CETP c.750+595C>G

Variant ID: 16-57006590-C-G

NM_000078.2(CETP):c.750+595C>G

This variant was identified in 49 publications

View GRCh38 version.




Publications:


Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease.

Cell Genomics
Zhou, Wei W; Kanai, Masahiro M; Wu, Kuan-Han H KH; Rasheed, Humaira H; Tsuo, Kristin K; Hirbo, Jibril B JB; Wang, Ying Y; Bhattacharya, Arjun A; Zhao, Huiling H; Namba, Shinichi S; Surakka, Ida I; Wolford, Brooke N BN; Lo Faro, Valeria V; Lopera-Maya, Esteban A EA; Läll, Kristi K; Favé, Marie-Julie MJ; Partanen, Juulia J JJ; Chapman, Sinéad B SB; Karjalainen, Juha J; Kurki, Mitja M; Maasha, Mutaamba M; Brumpton, Ben M BM; Chavan, Sameer S; Chen, Tzu-Ting TT; Daya, Michelle M; Ding, Yi Y; Feng, Yen-Chen A YA; Guare, Lindsay A LA; Gignoux, Christopher R CR; Graham, Sarah E SE; Hornsby, Whitney E WE; Ingold, Nathan N; Ismail, Said I SI; Johnson, Ruth R; Laisk, Triin T; Lin, Kuang K; Lv, Jun J; Millwood, Iona Y IY; Moreno-Grau, Sonia S; Nam, Kisung K; Palta, Priit P; Pandit, Anita A; Preuss, Michael H MH; Saad, Chadi C; Setia-Verma, Shefali S; Thorsteinsdottir, Unnur U; Uzunovic, Jasmina J; Verma, Anurag A; Zawistowski, Matthew M; Zhong, Xue X; Afifi, Nahla N; Al-Dabhani, Kawthar M KM; Al Thani, Asma A; Bradford, Yuki Y; Campbell, Archie A; Crooks, Kristy K; de Bock, Geertruida H GH; Damrauer, Scott M SM; Douville, Nicholas J NJ; Finer, Sarah S; Fritsche, Lars G LG; Fthenou, Eleni E; Gonzalez-Arroyo, Gilberto G; Griffiths, Christopher J CJ; Guo, Yu Y; Hunt, Karen A KA; Ioannidis, Alexander A; Jansonius, Nomdo M NM; Konuma, Takahiro T; Lee, Ming Ta Michael MTM; Lopez-Pineda, Arturo A; Matsuda, Yuta Y; Marioni, Riccardo E RE; Moatamed, Babak B; Nava-Aguilar, Marco A MA; Numakura, Kensuke K; Patil, Snehal S; Rafaels, Nicholas N; Richmond, Anne A; Rojas-Muñoz, Agustin A; Shortt, Jonathan A JA; Straub, Peter P; Tao, Ran R; Vanderwerff, Brett B; Vernekar, Manvi M; Veturi, Yogasudha Y; Barnes, Kathleen C KC; Boezen, Marike M; Chen, Zhengming Z; Chen, Chia-Yen CY; Cho, Judy J; Smith, George Davey GD; Finucane, Hilary K HK; Franke, Lude L; Gamazon, Eric R ER; Ganna, Andrea A; Gaunt, Tom R TR; Ge, Tian T; Huang, Hailiang H; Huffman, Jennifer J; Katsanis, Nicholas N; Koskela, Jukka T JT; Lajonchere, Clara C; Law, Matthew H MH; Li, Liming L; Lindgren, Cecilia M CM; Loos, Ruth J F RJF; MacGregor, Stuart S; Matsuda, Koichi K; Olsen, Catherine M CM; Porteous, David J DJ; Shavit, Jordan A JA; Snieder, Harold H; Takano, Tomohiro T; Trembath, Richard C RC; Vonk, Judith M JM; Whiteman, David C DC; Wicks, Stephen J SJ; Wijmenga, Cisca C; Wright, John J; Zheng, Jie J; Zhou, Xiang X; Awadalla, Philip P; Boehnke, Michael M; Bustamante, Carlos D CD; Cox, Nancy J NJ; Fatumo, Segun S; Geschwind, Daniel H DH; Hayward, Caroline C; Hveem, Kristian K; Kenny, Eimear E EE; Lee, Seunggeun S; Lin, Yen-Feng YF; Mbarek, Hamdi H; Mägi, Reedik R; Martin, Hilary C HC; Medland, Sarah E SE; Okada, Yukinori Y; Palotie, Aarno V AV; Pasaniuc, Bogdan B; Rader, Daniel J DJ; Ritchie, Marylyn D MD; Sanna, Serena S; Smoller, Jordan W JW; Stefansson, Kari K; van Heel, David A DA; Walters, Robin G RG; Zöllner, Sebastian S; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; , ; Martin, Alicia R AR; Willer, Cristen J CJ; Daly, Mark J MJ; Neale, Benjamin M BM
Publication Date: 2022-10-12

Variant appearance in text: rs7499892
PubMed Link: 36777996
Variant Present in the following documents:
  • Main text
  • mmc28.pdf
  • main.pdf
View BVdb publication page



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: rs7499892
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
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Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals.

Nature Communications
Huang, Qin Qin QQ; Sallah, Neneh N; Dunca, Diana D; Trivedi, Bhavi B; Hunt, Karen A KA; Hodgson, Sam S; Lambert, Samuel A SA; Arciero, Elena E; Wright, John J; Griffiths, Chris C; Trembath, Richard C RC; Hemingway, Harry H; Inouye, Michael M; Finer, Sarah S; van Heel, David A DA; Lumbers, R Thomas RT; Martin, Hilary C HC; Kuchenbaecker, Karoline K
Publication Date: 2022-08-09

Variant appearance in text: rs7499892
PubMed Link: 35945198
Variant Present in the following documents:
  • 41467_2022_32095_MOESM1_ESM.pdf
View BVdb publication page



A Nutrigenetic Update on CETP Gene-Diet Interactions on Lipid-Related Outcomes.

Current Atherosclerosis Reports
Wuni, Ramatu R; Kuhnle, Gunter G C GGC; Wynn-Jones, Alexandra Azzari AA; Vimaleswaran, Karani Santhanakrishnan KS
Publication Date: 2022-02

Variant appearance in text: rs7499892
PubMed Link: 35098451
Variant Present in the following documents:
  • Main text
  • 11883_2022_Article_987.pdf
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Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation.

Human Genetics
Longchamps, R J RJ; Yang, S Y SY; Castellani, C A CA; Shi, W W; Lane, J J; Grove, M L ML; Bartz, T M TM; Sarnowski, C C; Liu, C C; Burrows, K K; Guyatt, A L AL; Gaunt, T R TR; Kacprowski, T T; Yang, J J; De Jager, P L PL; Yu, L L; Bergman, A A; Xia, R R; Fornage, M M; Feitosa, M F MF; Wojczynski, M K MK; Kraja, A T AT; Province, M A MA; Amin, N N; Rivadeneira, F F; Tiemeier, H H; Uitterlinden, A G AG; Broer, L L; Van Meurs, J B J JBJ; Van Duijn, C M CM; Raffield, L M LM; Lange, L L; Rich, S S SS; Lemaitre, R N RN; Goodarzi, M O MO; Sitlani, C M CM; Mak, A C Y ACY; Bennett, D A DA; Rodriguez, S S; Murabito, J M JM; Lunetta, K L KL; Sotoodehnia, N N; Atzmon, G G; Ye, K K; Barzilai, N N; Brody, J A JA; Psaty, B M BM; Taylor, K D KD; Rotter, J I JI; Boerwinkle, E E; Pankratz, N N; Arking, D E DE
Publication Date: 2022-01

Variant appearance in text: rs7499892
PubMed Link: 34859289
Variant Present in the following documents:
  • 439_2021_2394_MOESM3_ESM.xlsx, sheet 4
View BVdb publication page



Generalizability of GWA-Identified Genetic Risk Variants for Metabolic Traits to Populations from the Arabian Peninsula.

Genes
Hebbar, Prashantha P; Abu-Farha, Mohamed M; Abubaker, Jehad J; Channanath, Arshad Mohamed AM; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-10-18

Variant appearance in text: rs7499892
PubMed Link: 34681031
Variant Present in the following documents:
  • Main text
  • genes-12-01637.pdf
View BVdb publication page



Cholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease.

Nature Communications
Schmidt, Amand F AF; Hunt, Nicholas B NB; Gordillo-Marañón, Maria M; Charoen, Pimphen P; Drenos, Fotios F; Kivimaki, Mika M; Lawlor, Deborah A DA; Giambartolomei, Claudia C; Papacosta, Olia O; Chaturvedi, Nishi N; Bis, Joshua C JC; O'Donnell, Christopher J CJ; Wannamethee, Goya G; Wong, Andrew A; Price, Jackie F JF; Hughes, Alun D AD; Gaunt, Tom R TR; Franceschini, Nora N; Mook-Kanamori, Dennis O DO; Zwierzyna, Magdalena M; Sofat, Reecha R; Hingorani, Aroon D AD; Finan, Chris C
Publication Date: 2021-09-24

Variant appearance in text: rs7499892
PubMed Link: 34561430
Variant Present in the following documents:
  • 41467_2021_25703_MOESM1_ESM.pdf
View BVdb publication page



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: rs7499892
PubMed Link: 32902719
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Gigascience
Chu, Benjamin B BB; Keys, Kevin L KL; German, Christopher A CA; Zhou, Hua H; Zhou, Jin J JJ; Sobel, Eric M EM; Sinsheimer, Janet S JS; Lange, Kenneth K
Publication Date: 2020-06-01

Variant appearance in text: rs7499892
PubMed Link: 32491161
Variant Present in the following documents:
  • Main text
  • giaa044_giga-d-19-00398_revision_1.pdf
  • giaa044.pdf
  • giaa044_giga-d-19-00398_original_submission.pdf
  • giaa044_giga-d-19-00398_revision_2.pdf
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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
Piko, Peter P; Fiatal, Szilvia S; Werissa, Nardos Abebe NA; Bekele, Bayu Begashaw BB; Racz, Gabor G; Kosa, Zsigmond Z; Sandor, Janos J; Adany, Roza R
Publication Date: 2020-01-03

Variant appearance in text: rs7499892
PubMed Link: 31947886
Variant Present in the following documents:
  • Main text
  • genes-11-00056.pdf
View BVdb publication page



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: rs7499892
PubMed Link: 31910446
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults.

Jama Cardiology
Björnsson, Eythór E; Thorleifsson, Guðmar G; Helgadóttir, Anna A; Guðnason, Thórarinn T; Guðbjartsson, Tómas T; Andersen, Karl K; Grétarsdóttir, Sólveig S; Ólafsson, Ísleifur Í; Tragante, Vinicius V; Ólafsson, Ólafur Hreiðar ÓH; Jónsdóttir, Birna B; Eyjólfsson, Guðmundur I GI; Sigurðardóttir, Ólöf Ó; Thorgeirsson, Guðmundur G; Guðbjartsson, Daníel F DF; Thorsteinsdóttir, Unnur U; Hólm, Hilma H; Stefánsson, Kári K
Publication Date: 2020-01-01

Variant appearance in text: rs7499892
PubMed Link: 31746962
Variant Present in the following documents:
  • jamacardiol-5-13-s001.pdf
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Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes.

Human Heredity
Yu, Youfei Y; Xia, Lu L; Lee, Seunggeun S; Zhou, Xiang X; Stringham, Heather M HM; Boehnke, Michael M; Mukherjee, Bhramar B
Publication Date: 2018

Variant appearance in text: rs7499892
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
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A PheWAS study of a large observational epidemiological cohort of African Americans from the REGARDS study.

Bmc Medical Genomics
Zhao, Xueyan X; Geng, Xin X; Srinivasasainagendra, Vinodh V; Chaudhary, Ninad N; Judd, Suzanne S; Wadley, Virginia V; Gutiérrez, Orlando M OM; Wang, Henry H; Lange, Ethan M EM; Lange, Leslie A LA; Woo, Daniel D; Unverzagt, Frederick W FW; Safford, Monika M; Cushman, Mary M; Limdi, Nita N; Quarells, Rakale R; Arnett, Donna K DK; Irvin, Marguerite R MR; Zhi, Degui D
Publication Date: 2019-01-31

Variant appearance in text: rs7499892
PubMed Link: 30704471
Variant Present in the following documents:
  • Main text
  • 12920_2018_Article_462.pdf
View BVdb publication page



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)
Peloso, Gina M GM; van der Lee, Sven J SJ; , ; Destefano, Anita L AL; Seshardi, Sudha S
Publication Date: 2018

Variant appearance in text: rs7499892
PubMed Link: 30422133
Variant Present in the following documents:
  • Main text
  • main.pdf
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs7499892
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



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

Nature Communications
Hall, Molly A MA; Wallace, John J; Lucas, Anastasia A; Kim, Dokyoon D; Basile, Anna O AO; Verma, Shefali S SS; McCarty, Cathy A CA; Brilliant, Murray H MH; Peissig, Peggy L PL; Kitchner, Terrie E TE; Verma, Anurag A; Pendergrass, Sarah A SA; Dudek, Scott M SM; Moore, Jason H JH; Ritchie, Marylyn D MD
Publication Date: 2017-10-27

Variant appearance in text: rs7499892
PubMed Link: 29079728
Variant Present in the following documents:
  • Main text
  • 41467_2017_Article_802.pdf
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Iterative hard thresholding for model selection in genome-wide association studies.

Genetic Epidemiology
Keys, Kevin L KL; Chen, Gary K GK; Lange, Kenneth K
Publication Date: 2017-12

Variant appearance in text: rs7499892
PubMed Link: 28875524
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Data In Brief
Pikó, Péter P; Fiatal, Szilvia S; Kósa, Zsigmond Z; Sándor, János J; Ádány, Róza R
Publication Date: 2017-10

Variant appearance in text: rs7499892
PubMed Link: 28795114
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Npj Aging And Mechanisms Of Disease
van Leeuwen, Elisabeth M EM; Huffman, Jennifer E JE; Bis, Joshua C JC; Isaacs, Aaron A; Mulder, Monique M; Sabo, Aniko A; Smith, Albert V AV; Demissie, Serkalem S; Manichaikul, Ani A; Brody, Jennifer A JA; Feitosa, Mary F MF; Duan, Qing Q; Schraut, Katharina E KE; Navarro, Pau P; van Vliet-Ostaptchouk, Jana V JV; Zhu, Gu G; Mbarek, Hamdi H; Trompet, Stella S; Verweij, Niek N; Lyytikäinen, Leo-Pekka LP; Deelen, Joris J; Nolte, Ilja M IM; van der Laan, Sander W SW; Davies, Gail G; Vermeij-Verdoold, Andrea Jm AJ; van Oosterhout, Andy Alj AA; Vergeer-Drop, Jeannette M JM; Arking, Dan E DE; Trochet, Holly H; , ; Medina-Gomez, Carolina C; Rivadeneira, Fernando F; Uitterlinden, Andre G AG; Dehghan, Abbas A; Franco, Oscar H OH; Sijbrands, Eric J EJ; Hofman, Albert A; White, Charles C CC; Mychaleckyj, Josyf C JC; Peloso, Gina M GM; Swertz, Morris A MA; , ; Willemsen, Gonneke G; de Geus, Eco J EJ; Milaneschi, Yuri Y; Penninx, Brenda Wjh BW; Ford, Ian I; Buckley, Brendan M BM; de Craen, Anton Jm AJ; Starr, John M JM; Deary, Ian J IJ; Pasterkamp, Gerard G; Oldehinkel, Albertine J AJ; Snieder, Harold H; Slagboom, P Eline PE; Nikus, Kjell K; Kähönen, Mika M; Lehtimäki, Terho T; Viikari, Jorma S JS; Raitakari, Olli T OT; van der Harst, Pim P; Jukema, J Wouter JW; Hottenga, Jouke-Jan JJ; Boomsma, Dorret I DI; Whitfield, John B JB; Montgomery, Grant G; Martin, Nicholas G NG; , ; Polasek, Ozren O; Vitart, Veronique V; Hayward, Caroline C; Kolcic, Ivana I; Wright, Alan F AF; Rudan, Igor I; Joshi, Peter K PK; Wilson, James F JF; Lange, Leslie A LA; Wilson, James G JG; Gudnason, Vilmundur V; Harris, Tamar B TB; Morrison, Alanna C AC; Borecki, Ingrid B IB; Rich, Stephen S SS; Padmanabhan, Sandosh S; Psaty, Bruce M BM; Rotter, Jerome I JI; Smith, Blair H BH; Boerwinkle, Eric E; Cupples, L Adrienne LA; van Duijn, Cornelia C
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 28721259
Variant Present in the following documents:
  • Main text
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Replication and fine-mapping of genetic predictors of lipid traits in African-Americans.

Journal Of Human Genetics
Feng, QiPing Q; Wei, Wei-Qi WQ; Levinson, Rebecca T RT; Mosley, Jonathan D JD; Stein, C Michael CM
Publication Date: 2017-10

Variant appearance in text: rs7499892
PubMed Link: 28539666
Variant Present in the following documents:
  • Main text
  • nihms870241.pdf
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c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One
Ganesan, Mala M; Nizamuddin, Sheikh S; Katkam, Shiva Krishna SK; Kumaraswami, Konda K; Hosad, Uday Kumar UK; Lobo, Limmy Loret LL; Kutala, Vijay Kumar VK; Thangaraj, Kumarasamy K
Publication Date: 2016

Variant appearance in text: rs7499892
PubMed Link: 27768712
Variant Present in the following documents:
  • Main text
  • pone.0164151.pdf
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Genetic variants in CETP increase risk of intracerebral hemorrhage.

Annals Of Neurology
Anderson, Christopher D CD; Falcone, Guido J GJ; Phuah, Chia-Ling CL; Radmanesh, Farid F; Brouwers, H Bart HB; Battey, Thomas W K TW; Biffi, Alessandro A; Peloso, Gina M GM; Liu, Dajiang J DJ; Ayres, Alison M AM; Goldstein, Joshua N JN; Viswanathan, Anand A; Greenberg, Steven M SM; Selim, Magdy M; Meschia, James F JF; Brown, Devin L DL; Worrall, Bradford B BB; Silliman, Scott L SL; Tirschwell, David L DL; Flaherty, Matthew L ML; Kraft, Peter P; Jagiella, Jeremiasz M JM; Schmidt, Helena H; Hansen, Björn M BM; Jimenez-Conde, Jordi J; Giralt-Steinhauer, Eva E; Elosua, Roberto R; Cuadrado-Godia, Elisa E; Soriano, Carolina C; van Nieuwenhuizen, Koen M KM; Klijn, Catharina J M CJ; Rannikmae, Kristiina K; Samarasekera, Neshika N; Al-Shahi Salman, Rustam R; Sudlow, Catherine L CL; Deary, Ian J IJ; Morotti, Andrea A; Pezzini, Alessandro A; Pera, Joanna J; Urbanik, Andrzej A; Pichler, Alexander A; Enzinger, Christian C; Norrving, Bo B; Montaner, Joan J; Fernandez-Cadenas, Israel I; Delgado, Pilar P; Roquer, Jaume J; Lindgren, Arne A; Slowik, Agnieszka A; Schmidt, Reinhold R; Kidwell, Chelsea S CS; Kittner, Steven J SJ; Waddy, Salina P SP; Langefeld, Carl D CD; Abecasis, Goncalo G; Willer, Cristen J CJ; Kathiresan, Sekar S; Woo, Daniel D; Rosand, Jonathan J; ,
Publication Date: 2016-11

Variant appearance in text: rs7499892
PubMed Link: 27717122
Variant Present in the following documents:
  • Main text
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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
Below, Jennifer E JE; Parra, Esteban J EJ; Gamazon, Eric R ER; Torres, Jason J; Krithika, S S; Candille, Sophie S; Lu, Yingchang Y; Manichakul, Ani A; Peralta-Romero, Jesus J; Duan, Qing Q; Li, Yun Y; Morris, Andrew P AP; Gottesman, Omri O; Bottinger, Erwin E; Wang, Xin-Qun XQ; Taylor, Kent D KD; Ida Chen, Y-D YD; Rotter, Jerome I JI; Rich, Stephen S SS; Loos, Ruth J F RJ; Tang, Hua H; Cox, Nancy J NJ; Cruz, Miguel M; Hanis, Craig L CL; Valladares-Salgado, Adan A
Publication Date: 2016-01-19

Variant appearance in text: rs7499892
PubMed Link: 26780889
Variant Present in the following documents:
  • Main text
  • srep19429-s1.pdf
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Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.

Heredity
Shirali, M M; Pong-Wong, R R; Navarro, P P; Knott, S S; Hayward, C C; Vitart, V V; Rudan, I I; Campbell, H H; Hastie, N D ND; Wright, A F AF; Haley, C S CS
Publication Date: 2016-03

Variant appearance in text: rs7499892
PubMed Link: 26696135
Variant Present in the following documents:
  • Main text
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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
Pirim, Dilek D; Wang, Xingbin X; Niemsiri, Vipavee V; Radwan, Zaheda H ZH; Bunker, Clareann H CH; Hokanson, John E JE; Hamman, Richard F RF; Barmada, M Michael MM; Demirci, F Yesim FY; Kamboh, M Ilyas MI
Publication Date: 2016-01

Variant appearance in text: rs7499892
PubMed Link: 26683795
Variant Present in the following documents:
  • Main text
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Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.

Human Molecular Genetics
Spiliopoulou, Athina A; Nagy, Reka R; Bermingham, Mairead L ML; Huffman, Jennifer E JE; Hayward, Caroline C; Vitart, Veronique V; Rudan, Igor I; Campbell, Harry H; Wright, Alan F AF; Wilson, James F JF; Pong-Wong, Ricardo R; Agakov, Felix F; Navarro, Pau P; Haley, Chris S CS
Publication Date: 2015-07-15

Variant appearance in text: rs7499892
PubMed Link: 25918167
Variant Present in the following documents:
  • Main text
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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
Shim, Heejung H; Chasman, Daniel I DI; Smith, Joshua D JD; Mora, Samia S; Ridker, Paul M PM; Nickerson, Deborah A DA; Krauss, Ronald M RM; Stephens, Matthew M
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 25898129
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Frontiers In Genetics
Laston, Sandra L SL; Voruganti, V Saroja VS; Haack, Karin K; Shah, Vallabh O VO; Bobelu, Arlene A; Bobelu, Jeanette J; Ghahate, Donica D; Harford, Antonia M AM; Paine, Susan S SS; Tentori, Francesca F; Cole, Shelley A SA; MacCluer, Jean W JW; Comuzzie, Anthony G AG; Zager, Philip G PG
Publication Date: 2015

Variant appearance in text: rs7499892
PubMed Link: 25688259
Variant Present in the following documents:
  • Main text
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New loci and coding variants confer risk for age-related macular degeneration in East Asians.

Nature Communications
Cheng, Ching-Yu CY; Yamashiro, Kenji K; Chen, Li Jia LJ; Ahn, Jeeyun J; Huang, Lulin L; Huang, Lvzhen L; Cheung, Chui Ming G CM; Miyake, Masahiro M; Cackett, Peter D PD; Yeo, Ian Y IY; Laude, Augustinus A; Mathur, Ranjana R; Pang, Junxiong J; Sim, Kar Seng KS; Koh, Adrian H AH; Chen, Peng P; Lee, Shu Yen SY; Wong, Doric D; Chan, Choi Mun CM; Loh, Boon Kwang BK; Sun, Yaoyao Y; Davila, Sonia S; Nakata, Isao I; Nakanishi, Hideo H; Akagi-Kurashige, Yumiko Y; Gotoh, Norimoto N; Tsujikawa, Akitaka A; Matsuda, Fumihiko F; Mori, Keisuke K; Yoneya, Shin S; Sakurada, Yoichi Y; Iijima, Hiroyuki H; Iida, Tomohiro T; Honda, Shigeru S; Lai, Timothy Yuk Yau TY; Tam, Pancy Oi Sin PO; Chen, Haoyu H; Tang, Shibo S; Ding, Xiaoyan X; Wen, Feng F; Lu, Fang F; Zhang, Xiongze X; Shi, Yi Y; Zhao, Peiquan P; Zhao, Bowen B; Sang, Jinghong J; Gong, Bo B; Dorajoo, Rajkumar R; Yuan, Jian-Min JM; Koh, Woon-Puay WP; van Dam, Rob M RM; Friedlander, Yechiel Y; Lin, Ying Y; Hibberd, Martin L ML; Foo, Jia Nee JN; Wang, Ningli N; Wong, Chang Hua CH; Tan, Gavin S GS; Park, Sang Jun SJ; Bhargava, Mayuri M; Gopal, Lingam L; Naing, Thet T; Liao, Jiemin J; Ong, Peng Guan PG; Mitchell, Paul P; Zhou, Peng P; Xie, Xuefeng X; Liang, Jinlong J; Mei, Junpu J; Jin, Xin X; Saw, Seang-Mei SM; Ozaki, Mineo M; Mizoguchi, Takanori T; Kurimoto, Yasuo Y; Woo, Se Joon SJ; Chung, Hum H; Yu, Hyeong-Gon HG; Shin, Joo Young JY; Park, Dong Ho DH; Kim, In Taek IT; Chang, Woohyok W; Sagong, Min M; Lee, Sang-Joon SJ; Kim, Hyun Woong HW; Lee, Ji Eun JE; Li, Yi Y; Liu, Jianjun J; Teo, Yik Ying YY; Heng, Chew Kiat CK; Lim, Tock Han TH; Yang, Suk-Kyun SK; Song, Kyuyoung K; Vithana, Eranga N EN; Aung, Tin T; Bei, Jin Xin JX; Zeng, Yi Xin YX; Tai, E Shyong ES; Li, Xiao Xin XX; Yang, Zhenglin Z; Park, Kyu-Hyung KH; Pang, Chi Pui CP; Yoshimura, Nagahisa N; Wong, Tien Yin TY; Khor, Chiea Chuen CC
Publication Date: 2015-01-28

Variant appearance in text: rs7499892
PubMed Link: 25629512
Variant Present in the following documents:
  • ncomms7063-s1.pdf
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MGAS: a powerful tool for multivariate gene-based genome-wide association analysis.

Bioinformatics (Oxford, England)
Van der Sluis, Sophie S; Dolan, Conor V CV; Li, Jiang J; Song, Youqiang Y; Sham, Pak P; Posthuma, Danielle D; Li, Miao-Xin MX
Publication Date: 2015-04-01

Variant appearance in text: rs7499892
PubMed Link: 25431328
Variant Present in the following documents:
  • Main text
  • btu783.pdf
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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
Carty, Cara L CL; Bhattacharjee, Samsiddhi S; Haessler, Jeff J; Cheng, Iona I; Hindorff, Lucia A LA; Aroda, Vanita V; Carlson, Christopher S CS; Hsu, Chun-Nan CN; Wilkens, Lynne L; Liu, Simin S; Selvin, Elizabeth E; Jackson, Rebecca R; North, Kari E KE; Peters, Ulrike U; Pankow, James S JS; Chatterjee, Nilanjan N; Kooperberg, Charles C
Publication Date: 2014-08

Variant appearance in text: rs7499892
PubMed Link: 25023634
Variant Present in the following documents:
  • Main text
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Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.

Genetic Epidemiology
Hellwege, Jacklyn N JN; Palmer, Nicholette D ND; Raffield, Laura M LM; Ng, Maggie C Y MC; Hawkins, Gregory A GA; Long, Jirong J; Lorenzo, Carlos C; Norris, Jill M JM; Ida Chen, Y-D YD; Speliotes, Elizabeth K EK; Rotter, Jerome I JI; Langefeld, Carl D CD; Wagenknecht, Lynne E LE; Bowden, Donald W DW
Publication Date: 2014-05

Variant appearance in text: rs7499892
PubMed Link: 24719370
Variant Present in the following documents:
  • Main text
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CETP gene polymorphisms and risk of coronary atherosclerosis in a Chinese population.

Lipids In Health And Disease
Wang, Jun J; Wang, Li Jun LJ; Zhong, Yong Y; Gu, Ping P; Shao, Jia Qing JQ; Jiang, Shi Sen SS; Gong, Jian Bin JB
Publication Date: 2013-11-27

Variant appearance in text: rs7499892
PubMed Link: 24283500
Variant Present in the following documents:
  • Main text
  • 1476-511X-12-176.pdf
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Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels.

Journal Of Lipid Research
Wu, Ying Y; Marvelle, Amanda F AF; Li, Jin J; Croteau-Chonka, Damien C DC; Feranil, Alan B AB; Kuzawa, Christopher W CW; Li, Yun Y; Adair, Linda S LS; Mohlke, Karen L KL
Publication Date: 2013-11

Variant appearance in text: rs7499892
PubMed Link: 24023260
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  • Main text
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Properties of local interactions and their potential value in complementing genome-wide association studies.

Plos One
Wei, Wenhua W; Gyenesei, Attila A; Semple, Colin A M CA; Haley, Chris S CS
Publication Date: 2013

Variant appearance in text: rs7499892
PubMed Link: 23940718
Variant Present in the following documents:
  • Main text
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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
Clifford, Andrew J AJ; Rincon, Gonzalo G; Owens, Janel E JE; Medrano, Juan F JF; Moshfegh, Alanna J AJ; Baer, David J DJ; Novotny, Janet A JA
Publication Date: 2013-05-08

Variant appearance in text: rs7499892
PubMed Link: 23656756
Variant Present in the following documents:
  • Main text
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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
Taylor, Kira C KC; Carty, Cara L CL; Dumitrescu, Logan L; Bůžková, Petra P; Cole, Shelley A SA; Hindorff, Lucia L; Schumacher, Fred R FR; Wilkens, Lynne R LR; Shohet, Ralph V RV; Quibrera, P Miguel PM; Johnson, Karen C KC; Henderson, Brian E BE; Haessler, Jeff J; Franceschini, Nora N; Eaton, Charles B CB; Duggan, David J DJ; Cochran, Barbara B; Cheng, Iona I; Carlson, Chris S CS; Brown-Gentry, Kristin K; Anderson, Garnet G; Ambite, Jose Luis JL; Haiman, Christopher C; Le Marchand, Loïc L; Kooperberg, Charles C; Crawford, Dana C DC; Buyske, Steven S; North, Kari E KE; Fornage, Myriam M; ,
Publication Date: 2013-05-01

Variant appearance in text: rs7499892
PubMed Link: 23634756
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  • Main text
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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
Wu, Ying Y; Waite, Lindsay L LL; Jackson, Anne U AU; Sheu, Wayne H-H WH; Buyske, Steven S; Absher, Devin D; Arnett, Donna K DK; Boerwinkle, Eric E; Bonnycastle, Lori L LL; Carty, Cara L CL; Cheng, Iona I; Cochran, Barbara B; Croteau-Chonka, Damien C DC; Dumitrescu, Logan L; Eaton, Charles B CB; Franceschini, Nora N; Guo, Xiuqing X; Henderson, Brian E BE; Hindorff, Lucia A LA; Kim, Eric E; Kinnunen, Leena L; Komulainen, Pirjo P; Lee, Wen-Jane WJ; Le Marchand, Loic L; Lin, Yi Y; Lindström, Jaana J; Lingaas-Holmen, Oddgeir O; Mitchell, Sabrina L SL; Narisu, Narisu N; Robinson, Jennifer G JG; Schumacher, Fred F; Stančáková, Alena A; Sundvall, Jouko J; Sung, Yun-Ju YJ; Swift, Amy J AJ; Wang, Wen-Chang WC; Wilkens, Lynne L; Wilsgaard, Tom T; Young, Alicia M AM; Adair, Linda S LS; Ballantyne, Christie M CM; Bůžková, Petra P; Chakravarti, Aravinda A; Collins, Francis S FS; Duggan, David D; Feranil, Alan B AB; Ho, Low-Tone LT; Hung, Yi-Jen YJ; Hunt, Steven C SC; Hveem, Kristian K; Juang, Jyh-Ming J JM; Kesäniemi, Antero Y AY; Kuusisto, Johanna J; Laakso, Markku M; Lakka, Timo A TA; Lee, I-Te IT; Leppert, Mark F MF; Matise, Tara C TC; Moilanen, Leena L; Njølstad, Inger I; Peters, Ulrike U; Quertermous, Thomas T; Rauramaa, Rainer R; Rotter, Jerome I JI; Saramies, Jouko J; Tuomilehto, Jaakko J; Uusitupa, Matti M; Wang, Tzung-Dau TD; Boehnke, Michael M; Haiman, Christopher A CA; Chen, Yii-Der I YD; Kooperberg, Charles C; Assimes, Themistocles L TL; Crawford, Dana C DC; Hsiung, Chao A CA; North, Kari E KE; Mohlke, Karen L KL
Publication Date: 2013-03

Variant appearance in text: rs7499892
PubMed Link: 23555291
Variant Present in the following documents:
  • Main text
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Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations.

Plos One
Elbers, Clara C CC; Guo, Yiran Y; Tragante, Vinicius V; van Iperen, Erik P A EP; Lanktree, Matthew B MB; Castillo, Berta Almoguera BA; Chen, Fang F; Yanek, Lisa R LR; Wojczynski, Mary K MK; Li, Yun R YR; Ferwerda, Bart B; Ballantyne, Christie M CM; Buxbaum, Sarah G SG; Chen, Yii-Der Ida YD; Chen, Wei-Min WM; Cupples, L Adrienne LA; Cushman, Mary M; Duan, Yanan Y; Duggan, David D; Evans, Michele K MK; Fernandes, Jyotika K JK; Fornage, Myriam M; Garcia, Melissa M; Garvey, W Timothy WT; Glazer, Nicole N; Gomez, Felicia F; Harris, Tamara B TB; Halder, Indrani I; Howard, Virginia J VJ; Keller, Margaux F MF; Kamboh, M Ilyas MI; Kooperberg, Charles C; Kritchevsky, Stephen B SB; LaCroix, Andrea A; Liu, Kiang K; Liu, Yongmei Y; Musunuru, Kiran K; Newman, Anne B AB; Onland-Moret, N Charlotte NC; Ordovas, Jose J; Peter, Inga I; Post, Wendy W; Redline, Susan S; Reis, Steven E SE; Saxena, Richa R; Schreiner, Pamela J PJ; Volcik, Kelly A KA; Wang, Xingbin X; Yusuf, Salim S; Zonderland, Alan B AB; Anand, Sonia S SS; Becker, Diane M DM; Psaty, Bruce B; Rader, Daniel J DJ; Reiner, Alex P AP; Rich, Stephen S SS; Rotter, Jerome I JI; Sale, Michèle M MM; Tsai, Michael Y MY; Borecki, Ingrid B IB; Hegele, Robert A RA; Kathiresan, Sekar S; Nalls, Michael A MA; Taylor, Herman A HA; Hakonarson, Hakon H; Sivapalaratnam, Suthesh S; Asselbergs, Folkert W FW; Drenos, Fotios F; Wilson, James G JG; Keating, Brendan J BJ
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 23236364
Variant Present in the following documents:
  • Main text
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A mixed-model approach for genome-wide association studies of correlated traits in structured populations.

Nature Genetics
Korte, Arthur A; Vilhjálmsson, Bjarni J BJ; Segura, Vincent V; Platt, Alexander A; Long, Quan Q; Nordborg, Magnus M
Publication Date: 2012-09

Variant appearance in text: rs7499892
PubMed Link: 22902788
Variant Present in the following documents:
  • NIHMS392993-supplement-1.pdf
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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.

Nature Genetics
Segura, Vincent V; Vilhjálmsson, Bjarni J BJ; Platt, Alexander A; Korte, Arthur A; Seren, Ümit Ü; Long, Quan Q; Nordborg, Magnus M
Publication Date: 2012-06-17

Variant appearance in text: rs7499892
PubMed Link: 22706313
Variant Present in the following documents:
  • Main text
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Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

Plos One
Musunuru, Kiran K; Romaine, Simon P R SP; Lettre, Guillaume G; Wilson, James G JG; Volcik, Kelly A KA; Tsai, Michael Y MY; Taylor, Herman A HA; Schreiner, Pamela J PJ; Rotter, Jerome I JI; Rich, Stephen S SS; Redline, Susan S; Psaty, Bruce M BM; Papanicolaou, George J GJ; Ordovas, Jose M JM; Liu, Kiang K; Krauss, Ronald M RM; Glazer, Nicole L NL; Gabriel, Stacey B SB; Fornage, Myriam M; Cupples, L Adrienne LA; Buxbaum, Sarah G SG; Boerwinkle, Eric E; Ballantyne, Christie M CM; Kathiresan, Sekar S; Rader, Daniel J DJ
Publication Date: 2012

Variant appearance in text: rs7499892
PubMed Link: 22629316
Variant Present in the following documents:
  • Main text
  • pone.0036473.pdf
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A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort.

Genome Research
Greenawalt, Danielle M DM; Dobrin, Radu R; Chudin, Eugene E; Hatoum, Ida J IJ; Suver, Christine C; Beaulaurier, John J; Zhang, Bin B; Castro, Victor V; Zhu, Jun J; Sieberts, Solveig K SK; Wang, Susanna S; Molony, Cliona C; Heymsfield, Steven B SB; Kemp, Daniel M DM; Reitman, Marc L ML; Lum, Pek Yee PY; Schadt, Eric E EE; Kaplan, Lee M LM
Publication Date: 2011-07

Variant appearance in text: rs7499892
PubMed Link: 21602305
Variant Present in the following documents:
  • Main text
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Genetic architecture of circulating lipid levels.

European Journal Of Human Genetics : Ejhg
Demirkan, Ayşe A; Amin, Najaf N; Isaacs, Aaron A; Jarvelin, Marjo-Riitta MR; Whitfield, John B JB; Wichmann, Heinz-Erich HE; Kyvik, Kirsten O H M KO; Rudan, Igor I; Gieger, Christian C; Hicks, Andrew A AA; Johansson, Åsa Å; Hottenga, Jouke-Jan JJ; Smith, Johannes J JJ; Wild, Sarah H SH; Pedersen, Nancy L NL; Willemsen, Gonneke G; Mangino, Massimo M; Hayward, Caroline C; Uitterlinden, André G AG; Hofman, Albert A; Witteman, Jacqueline J; Montgomery, Grant W GW; Pietiläinen, Kirsi H KH; Rantanen, Taina T; Kaprio, Jaakko J; Döring, Angela A; Pramstaller, Peter P PP; Gyllensten, Ulf U; de Geus, Eco J C EJ; Penninx, Brenda W BW; Wilson, James F JF; Rivadeneria, Fernando F; Magnusson, Patrik K E PK; Boomsma, Dorret I DI; Spector, Tim T; Campbell, Harry H; Hoehne, Birgit B; Martin, Nicholas G NG; Oostra, Ben A BA; McCarthy, Mark M; Peltonen-Palotie, Leena L; Aulchenko, Yurii Y; Visscher, Peter M PM; Ripatti, Samuli S; Janssens, A Cecile J W AC; van Duijn, Cornelia M CM; ,
Publication Date: 2011-07

Variant appearance in text: rs7499892
PubMed Link: 21448234
Variant Present in the following documents:
  • Main text
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Genetic causes of high and low serum HDL-cholesterol.

Journal Of Lipid Research
Weissglas-Volkov, Daphna D; Pajukanta, Päivi P
Publication Date: 2010-08

Variant appearance in text: rs7499892
PubMed Link: 20421590
Variant Present in the following documents:
  • Main text
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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
Ridker, Paul M PM; Paré, Guillaume G; Parker, Alex N AN; Zee, Robert Y L RY; Miletich, Joseph P JP; Chasman, Daniel I DI
Publication Date: 2009-02

Variant appearance in text: rs7499892
PubMed Link: 20031564
Variant Present in the following documents:
  • Main text
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Genome-wide association study of biochemical traits in Korcula Island, Croatia.

Croatian Medical Journal
Zemunik, Tatijana T; Boban, Mladen M; Lauc, Gordan G; Janković, Stipan S; Rotim, Kresimir K; Vatavuk, Zoran Z; Bencić, Goran G; Dogas, Zoran Z; Boraska, Vesna V; Torlak, Vesela V; Susac, Jelena J; Zobić, Ivana I; Rudan, Diana D; Pulanić, Drazen D; Modun, Darko D; Mudnić, Ivana I; Gunjaca, Grgo G; Budimir, Danijela D; Hayward, Caroline C; Vitart, Veronique V; Wright, Alan F AF; Campbell, Harry H; Rudan, Igor I
Publication Date: 2009-02

Variant appearance in text: rs7499892
PubMed Link: 19260141
Variant Present in the following documents:
  • Main text
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