CETP c.658+186C>A

Variant ID: 16-57005479-C-A

NM_000078.2(CETP):c.658+186C>A

This variant was identified in 67 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: CETP: 658+186C>A
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Pharmacokinetics and Genetic Factors of Atorvastatin in Healthy Korean Subjects.

Frontiers In Genetics
Kim, Serim S; Seo, Jong Do JD; Yun, Yeo-Min YM; Kim, Hanah H; Kim, Tae-Eun TE; Lee, Taeheon T; Lee, Tae-Rim TR; Lee, Jun Hyung JH; Cho, Eun-Hae EH; Ki, Chang-Seok CS
Publication Date: 2022

Variant appearance in text: rs1532624
PubMed Link: 35664336
Variant Present in the following documents:
  • DataSheet1.pdf
View BVdb publication page



The Prevalence of Pharmacogenomics Variants and Their Clinical Relevance Among the Pakistani Population.

Evolutionary Bioinformatics Online
Khan, Abdul Rafay AR; Shah, Sayed Hajan SH; Ajaz, Sadia S; Firasat, Sadaf S; Abid, Aiysha A; Raza, Ali A
Publication Date: 2022

Variant appearance in text: rs1532624
PubMed Link: 35497687
Variant Present in the following documents:
  • Main text
  • 10.1177_11769343221095834.pdf
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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: rs1532624
PubMed Link: 35098451
Variant Present in the following documents:
  • Main text
  • 11883_2022_Article_987.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: rs1532624
PubMed Link: 34561430
Variant Present in the following documents:
  • 41467_2021_25703_MOESM1_ESM.pdf
View BVdb publication page



Drug-Drug Interactions and Pharmacogenomic Evaluation in Colorectal Cancer Patients: The New Drug-PIN® System Comprehensive Approach.

Pharmaceuticals (Basel, Switzerland)
Roberto, Michela M; Rossi, Alessandro A; Panebianco, Martina M; Pomes, Leda Marina LM; Arrivi, Giulia G; Ierinò, Debora D; Simmaco, Maurizio M; Marchetti, Paolo P; Mazzuca, Federica F
Publication Date: 2021-01-15

Variant appearance in text: rs1532624
PubMed Link: 33467633
Variant Present in the following documents:
  • pharmaceuticals-14-00067-s001.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: rs1532624
PubMed Link: 32902719
Variant Present in the following documents:
  • Main text
View BVdb publication page



Role of Genetic Variations in the Hepatic Handling of Drugs.

International Journal Of Molecular Sciences
Marin, Jose J G JJG; Serrano, Maria A MA; Monte, Maria J MJ; Sanchez-Martin, Anabel A; Temprano, Alvaro G AG; Briz, Oscar O; Romero, Marta R MR
Publication Date: 2020-04-20

Variant appearance in text: rs1532624
PubMed Link: 32326111
Variant Present in the following documents:
  • Main text
  • ijms-21-02884.pdf
View BVdb publication page



Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Bmc Medical Genomics
Dron, Jacqueline S JS; Wang, Jian J; McIntyre, Adam D AD; Iacocca, Michael A MA; Robinson, John F JF; Ban, Matthew R MR; Cao, Henian H; Hegele, Robert A RA
Publication Date: 2020-02-10

Variant appearance in text: CETP: 658+186C>A
PubMed Link: 32041611
Variant Present in the following documents:
  • 12920_2020_669_MOESM1_ESM.xlsx, sheet 3
View BVdb publication page



Heterogeneity in the distribution of 159 drug-response related SNPs in world populations and their genetic relatedness.

Plos One
Ahsan, Tamim T; Urmi, Nusrat Jahan NJ; Sajib, Abu Ashfaqur AA
Publication Date: 2020

Variant appearance in text: rs1532624
PubMed Link: 31971968
Variant Present in the following documents:
  • Main text
  • pone.0228000.pdf
View BVdb publication page



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: rs1532624
PubMed Link: 31947886
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of RS708272 (CETP Gene Variant) with Lipid Profile Parameters and the Risk of Myocardial Infarction in the White Population of Western Siberia.

Biomolecules
Semaev, Sergey S; Shakhtshneider, Elena E; Orlov, Pavel P; Ivanoshchuk, Dinara D; Malyutina, Sophia S; Gafarov, Valery V; Ragino, Yuliya Y; Voevoda, Mikhail M
Publication Date: 2019-11-14

Variant appearance in text: rs1532624
PubMed Link: 31739638
Variant Present in the following documents:
  • Main text
  • biomolecules-09-00739.pdf
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The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population.

Journal Of Lipid Research
Nishida, Yuichiro Y; Hachiya, Tsuyoshi T; Hara, Megumi M; Shimanoe, Chisato C; Tanaka, Keitaro K; Sutoh, Yoichi Y; Shimizu, Atsushi A; Hishida, Asahi A; Tsukamoto, Mineko M; Kadomatsu, Yuka Y; Oze, Isao I; Koyanagi, Yuriko N YN; Kuriyama, Nagato N; Koyama, Teruhide T; Ibusuki, Rie R; Takezaki, Toshiro T; Ikezaki, Hiroaki H; Furusyo, Norihiro N; Takashima, Naoyuki N; Kadota, Aya A; Uemura, Hirokazu H; Katsuura-Kamano, Sakurako S; Suzuki, Sadao S; Nakagawa-Senda, Hiroko H; Kuriki, Kiyonori K; Mikami, Haruo H; Nakamura, Yohko Y; Momozawa, Yukihide Y; Kubo, Michiaki M; Nakatochi, Masahiro M; Naito, Mariko M; Wakai, Kenji K; ,
Publication Date: 2020-01

Variant appearance in text: rs1532624
PubMed Link: 31694877
Variant Present in the following documents:
  • Main text
View BVdb publication page



Introducing the first whole genomes of nationals from the United Arab Emirates.

Scientific Reports
AlSafar, Habiba S HS; Al-Ali, Mariam M; Elbait, Gihan Daw GD; Al-Maini, Mustafa H MH; Ruta, Dymitr D; Peramo, Braulio B; Henschel, Andreas A; Tay, Guan K GK
Publication Date: 2019-10-11

Variant appearance in text: rs1532624
PubMed Link: 31604968
Variant Present in the following documents:
  • 41598_2019_50876_MOESM1_ESM.xlsx, sheet 1
  • 41598_2019_50876_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Genetics and pharmacogenetics in the diagnosis and therapy of cardiovascular diseases.

Acta Bio-Medica : Atenei Parmensis
Krasi, Geraldo G; Precone, Vincenza V; Paolacci, Stefano S; Stuppia, Liborio L; Nodari, Savina S; Romeo, Francesco F; Perrone, Marco M; Bushati, Vilma V; Dautaj, Astrit A; Bertelli, Matteo M
Publication Date: 2019-09-30

Variant appearance in text: rs1532624
PubMed Link: 31577248
Variant Present in the following documents:
  • ACTA-90-7.pdf
View BVdb publication page



Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at CETP Locus in Indians.

Biomolecules
Prasad, Gauri G; Bandesh, Khushdeep K; Giri, Anil K AK; Kauser, Yasmeen Y; Chanda, Prakriti P; Parekatt, Vaisak V; Mathur, Sandeep S; Madhu, Sri Venkata SV; Venkatesh, Pradeep P; Bhansali, Anil A; Marwaha, Raman K RK; Basu, Analabha A; Tandon, Nikhil N; Bharadwaj, Dwaipayan D; ,
Publication Date: 2019-07-30

Variant appearance in text: rs1532624
PubMed Link: 31366177
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs1532624
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

International Journal Of Molecular Medicine
Yamada, Yoshiji Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Horibe, Hideki H; Fujimaki, Tetsuo T; Yasukochi, Yoshiki Y; Takeuchi, Ichiro I; Sakuma, Jun J
Publication Date: 2019-01

Variant appearance in text: rs1532624
PubMed Link: 30365130
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: CETP: 658+186C>A; rs1532624
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



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: rs1532624
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Relationship between CETP gene polymorphisms with coronary artery disease in Polish population.

Molecular Biology Reports
Iwanicka, Joanna J; Iwanicki, Tomasz T; Niemiec, Paweł P; Balcerzyk, Anna A; Krauze, Jolanta J; Górczyńska-Kosiorz, Sylwia S; Ochalska-Tyka, Anna A; Grzeszczak, Władysław W; Żak, Iwona I
Publication Date: 2018-12

Variant appearance in text: rs1532624
PubMed Link: 30178218
Variant Present in the following documents:
  • Main text
  • 11033_2018_Article_4342.pdf
View BVdb publication page



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

Nutrition & Metabolism
Mirmiran, Parvin P; Esfandiar, Zohre Z; Hosseini-Esfahani, Firoozeh F; Koochakpoor, Gelareh G; Daneshpour, Maryam S MS; Sedaghati-Khayat, Bahar B; Azizi, Fereidoun F
Publication Date: 2017

Variant appearance in text: rs1532624
PubMed Link: 29234452
Variant Present in the following documents:
  • Main text
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: rs1532624
PubMed Link: 29079728
Variant Present in the following documents:
  • 41467_2017_Article_802.pdf
View BVdb publication page



Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos.

Lipids In Health And Disease
Graff, Mariaelisa M; Emery, Leslie S LS; Justice, Anne E AE; Parra, Esteban E; Below, Jennifer E JE; Palmer, Nicholette D ND; Gao, Chuan C; Duan, Qing Q; Valladares-Salgado, Adan A; Cruz, Miguel M; Morrison, Alanna C AC; Boerwinkle, Eric E; Whitsel, Eric A EA; Kooperberg, Charles C; Reiner, Alex A; Li, Yun Y; Rodriguez, Carlos Jose CJ; Talavera, Gregory A GA; Langefeld, Carl D CD; Wagenknecht, Lynne E LE; Norris, Jill M JM; Taylor, Kent D KD; Papanicolaou, George G; Kenny, Eimear E; Loos, Ruth J F RJF; Chen, Yii-Der Ida YI; Laurie, Cathy C; Sofer, Tamar T; North, Kari E KE
Publication Date: 2017-10-12

Variant appearance in text: rs1532624
PubMed Link: 29025430
Variant Present in the following documents:
  • Main text
  • 12944_2017_Article_591.pdf
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: rs1532624
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: rs1532624
PubMed Link: 28721259
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Nature Communications
Southam, Lorraine L; Gilly, Arthur A; Süveges, Dániel D; Farmaki, Aliki-Eleni AE; Schwartzentruber, Jeremy J; Tachmazidou, Ioanna I; Matchan, Angela A; Rayner, Nigel W NW; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Xue, Yali Y; Dedoussis, George G; Zeggini, Eleftheria E
Publication Date: 2017-05-26

Variant appearance in text: rs1532624
PubMed Link: 28548082
Variant Present in the following documents:
  • Main text
  • ncomms15606-s1.pdf
  • ncomms15606.pdf
View BVdb publication page



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
Zhu, Yimin Y; Zhang, Dandan D; Zhou, Dan D; Li, Zhenli Z; Li, Zhiqiang Z; Fang, Le L; Yang, Min M; Shan, Zhongyan Z; Li, Hong H; Chen, Jianhua J; Zhou, Xianghai X; Ye, Wei W; Yu, Senhai S; Li, Huabin H; Cai, Libin L; Liu, Chengguo C; Zhang, Jie J; Wang, Lixin L; Lai, Yaxin Y; Ruan, Liansheng L; Sun, Zhanhang Z; Zhang, Shuai S; Wang, Hao H; Liu, Yi Y; Xu, Yuyang Y; Ling, Jie J; Xu, Chunxiao C; Zhang, Yan Y; Lv, Duo D; Yuan, Zheping Z; Zhang, Jing J; Zhang, Yingqi Y; Shi, Yongyong Y; Lai, Maode M
Publication Date: 2017-06

Variant appearance in text: rs1532624
PubMed Link: 28371326
Variant Present in the following documents:
  • Main text
  • JCMM-21-1106.pdf
View BVdb publication page



Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.

American Journal Of Human Genetics
Civelek, Mete M; Wu, Ying Y; Pan, Calvin C; Raulerson, Chelsea K CK; Ko, Arthur A; He, Aiqing A; Tilford, Charles C; Saleem, Niyas K NK; Stančáková, Alena A; Scott, Laura J LJ; Fuchsberger, Christian C; Stringham, Heather M HM; Jackson, Anne U AU; Narisu, Narisu N; Chines, Peter S PS; Small, Kerrin S KS; Kuusisto, Johanna J; Parks, Brian W BW; Pajukanta, Päivi P; Kirchgessner, Todd T; Collins, Francis S FS; Gargalovic, Peter S PS; Boehnke, Michael M; Laakso, Markku M; Mohlke, Karen L KL; Lusis, Aldons J AJ
Publication Date: 2017-03-02

Variant appearance in text: rs1532624
PubMed Link: 28257690
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs1532624
PubMed Link: 27768712
Variant Present in the following documents:
  • Main text
  • pone.0164151.pdf
View BVdb publication page



Analysis with the exome array identifies multiple new independent variants in lipid loci.

Human Molecular Genetics
Kanoni, Stavroula S; Masca, Nicholas G D NG; Stirrups, Kathleen E KE; Varga, Tibor V TV; Warren, Helen R HR; Scott, Robert A RA; Southam, Lorraine L; Zhang, Weihua W; Yaghootkar, Hanieh H; Müller-Nurasyid, Martina M; Couto Alves, Alexessander A; Strawbridge, Rona J RJ; Lataniotis, Lazaros L; An Hashim, Nikman N; Besse, Céline C; Boland, Anne A; Braund, Peter S PS; Connell, John M JM; Dominiczak, Anna A; Farmaki, Aliki-Eleni AE; Franks, Stephen S; Grallert, Harald H; Jansson, Jan-Håkan JH; Karaleftheri, Maria M; Keinänen-Kiukaanniemi, Sirkka S; Matchan, Angela A; Pasko, Dorota D; Peters, Annette A; Poulter, Neil N; Rayner, Nigel W NW; Renström, Frida F; Rolandsson, Olov O; Sabater-Lleal, Maria M; Sennblad, Bengt B; Sever, Peter P; Shields, Denis D; Silveira, Angela A; Stanton, Alice V AV; Strauch, Konstantin K; Tomaszewski, Maciej M; Tsafantakis, Emmanouil E; Waldenberger, Melanie M; Blakemore, Alexandra I F AI; Dedoussis, George G; Escher, Stefan A SA; Kooner, Jaspal S JS; McCarthy, Mark I MI; Palmer, Colin N A CN; , ; Hamsten, Anders A; Caulfield, Mark J MJ; Frayling, Timothy M TM; Tobin, Martin D MD; Jarvelin, Marjo-Riitta MR; Zeggini, Eleftheria E; Gieger, Christian C; Chambers, John C JC; Wareham, Nick J NJ; Munroe, Patricia B PB; Franks, Paul W PW; Samani, Nilesh J NJ; Deloukas, Panos P
Publication Date: 2016-09-15

Variant appearance in text: rs1532624
PubMed Link: 27466198
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: rs1532624
PubMed Link: 26683795
Variant Present in the following documents:
  • Main text
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Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs1532624
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
View BVdb publication page



The Rotterdam Study: 2016 objectives and design update.

European Journal Of Epidemiology
Hofman, Albert A; Brusselle, Guy G O GG; Darwish Murad, Sarwa S; van Duijn, Cornelia M CM; Franco, Oscar H OH; Goedegebure, André A; Ikram, M Arfan MA; Klaver, Caroline C W CC; Nijsten, Tamar E C TE; Peeters, Robin P RP; Stricker, Bruno H Ch BH; Tiemeier, Henning W HW; Uitterlinden, André G AG; Vernooij, Meike W MW
Publication Date: 2015-08

Variant appearance in text: rs1532624
PubMed Link: 26386597
Variant Present in the following documents:
  • Main text
View BVdb publication page



Regulation of cholesteryl ester transfer protein expression by upstream polymorphisms: reduced expression associated with rs247616.

Pharmacogenetics And Genomics
Suhy, Adam A; Hartmann, Katherine K; Papp, Audrey C AC; Wang, Danxin D; Sadee, Wolfgang W
Publication Date: 2015-08

Variant appearance in text: rs1532624
PubMed Link: 26061659
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs1532624
PubMed Link: 25918167
Variant Present in the following documents:
  • Main text
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Testing for genetic associations in arbitrarily structured populations.

Nature Genetics
Song, Minsun M; Hao, Wei W; Storey, John D JD
Publication Date: 2015-05

Variant appearance in text: rs1532624
PubMed Link: 25822090
Variant Present in the following documents:
  • NIHMS664591-supplement-1.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: rs1532624
PubMed Link: 25431328
Variant Present in the following documents:
  • Main text
  • btu783.pdf
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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: rs1532624
PubMed Link: 24719370
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  • Main text
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A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates.

Nature Communications
Tachmazidou, Ioanna I; Dedoussis, George G; Southam, Lorraine L; Farmaki, Aliki-Eleni AE; Ritchie, Graham R S GR; Xifara, Dionysia K DK; Matchan, Angela A; Hatzikotoulas, Konstantinos K; Rayner, Nigel W NW; Chen, Yuan Y; Pollin, Toni I TI; O'Connell, Jeffrey R JR; Yerges-Armstrong, Laura M LM; Kiagiadaki, Chrysoula C; Panoutsopoulou, Kalliope K; Schwartzentruber, Jeremy J; Moutsianas, Loukas L; , ; Tsafantakis, Emmanouil E; Tyler-Smith, Chris C; McVean, Gil G; Xue, Yali Y; Zeggini, Eleftheria E
Publication Date: 2013

Variant appearance in text: rs1532624
PubMed Link: 24343240
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: rs1532624
PubMed Link: 24283500
Variant Present in the following documents:
  • Main text
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Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data.

Plos One
Bryzgalov, Leonid O LO; Antontseva, Elena V EV; Matveeva, Marina Yu MY; Shilov, Alexander G AG; Kashina, Elena V EV; Mordvinov, Viatcheslav A VA; Merkulova, Tatyana I TI
Publication Date: 2013

Variant appearance in text: rs1532624
PubMed Link: 24205329
Variant Present in the following documents:
  • Main text
  • pone.0078833.pdf
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Do genetic modifiers of high-density lipoprotein cholesterol and triglyceride levels also modify their response to a lifestyle intervention in the setting of obesity and type-2 diabetes mellitus?: The Action for Health in Diabetes (Look AHEAD) study.

Circulation. Cardiovascular Genetics
Huggins, Gordon S GS; Papandonatos, George D GD; Erar, Bahar B; Belalcazar, L Maria LM; Brautbar, Ariel A; Ballantyne, Christie C; Kitabchi, Abbas E AE; Wagenknecht, Lynne E LE; Knowler, William C WC; Pownall, Henry J HJ; Wing, Rena R RR; Peter, Inga I; McCaffery, Jeanne M JM; ,
Publication Date: 2013-08

Variant appearance in text: rs1532624
PubMed Link: 23861364
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  • Main text
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Association analysis of dyslipidemia-related genes in diabetic nephropathy.

Plos One
McKay, Gareth J GJ; Savage, David A DA; Patterson, Christopher C CC; Lewis, Gareth G; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; ,
Publication Date: 2013

Variant appearance in text: rs1532624
PubMed Link: 23555584
Variant Present in the following documents:
  • Main text
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Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.

Journal Of Medical Genetics
Weissglas-Volkov, Daphna D; Aguilar-Salinas, Carlos A CA; Nikkola, Elina E; Deere, Kerry A KA; Cruz-Bautista, Ivette I; Arellano-Campos, Olimpia O; Muñoz-Hernandez, Linda Liliana LL; Gomez-Munguia, Lizeth L; Ordoñez-Sánchez, Maria Luisa ML; Reddy, Prasad M V Linga PM; Lusis, Aldons J AJ; Matikainen, Niina N; Taskinen, Marja-Riitta MR; Riba, Laura L; Cantor, Rita M RM; Sinsheimer, Janet S JS; Tusie-Luna, Teresa T; Pajukanta, Päivi P
Publication Date: 2013-05

Variant appearance in text: rs1532624
PubMed Link: 23505323
Variant Present in the following documents:
  • Main text
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Investigation of genetic risk factors for chronic adult diseases for association with preterm birth.

Human Genetics
Falah, Nadia N; McElroy, Jude J; Snegovskikh, Victoria V; Lockwood, Charles J CJ; Norwitz, Errol E; Murray, Jeffey C JC; Kuczynski, Edward E; Menon, Ramkumar R; Teramo, Kari K; Muglia, Louis J LJ; Morgan, Thomas T
Publication Date: 2013-01

Variant appearance in text: rs1532624
PubMed Link: 22972380
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: rs1532624
PubMed Link: 22902788
Variant Present in the following documents:
  • NIHMS392993-supplement-1.pdf
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High-throughput analysis of epistasis in genome-wide association studies with BiForce.

Bioinformatics (Oxford, England)
Gyenesei, Attila A; Moody, Jonathan J; Semple, Colin A M CA; Haley, Chris S CS; Wei, Wen-Hua WH
Publication Date: 2012-08-01

Variant appearance in text: rs1532624
PubMed Link: 22618535
Variant Present in the following documents:
  • Main text
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Advances in exercise, fitness, and performance genomics in 2011.

Medicine And Science In Sports And Exercise
Roth, Stephen M SM; Rankinen, Tuomo T; Hagberg, James M JM; Loos, Ruth J F RJ; Pérusse, Louis L; Sarzynski, Mark A MA; Wolfarth, Bernd B; Bouchard, Claude C
Publication Date: 2012-05

Variant appearance in text: rs1532624
PubMed Link: 22330029
Variant Present in the following documents:
  • Main text
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A Database of Gene-Environment Interactions Pertaining to Blood Lipid Traits, Cardiovascular Disease and Type 2 Diabetes.

Journal Of Data Mining In Genomics & Proteomics
Lee, Yu-Chi YC; Lai, Chao-Qiang CQ; Ordovas, Jose M JM; Parnell, Laurence D LD
Publication Date: 2011-01-01

Variant appearance in text: rs1532624
PubMed Link: 22328972
Variant Present in the following documents:
  • Main text
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GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.

Human Molecular Genetics
Benyamin, Beben B; Middelberg, Rita P RP; Lind, Penelope A PA; Valle, Anne M AM; Gordon, Scott S; Nyholt, Dale R DR; Medland, Sarah E SE; Henders, Anjali K AK; Heath, Andrew C AC; Madden, Pamela A F PA; Visscher, Peter M PM; O'Connor, Daniel T DT; Montgomery, Grant W GW; Martin, Nicholas G NG; Whitfield, John B JB
Publication Date: 2011-11-15

Variant appearance in text: rs1532624
PubMed Link: 21862451
Variant Present in the following documents:
  • Main text
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Implications of discoveries from genome-wide association studies in current cardiovascular practice.

World Journal Of Cardiology
Jeemon, Panniyammakal P; Pettigrew, Kerry K; Sainsbury, Christopher C; Prabhakaran, Dorairaj D; Padmanabhan, Sandosh S
Publication Date: 2011-07-26

Variant appearance in text: rs1532624
PubMed Link: 21860704
Variant Present in the following documents:
  • Main text
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Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.

Plos One
Turner, Stephen D SD; Berg, Richard L RL; Linneman, James G JG; Peissig, Peggy L PL; Crawford, Dana C DC; Denny, Joshua C JC; Roden, Dan M DM; McCarty, Catherine A CA; Ritchie, Marylyn D MD; Wilke, Russell A RA
Publication Date: 2011-05-11

Variant appearance in text: rs1532624
PubMed Link: 21589926
Variant Present in the following documents:
  • Main text
  • pone.0019586.pdf
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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
Ahmad, Tariq T; Chasman, Daniel I DI; Buring, Julie E JE; Lee, I-Min IM; Ridker, Paul M PM; Everett, Brendan M BM
Publication Date: 2011-02

Variant appearance in text: rs1532624
PubMed Link: 21252145
Variant Present in the following documents:
  • Main text
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Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.

Plos Genetics
Smith, Erin N EN; Chen, Wei W; Kähönen, Mika M; Kettunen, Johannes J; Lehtimäki, Terho T; Peltonen, Leena L; Raitakari, Olli T OT; Salem, Rany M RM; Schork, Nicholas J NJ; Shaw, Marian M; Srinivasan, Sathanur R SR; Topol, Eric J EJ; Viikari, Jorma S JS; Berenson, Gerald S GS; Murray, Sarah S SS
Publication Date: 2010-09-09

Variant appearance in text: rs1532624
PubMed Link: 20838585
Variant Present in the following documents:
  • Main text
  • pgen.1001094.pdf
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Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

Plos One
Zeller, Tanja T; Wild, Philipp P; Szymczak, Silke S; Rotival, Maxime M; Schillert, Arne A; Castagne, Raphaele R; Maouche, Seraya S; Germain, Marine M; Lackner, Karl K; Rossmann, Heidi H; Eleftheriadis, Medea M; Sinning, Christoph R CR; Schnabel, Renate B RB; Lubos, Edith E; Mennerich, Detlev D; Rust, Werner W; Perret, Claire C; Proust, Carole C; Nicaud, Viviane V; Loscalzo, Joseph J; Hübner, Norbert N; Tregouet, David D; Münzel, Thomas T; Ziegler, Andreas A; Tiret, Laurence L; Blankenberg, Stefan S; Cambien, François F
Publication Date: 2010-05-18

Variant appearance in text: rs1532624
PubMed Link: 20502693
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: rs1532624
PubMed Link: 20421590
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  • Main text
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The genetics of obesity and the metabolic syndrome.

Endocrine, Metabolic & Immune Disorders Drug Targets
Monda, Keri L KL; North, Kari E KE; Hunt, Steven C SC; Rao, D C DC; Province, Michael A MA; Kraja, Aldi T AT
Publication Date: 2010-06

Variant appearance in text: rs1532624
PubMed Link: 20406164
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  • Main text
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Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.

Plos Genetics
Igl, Wilmar W; Johansson, Asa A; Wilson, James F JF; Wild, Sarah H SH; Polasek, Ozren O; Hayward, Caroline C; Vitart, Veronique V; Hastie, Nicholas N; Rudan, Pavao P; Gnewuch, Carsten C; Schmitz, Gerd G; Meitinger, Thomas T; Pramstaller, Peter P PP; Hicks, Andrew A AA; Oostra, Ben A BA; van Duijn, Cornelia M CM; Rudan, Igor I; Wright, Alan A; Campbell, Harry H; Gyllensten, Ulf U; ,
Publication Date: 2010-01

Variant appearance in text: rs1532624
PubMed Link: 20066028
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: rs1532624
PubMed Link: 20031564
Variant Present in the following documents:
  • Main text
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Analysis of recently identified dyslipidemia alleles reveals two loci that contribute to risk for carotid artery disease.

Lipids In Health And Disease
Ronald, James J; Rajagopalan, Ramakrishnan R; Ranchalis, Jane E JE; Marshall, Julieann K JK; Hatsukami, Thomas S TS; Heagerty, Patrick J PJ; Jarvik, Gail P GP
Publication Date: 2009-12-01

Variant appearance in text: rs1532624
PubMed Link: 19951432
Variant Present in the following documents:
  • Main text
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TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population.

Journal Of Biomedical Science
Lins, Tulio C TC; Abreu, Breno S BS; Pereira, Rinaldo W RW
Publication Date: 2009-08-14

Variant appearance in text: rs1532624
PubMed Link: 19682379
Variant Present in the following documents:
  • Main text
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