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

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

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

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

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

9. Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

10. Author Correction: Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

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

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

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

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

16. Multiomic analysis of malignant pleural mesothelioma identifies molecular axes and specialized tumor profiles driving intertumor heterogeneity

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

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

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

20. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

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

23. A large‐scale exome array analysis of venous thromboembolism

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

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

26. Multi-ancestry polygenic risk scores for venous thromboembolism.

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

31. Plasma levels of complement components C5 and C9 are associated with thrombin generation

33. Constitutional DNA Polymorphisms Associated with the Plasma Imatinib Concentration in Chronic Myeloid Leukemia Patients.

34. Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes

36. Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

37. Feasibility of high-throughput sequencing in clinical routine cancer care: lessons from the cancer pilot project of the France Genomic Medicine 2025 plan

38. Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes

39. Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

41. Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation

46. STAT3 Mediates Nilotinib Response in KIT-Altered Melanoma: A Phase II Multicenter Trial of the French Skin Cancer Network

47. Sex specific associations in genome wide association analysis of renal cell carcinoma

48. Genomic landscape of human diversity across Madagascar

49. Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer”

50. An elevated level of Interleukin-17A in a Senegalese malaria cohort is associated with rs8193038 IL-17A genetic variant

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