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230 results on '"Clarimón J"'

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1. Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

2. Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project

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

5. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimerʼs and Parkinsonʼs diseases

6. Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups

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

10. A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

12. Does ALS‐FUS without FUS mutation represent ALS‐FET? Report of three cases

14. Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome

15. Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage

16. Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease

17. Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

18. Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease

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

20. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

21. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

22. Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

23. Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

27. Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

28. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

29. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

30. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

31. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

32. CXCR4involvement in neurodegenerative diseases

33. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer’s and Parkinson’s diseases

34. CXCR4 involvement in neurodegenerative diseases

35. Plasma and CSF biomarkers for the diagnosis of Alzheimer's disease in adults with Down syndrome: a cross-sectional study

36. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

37. Obesity and Alzheimer's disease, does the obesity paradox really exist? A magnetic resonance imaging study

38. Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

39. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

40. Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

41. Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

42. Immune-related genetic enrichment in frontotemporal dementia

43. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

44. Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

45. CSF sAPPß, YKL-40, and neurofilament light in frontotemporal lobar degeneration

46. Early diagnosis of amyotrophic lateral sclerosis mimic syndromes: pros and cons of current clinical diagnostic criteria

47. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

48. Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

49. Biomarkers in cerebral amyloid angiopathy-related inflammation

50. Shared Genetic Contribution to Ischemic Stroke and Alzheimer's Disease

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