Hélène Choquet to Humans
This is a "connection" page, showing publications Hélène Choquet has written about Humans.
Connection Strength
1.586
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Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma. Commun Biol. 2024 01 05; 7(1):33.
Score: 0.065
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Association of Behavioral and Clinical Risk Factors With Cataract: A Two-Sample Mendelian Randomization Study. Invest Ophthalmol Vis Sci. 2023 07 03; 64(10):19.
Score: 0.062
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Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine. HGG Adv. 2023 Jul 13; 4(3):100211.
Score: 0.062
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Association Between Myopic Refractive Error and Primary Open-Angle Glaucoma: A 2-Sample Mendelian Randomization Study. JAMA Ophthalmol. 2022 09 01; 140(9):864-871.
Score: 0.059
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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: 0.054
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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: 0.054
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Cigarette smoking behaviors and the importance of ethnicity and genetic ancestry. Transl Psychiatry. 2021 02 11; 11(1):120.
Score: 0.053
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A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness. Commun Biol. 2020 06 11; 3(1):301.
Score: 0.050
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Genetic and environmental factors underlying keratinocyte carcinoma risk. JCI Insight. 2020 05 21; 5(10).
Score: 0.050
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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: 0.049
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Clinical implications of recent advances in primary open-angle glaucoma genetics. Eye (Lond). 2020 01; 34(1):29-39.
Score: 0.048
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Routes of cannabis administration among females in the year before and during pregnancy: Results from a pilot project. Addict Behav. 2020 01; 100:106125.
Score: 0.048
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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: 0.044
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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: 0.042
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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: 0.041
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Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1. Free Radic Biol Med. 2016 Mar; 92:100-109.
Score: 0.037
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Genetics of cerebral cavernous malformations: current status and future prospects. J Neurosurg Sci. 2015 Sep; 59(3):211-20.
Score: 0.035
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Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Cerebrovasc Dis. 2014; 38(6):433-40.
Score: 0.034
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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: 0.032
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Examination of rare missense variants in the CHRNA5-A3-B4 gene cluster to level of response to alcohol in the San Diego Sibling Pair study. Alcohol Clin Exp Res. 2013 Aug; 37(8):1311-6.
Score: 0.030
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Contribution of common PCSK1 genetic variants to obesity in 8,359 subjects from multi-ethnic American population. PLoS One. 2013; 8(2):e57857.
Score: 0.030
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Genetic and functional characterization of PCSK1. Methods Mol Biol. 2011; 768:247-53.
Score: 0.026
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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: 0.026
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Adverse Childhood Experiences and Pregnancy Intentions among Pregnant Women Seeking Prenatal Care. Womens Health Issues. 2021 Mar-Apr; 31(2):100-106.
Score: 0.026
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The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects. Hum Mol Genet. 2009 Jul 01; 18(13):2495-501.
Score: 0.023
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Documentation of e-cigarette use and associations with smoking from 2012 to 2015 in an integrated healthcare delivery system. Prev Med. 2018 04; 109:113-118.
Score: 0.021
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Smoking Trends Among Adults With Behavioral Health Conditions in Integrated Health Care: A Retrospective Cohort Study. Psychiatr Serv. 2016 09 01; 67(9):996-1003.
Score: 0.019
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Drinking experience uncovers genetic influences on alcohol expectancies across adolescence. Addiction. 2015 Apr; 110(4):610-8.
Score: 0.018
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Dysregulation of septin cytoskeletal organization in the trabecular meshwork contributes to ocular hypertension. JCI Insight. 2024 Dec 06; 9(23).
Score: 0.017
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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: 0.017
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Structural framework to address variant-gene relationship in primary open-angle glaucoma. Vision Res. 2025 Jan; 226:108505.
Score: 0.017
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Visual Impairment, Eye Conditions, and Diagnoses of Neurodegeneration and Dementia. JAMA Netw Open. 2024 Jul 01; 7(7):e2424539.
Score: 0.017
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A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation. Commun Biol. 2024 Apr 06; 7(1):418.
Score: 0.016
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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: 0.016
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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: 0.016
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A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration. EBioMedicine. 2023 May; 91:104551.
Score: 0.015
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Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature. 2022 12; 612(7941):720-724.
Score: 0.015
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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: 0.014
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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: 0.014
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GLIS1 regulates trabecular meshwork function and intraocular pressure and is associated with glaucoma in humans. Nat Commun. 2021 08 12; 12(1):4877.
Score: 0.014
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Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Am J Hum Genet. 2021 05 06; 108(5):874-893.
Score: 0.013
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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: 0.013
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Nicotine and cannabis vaping among adolescents in treatment for substance use disorders. J Subst Abuse Treat. 2021 06; 125:108304.
Score: 0.013
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Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations. Commun Biol. 2020 12 14; 3(1):765.
Score: 0.013
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Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Cell. 2020 09 03; 182(5):1198-1213.e14.
Score: 0.013
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The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 2020 09 03; 182(5):1214-1231.e11.
Score: 0.013
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Trends and correlates of self-reported alcohol and nicotine use among women before and during pregnancy, 2009-2017. Drug Alcohol Depend. 2020 09 01; 214:108168.
Score: 0.013
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Correlates of Pregnant Women's Participation in a Substance Use Assessment and Counseling Intervention Integrated into Prenatal Care. Matern Child Health J. 2020 Apr; 24(4):423-431.
Score: 0.012
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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: 0.012
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Functional validity, role, and implications of heavy alcohol consumption genetic loci. Sci Adv. 2020 01; 6(3):eaay5034.
Score: 0.012
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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: 0.012
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Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications. Sci Rep. 2019 11 20; 9(1):17123.
Score: 0.012
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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Nat Genet. 2019 02; 51(2):237-244.
Score: 0.011
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A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. Genetics. 2018 10; 210(2):499-515.
Score: 0.011
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Do you vape? Leveraging electronic health records to assess clinician documentation of electronic nicotine delivery system use among adolescents and adults. Prev Med. 2017 Dec; 105:32-36.
Score: 0.010
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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human. Nature. 2012 Feb 19; 483(7389):350-4.
Score: 0.007
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Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity. Diabetes. 2012 Feb; 61(2):383-90.
Score: 0.007
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Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets. Mol Genet Metab. 2010 May; 100(1):77-82.
Score: 0.006
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TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia. Pathol Biol (Paris). 2010 Dec; 58(6):426-9.
Score: 0.006
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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: 0.005
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Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value. PLoS One. 2008 May 07; 3(5):e2031.
Score: 0.005
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Effects of TCF7L2 polymorphisms on obesity in European populations. Obesity (Silver Spring). 2008 Feb; 16(2):476-82.
Score: 0.005
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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: 0.005
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TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population. BMC Med Genet. 2007 Jun 25; 8:37.
Score: 0.005
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TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis. J Mol Med (Berl). 2007 Jul; 85(7):777-82.
Score: 0.005
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No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects. Diabetologia. 2007 Jan; 50(1):214-6.
Score: 0.005
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TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Diabetes. 2006 Nov; 55(11):3189-92.
Score: 0.005
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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: 0.005