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1. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

2. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

3. Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error

4. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.

5. Common genetic determinants of intraocular pressure and primary open-angle glaucoma.

6. Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease

7. Protective association of HLA‐DRB1 *04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences

8. Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer’s disease etiopathogenesis

9. Protective association of HLA-DRB1*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences

10. Alzheimers Dement

11. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

12. Rare missense variant (R251G) on APOE counterbalances the Alzheimer’s disease risk associated with APOE‐ε4

13. Genetics of PlGF plasma levels highlights a role of its receptors and supports the link between angiogenesis and immunity

14. ZCWPW1loss-of-function variants in Alzheimer’s Disease

15. Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy

16. Genome-Wide Meta-Analysis of Late-Onset Alzheimer’s Disease Using Rare Variant Imputation in 65,602 Subjects Identifies Novel Rare Variant Locus NCK2: The International Genomics of Alzheimer’s Project (IGAP)

17. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

18. TopMed‐imputed genome‐wide association study of Alzheimer’s disease in more than 100,000 European samples from the EADB project

19. SORL1 ‐variant carriers in ADES‐ADSP: A higher level of variant pathogenicity associates with earlier age at onset of Alzheimer's disease

20. Novel genetic effects on amyloid and tau protein levels in cerebrospinal fluid

21. Integration of demographics, genetics, imaging and metabolomics data to identify Alzheimer’s disease patients

22. Exome sequencing identifies three novel AD‐associated genes

23. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

24. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

25. Common variants in Alzheimers disease: Novel association of six genetic variants with AD and risk stratification by polygenic risk scores

26. Genetics of Alzheimer's disease: where we are, and where we are going

27. Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

28. Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

29. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

30. Identification of additional risk loci for stroke and small vessel disease

31. A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

32. Genetic Risk Factors for Complex Forms of Alzheimer’s Disease

33. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

34. P1-272: MULTI-OMICS DATA INTEGRATION TO CLASSIFY ALZHEIMER'S DISEASE, MILD COGNITIVE IMPAIRMENT AND COGNITIVELY NORMAL INDIVIDUALS FROM THE ADNI DATASET

35. The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

36. SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease

37. Convergent genetic and expression data implicate immunity in Alzheimer's disease

38. Strategies for Phasing and Imputation in a Population Isolate

39. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

40. SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

41. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression

42. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer’s disease

43. Contribution to Alzheimer's disease risk of rare variants in TREM_2, SORL_1, and ABCA_7 in 1779 cases and 1273 controls

44. A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

45. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

46. O2-10-06: GENOME-WIDE META-ANALYSIS OF LATE-ONSET ALZHEIMER'S DISEASE USING RARE VARIANT IMPUTATION IN 64,859 SUBJECTS IDENTIFIES RISK LOCI WITH ROLES IN INNATE IMMUNITY AND CARDIOVASCULAR TRAITS: THE INTERNATIONAL GENOMICS OF ALZHEIMER'S PROJECT (IGAP)

47. Using Phenotypic Heterogeneity to Increase the Power of Genome-Wide Association Studies: Application to Age at Onset of Ischaemic Stroke Subphenotypes

48. Biallelic Variants in UBA5 Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy

49. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

50. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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