Publications:

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Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.

Lipids In Health And Disease

R Pranavchand, BM Reddy

Publication Date: 2017-06-13

Variant appearance in text: rs664059

PubMed Link: 28610615

Variant Present in the following documents:

• 12944_2017_507_MOESM4_ESM.docx
• aaaaaMain text

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: rs664059

PubMed Link: 28257648

Variant Present in the following documents:

• 40246_2017_99_MOESM3_ESM.docx
• 40246_2017_99_MOESM4_ESM.docx
• aaaaaMain text

View BVdb publication page

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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: rs664059

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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Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.

Scientific Reports

W Wen, N Kato, JY Hwang, X Guo, Y Tabara, H Li, R Dorajoo, X Yang, FJ Tsai, S Li, Y Wu, T Wu, S Kim, X Guo, J Liang, D Shungin, LS Adair, K Akiyama, M Allison, Q Cai, LC Chang, CH Chen, YT Chen, YS Cho, BY Choi, Y Gao, MJ Go, D Gu, BG Han, M He, JE Hixson, Y Hu, T Huang, M Isono, KJ Jung, D Kang, YJ Kim, Y Kita, J Lee, NR Lee, J Lee, Y Wang, JJ Liu, J Long, S Moon, Y Nakamura, M Nakatochi, K Ohnaka, D Rao, J Shi, JW Sull, A Tan, H Ueshima, C Wu, YB Xiang, K Yamamoto, J Yao, X Ye, M Yokota, X Zhang, Y Zheng, L Qi, JI Rotter, SH Jee, D Lin, KL Mohlke, J He, Z Mo, JY Wu, ES Tai, X Lin, T Miki, BJ Kim, F Takeuchi, W Zheng, XO Shu

Publication Date: 2016-01-20

Variant appearance in text: rs664059

PubMed Link: 26785701

Variant Present in the following documents:

• srep17958-s10.xls
• srep17958-s11.xls
• srep17958-s12.xls
• srep17958-s15.xls
• srep17958-s9.xls

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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: rs664059

PubMed Link: 26780889

Variant Present in the following documents:

• srep19429-s3.xls

View BVdb publication page

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APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.

Bmc Medical Genetics

C Dussaillant, V Serrano, A Maiz, S Eyheramendy, LR Cataldo, M Chavez, SV Smalley, M Fuentes, A Rigotti, L Rubio, CF Lagos, JA Martinez, JL Santos

Publication Date: 2012-11-15

Variant appearance in text: rs664059

PubMed Link: 23151256

Variant Present in the following documents:

• 1471-2350-13-106-S1.docx

View BVdb publication page

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Genome-wide association of lipid-lowering response to statins in combined study populations.

Plos One

MJ Barber, LM Mangravite, CL Hyde, DI Chasman, JD Smith, CA McCarty, X Li, RA Wilke, MJ Rieder, PT Williams, PM Ridker, A Chatterjee, JI Rotter, DA Nickerson, M Stephens, RM Krauss

Publication Date: 2010-03-22

Variant appearance in text: rs664059

PubMed Link: 20339536

Variant Present in the following documents:

• pone.0009763.s008.xls

View BVdb publication page

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Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.

Genomics

M Olivier, X Wang, R Cole, B Gau, J Kim, EM Rubin, LA Pennacchio

Publication Date: 2004-05

Variant appearance in text: rs664059

PubMed Link: 15081120

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.144-1199G>A	-	intron_variant	-	1/9
ENST00000375445.3	c.144-1199G>A	-	intron_variant	-	1/9
NM_001159736.1	c.144-1199G>A	-	intron_variant	-	1/9
NM_032725.4	c.144-1199G>A	-	intron_variant	-	1/9