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5. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

6. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

7. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

8. Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults

9. Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

10. Genome-wide physical activity interactions in adiposity:a meta-analysis of 200,452 adults

11. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

12. Genome-wide physical activity interactions in adiposity. A meta-analysis of 200,452 adults

13. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

14. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

15. Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

16. PCSK9 genetic variants and risk of type 2 diabetes: A mendelian randomisation study

17. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

23. Prognostic factors associated with healing of venous leg ulcers: a multicentre, prospective, cohort study.

24. Ischemic Digital Ulcers Affect Hand Disability and Pain in Systemic Sclerosis

25. Biologie, épidémiologie et immunologie du paludisme

26. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

27. Exome-Wide Association Study on Alanine Aminotransferase Identifies Sequence Variants in the GPAM and APOE Associated With Fatty Liver Disease

28. A Federated Database for Obesity Research: An IMI-SOPHIA Study.

29. A comparison of changes in bone turnover markers after gastric bypass and sleeve gastrectomy, and their association with markers of interest.

30. PSD3 downregulation confers protection against fatty liver disease.

31. Exome-Wide Association Study on Alanine Aminotransferase Identifies Sequence Variants in the GPAM and APOE Associated With Fatty Liver Disease.

32. Hepatic Molecular Signatures Highlight the Sexual Dimorphism of Nonalcoholic Steatohepatitis (NASH).

33. NASH-related increases in plasma bile acid levels depend on insulin resistance.

34. Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9.

35. Hepatic transcriptomic signatures of statin treatment are associated with impaired glucose homeostasis in severely obese patients.

36. CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability.

37. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

38. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.

39. An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.

40. Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

41. Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.

42. Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

43. Obtaining Correct Ankle Alignment Using Intraoperative External Fixation for Ankle Arthrodesis.

44. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study.

45. Incidence and Predictive Factors of Postprandial Hyperinsulinemic Hypoglycemia After Roux-en-Y Gastric Bypass: A Five year Longitudinal Study.

46. The genetic architecture of type 2 diabetes.

47. Eating Behavior, Low-Frequency Functional Mutations in the Melanocortin-4 Receptor (MC4R) Gene, and Outcomes of Bariatric Operations: A 6-Year Prospective Study.

48. Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms.

49. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.

50. Revision surgery for lumbar pseudarthrosis.

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