Publications:

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A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context.

Nature Communications

A Gallois, J Mefford, A Ko, A Vaysse, H Julienne, M Ala-Korpela, M Laakso, N Zaitlen, P Pajukanta, H Aschard

Publication Date: 2019-10-21

Variant appearance in text: rs180326

PubMed Link: 31636271

Variant Present in the following documents:

• 41467_2019_12703_MOESM3_ESM.xlsx

View BVdb publication page

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

Journal Of Cellular And Molecular Medicine

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

Publication Date: 2017-06

Variant appearance in text: rs180326

PubMed Link: 28371326

Variant Present in the following documents:

• Main text
• JCMM-21-1106-s001.docx

View BVdb publication page

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Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.

Human Genomics

R Pranavchand, AS Kumar, BM Reddy

Publication Date: 2017-03-04

Variant appearance in text: rs180326

PubMed Link: 28257648

Variant Present in the following documents:

• Main text

View BVdb publication page

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

Plos One

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

Publication Date: 2017

Variant appearance in text: rs180326

PubMed Link: 28245265

Variant Present in the following documents:

• pone.0172880.s002.xlsx

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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: rs180326

PubMed Link: 27827461

Variant Present in the following documents:

• srep36830-s1.pdf

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Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Plos One

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

Publication Date: 2016

Variant appearance in text: rs180326

PubMed Link: 27257688

Variant Present in the following documents:

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

View BVdb publication page

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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: rs180326

PubMed Link: 26776183

Variant Present in the following documents:

• NIHMS742521-supplement-2.pdf

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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: rs180326

PubMed Link: 25688259

Variant Present in the following documents:

• Main text

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Association between the MLX interacting protein-like, BUD13 homolog and zinc finger protein 259 gene polymorphisms and serum lipid levels.

Scientific Reports

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

Publication Date: 2014-07-03

Variant appearance in text: rs180326

PubMed Link: 24989072

Variant Present in the following documents:

• Main text

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A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.

European Journal Of Human Genetics : Ejhg

M Hirokawa, H Morita, T Tajima, A Takahashi, K Ashikawa, F Miya, D Shigemizu, K Ozaki, Y Sakata, D Nakatani, S Suna, Y Imai, T Tanaka, T Tsunoda, K Matsuda, T Kadowaki, Y Nakamura, R Nagai, I Komuro, M Kubo

Publication Date: 2015-03

Variant appearance in text: rs180326

PubMed Link: 24916648

Variant Present in the following documents:

• ejhg2014110x4.pdf

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

Journal Of Cellular And Molecular Medicine

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

Publication Date: 2014-07

Variant appearance in text: rs180326

PubMed Link: 24780069

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of genetic variants influencing lipid levels with coronary artery disease in Japanese individuals.

Plos One

F Takeuchi, M Isono, T Katsuya, M Yokota, K Yamamoto, T Nabika, K Shimokawa, E Nakashima, T Sugiyama, H Rakugi, S Yamaguchi, T Ogihara, Y Yamori, N Kato

Publication Date: 2012

Variant appearance in text: rs180326

PubMed Link: 23050023

Variant Present in the following documents:

• pone.0046385.s003.xls
• pone.0046385.s004.xls
• pone.0046385.s005.xls

View BVdb publication page

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A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides.

Plos One

TR Braun, LF Been, A Singhal, J Worsham, S Ralhan, GS Wander, JC Chambers, JS Kooner, CE Aston, DK Sanghera

Publication Date: 2012

Variant appearance in text: rs180326

PubMed Link: 22623978

Variant Present in the following documents:

• Main text

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Genome-wide association study identifies common variants associated with circulating vitamin E levels.

Human Molecular Genetics

JM Major, K Yu, W Wheeler, H Zhang, MC Cornelis, ME Wright, M Yeager, K Snyder, SJ Weinstein, A Mondul, H Eliassen, M Purdue, A Hazra, CA McCarty, S Hendrickson, J Virtamo, D Hunter, S Chanock, P Kraft, D Albanes

Publication Date: 2011-10-01

Variant appearance in text: rs180326

PubMed Link: 21729881

Variant Present in the following documents:

• Main text

View BVdb publication page

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Alternative transcript annotations:

Transcript	cDNA	Protein	Consequence	Exon	Intron
ENST00000260210.4	c.1766+3159C>A	-	intron_variant	-	9/9
ENST00000375445.3	c.1364+3159C>A	-	intron_variant	-	9/9
ENST00000419189.1	c.*186+3159C>A	-	intron_variant,NMD_transcript_variant	-	3/3
NM_001159736.1	c.1364+3159C>A	-	intron_variant	-	9/9
NM_032725.4	c.1766+3159C>A	-	intron_variant	-	9/9