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22 results on '"Hardy, J. (John)"'

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1. Investigation of autosomal genetic sex differences in Parkinson’s disease

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

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

4. Moving beyond neurons:the role of cell type-specific gene regulation in Parkinson’s disease heritability

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

6. Alzheimer's disease in Down syndrome: An overlooked population for prevention trials

7. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

8. Novel genetic loci associated with hippocampal volume

9. ABCA7 p.G215S as potential protective factor for Alzheimer's disease

10. The transcriptional landscape of age in human peripheral blood

11. Polygenic overlap between C-reactive protein, plasma lipids, and Alzheimer disease

12. Common genetic variants influence human subcortical brain structures

13. Frontotemporal dementia and its subtypes: A genome-wide association study

14. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

15. The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data

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

17. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism

18. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study

19. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

20. Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease

21. Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease

22. Amyloid precursor protein gene mutation in early-onset Alzheimer's disease.

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