Hu, K Yu, Y Wang, CYY Cheung, F Wang, J Huang, Q Fan, Q Cai, S Chen, J Shi, X Yang, W Zhao, WH Sheu, SS Cherny, M He, AB Feranil, LS Adair, P Gordon-Larsen, S Du, R Varma, YI Chen, XO Shu, KSL Lam, TY Wong, SK Ganesh, Z Mo, K Hveem, LG Fritsche, JB Nielsen, HF Tse, Y Huo, CY Cheng, YE Chen, W Zheng, ES Tai, W Gao, X Lin, W Huang, G Abecasis, , S Kathiresan, KL Mohlke, T Wu, PC Sham, D Gu, CJ Willer

Publication Date: 2017-12

Variant appearance in text: rs10790162

PubMed Link: 29083407

Variant Present in the following documents:

• NIHMS909133-supplement-2.xlsx

View BVdb publication page

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Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.

Plos One

LC Pilling, JL Atkins, MO Duff, RN Beaumont, SE Jones, J Tyrrell, CL Kuo, KS Ruth, MA Tuke, H Yaghootkar, AR Wood, A Murray, MN Weedon, LW Harries, GA Kuchel, L Ferrucci, TM Frayling, D Melzer

Publication Date: 2017

Variant appearance in text: rs10790162

PubMed Link: 28957414

Variant Present in the following documents:

• pone.0185083.s004.xlsx

View BVdb publication page

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Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.

Scientific Reports

S Jäger, S Wahl, J Kröger, S Sharma, P Hoffmann, A Floegel, T Pischon, C Prehn, J Adamski, M Müller-Nurasyid, M Waldenberger, K Strauch, A Peters, C Gieger, K Suhre, H Grallert, H Boeing, MB Schulze, K Meidtner

Publication Date: 2017-07-20

Variant appearance in text: rs10790162

PubMed Link: 28729637

Variant Present in the following documents:

• 41598_2017_6158_MOESM1_ESM.pdf
• aaaaaMain text

View BVdb publication page

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Association of BUD13 polymorphisms with metabolic syndrome in Chinese population: a case-control study.

Lipids In Health And Disease

L Zhang, Y You, Y Wu, Y Zhang, M Wang, Y Song, X Liu, C Kou

Publication Date: 2017-06-28

Variant appearance in text: rs10790162

PubMed Link: 28659142

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs10790162

PubMed Link: 28610615

Variant Present in the following documents:

• 12944_2017_507_MOESM4_ESM.docx

View BVdb publication page

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Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.

Oncotarget

Y Yamada, J Sakuma, I Takeuchi, Y Yasukochi, K Kato, M Oguri, T Fujimaki, H Horibe, M Muramatsu, M Sawabe, Y Fujiwara, Y Taniguchi, S Obuchi, H Kawai, S Shinkai, S Mori, T Arai, M Tanaka

Publication Date: 2017-06-13

Variant appearance in text: rs10790162

PubMed Link: 28473662

Variant Present in the following documents:

• Main text
• oncotarget-08-38950-s002.docx
• oncotarget-08-38950-s003.docx
• oncotarget-08-38950-s006.docx
• oncotarget-08-38950-s009.docx
• oncotarget-08-38950-s012.docx
• oncotarget-08-38950-s013.docx
• oncotarget-08-38950-s015.docx
• oncotarget-08-38950-s016.docx
• oncotarget-08-38950-s018.docx
• oncotarget-08-38950-s019.docx

View BVdb publication page

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Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions.

Circulation

D Saleheen, W Zhao, R Young, CP Nelson, W Ho, JF Ferguson, A Rasheed, K Ou, ST Nurnberg, RC Bauer, A Goel, R Do, AFR Stewart, J Hartiala, W Zhang, G Thorleifsson, RJ Strawbridge, J Sinisalo, S Kanoni, S Sedaghat, E Marouli, K Kristiansson, J Hua Zhao, R Scott, D Gauguier, SH Shah, AV Smith, N van Zuydam, AJ Cox, C Willenborg, T Kessler, L Zeng, MA Province, A Ganna, L Lind, NL Pedersen, CC White, A Joensuu, M Edi Kleber, AS Hall, W März, V Salomaa, C O'Donnell, E Ingelsson, MF Feitosa, J Erdmann, DW Bowden, CNA Palmer, V Gudnason, U Faire, P Zalloua, N Wareham, JR Thompson, K Kuulasmaa, G Dedoussis, M Perola, A Dehghan, JC Chambers, J Kooner, H Allayee, P Deloukas, R McPherson, K Stefansson, H Schunkert, S Kathiresan, M Farrall, P Marcel Frossard, DJ Rader, NJ Samani, MP Reilly

Publication Date: 2017-06-13

Variant appearance in text: rs10790162

PubMed Link: 28461624

Variant Present in the following documents:

• NIHMS870560-supplement-Final_Supplementary_Material.pdf

View BVdb publication page

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Mendelian Randomization Implicates High-Density Lipoprotein Cholesterol-Associated Mechanisms in Etiology of Age-Related Macular Degeneration.

Ophthalmology

S Burgess, G Davey Smith

Publication Date: 2017-08

Variant appearance in text: rs10790162

PubMed Link: 28456421

Variant Present in the following documents:

• Main text

View BVdb publication page

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Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.

Journal Of Cellular And Molecular Medicine

Y Zhu, D Zhang, D Zhou, Z Li, Z Li, L Fang, M Yang, Z Shan, H Li, J Chen, X Zhou, W Ye, S Yu, H Li, L Cai, C Liu, J Zhang, L Wang, Y Lai, L Ruan, Z Sun, S Zhang, H Wang, Y Liu, Y Xu, J Ling, C Xu, Y Zhang, D Lv, Z Yuan, J Zhang, Y Zhang, Y Shi, M Lai

Publication Date: 2017-06

Variant appearance in text: rs10790162

PubMed Link: 28371326

Variant Present in the following documents:

• JCMM-21-1106-s002.xlsx

View BVdb publication page

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Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.

Plos One

EJ Parra, A Mazurek, CR Gignoux, A Sockell, M Agostino, AP Morris, LE Petty, CL Hanis, NJ Cox, A Valladares-Salgado, JE Below, M Cruz

Publication Date: 2017

Variant appearance in text: rs10790162

PubMed Link: 28245265

Variant Present in the following documents:

• pone.0172880.s002.xlsx

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

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: rs10790162

PubMed Link: 28099408

Variant Present in the following documents:

• Main text

View BVdb publication page

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Novel genetic loci associated with long-term deterioration in blood lipid concentrations and coronary artery disease in European adults.

International Journal Of Epidemiology

TV Varga, A Kurbasic, M Aine, P Eriksson, A Ali, G Hindy, S Gustafsson, J Luan, D Shungin, Y Chen, CA Schulz, PM Nilsson, G Hallmans, I Barroso, P Deloukas, C Langenberg, RA Scott, NJ Wareham, L Lind, E Ingelsson, O Melander, M Orho-Melander, F Renström, PW Franks

Publication Date: 2017-08-01

Variant appearance in text: rs10790162

PubMed Link: 27864399

Variant Present in the following documents:

• dyw245_supplementary_method_2.docx
• dyw245_supplementary_table_7.xlsx

View BVdb publication page

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

Scientific Reports

E Lin, PH Kuo, YL Liu, AC Yang, CF Kao, SJ Tsai

Publication Date: 2016-11-09

Variant appearance in text: rs10790162

PubMed Link: 27827461

Variant Present in the following documents:

• Main text
• srep36830-s1.pdf

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

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: rs10790162

PubMed Link: 27411854

Variant Present in the following documents:

• Main text

View BVdb publication page

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A Genome-Wide mQTL Analysis in Human Adipose Tissue Identifies Genetic Variants Associated with DNA Methylation, Gene Expression and Metabolic Traits.

Plos One

P Volkov, AH Olsson, L Gillberg, SW Jørgensen, C Brøns, KF Eriksson, L Groop, PA Jansson, E Nilsson, T Rönn, A Vaag, C Ling

Publication Date: 2016

Variant appearance in text: rs10790162

PubMed Link: 27322064

Variant Present in the following documents:

• pone.0157776.s004.xlsx

View BVdb publication page

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Genetics of Insulin Resistance and the Metabolic Syndrome.

Current Cardiology Reports

AE Brown, M Walker

Publication Date: 2016-08

Variant appearance in text: rs10790162

PubMed Link: 27312935

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

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

Publication Date: 2016

Variant appearance in text: rs10790162

PubMed Link: 27257688

Variant Present in the following documents:

• Main text
• pone.0153720.s002.docx
• pone.0153720.s003.xlsx

View BVdb publication page

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Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.

Scientific Reports

JE Below, EJ Parra, ER Gamazon, J Torres, S Krithika, S Candille, Y Lu, A Manichakul, J Peralta-Romero, Q Duan, Y Li, AP Morris, O Gottesman, E Bottinger, XQ Wang, KD Taylor, YD Ida Chen, JI Rotter, SS Rich, RJ Loos, H Tang, NJ Cox, M Cruz, CL Hanis, A Valladares-Salgado

Publication Date: 2016-01-19

Variant appearance in text: rs10790162

PubMed Link: 26780889

Variant Present in the following documents:

• Main text
• srep19429-s1.pdf
• srep19429-s2.xls
• srep19429-s3.xls

View BVdb publication page

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INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing

A Verma, JB Leader, SS Verma, A Frase, J Wallace, S Dudek, DR Lavage, CV Van Hout, FE Dewey, J Penn, A Lopez, JD Overton, DJ Carey, DH Ledbetter, HL Kirchner, MD Ritchie, SA Pendergrass

Publication Date: 2016

Variant appearance in text: rs10790162

PubMed Link: 26776183

Variant Present in the following documents:

• NIHMS742521-supplement-2.pdf

View BVdb publication page

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Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome.

Molecular Genetics And Metabolism

F Tekola-Ayele, AP Doumatey, D Shriner, AR Bentley, G Chen, J Zhou, O Fasanmade, T Johnson, J Oli, G Okafor, BA Eghan, K Agyenim-Boateng, C Adebamowo, A Amoah, J Acheampong, A Adeyemo, CN Rotimi

Publication Date: 2015-12

Variant appearance in text: rs10790162

PubMed Link: 26507551

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

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

Publication Date: 2014-12

Variant appearance in text: rs10790162

PubMed Link: 25705157

Variant Present in the following documents:

• gni-12-187-s001.pdf

View BVdb publication page

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Burden of disease variants in participants of the Long Life Family Study.

Aging

M Stevenson, H Bae, N Schupf, S Andersen, Q Zhang, T Perls, P Sebastiani

Publication Date: 2015-02

Variant appearance in text: rs10790162

PubMed Link: 25664523

Variant Present in the following documents:

• aging-07-0123-s001.docx

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

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

Publication Date: 2014-07-03

Variant appearance in text: rs10790162

PubMed Link: 24989072

Variant Present in the following documents:

• Main text
• srep05565-s1.doc

View BVdb publication page

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Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine

LH Aung, RX Yin, DF Wu, W Wang, CW Liu, SL Pan

Publication Date: 2014-07

Variant appearance in text: rs10790162

PubMed Link: 24780069

Variant Present in the following documents:

• Main text
• jcmm0018-1417-SD1.doc

View BVdb publication page

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Biobanking across the phenome - at the center of chronic disease research.

Bmc Public Health

M Imboden, NM Probst-Hensch

Publication Date: 2013-11-25

Variant appearance in text: rs10790162

PubMed Link: 24274136

Variant Present in the following documents:

• 1471-2458-13-1094-S2.xlsx

View BVdb publication page

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Common variants associated with plasma triglycerides and risk for coronary artery disease.

Nature Genetics

R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, S Gustafsson, S Kanoni, A Ganna, J Chen, ML Buchkovich, S Mora, JS Beckmann, JL Bragg-Gresham, HY Chang, A Demirkan, HM Den Hertog, LA Donnelly, GB Ehret, T Esko, MF Feitosa, T Ferreira, K Fischer, P Fontanillas, RM Fraser, DF Freitag, D Gurdasani, K Heikkilä, E Hyppönen, A Isaacs, AU Jackson, A Johansson, T Johnson, M Kaakinen, J Kettunen, ME Kleber, X Li, J Luan, LP Lyytikäinen, PK Magnusson, M Mangino, E Mihailov, ME Montasser, M Müller-Nurasyid, IM Nolte, JR O'Connell, CD Palmer, M Perola, AK Petersen, S Sanna, R Saxena, SK Service, S Shah, D Shungin, C Sidore, C Song, RJ Strawbridge, I Surakka, T Tanaka, TM Teslovich, G Thorleifsson, EG Van den Herik, BF Voight, KA Volcik, LL Waite, A Wong, Y Wu, W Zhang, D Absher, G Asiki, I Barroso, LF Been, JL Bolton, LL Bonnycastle, P Brambilla, MS Burnett, G Cesana, M Dimitriou, AS Doney, A Döring, P Elliott, SE Epstein, GI Eyjolfsson, B Gigante, MO Goodarzi, H Grallert, ML Gravito, CJ Groves, G Hallmans, AL Hartikainen, C Hayward, D Hernandez, AA Hicks, H Holm, YJ Hung, T Illig, MR Jones, P Kaleebu, JJ Kastelein, KT Khaw, E Kim, N Klopp, P Komulainen, M Kumari, C Langenberg, T Lehtimäki, SY Lin, J Lindström, RJ Loos, F Mach, WL McArdle, C Meisinger, BD Mitchell, G Müller, R Nagaraja, N Narisu, TV Nieminen, RN Nsubuga, I Olafsson, KK Ong, A Palotie, T Papamarkou, C Pomilla, A Pouta, DJ Rader, MP Reilly, PM Ridker, F Rivadeneira, I Rudan, A Ruokonen, N Samani, H Scharnagl, J Seeley, K Silander, A Stančáková, K Stirrups, AJ Swift, L Tiret, AG Uitterlinden, LJ van Pelt, S Vedantam, N Wainwright, C Wijmenga, SH Wild, G Willemsen, T Wilsgaard, JF Wilson, EH Young, JH Zhao, LS Adair, D Arveiler, TL Assimes, S Bandinelli, F Bennett, M Bochud, BO Boehm, DI Boomsma, IB Borecki, SR Bornstein, P Bovet, M Burnier, H Campbell, A Chakravarti, JC Chambers, YD Chen, FS Collins, RS Cooper, J Danesh, G Dedoussis, U de Faire, AB Feranil, J Ferrières, L Ferrucci, NB Freimer, C Gieger, LC Groop, V Gudnason, U Gyllensten, A Hamsten, TB Harris, A Hingorani, JN Hirschhorn, A Hofman, GK Hovingh, CA Hsiung, SE Humphries, SC Hunt, K Hveem, C Iribarren, MR Järvelin, A Jula, M Kähönen, J Kaprio, A Kesäniemi, M Kivimaki, JS Kooner, PJ Koudstaal, RM Krauss, D Kuh, J Kuusisto, KO Kyvik, M Laakso, TA Lakka, L Lind, CM Lindgren, NG Martin, W März, MI McCarthy, CA McKenzie, P Meneton, A Metspalu, L Moilanen, AD Morris, PB Munroe, I Njølstad, NL Pedersen, C Power, PP Pramstaller, JF Price, BM Psaty, T Quertermous, R Rauramaa, D Saleheen, V Salomaa, DK Sanghera, J Saramies, PE Schwarz, WH Sheu, AR Shuldiner, A Siegbahn, TD Spector, K Stefansson, DP Strachan, BO Tayo, E Tremoli, J Tuomilehto, M Uusitupa, CM van Duijn, P Vollenweider, L Wallentin, NJ Wareham, JB Whitfield, BH Wolffenbuttel, D Altshuler, JM Ordovas, E Boerwinkle, CN Palmer, U Thorsteinsdottir, DI Chasman, JI Rotter, PW Franks, S Ripatti, LA Cupples, MS Sandhu, SS Rich, M Boehnke, P Deloukas, KL Mohlke, E Ingelsson, GR Abecasis, MJ Daly, BM Neale, S Kathiresan

Publication Date: 2013-11

Variant appearance in text: rs10790162

PubMed Link: 24097064

Variant Present in the following documents:

• Main text
• NIHMS524704-supplement-1.pdf

View BVdb publication page

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Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.

Circulation. Cardiovascular Genetics

K Kristiansson, M Perola, E Tikkanen, J Kettunen, I Surakka, AS Havulinna, A Stancáková, C Barnes, E Widen, E Kajantie, JG Eriksson, J Viikari, M Kähönen, T Lehtimäki, OT Raitakari, AL Hartikainen, A Ruokonen, A Pouta, A Jula, AJ Kangas, P Soininen, M Ala-Korpela, S Männistö, P Jousilahti, LL Bonnycastle, MR Järvelin, J Kuusisto, FS Collins, M Laakso, ME Hurles, A Palotie, L Peltonen, S Ripatti, V Salomaa

Publication Date: 2012-04-01

Variant appearance in text: rs10790162

PubMed Link: 22399527

Variant Present in the following documents:

• NIHMS47601-supplement-supp_data.pdf

View BVdb publication page

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Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

Nature Genetics

J Kettunen, T Tukiainen, AP Sarin, A Ortega-Alonso, E Tikkanen, LP Lyytikäinen, AJ Kangas, P Soininen, P Würtz, K Silander, DM Dick, RJ Rose, MJ Savolainen, J Viikari, M Kähönen, T Lehtimäki, KH Pietiläinen, M Inouye, MI McCarthy, A Jula, J Eriksson, OT Raitakari, V Salomaa, J Kaprio, MR Järvelin, L Peltonen, M Perola, NB Freimer, M Ala-Korpela, A Palotie, S Ripatti

Publication Date: 2012-01-29

Variant appearance in text: rs10790162

PubMed Link: 22286219

Variant Present in the following documents:

• NIHMS444574-supplement-supplementary_table_2.xlsx

View BVdb publication page

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A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.

Diabetes

AT Kraja, D Vaidya, JS Pankow, MO Goodarzi, TL Assimes, IJ Kullo, U Sovio, RA Mathias, YV Sun, N Franceschini, D Absher, G Li, Q Zhang, MF Feitosa, NL Glazer, T Haritunians, AL Hartikainen, JW Knowles, KE North, C Iribarren, B Kral, L Yanek, PF O'Reilly, MI McCarthy, C Jaquish, DJ Couper, A Chakravarti, BM Psaty, LC Becker, MA Province, E Boerwinkle, T Quertermous, L Palotie, MR Jarvelin, DM Becker, SL Kardia, JI Rotter, YD Chen, IB Borecki

Publication Date: 2011-04

Variant appearance in text: rs10790162

PubMed Link: 21386085

Variant Present in the following documents:

• Main text

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Genome-wide association of lipid-lowering response to statins in combined study populations.

Plos One

MJ Barber, LM Mangravite, CL Hyde, DI Chasman, JD Smith, CA McCarty, X Li, RA Wilke, MJ Rieder, PT Williams, PM Ridker, A Chatterjee, JI Rotter, DA Nickerson, M Stephens, RM Krauss

Publication Date: 2010-03-22

Variant appearance in text: rs10790162

PubMed Link: 20339536

Variant Present in the following documents:

• pone.0009763.s008.xls

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000260210.4	c.237+1741T>C	-	intron_variant	-	2/9
ENST00000375445.3	c.237+1741T>C	-	intron_variant	-	2/9
NM_001159736.1	c.237+1741T>C	-	intron_variant	-	2/9
NM_032725.4	c.237+1741T>C	-	intron_variant	-	2/9