Publications:

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Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity.

Gigascience

BB Chu, KL Keys, CA German, H Zhou, JJ Zhou, EM Sobel, JS Sinsheimer, K Lange

Publication Date: 2020-06-01

Variant appearance in text: rs7499892

PubMed Link: 32491161

Variant Present in the following documents:

• Main text

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The Effect of Haplotypes in the CETP and LIPC Genes on the Triglycerides to HDL-C Ratio and Its Components in the Roma and Hungarian General Populations.

Genes

P Piko, S Fiatal, NA Werissa, BB Bekele, G Racz, Z Kosa, J Sandor, R Adany

Publication Date: 2020-01-03

Variant appearance in text: rs7499892

PubMed Link: 31947886

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

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

Publication Date: 2020

Variant appearance in text: rs7499892

PubMed Link: 31910446

Variant Present in the following documents:

• Main text

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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: rs7499892

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: rs7499892

PubMed Link: 31551420

Variant Present in the following documents:

• 41467_2019_12026_MOESM2_ESM.pdf

View BVdb publication page

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Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes.

Human Heredity

Y Yu, L Xia, S Lee, X Zhou, HM Stringham, M Boehnke, B Mukherjee

Publication Date: 2018

Variant appearance in text: rs7499892

PubMed Link: 31132756

Variant Present in the following documents:

• Main text

View BVdb publication page

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A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study.

Bmc Medical Genomics

X Zhao, X Geng, V Srinivasasainagendra, N Chaudhary, S Judd, V Wadley, OM Gutiérrez, H Wang, EM Lange, LA Lange, D Woo, FW Unverzagt, M Safford, M Cushman, N Limdi, R Quarells, DK Arnett, MR Irvin, D Zhi

Publication Date: 2019-01-31

Variant appearance in text: rs7499892

PubMed Link: 30704471

Variant Present in the following documents:

• Main text

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Gene-Based Elevated Triglycerides and Type 2 Diabetes Mellitus Risk in the Women's Genome Health Study.

Arteriosclerosis, Thrombosis, And Vascular Biology

S Ahmad, S Mora, PM Ridker, FB Hu, DI Chasman

Publication Date: 2019-01

Variant appearance in text: rs7499892

PubMed Link: 30565958

Variant Present in the following documents:

• NIHMS1512616-supplement-Supplemental_Material.pdf

View BVdb publication page

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Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease.

Alzheimer'S & Dementia (Amsterdam, Netherlands)

GM Peloso, SJ van der Lee, , AL Destefano, S Seshardi

Publication Date: 2018

Variant appearance in text: rs7499892

PubMed Link: 30422133

Variant Present in the following documents:

• Main text

View BVdb publication page

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The role of genetic variation of human metabolism for BMI, mental traits and mental disorders.

Molecular Metabolism

J Hebebrand, T Peters, D Schijven, M Hebebrand, C Grasemann, TW Winkler, IM Heid, J Antel, M Föcker, L Tegeler, L Brauner, RAH Adan, JJ Luykx, CU Correll, IR König, A Hinney, L Libuda

Publication Date: 2018-06

Variant appearance in text: rs7499892

PubMed Link: 29673576

Variant Present in the following documents:

• mmc1.xlsx

View BVdb publication page

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Genetic variations of cholesteryl ester transfer protein and diet interactions in relation to lipid profiles and coronary heart disease: a systematic review.

Nutrition & Metabolism

P Mirmiran, Z Esfandiar, F Hosseini-Esfahani, G Koochakpoor, MS Daneshpour, B Sedaghati-Khayat, F Azizi

Publication Date: 2017

Variant appearance in text: rs7499892

PubMed Link: 29234452

Variant Present in the following documents:

• 12986_2017_231_MOESM1_ESM.docx

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: rs7499892

PubMed Link: 29084231

Variant Present in the following documents:

• pgen.1007079.s010.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: rs7499892

PubMed Link: 29083407

Variant Present in the following documents:

• NIHMS909133-supplement-1.docx
• NIHMS909133-supplement-2.xlsx

View BVdb publication page

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PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.

Nature Communications

MA Hall, J Wallace, A Lucas, D Kim, AO Basile, SS Verma, CA McCarty, MH Brilliant, PL Peissig, TE Kitchner, A Verma, SA Pendergrass, SM Dudek, JH Moore, MD Ritchie

Publication Date: 2017-10-27

Variant appearance in text: rs7499892

PubMed Link: 29079728

Variant Present in the following documents:

• Main text

View BVdb publication page

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Iterative hard thresholding for model selection in genome-wide association studies.

Genetic Epidemiology

KL Keys, GK Chen, K Lange

Publication Date: 2017-12

Variant appearance in text: rs7499892

PubMed Link: 28875524

Variant Present in the following documents:

• Main text
• NIHMS898446-supplement-Supp_TableS1-2.docx

View BVdb publication page

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A Scalable Bayesian Method for Integrating Functional Information in Genome-wide Association Studies.

American Journal Of Human Genetics

J Yang, LG Fritsche, X Zhou, G Abecasis,

Publication Date: 2017-09-07

Variant appearance in text: rs7499892

PubMed Link: 28844487

Variant Present in the following documents:

• mmc1.pdf
• mmc2.pdf

View BVdb publication page

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Data to genetic risk assessment on high-density cholesterol level associated polymorphisms in Hungarian general and Roma populations.

Data In Brief

P Pikó, S Fiatal, Z Kósa, J Sándor, R Ádány

Publication Date: 2017-10

Variant appearance in text: rs7499892

PubMed Link: 28795114

Variant Present in the following documents:

• Main text

View BVdb publication page

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Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C.

Npj Aging And Mechanisms Of Disease

EM van Leeuwen, JE Huffman, JC Bis, A Isaacs, M Mulder, A Sabo, AV Smith, S Demissie, A Manichaikul, JA Brody, MF Feitosa, Q Duan, KE Schraut, P Navarro, JV van Vliet-Ostaptchouk, G Zhu, H Mbarek, S Trompet, N Verweij, LP Lyytikäinen, J Deelen, IM Nolte, SW van der Laan, G Davies, AJ Vermeij-Verdoold, AA van Oosterhout, JM Vergeer-Drop, DE Arking, H Trochet, , C Medina-Gomez, F Rivadeneira, AG Uitterlinden, A Dehghan, OH Franco, EJ Sijbrands, A Hofman, CC White, JC Mychaleckyj, GM Peloso, MA Swertz, , G Willemsen, EJ de Geus, Y Milaneschi, BW Penninx, I Ford, BM Buckley, AJ de Craen, JM Starr, IJ Deary, G Pasterkamp, AJ Oldehinkel, H Snieder, PE Slagboom, K Nikus, M Kähönen, T Lehtimäki, JS Viikari, OT Raitakari, P van der Harst, JW Jukema, JJ Hottenga, DI Boomsma, JB Whitfield, G Montgomery, NG Martin, , O Polasek, V Vitart, C Hayward, I Kolcic, AF Wright, I Rudan, PK Joshi, JF Wilson, LA Lange, JG Wilson, V Gudnason, TB Harris, AC Morrison, IB Borecki, SS Rich, S Padmanabhan, BM Psaty, JI Rotter, BH Smith, E Boerwinkle, LA Cupples, C van Duijn

Publication Date: 2015

Variant appearance in text: rs7499892

PubMed Link: 28721259

Variant Present in the following documents:

• Main text
• npjamd201511-s1.doc

View BVdb publication page

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Replication and fine-mapping of genetic predictors of lipid traits in African-Americans.

Journal Of Human Genetics

Q Feng, WQ Wei, RT Levinson, JD Mosley, CM Stein

Publication Date: 2017-10

Variant appearance in text: rs7499892

PubMed Link: 28539666

Variant Present in the following documents:

• Main text

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: rs7499892

PubMed Link: 28473662

Variant Present in the following documents:

• oncotarget-08-38950-s002.docx
• oncotarget-08-38950-s013.docx
• oncotarget-08-38950-s016.docx
• oncotarget-08-38950-s019.docx

View BVdb publication page

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Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.

Human Molecular Genetics

N Zubair, M Graff, J Luis Ambite, WS Bush, G Kichaev, Y Lu, A Manichaikul, WH Sheu, D Absher, TL Assimes, SJ Bielinski, EP Bottinger, P Buzkova, LM Chuang, RH Chung, B Cochran, L Dumitrescu, O Gottesman, JW Haessler, C Haiman, G Heiss, CA Hsiung, YJ Hung, CM Hwu, JJ Juang, L Le Marchand, IT Lee, WJ Lee, LA Lin, D Lin, SY Lin, RH Mackey, LW Martin, B Pasaniuc, U Peters, I Predazzi, T Quertermous, AP Reiner, J Robinson, JI Rotter, KK Ryckman, PJ Schreiner, E Stahl, R Tao, MY Tsai, LL Waite, TD Wang, S Buyske, YD Ida Chen, I Cheng, DC Crawford, RJF Loos, SS Rich, M Fornage, KE North, C Kooperberg, CL Carty

Publication Date: 2016-12-15

Variant appearance in text: rs7499892

PubMed Link: 28426890

Variant Present in the following documents:

• ddw358_supp.docx

View BVdb publication page

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Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).

Human Genetics

Z Wang, A Manichukal, DC Goff, S Mora, JM Ordovas, NM Pajewski, WS Post, JI Rotter, MM Sale, SA Santorico, D Siscovick, MY Tsai, DK Arnett, S Rich, AC Frazier-Wood

Publication Date: 2017-06

Variant appearance in text: rs7499892

PubMed Link: 28352986

Variant Present in the following documents:

• 439_2017_1782_MOESM1_ESM.docx

View BVdb publication page

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Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.

Genome Medicine

R Nagy, TS Boutin, J Marten, JE Huffman, SM Kerr, A Campbell, L Evenden, J Gibson, C Amador, DM Howard, P Navarro, A Morris, IJ Deary, LJ Hocking, S Padmanabhan, BH Smith, P Joshi, JF Wilson, ND Hastie, AF Wright, AM McIntosh, DJ Porteous, CS Haley, V Vitart, C Hayward

Publication Date: 2017-03-07

Variant appearance in text: rs7499892

PubMed Link: 28270201

Variant Present in the following documents:

• 13073_2017_414_MOESM9_ESM.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: rs7499892

PubMed Link: 27827461

Variant Present in the following documents:

• srep36830-s1.pdf

View BVdb publication page

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c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One

M Ganesan, S Nizamuddin, SK Katkam, K Kumaraswami, UK Hosad, LL Lobo, VK Kutala, K Thangaraj

Publication Date: 2016

Variant appearance in text: rs7499892

PubMed Link: 27768712

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variants in CETP increase risk of intracerebral hemorrhage.

Annals Of Neurology

CD Anderson, GJ Falcone, CL Phuah, F Radmanesh, HB Brouwers, TW Battey, A Biffi, GM Peloso, DJ Liu, AM Ayres, JN Goldstein, A Viswanathan, SM Greenberg, M Selim, JF Meschia, DL Brown, BB Worrall, SL Silliman, DL Tirschwell, ML Flaherty, P Kraft, JM Jagiella, H Schmidt, BM Hansen, J Jimenez-Conde, E Giralt-Steinhauer, R Elosua, E Cuadrado-Godia, C Soriano, KM van Nieuwenhuizen, CJ Klijn, K Rannikmae, N Samarasekera, R Al-Shahi Salman, CL Sudlow, IJ Deary, A Morotti, A Pezzini, J Pera, A Urbanik, A Pichler, C Enzinger, B Norrving, J Montaner, I Fernandez-Cadenas, P Delgado, J Roquer, A Lindgren, A Slowik, R Schmidt, CS Kidwell, SJ Kittner, SP Waddy, CD Langefeld, G Abecasis, CJ Willer, S Kathiresan, D Woo, J Rosand,

Publication Date: 2016-11

Variant appearance in text: rs7499892

PubMed Link: 27717122

Variant Present in the following documents:

• Main text

View BVdb publication page

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Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.

Nature Genetics

V Iotchkova, J Huang, JA Morris, D Jain, C Barbieri, K Walter, JL Min, L Chen, W Astle, M Cocca, P Deelen, H Elding, AE Farmaki, CS Franklin, M Franberg, TR Gaunt, A Hofman, T Jiang, ME Kleber, G Lachance, J Luan, G Malerba, A Matchan, D Mead, Y Memari, I Ntalla, K Panoutsopoulou, R Pazoki, JRB Perry, F Rivadeneira, M Sabater-Lleal, B Sennblad, SY Shin, L Southam, M Traglia, F van Dijk, EM van Leeuwen, G Zaza, W Zhang, , N Amin, A Butterworth, JC Chambers, G Dedoussis, A Dehghan, OH Franco, L Franke, M Frontini, G Gambaro, P Gasparini, A Hamsten, A Issacs, JS Kooner, C Kooperberg, C Langenberg, W Marz, RA Scott, MA Swertz, D Toniolo, AG Uitterlinden, CM van Duijn, H Watkins, E Zeggini, MT Maurano, NJ Timpson, AP Reiner, PL Auer, N Soranzo

Publication Date: 2016-11

Variant appearance in text: rs7499892

PubMed Link: 27668658

Variant Present in the following documents:

• NIHMS71079-supplement-Supplementary_Data.pdf

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: rs7499892

PubMed Link: 26780889

Variant Present in the following documents:

• Main text
• srep19429-s1.pdf
• srep19429-s3.xls
• srep19429-s5.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: rs7499892

PubMed Link: 26776183

Variant Present in the following documents:

• NIHMS742521-supplement-2.pdf

View BVdb publication page

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Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Heredity

M Shirali, R Pong-Wong, P Navarro, S Knott, C Hayward, V Vitart, I Rudan, H Campbell, ND Hastie, AF Wright, CS Haley

Publication Date: 2016-03

Variant appearance in text: rs7499892

PubMed Link: 26696135

Variant Present in the following documents:

• Main text
• hdy2015107x1.docx

View BVdb publication page

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Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Metabolism: Clinical And Experimental

D Pirim, X Wang, V Niemsiri, ZH Radwan, CH Bunker, JE Hokanson, RF Hamman, MM Barmada, FY Demirci, MI Kamboh

Publication Date: 2016-01

Variant appearance in text: rs7499892

PubMed Link: 26683795

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.

Human Molecular Genetics

A Spiliopoulou, R Nagy, ML Bermingham, JE Huffman, C Hayward, V Vitart, I Rudan, H Campbell, AF Wright, JF Wilson, R Pong-Wong, F Agakov, P Navarro, CS Haley

Publication Date: 2015-07-15

Variant appearance in text: rs7499892

PubMed Link: 25918167

Variant Present in the following documents:

• Main text

View BVdb publication page

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A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians.

Plos One

H Shim, DI Chasman, JD Smith, S Mora, PM Ridker, DA Nickerson, RM Krauss, M Stephens

Publication Date: 2015

Variant appearance in text: rs7499892

PubMed Link: 25898129

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetics of kidney disease and related cardiometabolic phenotypes in Zuni Indians: the Zuni Kidney Project.

Frontiers In Genetics

SL Laston, VS Voruganti, K Haack, VO Shah, A Bobelu, J Bobelu, D Ghahate, AM Harford, SS Paine, F Tentori, SA Cole, JW MacCluer, AG Comuzzie, PG Zager

Publication Date: 2015

Variant appearance in text: rs7499892

PubMed Link: 25688259

Variant Present in the following documents:

• Main text

View BVdb publication page

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New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nature Communications

CY Cheng, K Yamashiro, LJ Chen, J Ahn, L Huang, L Huang, CM Cheung, M Miyake, PD Cackett, IY Yeo, A Laude, R Mathur, J Pang, KS Sim, AH Koh, P Chen, SY Lee, D Wong, CM Chan, BK Loh, Y Sun, S Davila, I Nakata, H Nakanishi, Y Akagi-Kurashige, N Gotoh, A Tsujikawa, F Matsuda, K Mori, S Yoneya, Y Sakurada, H Iijima, T Iida, S Honda, TY Lai, PO Tam, H Chen, S Tang, X Ding, F Wen, F Lu, X Zhang, Y Shi, P Zhao, B Zhao, J Sang, B Gong, R Dorajoo, JM Yuan, WP Koh, RM van Dam, Y Friedlander, Y Lin, ML Hibberd, JN Foo, N Wang, CH Wong, GS Tan, SJ Park, M Bhargava, L Gopal, T Naing, J Liao, PG Ong, P Mitchell, P Zhou, X Xie, J Liang, J Mei, X Jin, SM Saw, M Ozaki, T Mizoguchi, Y Kurimoto, SJ Woo, H Chung, HG Yu, JY Shin, DH Park, IT Kim, W Chang, M Sagong, SJ Lee, HW Kim, JE Lee, Y Li, J Liu, YY Teo, CK Heng, TH Lim, SK Yang, K Song, EN Vithana, T Aung, JX Bei, YX Zeng, ES Tai, XX Li, Z Yang, KH Park, CP Pang, N Yoshimura, TY Wong, CC Khor

Publication Date: 2015-01-28

Variant appearance in text: rs7499892

PubMed Link: 25629512

Variant Present in the following documents:

• ncomms7063-s1.pdf

View BVdb publication page

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Association between CETP, MLXIPL, and TOMM40 polymorphisms and serum lipid levels in a Latvian population.

Meta Gene

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

Publication Date: 2014-12

Variant appearance in text: rs7499892

PubMed Link: 25606439

Variant Present in the following documents:

• mmc2.docx

View BVdb publication page

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MGAS: a powerful tool for multivariate gene-based genome-wide association analysis.

Bioinformatics (Oxford, England)

S Van der Sluis, CV Dolan, J Li, Y Song, P Sham, D Posthuma, MX Li

Publication Date: 2015-04-01

Variant appearance in text: rs7499892

PubMed Link: 25431328

Variant Present in the following documents:

• Main text

View BVdb publication page

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Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology study.

Circulation. Cardiovascular Genetics

CL Carty, S Bhattacharjee, J Haessler, I Cheng, LA Hindorff, V Aroda, CS Carlson, CN Hsu, L Wilkens, S Liu, E Selvin, R Jackson, KE North, U Peters, JS Pankow, N Chatterjee, C Kooperberg

Publication Date: 2014-08

Variant appearance in text: rs7499892

PubMed Link: 25023634

Variant Present in the following documents:

• Main text
• NIHMS614064-supplement-000386_-_PAP.pdf

View BVdb publication page

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Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.

Genetic Epidemiology

JN Hellwege, ND Palmer, LM Raffield, MC Ng, GA Hawkins, J Long, C Lorenzo, JM Norris, YD Ida Chen, EK Speliotes, JI Rotter, CD Langefeld, LE Wagenknecht, DW Bowden

Publication Date: 2014-05

Variant appearance in text: rs7499892

PubMed Link: 24719370

Variant Present in the following documents:

• Main text
• NIHMS649741-supplement-supplemental_tables.docx

View BVdb publication page

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CETP gene polymorphisms and risk of coronary atherosclerosis in a Chinese population.

Lipids In Health And Disease

J Wang, LJ Wang, Y Zhong, P Gu, JQ Shao, SS Jiang, JB Gong

Publication Date: 2013-11-27

Variant appearance in text: rs7499892

PubMed Link: 24283500

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels.

Journal Of Lipid Research

Y Wu, AF Marvelle, J Li, DC Croteau-Chonka, AB Feranil, CW Kuzawa, Y Li, LS Adair, KL Mohlke

Publication Date: 2013-11

Variant appearance in text: rs7499892

PubMed Link: 24023260

Variant Present in the following documents:

• Main text

View BVdb publication page

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Properties of local interactions and their potential value in complementing genome-wide association studies.

Plos One

W Wei, A Gyenesei, CA Semple, CS Haley

Publication Date: 2013

Variant appearance in text: rs7499892

PubMed Link: 23940718

Variant Present in the following documents:

• Main text
• pone.0071203.s003.xlsx

View BVdb publication page

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Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adults.

Lipids In Health And Disease

AJ Clifford, G Rincon, JE Owens, JF Medrano, AJ Moshfegh, DJ Baer, JA Novotny

Publication Date: 2013-05-08

Variant appearance in text: rs7499892

PubMed Link: 23656756

Variant Present in the following documents:

• Main text

View BVdb publication page

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Investigation of gene-by-sex interactions for lipid traits in diverse populations from the population architecture using genomics and epidemiology study.

Bmc Genetics

KC Taylor, CL Carty, L Dumitrescu, P Bůžková, SA Cole, L Hindorff, FR Schumacher, LR Wilkens, RV Shohet, PM Quibrera, KC Johnson, BE Henderson, J Haessler, N Franceschini, CB Eaton, DJ Duggan, B Cochran, I Cheng, CS Carlson, K Brown-Gentry, G Anderson, JL Ambite, C Haiman, L Le Marchand, C Kooperberg, DC Crawford, S Buyske, KE North, M Fornage,

Publication Date: 2013-05-01

Variant appearance in text: rs7499892

PubMed Link: 23634756

Variant Present in the following documents:

• Main text

View BVdb publication page

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Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.

Plos Genetics

Y Wu, LL Waite, AU Jackson, WH Sheu, S Buyske, D Absher, DK Arnett, E Boerwinkle, LL Bonnycastle, CL Carty, I Cheng, B Cochran, DC Croteau-Chonka, L Dumitrescu, CB Eaton, N Franceschini, X Guo, BE Henderson, LA Hindorff, E Kim, L Kinnunen, P Komulainen, WJ Lee, L Le Marchand, Y Lin, J Lindström, O Lingaas-Holmen, SL Mitchell, N Narisu, JG Robinson, F Schumacher, A Stančáková, J Sundvall, YJ Sung, AJ Swift, WC Wang, L Wilkens, T Wilsgaard, AM Young, LS Adair, CM Ballantyne, P Bůžková, A Chakravarti, FS Collins, D Duggan, AB Feranil, LT Ho, YJ Hung, SC Hunt, K Hveem, JM Juang, AY Kesäniemi, J Kuusisto, M Laakso, TA Lakka, IT Lee, MF Leppert, TC Matise, L Moilanen, I Njølstad, U Peters, T Quertermous, R Rauramaa, JI Rotter, J Saramies, J Tuomilehto, M Uusitupa, TD Wang, M Boehnke, CA Haiman, YD Chen, C Kooperberg, TL Assimes, DC Crawford, CA Hsiung, KE North, KL Mohlke

Publication Date: 2013-03

Variant appearance in text: rs7499892

PubMed Link: 23555291

Variant Present in the following documents:

• Main text

View BVdb publication page

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Seven new loci associated with age-related macular degeneration.

Nature Genetics

LG Fritsche, W Chen, M Schu, BL Yaspan, Y Yu, G Thorleifsson, DJ Zack, S Arakawa, V Cipriani, S Ripke, RP Igo, GH Buitendijk, X Sim, DE Weeks, RH Guymer, JE Merriam, PJ Francis, G Hannum, A Agarwal, AM Armbrecht, I Audo, T Aung, GR Barile, M Benchaboune, AC Bird, PN Bishop, KE Branham, M Brooks, AJ Brucker, WH Cade, MS Cain, PA Campochiaro, CC Chan, CY Cheng, EY Chew, KA Chin, I Chowers, DG Clayton, R Cojocaru, YP Conley, BK Cornes, MJ Daly, B Dhillon, AO Edwards, E Evangelou, J Fagerness, HA Ferreyra, JS Friedman, A Geirsdottir, RJ George, C Gieger, N Gupta, SA Hagstrom, SP Harding, C Haritoglou, JR Heckenlively, FG Holz, G Hughes, JP Ioannidis, T Ishibashi, P Joseph, G Jun, Y Kamatani, N Katsanis, C N Keilhauer, JC Khan, IK Kim, Y Kiyohara, BE Klein, R Klein, JL Kovach, I Kozak, CJ Lee, KE Lee, P Lichtner, AJ Lotery, T Meitinger, P Mitchell, S Mohand-Saïd, AT Moore, DJ Morgan, MA Morrison, CE Myers, AC Naj, Y Nakamura, Y Okada, A Orlin, MC Ortube, MI Othman, C Pappas, KH Park, GJ Pauer, NS Peachey, O Poch, RR Priya, R Reynolds, AJ Richardson, R Ripp, G Rudolph, E Ryu, JA Sahel, DA Schaumberg, HP Scholl, SG Schwartz, WK Scott, H Shahid, H Sigurdsson, G Silvestri, TA Sivakumaran, RT Smith, L Sobrin, EH Souied, DE Stambolian, H Stefansson, GM Sturgill-Short, A Takahashi, N Tosakulwong, BJ Truitt, EE Tsironi, AG Uitterlinden, CM van Duijn, L Vijaya, JR Vingerling, EN Vithana, AR Webster, HE Wichmann, TW Winkler, TY Wong, AF Wright, D Zelenika, M Zhang, L Zhao, K Zhang, ML Klein, GS Hageman, GM Lathrop, K Stefansson, R Allikmets, PN Baird, MB Gorin, JJ Wang, CC Klaver, JM Seddon, MA Pericak-Vance, SK Iyengar, JR Yates, A Swaroop, BH Weber, M Kubo, MM Deangelis, T Léveillard, U Thorsteinsdottir, JL Haines, LA Farrer, IM Heid, GR Abecasis,

Publication Date: 2013-04

Variant appearance in text: rs7499892

PubMed Link: 23455636

Variant Present in the following documents:

• NIHMS474886-supplement-1.pdf

View BVdb publication page

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Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.

Plos One

CC Elbers, Y Guo, V Tragante, EP van Iperen, MB Lanktree, BA Castillo, F Chen, LR Yanek, MK Wojczynski, YR Li, B Ferwerda, CM Ballantyne, SG Buxbaum, YD Chen, WM Chen, LA Cupples, M Cushman, Y Duan, D Duggan, MK Evans, JK Fernandes, M Fornage, M Garcia, WT Garvey, N Glazer, F Gomez, TB Harris, I Halder, VJ Howard, MF Keller, MI Kamboh, C Kooperberg, SB Kritchevsky, A LaCroix, K Liu, Y Liu, K Musunuru, AB Newman, NC Onland-Moret, J Ordovas, I Peter, W Post, S Redline, SE Reis, R Saxena, PJ Schreiner, KA Volcik, X Wang, S Yusuf, AB Zonderland, SS Anand, DM Becker, B Psaty, DJ Rader, AP Reiner, SS Rich, JI Rotter, MM Sale, MY Tsai, IB Borecki, RA Hegele, S Kathiresan, MA Nalls, HA Taylor, H Hakonarson, S Sivapalaratnam, FW Asselbergs, F Drenos, JG Wilson, BJ Keating

Publication Date: 2012

Variant appearance in text: rs7499892

PubMed Link: 23236364

Variant Present in the following documents:

• Main text
• pone.0050198.s007.xlsx

View BVdb publication page

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Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

American Journal Of Human Genetics

FW Asselbergs, Y Guo, EP van Iperen, S Sivapalaratnam, V Tragante, MB Lanktree, LA Lange, B Almoguera, YE Appelman, J Barnard, J Baumert, AL Beitelshees, TR Bhangale, YD Chen, TR Gaunt, Y Gong, JC Hopewell, T Johnson, ME Kleber, TY Langaee, M Li, YR Li, K Liu, CW McDonough, MF Meijs, RP Middelberg, K Musunuru, CP Nelson, JR O'Connell, S Padmanabhan, JS Pankow, N Pankratz, S Rafelt, R Rajagopalan, SP Romaine, NJ Schork, J Shaffer, H Shen, EN Smith, SE Tischfield, PJ van der Most, JV van Vliet-Ostaptchouk, N Verweij, KA Volcik, L Zhang, KR Bailey, KM Bailey, F Bauer, JM Boer, PS Braund, A Burt, PR Burton, SG Buxbaum, W Chen, RM Cooper-Dehoff, LA Cupples, JS deJong, C Delles, D Duggan, M Fornage, CE Furlong, N Glazer, JG Gums, C Hastie, MV Holmes, T Illig, SA Kirkland, M Kivimaki, R Klein, BE Klein, C Kooperberg, K Kottke-Marchant, M Kumari, AZ LaCroix, L Mallela, G Murugesan, J Ordovas, WH Ouwehand, WS Post, R Saxena, H Scharnagl, PJ Schreiner, T Shah, DC Shields, D Shimbo, SR Srinivasan, RP Stolk, DI Swerdlow, HA Taylor, EJ Topol, E Toskala, JL van Pelt, J van Setten, S Yusuf, JC Whittaker, AH Zwinderman, , SS Anand, AJ Balmforth, GS Berenson, CR Bezzina, BO Boehm, E Boerwinkle, JP Casas, MJ Caulfield, R Clarke, JM Connell, KJ Cruickshanks, KW Davidson, IN Day, PI de Bakker, PA Doevendans, AF Dominiczak, AS Hall, CA Hartman, C Hengstenberg, HL Hillege, MH Hofker, SE Humphries, GP Jarvik, JA Johnson, BM Kaess, S Kathiresan, W Koenig, DA Lawlor, W März, O Melander, BD Mitchell, GW Montgomery, PB Munroe, SS Murray, SJ Newhouse, NC Onland-Moret, N Poulter, B Psaty, S Redline, SS Rich, JI Rotter, H Schunkert, P Sever, AR Shuldiner, RL Silverstein, A Stanton, B Thorand, MD Trip, MY Tsai, P van der Harst, E van der Schoot, YT van der Schouw, WM Verschuren, H Watkins, AA Wilde, BH Wolffenbuttel, JB Whitfield, GK Hovingh, CM Ballantyne, C Wijmenga, MP Reilly, NG Martin, JG Wilson, DJ Rader, NJ Samani, AP Reiner, RA Hegele, JJ Kastelein, AD Hingorani, PJ Talmud, H Hakonarson, CC Elbers, BJ Keating, F Drenos

Publication Date: 2012-11-02

Variant appearance in text: rs7499892

PubMed Link: 23063622

Variant Present in the following documents:

• mmc4.xls
• mmc5.xls
• mmc6.xls
• mmc7.xls

View BVdb publication page

---

A mixed-model approach for genome-wide association studies of correlated traits in structured populations.

Nature Genetics

A Korte, BJ Vilhjálmsson, V Segura, A Platt, Q Long, M Nordborg

Publication Date: 2012-09

Variant appearance in text: rs7499892

PubMed Link: 22902788

Variant Present in the following documents:

• NIHMS392993-supplement-1.pdf

View BVdb publication page

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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.

Nature Genetics

V Segura, BJ Vilhjálmsson, A Platt, A Korte, Ü Seren, Q Long, M Nordborg

Publication Date: 2012-06-17

Variant appearance in text: rs7499892

PubMed Link: 22706313

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

Plos One

K Musunuru, SP Romaine, G Lettre, JG Wilson, KA Volcik, MY Tsai, HA Taylor, PJ Schreiner, JI Rotter, SS Rich, S Redline, BM Psaty, GJ Papanicolaou, JM Ordovas, K Liu, RM Krauss, NL Glazer, SB Gabriel, M Fornage, LA Cupples, SG Buxbaum, E Boerwinkle, CM Ballantyne, S Kathiresan, DJ Rader

Publication Date: 2012

Variant appearance in text: rs7499892

PubMed Link: 22629316

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma.

Cancer Discovery

J Shi, N Chatterjee, M Rotunno, Y Wang, AC Pesatori, D Consonni, P Li, W Wheeler, P Broderick, M Henrion, T Eisen, Z Wang, W Chen, Q Dong, D Albanes, M Thun, MR Spitz, PA Bertazzi, NE Caporaso, SJ Chanock, CI Amos, RS Houlston, MT Landi

Publication Date: 2012-02

Variant appearance in text: rs7499892

PubMed Link: 22585858

Variant Present in the following documents:

• NIHMS343818-supplement-1.pdf

View BVdb publication page

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Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk.

Plos One

AC Papp, JK Pinsonneault, D Wang, LC Newman, Y Gong, JA Johnson, CJ Pepine, M Kumari, AD Hingorani, PJ Talmud, S Shah, SE Humphries, W Sadee

Publication Date: 2012

Variant appearance in text: rs7499892

PubMed Link: 22403620

Variant Present in the following documents:

• pone.0031930.s009.docx
• pone.0031930.s010.docx

View BVdb publication page

---

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

Plos Genetics

A Demirkan, CM van Duijn, P Ugocsai, A Isaacs, PP Pramstaller, G Liebisch, JF Wilson, Å Johansson, I Rudan, YS Aulchenko, AV Kirichenko, AC Janssens, RC Jansen, C Gnewuch, FS Domingues, C Pattaro, SH Wild, I Jonasson, O Polasek, IV Zorkoltseva, A Hofman, LC Karssen, M Struchalin, J Floyd, W Igl, Z Biloglav, L Broer, A Pfeufer, I Pichler, S Campbell, G Zaboli, I Kolcic, F Rivadeneira, J Huffman, ND Hastie, A Uitterlinden, L Franke, CS Franklin, V Vitart, , CP Nelson, M Preuss, , JC Bis, CJ O'Donnell, N Franceschini, , JC Witteman, T Axenovich, BA Oostra, T Meitinger, AA Hicks, C Hayward, AF Wright, U Gyllensten, H Campbell, G Schmitz,

Publication Date: 2012

Variant appearance in text: rs7499892

PubMed Link: 22359512

Variant Present in the following documents:

• pgen.1002490.s009.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: rs7499892

PubMed Link: 22286219

Variant Present in the following documents:

• NIHMS444574-supplement-supplementary_table_2.xlsx

View BVdb publication page

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A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort.

Genome Research

DM Greenawalt, R Dobrin, E Chudin, IJ Hatoum, C Suver, J Beaulaurier, B Zhang, V Castro, J Zhu, SK Sieberts, S Wang, C Molony, SB Heymsfield, DM Kemp, ML Reitman, PY Lum, EE Schadt, LM Kaplan

Publication Date: 2011-07

Variant appearance in text: rs7499892

PubMed Link: 21602305

Variant Present in the following documents:

• Main text

View BVdb publication page

---

Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Plos One

SD Turner, RL Berg, JG Linneman, PL Peissig, DC Crawford, JC Denny, DM Roden, CA McCarty, MD Ritchie, RA Wilke

Publication Date: 2011-05-11

Variant appearance in text: rs7499892

PubMed Link: 21589926

Variant Present in the following documents:

• pone.0019586.s004.pdf

View BVdb publication page

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Genetic architecture of circulating lipid levels.

European Journal Of Human Genetics : Ejhg

A Demirkan, N Amin, A Isaacs, MR Jarvelin, JB Whitfield, HE Wichmann, KO Kyvik, I Rudan, C Gieger, AA Hicks, Å Johansson, JJ Hottenga, JJ Smith, SH Wild, NL Pedersen, G Willemsen, M Mangino, C Hayward, AG Uitterlinden, A Hofman, J Witteman, GW Montgomery, KH Pietiläinen, T Rantanen, J Kaprio, A Döring, PP Pramstaller, U Gyllensten, EJ de Geus, BW Penninx, JF Wilson, F Rivadeneria, PK Magnusson, DI Boomsma, T Spector, H Campbell, B Hoehne, NG Martin, BA Oostra, M McCarthy, L Peltonen-Palotie, Y Aulchenko, PM Visscher, S Ripatti, AC Janssens, CM van Duijn,

Publication Date: 2011-07

Variant appearance in text: rs7499892

PubMed Link: 21448234

Variant Present in the following documents:

• Main text
• ejhg201121x5.doc

View BVdb publication page

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Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.

Plos Genetics

G Lettre, CD Palmer, T Young, KG Ejebe, H Allayee, EJ Benjamin, F Bennett, DW Bowden, A Chakravarti, A Dreisbach, DN Farlow, AR Folsom, M Fornage, T Forrester, E Fox, CA Haiman, J Hartiala, TB Harris, SL Hazen, SR Heckbert, BE Henderson, JN Hirschhorn, BJ Keating, SB Kritchevsky, E Larkin, M Li, ME Rudock, CA McKenzie, JB Meigs, YA Meng, TH Mosley, AB Newman, CH Newton-Cheh, DN Paltoo, GJ Papanicolaou, N Patterson, WS Post, BM Psaty, AN Qasim, L Qu, DJ Rader, S Redline, MP Reilly, AP Reiner, SS Rich, JI Rotter, Y Liu, P Shrader, DS Siscovick, WH Tang, HA Taylor, RP Tracy, RS Vasan, KM Waters, R Wilks, JG Wilson, RR Fabsitz, SB Gabriel, S Kathiresan, E Boerwinkle

Publication Date: 2011-02-10

Variant appearance in text: rs7499892

PubMed Link: 21347282

Variant Present in the following documents:

• pgen.1001300.s017.doc

View BVdb publication page

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Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.

Circulation. Cardiovascular Genetics

AC Edmondson, PS Braund, IM Stylianou, AV Khera, CP Nelson, ML Wolfe, SL Derohannessian, BJ Keating, L Qu, J He, MD Tobin, M Tomaszewski, J Baumert, N Klopp, A Döring, B Thorand, M Li, MP Reilly, W Koenig, NJ Samani, DJ Rader

Publication Date: 2011-04

Variant appearance in text: rs7499892

PubMed Link: 21303902

Variant Present in the following documents:

• NIHMS280051-supplement-1.pdf

View BVdb publication page

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Physical activity modifies the effect of LPL, LIPC, and CETP polymorphisms on HDL-C levels and the risk of myocardial infarction in women of European ancestry.

Circulation. Cardiovascular Genetics

T Ahmad, DI Chasman, JE Buring, IM Lee, PM Ridker, BM Everett

Publication Date: 2011-02

Variant appearance in text: rs7499892

PubMed Link: 21252145

Variant Present in the following documents:

• NIHMS260598-supplement-Supplemental.doc

View BVdb publication page

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Genetic causes of high and low serum HDL-cholesterol.

Journal Of Lipid Research

D Weissglas-Volkov, P Pajukanta

Publication Date: 2010-08

Variant appearance in text: rs7499892

PubMed Link: 20421590

Variant Present in the following documents:

• Main text

View BVdb publication page

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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: rs7499892

PubMed Link: 20339536

Variant Present in the following documents:

• pone.0009763.s005.xls
• pone.0009763.s007.xls

View BVdb publication page

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Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.

Circulation. Cardiovascular Genetics

PM Ridker, G Paré, AN Parker, RY Zee, JP Miletich, DI Chasman

Publication Date: 2009-02

Variant appearance in text: rs7499892

PubMed Link: 20031564

Variant Present in the following documents:

• Main text

View BVdb publication page

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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

Plos Genetics

DI Chasman, G Paré, S Mora, JC Hopewell, G Peloso, R Clarke, LA Cupples, A Hamsten, S Kathiresan, A Mälarstig, JM Ordovas, S Ripatti, AN Parker, JP Miletich, PM Ridker

Publication Date: 2009-11

Variant appearance in text: rs7499892

PubMed Link: 19936222

Variant Present in the following documents:

• pgen.1000730.s004.pdf
• pgen.1000730.s005.doc
• pgen.1000730.s007.doc
• pgen.1000730.s008.doc

View BVdb publication page

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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

American Journal Of Human Genetics

PJ Talmud, F Drenos, S Shah, T Shah, J Palmen, C Verzilli, TR Gaunt, J Pallas, R Lovering, K Li, JP Casas, R Sofat, M Kumari, S Rodriguez, T Johnson, SJ Newhouse, A Dominiczak, NJ Samani, M Caulfield, P Sever, A Stanton, DC Shields, S Padmanabhan, O Melander, C Hastie, C Delles, S Ebrahim, MG Marmot, GD Smith, DA Lawlor, PB Munroe, IN Day, M Kivimaki, J Whittaker, SE Humphries, AD Hingorani, , ,

Publication Date: 2009-11

Variant appearance in text: rs7499892

PubMed Link: 19913121

Variant Present in the following documents:

• mmc1.pdf
• mmc2.xls

View BVdb publication page

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Genome-wide association study of biochemical traits in Korcula Island, Croatia.

Croatian Medical Journal

T Zemunik, M Boban, G Lauc, S Janković, K Rotim, Z Vatavuk, G Bencić, Z Dogas, V Boraska, V Torlak, J Susac, I Zobić, D Rudan, D Pulanić, D Modun, I Mudnić, G Gunjaca, D Budimir, C Hayward, V Vitart, AF Wright, H Campbell, I Rudan

Publication Date: 2009-02

Variant appearance in text: rs7499892

PubMed Link: 19260141

Variant Present in the following documents:

• Main text

View BVdb publication page

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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.

Nature Genetics

YS Aulchenko, S Ripatti, I Lindqvist, D Boomsma, IM Heid, PP Pramstaller, BW Penninx, AC Janssens, JF Wilson, T Spector, NG Martin, NL Pedersen, KO Kyvik, J Kaprio, A Hofman, NB Freimer, MR Jarvelin, U Gyllensten, H Campbell, I Rudan, A Johansson, F Marroni, C Hayward, V Vitart, I Jonasson, C Pattaro, A Wright, N Hastie, I Pichler, AA Hicks, M Falchi, G Willemsen, JJ Hottenga, EJ de Geus, GW Montgomery, J Whitfield, P Magnusson, J Saharinen, M Perola, K Silander, A Isaacs, EJ Sijbrands, AG Uitterlinden, JC Witteman, BA Oostra, P Elliott, A Ruokonen, C Sabatti, C Gieger, T Meitinger, F Kronenberg, A Döring, HE Wichmann, JH Smit, MI McCarthy, CM van Duijn, L Peltonen,

Publication Date: 2009-01

Variant appearance in text: rs7499892

PubMed Link: 19060911

Variant Present in the following documents:

• NIHMS4347-supplement-figures_and_ta.pdf

View BVdb publication page

---

Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000200676.3	c.750+595C>T	-	intron_variant	-	8/15
ENST00000379780.2	c.750+595C>T	-	intron_variant	-	8/14
ENST00000566128.1	c.555+595C>T	-	intron_variant	-	8/15
ENST00000569082.1	n.852+595C>T	-	intron_variant,non_coding_transcript_variant	-	8/8
NM_000078.3	c.750+595C>T	-	intron_variant	-	8/15
NM_001286085.2	c.750+595C>T	-	intron_variant	-	8/14