Publications:

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Effects of Obesity and Family History of Diabetes on the Association of CETP rs6499861 with HDL-C Level in Korean Populations.

Journal Of Lipid And Atherosclerosis

JW Sull, S Kim, SH Jee

Publication Date: 2019-09

Variant appearance in text: rs12708980

PubMed Link: 32821715

Variant Present in the following documents:

• Main text

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

Scientific Reports

HS Lee, Y Kim, T Park

Publication Date: 2018-04-09

Variant appearance in text: rs12708980

PubMed Link: 29632305

Variant Present in the following documents:

• 41598_2018_23074_MOESM1_ESM.docx
• aaaaaMain text

View BVdb publication page

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From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results.

Plos One

E Cirillo, M Kutmon, M Gonzalez Hernandez, T Hooimeijer, ME Adriaens, LMT Eijssen, LD Parnell, SL Coort, CT Evelo

Publication Date: 2018

Variant appearance in text: rs12708980

PubMed Link: 29617380

Variant Present in the following documents:

• Complete_dissertation.pdf

View BVdb publication page

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Identifying potentially common genes between dyslipidemia and osteoporosis using novel analytical approaches.

Molecular Genetics And Genomics : Mgg

X Lin, C Peng, J Greenbaum, ZF Li, KH Wu, ZX Ao, T Zhang, J Shen, HW Deng

Publication Date: 2018-06

Variant appearance in text: rs12708980

PubMed Link: 29327327

Variant Present in the following documents:

• Main text

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: rs12708980

PubMed Link: 29084231

Variant Present in the following documents:

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

View BVdb publication page

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A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration.

Scientific Reports

K Kawashima-Kumagai, K Yamashiro, M Yoshikawa, M Miyake, GCC Ming, Q Fan, JY Koh, M Saito, M Sugahara-Kuroda, M Oishi, Y Akagi-Kurashige, I Nakata, H Nakanishi, N Gotoh, A Oishi, H Tamura, S Ooto, A Tsujikawa, Y Kurimoto, T Sekiryu, F Matsuda, CC Khor, CY Cheng, TY Wong, N Yoshimura

Publication Date: 2017-08-03

Variant appearance in text: rs12708980

PubMed Link: 28775256

Variant Present in the following documents:

• 41598_2017_7526_MOESM1_ESM.xls

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

Journal Of Cellular And Molecular Medicine

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

Publication Date: 2017-06

Variant appearance in text: rs12708980

PubMed Link: 28371326

Variant Present in the following documents:

• JCMM-21-1106-s002.xlsx

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: rs12708980

PubMed Link: 27768712

Variant Present in the following documents:

• Main text

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: rs12708980

PubMed Link: 26780889

Variant Present in the following documents:

• srep19429-s3.xls

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: rs12708980

PubMed Link: 26683795

Variant Present in the following documents:

• Main text

View BVdb publication page

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Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

European Journal Of Human Genetics : Ejhg

X Wang, CY Cheng, J Liao, X Sim, J Liu, KS Chia, ES Tai, P Little, CC Khor, T Aung, TY Wong, YY Teo

Publication Date: 2016-04

Variant appearance in text: rs12708980

PubMed Link: 26130488

Variant Present in the following documents:

• ejhg2015150x4.xls

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On the analysis of a repeated measure design in genome-wide association analysis.

International Journal Of Environmental Research And Public Health

Y Lee, S Park, S Moon, J Lee, RC Elston, W Lee, S Won

Publication Date: 2014-11-28

Variant appearance in text: rs12708980

PubMed Link: 25464127

Variant Present in the following documents:

• Main text

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Cis and trans effects of human genomic variants on gene expression.

Plos Genetics

J Bryois, A Buil, DM Evans, JP Kemp, SB Montgomery, DF Conrad, KM Ho, S Ring, M Hurles, P Deloukas, G Davey Smith, ET Dermitzakis

Publication Date: 2014-07

Variant appearance in text: rs12708980

PubMed Link: 25010687

Variant Present in the following documents:

• pgen.1004461.s012.xlsx

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Genetic risk score and adiposity interact to influence triglyceride levels in a cohort of Filipino women.

Nutrition & Diabetes

N Zubair, EJ Mayer-Davis, MA Mendez, KL Mohlke, KE North, LS Adair

Publication Date: 2014-06-16

Variant appearance in text: rs12708980

PubMed Link: 24932782

Variant Present in the following documents:

• Main text

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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: rs12708980

PubMed Link: 23940718

Variant Present in the following documents:

• Main text

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: rs12708980

PubMed Link: 23656756

Variant Present in the following documents:

• Main text

View BVdb publication page

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Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population.

Genomics & Informatics

MJ Go, JY Hwang, DJ Kim, HJ Lee, HB Jang, KH Park, J Song, JY Lee

Publication Date: 2012-06

Variant appearance in text: rs12708980

PubMed Link: 23105936

Variant Present in the following documents:

• Main text

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: rs12708980

PubMed Link: 22403620

Variant Present in the following documents:

• pone.0031930.s010.docx

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

Science (New York, N.Y.)

LJ Scott, KL Mohlke, LL Bonnycastle, CJ Willer, Y Li, WL Duren, MR Erdos, HM Stringham, PS Chines, AU Jackson, L Prokunina-Olsson, CJ Ding, AJ Swift, N Narisu, T Hu, R Pruim, R Xiao, XY Li, KN Conneely, NL Riebow, AG Sprau, M Tong, PP White, KN Hetrick, MW Barnhart, CW Bark, JL Goldstein, L Watkins, F Xiang, J Saramies, TA Buchanan, RM Watanabe, TT Valle, L Kinnunen, GR Abecasis, EW Pugh, KF Doheny, RN Bergman, J Tuomilehto, FS Collins, M Boehnke

Publication Date: 2007-06-01

Variant appearance in text: rs12708980

PubMed Link: 17463248

Variant Present in the following documents:

• NIHMS322992-supplement-Scott2007_supp.pdf

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000200676.3	c.1146+212T>G	-	intron_variant	-	11/15
ENST00000379780.2	c.966+212T>G	-	intron_variant	-	10/14
ENST00000566128.1	c.951+212T>G	-	intron_variant	-	11/15
NM_000078.3	c.1146+212T>G	-	intron_variant	-	11/15
NM_001286085.2	c.966+212T>G	-	intron_variant	-	10/14