Hélène Choquet to Genetic Predisposition to Disease
This is a "connection" page, showing publications Hélène Choquet has written about Genetic Predisposition to Disease.
Connection Strength
4.876
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New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis. Commun Biol. 2021 07 22; 4(1):864.
Score: 0.662
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A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects. Nat Commun. 2021 06 14; 12(1):3595.
Score: 0.657
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Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity. Methods Mol Biol. 2020; 2152:77-84.
Score: 0.594
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A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. Nat Commun. 2017 12 13; 8(1):2108.
Score: 0.515
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Genetics of cerebral cavernous malformations: current status and future prospects. J Neurosurg Sci. 2015 Sep; 59(3):211-20.
Score: 0.429
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Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries. Nat Genet. 2024 Dec; 56(12):2659-2671.
Score: 0.209
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Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine. HGG Adv. 2023 Jul 13; 4(3):100211.
Score: 0.188
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Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. 2022 12; 612(7941):720-724.
Score: 0.182
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The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 2020 09 03; 182(5):1214-1231.e11.
Score: 0.156
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Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Nat Genet. 2020 04; 52(4):401-407.
Score: 0.151
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Functional validity, role, and implications of heavy alcohol consumption genetic loci. Sci Adv. 2020 01; 6(3):eaay5034.
Score: 0.149
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A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Nat Commun. 2018 06 11; 9(1):2278.
Score: 0.133
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Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. Mol Psychiatry. 2017 09; 22(9):1359-1367.
Score: 0.124
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Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutation. Cerebrovasc Dis. 2014; 37(1):57-63.
Score: 0.098
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Genetic and functional characterization of PCSK1. Methods Mol Biol. 2011; 768:247-53.
Score: 0.080
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Lack of association of CD36 SNPs with early onset obesity: a meta-analysis in 9,973 European subjects. Obesity (Silver Spring). 2011 Apr; 19(4):833-9.
Score: 0.078
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The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies. BMC Med Genet. 2008 May 22; 9:45.
Score: 0.066
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Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study. J Mol Med (Berl). 2008 Mar; 86(3):341-8.
Score: 0.065
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Structural framework to address variant-gene relationship in primary open-angle glaucoma. Vision Res. 2025 Jan; 226:108505.
Score: 0.052
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European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nat Commun. 2023 10 04; 14(1):6172.
Score: 0.048
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Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nat Genet. 2023 07; 55(7):1116-1125.
Score: 0.047
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Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. Commun Biol. 2022 04 21; 5(1):386.
Score: 0.044
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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Am J Hum Genet. 2021 10 07; 108(10):1836-1851.
Score: 0.042
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A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Commun Biol. 2021 03 01; 4(1):266.
Score: 0.040
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. PLoS Genet. 2019 12; 15(12):e1008500.
Score: 0.037
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Effects of TCF7L2 polymorphisms on obesity in European populations. Obesity (Silver Spring). 2008 Feb; 16(2):476-82.
Score: 0.016
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Transcription factor TCF7L2 genetic study in the French population: expression in human beta-cells and adipose tissue and strong association with type 2 diabetes. Diabetes. 2006 Oct; 55(10):2903-8.
Score: 0.015