APOB c.8216C>A ;(p.P2739Q)

Variant ID: 2-21231524-G-T

NM_000384.2(APOB):c.8216C>A;(p.P2739Q)

This variant was identified in 50 publications

View GRCh38 version.




Publications:


Association of triglyceride levels and prostate cancer: a Mendelian randomization study.

Bmc Urology
Zhu, Shusheng S; Hu, Xia X; Fan, Yanpeng Y
Publication Date: 2022-10-31

Variant appearance in text: rs676210
PubMed Link: 36316671
Variant Present in the following documents:
  • Main text
  • 12894_2022_Article_1120.pdf
View BVdb publication page



Population-based meta-analysis and gene-set enrichment identifies FXR/RXR pathway as common to fatty liver disease and serum lipids.

Hepatology Communications
Handelman, Samuel K SK; Puentes, Yindra M YM; Kuppa, Annapurna A; Chen, Yanhua Y; Du, Xiaomeng X; Feitosa, Mary F MF; Palmer, Nicholette D ND; Speliotes, Elizabeth K EK
Publication Date: 2022-11

Variant appearance in text: rs676210
PubMed Link: 36098472
Variant Present in the following documents:
  • Main text
  • HEP4-6-3120-s001.xlsx, sheet 7
  • HEP4-6-3120.pdf
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The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population.

Frontiers In Genetics
Yang, Lincheng L; Pu, Tian T; Zhang, Yan Y; Yan, Hua H; Yu, Haiyi H; Gao, Wei W
Publication Date: 2022

Variant appearance in text: rs676210
PubMed Link: 35480303
Variant Present in the following documents:
  • Main text
  • fgene-13-875269.pdf
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Inferred expression regulator activities suggest genes mediating cardiometabolic genetic signals.

Plos Computational Biology
Hoskins, Jason W JW; Chung, Charles C CC; O'Brien, Aidan A; Zhong, Jun J; Connelly, Katelyn K; Collins, Irene I; Shi, Jianxin J; Amundadottir, Laufey T LT
Publication Date: 2021-11

Variant appearance in text: rs676210
PubMed Link: 34793442
Variant Present in the following documents:
  • Main text
  • pcbi.1009563.pdf
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Case Report: A Clinical and Genetic Analysis of Childhood Growth Hormone Deficiency With Familial Hypercholesterolemia.

Frontiers In Endocrinology
Yang, Shengmin S; Ke, Xiaoan X; Liang, Hanting H; Li, Ran R; Zhu, Huijuan H
Publication Date: 2021

Variant appearance in text: rs676210
PubMed Link: 34220717
Variant Present in the following documents:
  • Main text
  • fendo-12-691490.pdf
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ApoB gene polymorphism (rs676210) and its pharmacogenetics impact on atorvastatin response among Iraqi population with coronary artery disease.

Journal, Genetic Engineering & Biotechnology
Abdulfattah, Shaimaa Y SY; Al-Awadi, Salwa J SJ
Publication Date: 2021-06-22

Variant appearance in text: rs676210
PubMed Link: 34156559
Variant Present in the following documents:
  • Main text
  • 43141_2021_Article_193.pdf
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Association of apolipoprotein B XbaI (rs693) polymorphism and gallstone disease risk based on a comprehensive analysis.

Genes And Environment : The Official Journal Of The Japanese Environmental Mutagen Society
Zhu, Haifeng H; Yu, Linhai L; Feng, Linsong L
Publication Date: 2021-05-03

Variant appearance in text: rs676210
PubMed Link: 33941261
Variant Present in the following documents:
  • Main text
View BVdb publication page



Susceptibility of ApoB and PCSK9 Genetic Polymorphisms to Diabetic Kidney Disease Among Chinese Diabetic Patients.

Frontiers In Medicine
Ma, Liang L; Wang, Shaoting S; Zhao, Hailing H; Yu, Meijie M; Deng, Xiangling X; Jiang, Yongwei Y; Cao, Yongtong Y; Li, Ping P; Niu, Wenquan W
Publication Date: 2021

Variant appearance in text: rs676210
PubMed Link: 33889589
Variant Present in the following documents:
  • Main text
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Influence of multiple apolipoprotein A-I and B genetic variations on insulin resistance and metabolic syndrome in obstructive sleep apnea.

Nutrition & Metabolism
Li, Xinyi X; Fu, Zhihui Z; Xu, Huajun H; Zou, Jianyin J; Zhu, Huaming H; Li, Zhiqiang Z; Su, Kaiming K; Huai, De ; Yi, Hongliang H; Guan, Jian J; Yin, Shankai S
Publication Date: 2020

Variant appearance in text: rs676210
PubMed Link: 33005209
Variant Present in the following documents:
  • Main text
  • 12986_2020_Article_501.pdf
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In-depth plasma proteomics reveals increase in circulating PD-1 during anti-PD-1 immunotherapy in patients with metastatic cutaneous melanoma.

Journal For Immunotherapy Of Cancer
Babačić, Haris H; Lehtiö, Janne J; Pico de Coaña, Yago Y; Pernemalm, Maria M; Eriksson, Hanna H
Publication Date: 2020-05

Variant appearance in text: rs676210
PubMed Link: 32457125
Variant Present in the following documents:
  • jitc-2019-000204supp003.xlsx, sheet 3
View BVdb publication page



Gene-environment interactions due to quantile-specific heritability of triglyceride and VLDL concentrations.

Scientific Reports
Williams, Paul T PT
Publication Date: 2020-03-11

Variant appearance in text: rs676210
PubMed Link: 32161301
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polygenic Hyperlipidemias and Coronary Artery Disease Risk.

Circulation. Genomic And Precision Medicine
Ripatti, Pietari P; Rämö, Joel T JT; Mars, Nina J NJ; Fu, Yu Y; Lin, Jake J; Söderlund, Sanni S; Benner, Christian C; Surakka, Ida I; Kiiskinen, Tuomo T; Havulinna, Aki S AS; Palta, Priit P; Freimer, Nelson B NB; Widén, Elisabeth E; Salomaa, Veikko V; Tukiainen, Taru T; Pirinen, Matti M; Palotie, Aarno A; Taskinen, Marja-Riitta MR; Ripatti, Samuli S; ,
Publication Date: 2020-04

Variant appearance in text: rs676210
PubMed Link: 32154731
Variant Present in the following documents:
  • hcg-13-e002725-s001.pdf
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COPD-dependent effects of genetic variation in key inflammation pathway genes on lung cancer risk.

International Journal Of Cancer
Watza, Donovan D; Lusk, Christine M CM; Dyson, Gregory G; Purrington, Kristen S KS; Wenzlaff, Angela S AS; Neslund-Dudas, Christine C; Soubani, Ayman O AO; Gadgeel, Shirish M SM; Schwartz, Ann G AG
Publication Date: 2020-08-01

Variant appearance in text: rs676210
PubMed Link: 31709530
Variant Present in the following documents:
  • Main text
View BVdb publication page



The transferability of lipid loci across African, Asian and European cohorts.

Nature Communications
Kuchenbaecker, Karoline K; Telkar, Nikita N; Reiker, Theresa T; Walters, Robin G RG; Lin, Kuang K; Eriksson, Anders A; Gurdasani, Deepti D; Gilly, Arthur A; Southam, Lorraine L; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Seeley, Janet J; Kamali, Anatoli A; Asiki, Gershim G; Millwood, Iona Y IY; Holmes, Michael M; Du, Huaidong H; Guo, Yu Y; Kumari, Meena M; Dedoussis, George G; Li, Liming L; Chen, Zhengming Z; Sandhu, Manjinder S MS; Zeggini, Eleftheria E; ,
Publication Date: 2019-09-24

Variant appearance in text: rs676210
PubMed Link: 31551420
Variant Present in the following documents:
  • 41467_2019_12026_MOESM1_ESM.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: rs676210
PubMed Link: 31132756
Variant Present in the following documents:
  • Main text
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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs676210
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
View BVdb publication page



Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report.

Bmc Neurology
Zhang, Xiaoqian X; Zhang, Lei L; Wu, Yanqing Y; Li, Gang G; Chen, Shengcai S; Xia, Yuanpeng Y; Li, Hongge H
Publication Date: 2018-11-29

Variant appearance in text: rs676210
PubMed Link: 30497413
Variant Present in the following documents:
  • 12883_2018_1199_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



The relationship between apolipoprotein genes polymorphisms and susceptibility to osteonecrosis of the femoral head: a meta-analysis.

Lipids In Health And Disease
Hao, Yangquan Y; Guo, Hao H; Xu, Zhaochen Z; Qi, Handeng H; Wang, Yugui Y; Lu, Chao C; Liu, Jie J; Yuan, Puwei P
Publication Date: 2018-08-17

Variant appearance in text: rs676210
PubMed Link: 30119683
Variant Present in the following documents:
  • Main text
  • 12944_2018_Article_827.pdf
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Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.

Journal Of Lipid Research
Zhou, Yitian Y; Mägi, Reedik R; Milani, Lili L; Lauschke, Volker M VM
Publication Date: 2018-10

Variant appearance in text: rs676210
PubMed Link: 30076208
Variant Present in the following documents:
  • 10.1194_P086710_jlr.P086710-4.xlsx, sheet 1
View BVdb publication page



GWAS Reveal Targets in Vessel Wall Pathways to Treat Coronary Artery Disease.

Frontiers In Cardiovascular Medicine
Turner, Adam W AW; Wong, Doris D; Dreisbach, Caitlin N CN; Miller, Clint L CL
Publication Date: 2018

Variant appearance in text: rs676210
PubMed Link: 29988570
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association mapping from sequencing reads using k-mers.

Elife
Rahman, Atif A; Hallgrímsdóttir, Ingileif I; Eisen, Michael M; Pachter, Lior L
Publication Date: 2018-06-13

Variant appearance in text: rs676210
PubMed Link: 29897334
Variant Present in the following documents:
  • Main text
  • elife-32920.pdf
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Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population.

Oncotarget
Zhou, Feng F; Guo, Tie T; Zhou, Lv L; Zhou, Yanhui Y; Yu, Dan D
Publication Date: 2018-01-05

Variant appearance in text: rs676210
PubMed Link: 29416768
Variant Present in the following documents:
  • Main text
  • oncotarget-09-2249.pdf
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APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism.

Bmc Gastroenterology
Harada, Rie R; Kimura, Masako M; Sato, Yasushi Y; Taniguchi, Tatsuya T; Tomonari, Tetsu T; Tanaka, Takahiro T; Tanaka, Hironori H; Muguruma, Naoki N; Shinomiya, Hirohiko H; Honda, Hirohito H; Imoto, Issei I; Sogabe, Masahiro M; Okahisa, Toshiya T; Takayama, Tetsuji T
Publication Date: 2018-01-30

Variant appearance in text: rs676210
PubMed Link: 29382324
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomic determinants of long-term cardiometabolic complications in childhood acute lymphoblastic leukemia survivors.

Bmc Cancer
England, Jade J; Drouin, Simon S; Beaulieu, Patrick P; St-Onge, Pascal P; Krajinovic, Maja M; Laverdière, Caroline C; Levy, Emile E; Marcil, Valérie V; Sinnett, Daniel D
Publication Date: 2017-11-10

Variant appearance in text: rs676210
PubMed Link: 29126409
Variant Present in the following documents:
  • Main text
  • 12885_2017_Article_3722.pdf
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Association analysis of APO gene polymorphisms with ischemic stroke risk: a case-control study in a Chinese Han population.

Oncotarget
Xiao, Rongjun R; Sun, Shuaiqi S; Zhang, Jiayi J; Ouyang, Yongri Y; Zhang, Ning N; Yang, Min M; Jin, Tianbo T; Xia, Ying Y
Publication Date: 2017-09-01

Variant appearance in text: rs676210
PubMed Link: 28947988
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between polymorphisms in the APOB gene and hyperlipidemia in the Chinese Yugur population.

Brazilian Journal Of Medical And Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
Gu, Q-L QL; Han, Y Y; Lan, Y-M YM; Li, Y Y; Kou, W W; Zhou, Y-S YS; Hai, X-J XJ; Yan, B B; Ci, C-H CH
Publication Date: 2017-09-12

Variant appearance in text: rs676210
PubMed Link: 28902930
Variant Present in the following documents:
  • Main text
  • 1414-431X-bjmbr-1414-431X20176613.pdf
View BVdb publication page



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: rs676210
PubMed Link: 28875524
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gallbladder cancer epidemiology, pathogenesis and molecular genetics: Recent update.

World Journal Of Gastroenterology
Sharma, Aarti A; Sharma, Kiran Lata KL; Gupta, Annapurna A; Yadav, Alka A; Kumar, Ashok A
Publication Date: 2017-06-14

Variant appearance in text: rs676210
PubMed Link: 28652652
Variant Present in the following documents:
  • Main text
  • WJG-23-3978.pdf
View BVdb publication page



Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).

Human Genetics
Wang, Zhe Z; Manichukal, Ani A; Goff, David C DC; Mora, Samia S; Ordovas, Jose M JM; Pajewski, Nicholas M NM; Post, Wendy S WS; Rotter, Jerome I JI; Sale, Michele M MM; Santorico, Stephanie A SA; Siscovick, David D; Tsai, Michael Y MY; Arnett, Donna K DK; Rich, Stephen S; Frazier-Wood, Alexis C AC
Publication Date: 2017-06

Variant appearance in text: rs676210
PubMed Link: 28352986
Variant Present in the following documents:
  • Main text
  • 439_2017_Article_1782.pdf
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Imputing Phenotypes for Genome-wide Association Studies.

American Journal Of Human Genetics
Hormozdiari, Farhad F; Kang, Eun Yong EY; Bilow, Michael M; Ben-David, Eyal E; Vulpe, Chris C; McLachlan, Stela S; Lusis, Aldons J AJ; Han, Buhm B; Eskin, Eleazar E
Publication Date: 2016-07-07

Variant appearance in text: rs676210
PubMed Link: 27292110
Variant Present in the following documents:
  • Main text
View BVdb publication page



Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk.

Human Genetics
Tragante, Vinicius V; Asselbergs, Folkert W FW; Swerdlow, Daniel I DI; Palmer, Tom M TM; Moore, Jason H JH; de Bakker, Paul I W PIW; Keating, Brendan J BJ; Holmes, Michael V MV
Publication Date: 2016-05

Variant appearance in text: rs676210
PubMed Link: 26946290
Variant Present in the following documents:
  • Main text
  • 439_2016_Article_1647.pdf
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Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs676210
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



Polymorphisms in ApoB gene are associated with risk of myocardial infarction and serum ApoB levels in a Chinese population.

International Journal Of Clinical And Experimental Medicine
Liu, Changqing C; Yang, Jing J; Han, Wei W; Zhang, Qi Q; Shang, Xiaoming X; Li, Xia X; Lu, Feng F; Liu, Xiaokun X
Publication Date: 2015

Variant appearance in text: rs676210
PubMed Link: 26629186
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic association of the ApoB and ApoA1 gene polymorphisms with the risk for alcohol-induced osteonecrosis of femoral head.

International Journal Of Clinical And Experimental Pathology
Wang, Yuan Y; Cao, Yuju Y; Li, Yizhou Y; Guo, Yongchang Y; Wang, Quanjian Q; Yang, Min M; Zhang, Ning N; Jin, Tianbo T; Wang, Jianzhong J
Publication Date: 2015

Variant appearance in text: rs676210
PubMed Link: 26617857
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evidence for Clinical Implementation of Pharmacogenomics in Cardiac Drugs.

Mayo Clinic Proceedings
Kaufman, Amy L AL; Spitz, Jared J; Jacobs, Michael M; Sorrentino, Matthew M; Yuen, Shennin S; Danahey, Keith K; Saner, Donald D; Klein, Teri E TE; Altman, Russ B RB; Ratain, Mark J MJ; O'Donnell, Peter H PH
Publication Date: 2015-06

Variant appearance in text: rs676210
PubMed Link: 26046407
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs676210
PubMed Link: 25822090
Variant Present in the following documents:
  • NIHMS664591-supplement-1.pdf
View BVdb publication page



Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions.

Plos One
Yu, Fuli F; Lu, Jian J; Liu, Xiaoming X; Gazave, Elodie E; Chang, Diana D; Raj, Srilakshmi S; Hunter-Zinck, Haley H; Blekhman, Ran R; Arbiza, Leonardo L; Van Hout, Cris C; Morrison, Alanna A; Johnson, Andrew D AD; Bis, Joshua J; Cupples, L Adrienne LA; Psaty, Bruce M BM; Muzny, Donna D; Yu, Jin J; Gibbs, Richard A RA; Keinan, Alon A; Clark, Andrew G AG; Boerwinkle, Eric E
Publication Date: 2015

Variant appearance in text: rs676210
PubMed Link: 25807536
Variant Present in the following documents:
  • pone.0121644.s002.xls, sheet 1
View BVdb publication page



Gene polymorphisms and gene scores linked to low serum carotenoid status and their associations with metabolic disturbance and depressive symptoms in African-American adults.

The British Journal Of Nutrition
Beydoun, May A MA; Nalls, Michael A MA; Canas, J Atilio JA; Evans, Michele K MK; Zonderman, Alan B AB
Publication Date: 2014-09-28

Variant appearance in text: rs676210
PubMed Link: 25201307
Variant Present in the following documents:
  • Main text
View BVdb publication page



The roles of genetic polymorphisms and human immunodeficiency virus infection in lipid metabolism.

Biomed Research International
de Almeida, Elaine Regina Delicato ER; Reiche, Edna Maria Vissoci EM; Kallaur, Ana Paula AP; Flauzino, Tamires T; Watanabe, Maria Angelica Ehara MA
Publication Date: 2013

Variant appearance in text: rs676210
PubMed Link: 24319689
Variant Present in the following documents:
  • Main text
  • BMRI2013-836790.pdf
View BVdb publication page



Assessment of computational methods for predicting the effects of missense mutations in human cancers.

Bmc Genomics
Gnad, Florian F; Baucom, Albion A; Mukhyala, Kiran K; Manning, Gerard G; Zhang, Zemin Z
Publication Date: 2013

Variant appearance in text: rs676210
PubMed Link: 23819521
Variant Present in the following documents:
  • 1471-2164-14-S3-S7-S1.xlsx, sheet 2
View BVdb publication page



Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

Plos One
Wood, Andrew R AR; Perry, John R B JR; Tanaka, Toshiko T; Hernandez, Dena G DG; Zheng, Hou-Feng HF; Melzer, David D; Gibbs, J Raphael JR; Nalls, Michael A MA; Weedon, Michael N MN; Spector, Tim D TD; Richards, J Brent JB; Bandinelli, Stefania S; Ferrucci, Luigi L; Singleton, Andrew B AB; Frayling, Timothy M TM
Publication Date: 2013

Variant appearance in text: rs676210
PubMed Link: 23696881
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity.

Human Genetics
Frazier-Wood, Alexis C AC; Manichaikul, Ani A; Aslibekyan, Stella S; Borecki, Ingrid B IB; Goff, David C DC; Hopkins, Paul N PN; Lai, Chao-Qiang CQ; Ordovas, Jose M JM; Post, Wendy S WS; Rich, Stephen S SS; Sale, Michèle M MM; Siscovick, David D; Straka, Robert J RJ; Tiwari, Hemant K HK; Tsai, Michael Y MY; Rotter, Jerome I JI; Arnett, Donna K DK
Publication Date: 2013-04

Variant appearance in text: rs676210
PubMed Link: 23263444
Variant Present in the following documents:
  • Main text
View BVdb publication page



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

Plos One
Takeuchi, Fumihiko F; Isono, Masato M; Katsuya, Tomohiro T; Yokota, Mitsuhiro M; Yamamoto, Ken K; Nabika, Toru T; Shimokawa, Kazuro K; Nakashima, Eitaro E; Sugiyama, Takao T; Rakugi, Hiromi H; Yamaguchi, Shuhei S; Ogihara, Toshio T; Yamori, Yukio Y; Kato, Norihiro N
Publication Date: 2012

Variant appearance in text: rs676210
PubMed Link: 23050023
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: rs676210
PubMed Link: 22902788
Variant Present in the following documents:
  • Main text
  • NIHMS392993-supplement-1.pdf
View BVdb publication page



Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol.

Circulation. Cardiovascular Genetics
Edmondson, Andrew C AC; Braund, Peter S PS; Stylianou, Ioannis M IM; Khera, Amit V AV; Nelson, Christopher P CP; Wolfe, Megan L ML; Derohannessian, Stephanie L SL; Keating, Brendan J BJ; Qu, Liming L; He, Jing J; Tobin, Martin D MD; Tomaszewski, Maciej M; Baumert, Jens J; Klopp, Norman N; Döring, Angela A; Thorand, Barbara B; Li, Mingyao M; Reilly, Muredach P MP; Koenig, Wolfgang W; Samani, Nilesh J NJ; Rader, Daniel J DJ
Publication Date: 2011-04

Variant appearance in text: rs676210
PubMed Link: 21303902
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic associations of brain structural networks in schizophrenia: a preliminary study.

Biological Psychiatry
Jagannathan, Kanchana K; Calhoun, Vince D VD; Gelernter, Joel J; Stevens, Michael C MC; Liu, Jingyu J; Bolognani, Federico F; Windemuth, Andreas A; Ruaño, Gualberto G; Assaf, Michal M; Pearlson, Godfrey D GD
Publication Date: 2010-10-01

Variant appearance in text: rs676210
PubMed Link: 20691427
Variant Present in the following documents:
  • Main text
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Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.

Plos Genetics
Chasman, Daniel I DI; Paré, Guillaume G; Mora, Samia S; Hopewell, Jemma C JC; Peloso, Gina G; Clarke, Robert R; Cupples, L Adrienne LA; Hamsten, Anders A; Kathiresan, Sekar S; Mälarstig, Anders A; Ordovas, José M JM; Ripatti, Samuli S; Parker, Alex N AN; Miletich, Joseph P JP; Ridker, Paul M PM
Publication Date: 2009-11

Variant appearance in text: rs676210
PubMed Link: 19936222
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic variation in healthy oldest-old.

Plos One
Halaschek-Wiener, Julius J; Amirabbasi-Beik, Mahsa M; Monfared, Nasim N; Pieczyk, Markus M; Sailer, Christian C; Kollar, Anita A; Thomas, Ruth R; Agalaridis, Georgios G; Yamada, So S; Oliveira, Lisa L; Collins, Jennifer A JA; Meneilly, Graydon G; Marra, Marco A MA; Madden, Kenneth M KM; Le, Nhu D ND; Connors, Joseph M JM; Brooks-Wilson, Angela R AR
Publication Date: 2009-08-14

Variant appearance in text: rs676210
PubMed Link: 19680556
Variant Present in the following documents:
  • pone.0006641.s001.xls, sheet 1
View BVdb publication page



Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15

Variant appearance in text: rs676210
PubMed Link: 19336475
Variant Present in the following documents:
  • ddp159_1.pdf
View BVdb publication page



Polymorphisms of genes in the lipid metabolism pathway and risk of biliary tract cancers and stones: a population-based case-control study in Shanghai, China.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Andreotti, Gabriella G; Chen, Jinbo J; Gao, Yu-Tang YT; Rashid, Asif A; Chen, Bingshu E BE; Rosenberg, Philip P; Sakoda, Lori C LC; Deng, Jie J; Shen, Ming-Chang MC; Wang, Bing-Sheng BS; Han, Tian-Quan TQ; Zhang, Bai-He BH; Yeager, Meredith M; Welch, Robert R; Chanock, Stephen S; Fraumeni, Joseph F JF; Hsing, Ann W AW
Publication Date: 2008-03

Variant appearance in text: rs676210
PubMed Link: 18296645
Variant Present in the following documents:
  • Main text
View BVdb publication page