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1. Towards cascading genetic risk in Alzheimers disease.

2. Investigation of the genetic aetiology of Lewy body diseases with and without dementia

7. Neurobiology of Dementia and Other Neurodegenerative Disorders

8. Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

10. Genome-wide determinants of mortality and motor progression in Parkinson’s disease

11. Profiling complex repeat expansions in RFC1 in Parkinson’s disease

13. Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)

14. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

15. Aβ efflux impairment and inflammation linked to cerebrovascular accumulation of amyloid-forming amylin secreted from pancreas

16. Application Experiences on a GPU-Accelerated Arm-based HPC Testbed

18. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

19. An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer's disease.

20. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

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

23. Stratified analyses refine association between TLR7 rare variants and severe COVID-19

24. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

30. AD-linked R47H-TREM2 mutation induces disease-enhancing microglial states via AKT hyperactivation

31. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

32. The β-Secretase BACE1 in Alzheimer’s Disease

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

34. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

35. Impact of an Intensive Multi-Disciplinary STEM Enrichment Program on Underrepresented Minority Student Success

36. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

40. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

41. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

42. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

44. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

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

46. Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study.

48. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

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