74 results on '"Leung, Yuk Yee"'
Search Results
2. Using INFERNO to Infer the Molecular Mechanisms Underlying Noncoding Genetic Associations
3. NIA Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS): 2023 Update
4. The NIA Genetics of Alzheimer’s Disease Data Storage Site API: a toolkit for exploring Alzheimer’s disease genetics and genomic annotations
5. Identification of rare coding variants associated with Alzheimer’s disease.
6. hipFG: High-throughput harmonization and integration pipeline for functional genomics data
7. NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge
8. Transferability of a European-derived Alzheimer’s Disease Genetic Risk Score across Multi-Ancestry Populations
9. Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer’s Diseases Sequencing Project Subjects
10. Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project
11. Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifiesLRRC4C, LHX5-AS1and nominates ancestry-specific lociPTPRK,GRB14, andKIAA0825as novel risk loci for Alzheimer’s disease: the Alzheimer’s Disease Genetics Consortium
12. hipFG: High-throughput harmonization and integration pipeline for functional genomics data
13. ApoJ/Clusterin concentrations are determinants of cerebrospinal fluid cholesterol efflux capacity and reduced levels are associated with Alzheimer’s disease
14. NIA Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS): 2022 Update
15. A Haptoglobin (HP) Exon Deletion Polymorphism Alters the Effect of APOE Alleles on Alzheimer’s Disease in European‐Descent People with APOEε4
16. NIAGADS Alzheimer’s Genomics Database: version GRCh38
17. Rare Genetic Risk in Progressive Supranuclear Palsy
18. Spatial Distribution of Rare Missense Variants Within Protein Structures is Associated with AD Risk
19. The Alzheimer’s Disease Sequencing Project Follow Up Study (ADSP‐FUS): increasing ethnic diversity in Alzheimer’s disease (AD) genetics research.
20. Polygenic Risk Scores in Alzheimer’s Disease Genetics: Methodology, Applications, Inclusion, and Diversity
21. Omnibus and robust deconvolution scheme for bulk RNA sequencing data integrating multiple single-cell reference sets and prior biological knowledge
22. Scalable approaches for functional analyses of whole-genome sequencing non-coding variants
23. In Silico Identification of RNA Modifications from High-Throughput Sequencing Data Using HAMR
24. InteRD: The Integrated and Robust Deconvolution
25. Genome‐wide association and multi‐omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women
26. Corrigendum: An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease–related patterns
27. A comparative study of structural variant calling strategies using the Alzheimer’s Disease Sequencing Project’s whole genome family data
28. Alzheimer’s Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer’s Disease
29. An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease–related patterns
30. FILER: a framework for harmonizing and querying large-scale functional genomics knowledge
31. Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
32. An Association Test of the Spatial Distribution of Rare Missense Variants within Protein Structures Improves Statistical Power of Sequencing Studies
33. Genome-Wide Meta-Analysis of Late-Onset Alzheimer’s Disease Using Rare Variant Imputation in 65,602 Subjects Identifies Novel Rare Variant Locus NCK2: The International Genomics of Alzheimer’s Project (IGAP)
34. FILER: large-scale, harmonized FunctIonaL gEnomics Repository
35. Genome‐wide profiling of the noncoding regulatory mechanisms in Alzheimer’s disease
36. Alzheimer’s disease variant portal (ADVP): Harmonized genetics data and evidence collection for Alzheimer’s disease
37. NIA genetics of Alzheimer’s disease data storage site (NIAGADS): Update 2020
38. Alzheimer’s Disease variant portal (ADVP): a catalog of genetic findings for Alzheimer’s Disease
39. NIAGADS Alzheimer’s GenomicsDB: A resource for exploring Alzheimer’s Disease genetic and genomic knowledge
40. SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants
41. SparkINFERNO: A scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants
42. HiPR: High-throughput probabilistic RNA structure inference
43. Inferring the Molecular Mechanisms of Noncoding Alzheimer’s Disease-Associated Genetic Variants
44. P3-122: INFERRING THE NONCODING REGULATORY MECHANISMS UNDERLYING GENETIC SUSCEPTIBILITY CONTRIBUTED BY DIFFERENT CSF ENDOPHENOTYPES IN AD
45. P1-134: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): ALZHEIMER'S GENOMICS DATABASE - 2019 UPDATE
46. P4-090: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): UPDATE 2019
47. VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project
48. VCPA: genomic variant calling pipeline and data management tool for Alzheimer’s Disease Sequencing Project
49. Inferring the molecular mechanisms of noncoding Alzheimer’s disease-associated genetic variants
50. DASHR 2.0: integrated database of human small non-coding RNA genes and mature products
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.