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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Disease and ISL1[original query]
Common variation in ISL1 confers genetic susceptibility for human congenital heart disease.
PloS one 2010 5 (5): e10855.
Stevens Kristen N, Hakonarson Hakon, Kim Cecilia E, Doevendans Pieter A, Koeleman Bobby P C, Mital Seema, Raue Jennifer, Glessner Joseph T, Coles John G, Moreno Victor, Granger Anne, Gruber Stephen B, Gruber Peter
ISL1 common variant rs1017 is not associated with susceptibility to congenital heart disease in a Chinese population.
Genetic testing and molecular biomarkers 2012 Jul 16 (7): 679-83.
Xue Lei, Wang Xiaowei, Xu Jing, Xu Xiaohan, Liu Xiang, Hu Zhibin, Shen Hongbing, Chen Yijia
Genome-wide association scan of dental caries in the permanent dentition. GWAS Catalog
BMC oral health 2012 Dec 12 (1): 1.
Wang X, Shaffer JR, Zeng Z, Begum F, Vieira AR, Noel J, Anjomshoaa I, Cuenco KT, Lee MK, Beck J, Boerwinkle E, Cornelis MC, Hu FB, Crosslin DR, Laurie CC, Nelson SC, Doheny KF, Pugh EW, Polk DE, Weyant RJ, Crout R, McNeil DW, Weeks DE, Feingold E, Marazita ML
Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.
Pediatric cardiology 2013 Apr 34 (4): 938-41.
Cresci Monica, Vecoli Cecilia, Foffa Ilenia, Pulignani Silvia, Ait-Ali Lamia, Andreassi Maria Graz
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activity.
European journal of heart failure 2012 Nov .
Friedrich FW, Dilanian G, Khattar P, Juhr D, Gueneau L, Charron P, Fressart V, Vilquin JT, Isnard R, Gouya L, Richard P, Hammoudi N, Komajda M, Bonne G, Eschenhagen T, Dubourg O, Villard E, Carrier L
Genetic variations of ISL1 associated with human congenital heart disease in Chinese Han people.
Genetics and molecular research : GMR 2014 13 (1): 1329-38.
Luo Z L, Sun H, Yang Z Q, Ma Y H, Gu Y, He Y Q, Wei D, Xia L B, Yang B H, Guo
BER gene polymorphisms associated with key molecular events in bladder cancer.
Experimental oncology 2018 Dec 40 (4): 288-298.
Smal M P, Kuzhir T D, Savina N V, Nikitchenko N V, Rolevich A I, Krasny S A, Goncharova R
Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis.
Medicine 2020 Jan 99 (2): e18715.
Ding Zhaohong, Yang Wenke, Yi Kang, Ding Yunhan, Zhou Dan, Xie Xiaodong, You T
Identification and functional analysis of genetic variants of ISL1 gene promoter in human atrial septal defects.
The journal of gene medicine 2022 9 24 (12): e3450.
Yin Xiu-Yun, Chen Huan-Xin, Chen Zhuo, Yang Qin, Han Jun, He Guo-W
Genetic studies in the Pakistani population reveal novel associations with ventricular septal defects (VSDs).
BMC pediatrics 2023 2 23 (1): 67.
Sarwar Sumbal, Shabana , Sajjad Khadija, Hasnain Shahi
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