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178 results on '"Singleton, Andrew"'

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

3. Harnessing diversity to study Alzheimer’s disease: A new iPSC resource from the NIH CARD and ADNI

4. A biological definition of neuronal α-synuclein disease: towards an integrated staging system for research

5. omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases

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

7. A fully automated FAIMS-DIA mass spectrometry-based proteomic pipeline

9. MAPT allele and haplotype frequencies in Nigerian Africans: Population distribution and association with Parkinson's disease risk and age at onset

10. Application of Aligned-UMAP to longitudinal biomedical studies

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

12. The Foundational Data Initiative for Parkinson Disease: Enabling efficient translation from genetic maps to mechanism

14. Application of Aligned-UMAP to Longitudinal Biomedical Studies

15. The East Asian Parkinson Disease Genomics Consortium

16. The commercial genetic testing landscape for Parkinson's disease

18. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

20. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

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

23. Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson’s disease

24. Comprehensive assessment of PINK1 variants in Parkinson's disease

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

28. Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

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

30. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

34. Heritability and genetic variance of dementia with Lewy bodies

35. Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)

36. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation

37. A comprehensive screening of copy number variability in dementia with Lewy bodies

38. Genetic and Phenotypic Characterisation of Autosomal Recessive Parkinson's Disease in a Large Multicentre Cohort

39. LRP10 in α-synucleinopathies

40. LRP10 in α-synucleinopathies

41. LRP10 in α-synucleinopathies

43. Quantitative Interaction Proteomics of Neurodegenerative Disease Proteins

44. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3

46. Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

47. Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease

48. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

49. Genome-Wide Analyses Identify KIF5A as a Novel ALS Gene

50. Genetic risk factors in Finnish patients with Parkinson's disease

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