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1. Depressive symptoms and sex differences in the risk of post-COVID-19 persistent symptoms: a prospective population-based cohort study

2. Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.

5. Human genetic structure in Northwest France provides new insights into West European historical demography

6. Microsatellite instability at U2AF-binding polypyrimidic tract sites perturbs alternative splicing during colorectal cancer initiation

8. Positive selection in the genomes of two Papua New Guinean populations at distinct altitude levels

10. TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

11. SARS-CoV-2 infection prevalence and associated factors among primary healthcare workers in France after the third COVID-19 wave

12. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

15. Risperidone response in patients with schizophrenia drives DNA methylation changes in immune and neuronal systems

16. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.

17. Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders

18. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

19. Definition of a concentration and RNA extraction protocol for optimal whole genome sequencing of SARS-CoV-2 in wastewater (ANRS0160)

22. Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

23. Genome-wide investigation of exogenous female hormones, genetic variation, and venous thromboembolism risk

26. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

27. High diagnostic potential of short and long read genome sequencing with transcriptome analysis in exome-negative developmental disorders

28. A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

29. Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening

30. DLK1/DIO3 locus upregulation by a β-catenin-dependent enhancer drives cell proliferation and liver tumorigenesis

31. PIntMF: Penalized Integrative Matrix Factorization Method for Multi-Omics Data

32. Mutations and variants of ONECUT1 in diabetes

34. Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

36. High heritability does not imply accurate prediction under the small additive effects hypothesis

37. Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism

38. Prediction of Breast Cancer Treatment-Induced Fatigue by Machine Learning Using Genome Wide Association Data

39. Machine Learning-Based Urine Peptidome Analysis to Predict and Understand Mechanisms of Progression to Kidney Failure

41. Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease

43. Measuring the efficiency of purging by non-random mating in human populations

44. Plasma levels of Complement components C5 and C9 are associated with thrombin generation

45. Depressive symptoms and sex differences in the risk of post-COVID-19 persistent symptoms: A prospective population-based cohort study

46. Antithrombin, PC (Protein C), and PS (Protein S): Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

47. A meta-analysis of genome-wide association studies identifies multiple longevity genes.

48. Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

49. Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays

50. Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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