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4. Clinical utility of whole-genome sequencing in a large ALS cohort

5. Common genetic variants influence human subcortical brain structures

7. Genome-wide screen identifies rs646776 near sortilin as a regulator for progranulin levels in human plasma

8. Genetic comorbidities in Parkinsonʼs disease

9. Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

10. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease

11. Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

12. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinsonʼs disease with a sexual dimorphism

14. Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci

15. Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities

16. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease

17. Differences in the Presentation and Progression of Parkinson's Disease by Sex

19. Analysis of shared heritability in common disorders of the brain

22. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

23. LRP10 in α-synucleinopathies

24. Analysis of shared heritability in common disorders of the brain

25. Analysis of shared heritability in common disorders of the brain

26. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer’s Disease

27. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease

28. LRP10 in α-synucleinopathies

29. A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy

30. The transcriptional landscape of age in human peripheral blood

31. Mutations in the GCH1 Gene Are Associated with Parkinson Disease (S17.001)

32. Identifying likely causal connections between gene expression levels using a Mendelian randomization approach

35. Exome Sequencing Identifies a Novel TRPV4 Mutation in a CMT2C Family

36. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

37. Differences in the Presentation and Progression of Parkinson's Disease by Sex

38. Analysis of shared heritability in common disorders of the brain

39. Analysis of shared heritability in common disorders of the brain

40. Analysis of shared heritability in common disorders of the brain

41. Analysis of shared heritability in common disorders of the brain

42. Intermediate HTT CAG repeats worsen disease severity in amyotrophic lateral sclerosis.

43. Differences in the Presentation and Progression of Parkinson's Disease by Sex.

44. Analysis of shared heritability in common disorders of the brain.

45. Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.

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