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1. Genetic variants for head size share genes and pathways with cancer

2. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

4. Whole genome‐wide sequence analysis of long‐lived families (Long‐Life Family Study) identifies MTUS2 gene associated with late‐onset Alzheimer's disease

5. CYP1B1-RMDN2 Alzheimer’s disease endophenotype locus identified for cerebral tau PET

6. Identification of a specific APOE transcript and functional elements associated with Alzheimer’s disease

11. Cell subtype-specific effects of genetic variation in the Alzheimer’s disease brain

12. Xenografted human iPSC-derived neurons with the familial Alzheimer’s disease APPV717I mutation reveal dysregulated transcriptome signatures linked to synaptic function and implicate LINGO2 as a disease signaling mediator

14. Multi-tissue epigenetic analysis identifies distinct associations underlying insulin resistance and Alzheimer’s disease at CPT1A locus

15. Microglia states and nomenclature: A field at its crossroads

16. Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning

18. Chemokine-mediated cell migration into the central nervous system in progressive multifocal leukoencephalopathy

20. Osteopontin drives neuroinflammation and cell loss in MAPT-N279K frontotemporal dementia patient neurons

23. INPP5D regulates inflammasome activation in human microglia

26. Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population

27. Sex-Specific Association of the X Chromosome With Cognitive Change and Tau Pathology in Aging and Alzheimer Disease

28. Serum metabolomic biomarkers of perceptual speed in cognitively normal and mildly impaired subjects with fasting state stratification.

30. Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer’s disease risk gene SORL1

31. Cerebral small vessel disease genomics and its implications across the lifespan.

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

34. Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans.

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

36. A saturated map of common genetic variants associated with human height

37. From the prodromal stage of multiple sclerosis to disease prevention

39. A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

40. FMNL2 regulates gliovascular interactions and is associated with vascular risk factors and cerebrovascular pathology in Alzheimer’s disease

43. Early complement genes are associated with visual system degeneration in multiple sclerosis.

44. A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

45. CpG-related SNPs in the MS4A region have a dose-dependent effect on risk of late-onset Alzheimer disease.

46. Integrating Gene and Protein Expression Reveals Perturbed Functional Networks in Alzheimer’s Disease

47. Genome‐wide association studies of alcohol dependence, DSM‐IV criterion count and individual criteria

48. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

49. Altered bile acid profile associates with cognitive impairment in Alzheimer's disease—An emerging role for gut microbiome

50. Sex-specific genetic predictors of Alzheimer’s disease biomarkers

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