194 results on '"Choquet, Hélène"'
Search Results
2. A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
3. Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
4. Omega-3 Polyunsaturated Fatty Acids as a Protective Factor for Myopia
5. Structural framework to address variant-gene relationship in primary open-angle glaucoma
6. Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci
7. Socio-Demographic and Preoperative Clinical Factors Associated With 5-Year Weight Trajectories After Roux-en-Y Gastric Bypass and Sleeve Gastrectomy
8. Association between lifetime smoking and cutaneous squamous cell carcinoma: A 2-sample Mendelian randomization study
9. European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
10. Transcriptome-wide association study identifies novel candidate susceptibility genes for migraine
11. 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
12. Genetic diversity fuels gene discovery for tobacco and alcohol use
13. Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
14. Genome-wide meta-analysis identifies 22 loci for normal tension glaucoma with significant overlap with high tension glaucoma.
15. Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways
16. Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
17. Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
18. Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
19. The Polygenic and Monogenic Basis of Blood Traits and Diseases
20. Clinical implications of recent advances in primary open-angle glaucoma genetics
21. GLIS1 regulates trabecular meshwork function and intraocular pressure and is associated with glaucoma in humans
22. A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus
23. New and sex-specific migraine susceptibility loci identified from a multiethnic genome-wide meta-analysis
24. Cigarette smoking behaviors and the importance of ethnicity and genetic ancestry
25. Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations
26. A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness
27. Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1
28. A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia
29. Genetically Predicted Serum Vitamin C Levels and Cutaneous Squamous Cell Carcinoma Risk
30. 10 Years of GWAS in intraocular pressure.
31. 10Years of GWAS in intraocular pressure.
32. Meta-analysis and functional effects of the SLC30A8 rs13266634 polymorphism on isolated human pancreatic islets
33. Polymorphisms in Inflammatory and Immune Response Genes Associated with Cerebral Cavernous Malformation Type 1 Severity
34. Association of Cardiovascular Risk Factors with Disease Severity in Cerebral Cavernous Malformation Type 1 Subjects with the Common Hispanic Mutation
35. Association Between Myopic Refractive Error and Primary Open-Angle Glaucoma: A 2-Sample Mendelian Randomization Study.
36. Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.
37. Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study
38. TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis
39. 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
40. Visual Impairment, Eye Conditions, and Diagnoses of Neurodegeneration and Dementia.
41. Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human
42. Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity
43. The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects
44. Full title: A large‐scale transcriptome‐wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine‐mapping.
45. TCF7L2 Variation Predicts Hyperglycemia Incidence in a French General Population: The Data From an Epidemiological Study on the Insulin Resistance Syndrome (DESIR) Study
46. Transcription Factor TCF7L2 Genetic Study in the French Population: Expression in Human β-Cells and Adipose Tissue and Strong Association With Type 2 Diabetes
47. Untitled.
48. A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects.
49. Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images.
50. The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies
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