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95 results on '"Schellenberg G.D."'

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1. New insights into the genetic etiology of Alzheimer's disease and related dementias

2. Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice

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

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

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

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

8. Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation (Molecular Psychiatry, (2018), 10.1038/s41380-018-0112-7)

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

10. A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

11. Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study

13. Apolipoprotein E genotypes and outcome from out of hospital cardiac arrest

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

15. Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

17. Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

18. Clinical/Scientific Notes: The Alzheimer's disease sequencing project: Study design and sample selection

19. A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

20. A novel Alzheimer disease locus located near the gene encoding tau protein

23. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

24. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

25. Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

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

27. Identification of risk loci with shared effects on five major psychiatric disorders:a genome-wide analysis

28. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

29. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

30. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

31. APP Processing Genes and Cerebrospinal Fluid APP Cleavage Product Levels in Alzheimer’s Disease

32. Functional impact of global rare copy number variation in autism spectrum disorders

33. A genome-wide scan for common alleles affecting risk for autism

34. Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

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

36. A genome-wide linkage and association scan reveals novel loci for autism

37. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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

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

42. Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease

46. Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: Evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14

47. Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large veterans affairs cooperative study sample

48. Association of NOTCH4 with schizophrenia in VA coop study #366

49. Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample

50. A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration

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