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Connection

Hélène Choquet to Male

This is a "connection" page, showing publications Hélène Choquet has written about Male.
Connection Strength

1.006
  1. 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.
    View in: PubMed
    Score: 0.078
  2. New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis. Commun Biol. 2021 07 22; 4(1):864.
    View in: PubMed
    Score: 0.073
  3. 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.
    View in: PubMed
    Score: 0.067
  4. A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Nat Commun. 2018 06 11; 9(1):2278.
    View in: PubMed
    Score: 0.059
  5. A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. Nat Commun. 2017 12 13; 8(1):2108.
    View in: PubMed
    Score: 0.057
  6. 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.
    View in: PubMed
    Score: 0.054
  7. 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.
    View in: PubMed
    Score: 0.050
  8. Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity. Cerebrovasc Dis. 2014; 38(6):433-40.
    View in: PubMed
    Score: 0.046
  9. 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.
    View in: PubMed
    Score: 0.043
  10. 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.
    View in: PubMed
    Score: 0.041
  11. 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.
    View in: PubMed
    Score: 0.034
  12. 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.
    View in: PubMed
    Score: 0.031
  13. 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.
    View in: PubMed
    Score: 0.029
  14. 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.
    View in: PubMed
    Score: 0.025
  15. Drinking experience uncovers genetic influences on alcohol expectancies across adolescence. Addiction. 2015 Apr; 110(4):610-8.
    View in: PubMed
    Score: 0.023
  16. Dysregulation of septin cytoskeletal organization in the trabecular meshwork contributes to ocular hypertension. JCI Insight. 2024 Dec 06; 9(23).
    View in: PubMed
    Score: 0.023
  17. Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries. Nat Genet. 2024 Dec; 56(12):2659-2671.
    View in: PubMed
    Score: 0.023
  18. Visual Impairment, Eye Conditions, and Diagnoses of Neurodegeneration and Dementia. JAMA Netw Open. 2024 Jul 01; 7(7):e2424539.
    View in: PubMed
    Score: 0.022
  19. 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.
    View in: PubMed
    Score: 0.018
  20. Nicotine and cannabis vaping among adolescents in treatment for substance use disorders. J Subst Abuse Treat. 2021 06; 125:108304.
    View in: PubMed
    Score: 0.018
  21. 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.
    View in: PubMed
    Score: 0.017
  22. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell. 2020 09 03; 182(5):1214-1231.e11.
    View in: PubMed
    Score: 0.017
  23. 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.
    View in: PubMed
    Score: 0.017
  24. Functional validity, role, and implications of heavy alcohol consumption genetic loci. Sci Adv. 2020 01; 6(3):eaay5034.
    View in: PubMed
    Score: 0.016
  25. 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.
    View in: PubMed
    Score: 0.016
  26. 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.
    View in: PubMed
    Score: 0.015
  27. A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. Genetics. 2018 10; 210(2):499-515.
    View in: PubMed
    Score: 0.015
  28. 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.
    View in: PubMed
    Score: 0.014
  29. Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity. Diabetes. 2012 Feb; 61(2):383-90.
    View in: PubMed
    Score: 0.009
  30. TCF7L2 is associated with type 2 diabetes in nonobese individuals from Tunisia. Pathol Biol (Paris). 2010 Dec; 58(6):426-9.
    View in: PubMed
    Score: 0.008
  31. 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.
    View in: PubMed
    Score: 0.007
  32. Effects of TCF7L2 polymorphisms on obesity in European populations. Obesity (Silver Spring). 2008 Feb; 16(2):476-82.
    View in: PubMed
    Score: 0.007
  33. 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.
    View in: PubMed
    Score: 0.007
  34. TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population. BMC Med Genet. 2007 Jun 25; 8:37.
    View in: PubMed
    Score: 0.007
  35. 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.
    View in: PubMed
    Score: 0.007
  36. 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.
    View in: PubMed
    Score: 0.007
  37. 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.
    View in: PubMed
    Score: 0.007

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