74 results on '"Adam C Naj"'
Search Results
2. A Haptoglobin (HP) Exon Deletion Polymorphism Alters the Effect of APOE Alleles on Alzheimer’s Disease in European‐Descent People with APOEε4
3. Identifying context‐specific genetic variants and molecular pathways associated with resilience to Alzheimer’s disease in the induced immune response
4. Spatial Distribution of Rare Missense Variants Within Protein Structures is Associated with AD Risk
5. The Alzheimer’s Disease Sequencing Project Follow Up Study (ADSP‐FUS): increasing ethnic diversity in Alzheimer’s disease (AD) genetics research
6. Modeling gene expression on the X chromosome in the brain for transcriptome‐wide association studies
7. Leveraging the use of meta‐analysis summary statistics to improve gene expression prediction models
8. Genetic insights of all‐cause and vascular dementia through genome‐wide association studies
9. NIA Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS): 2022 Update
10. Genome‐wide meta‐analysis of late‐onset Alzheimer’s disease using rare variant imputation in 65,602 subjects identifies risk loci with roles in memory, neurodevelopment, and cardiometabolic traits: The international genomics of Alzheimer’s project (IGAP)
11. Assessing whole genome sequencing variation for Alzheimer’s disease in 4707 individuals from the Alzheimer’s Disease Sequencing Project (ADSP)
12. Pleiotropy analyses using TADs identify genomic regions affecting risk of AD and stroke
13. Tissue‐specific genetically regulated expression in late‐onset Alzheimer’s disease implicates risk genes within known and 30 novel loci
14. Mapping Alzheimer disease–associated regions in the African American population
15. Structural characterization of rare missense variants within known neurodegenerative disease proteins
16. NIA genetics of Alzheimer’s disease data storage site (NIAGADS): Update 2020
17. Comparative trans‐ethnic meta‐analysis of whole exome sequencing variation for Alzheimer’s disease (AD) in 18,402 individuals of the Alzheimer’s Disease Sequencing Project (ADSP)
18. Alzheimer’s disease variant portal (ADVP): Harmonized genetics data and evidence collection for Alzheimer’s disease
19. The Alzheimer’s disease sequencing project–follow up study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with addition of potential new cohorts
20. NIAGADS: The NIA Genetics of Alzheimer's Disease Data Storage Site
21. P4‐240: STOP‐GAIN VARIANT IN MICROGLIA‐EXPRESSED GENE GMIP IS ASSOCIATED WITH EARLY‐ONSET ALZHEIMER'S DISEASE
22. P1‐156: GENE‐BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE
23. P4‐044: THE GCAD CLOUD‐BASED WORKFLOW FOR PROCESSING WHOLE EXOME AND WHOLE GENOME DATA FROM THE ALZHEIMER'S DISEASE SEQUENCING PROJECT
24. P1‐157: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): UPDATE 2018
25. P3‐108: IDENTIFICATION OF MITOCHONDRIAL VARIANTS ASSOCIATED WITH LATE‐ONSET ALZHEIMER'S DISEASE
26. P1‐149: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2018
27. P3-123: IDENTIFICATION OF GENES MODIFYING AGE-AT-ONSET OF ALZHEIMER'S DISEASE IN THE ALZHEIMER'S DISEASE GENETICS CONSORTIUM (ADGC) COHORTS
28. P4-094: EXOME-WIDE ANALYSIS IDENTIFIES NOVEL SEX-SPECIFIC CANDIDATE GENES FOR ALZHEIMER DISEASE
29. Convergent genetic and expression data implicate immunity in Alzheimer's disease
30. [P3–090]: THE ALZHEIMER's DISEASE SEQUENCING PROJECT (ADSP) DATA UPDATE 2017
31. [P3–065]: POST‐VARIANT CALLING QUALITY CONTROL (QC) PIPELINE AND MULTI‐PIPELINE GENOTYPE CONSENSUS CALLER FOR LARGE‐SCALE WHOLE GENOME AND WHOLE EXOME SEQUENCING STUDIES
32. [P3–097]: NIA GENETICS OF ALZHEIMER's DISEASE DATA STORAGE SITE (NIAGADS): 2017
33. [O2–08–02]: SEX‐SPECIFIC ANALYSIS OF THE ADSP CASE‐CONTROL WHOLE‐EXOME SEQUENCING DATASET
34. [O1–03–01]: GENOME‐WIDE RARE VARIANT IMPUTATION AND TISSUE‐SPECIFIC TRANSCRIPTOMIC ANALYSIS IDENTIFY NOVEL RARE VARIANT CANDIDATE LOCI IN LATE‐ONSET ALZHEIMER's DISEASE: THE ALZHEIMER's DISEASE GENETICS CONSORTIUM
35. O2-10-06: GENOME-WIDE META-ANALYSIS OF LATE-ONSET ALZHEIMER'S DISEASE USING RARE VARIANT IMPUTATION IN 64,859 SUBJECTS IDENTIFIES RISK LOCI WITH ROLES IN INNATE IMMUNITY AND CARDIOVASCULAR TRAITS: THE INTERNATIONAL GENOMICS OF ALZHEIMER'S PROJECT (IGAP)
36. P4-097: RARE VARIANTS IN FAMILIAL LATE-ONSET ALZHEIMER'S DISEASE IDENTIFIED FROM LARGE SCALE WHOLE GENOME SEQUENCING
37. P2-151: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT - FOLLOW UP STUDY (ADSP-FUS): INCREASING ETHNIC DIVERSITY IN ALZHEIMER'S GENETICS RESEARCH
38. P4-090: NIA GENETICS OF ALZHEIMER'S DISEASE DATA STORAGE SITE (NIAGADS): UPDATE 2019
39. P3-129: SOMATIC LOSS OF Y CHROMOSOME IN THE ADGC COHORTS
40. Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation
41. Genome‐wide association study of the rate of cognitive decline in Alzheimer's disease
42. F1‐01‐02: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe Genotype Backgrounds
43. P1‐018: Rare Deleterious And Loss‐of‐Function Variants in OPRL1 and GAS2L2 Contribute to the Risk of Late‐Onset Alzheimer’s Disease: Alzheimer’s Disease Sequencing Project Case‐Control Study
44. O1‐03‐03: Identification of Novel Candidate Genes for Early‐Onset Alzheimer's Disease Through Integrated Whole‐Exome Sequencing and Exome Chip Array Association Analysis
45. P2‐077: Alzheimer's Disease Sequencing Project: Search for Alzheimer's Disease Resilience Genes That May Modify Disease Susceptibility in Specific Apoe Genotype Backgrounds
46. S4‐02‐01: Alzheimer's Disease Sequencing Project: Case‐Control Analyses
47. O1‐03‐05: High‐Resolution Imputation in Genome‐Wide Association Studies of Late‐Onset Alzheimer's Disease Identifies Novel Rare Variant Associations
48. P3‐093: NIA Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS): 2016 Update
49. O4‐12‐01: Integrating human protein‐protein interaction network with results from gwas in whites and african‐americans identifies common genes underlying late‐onset Alzheimer's disease
50. O3‐05‐03: Multiple deletion copy number variants (CNVs) are associated with late‐onset Alzheimer's disease: The Alzheimer's disease genetics consortium
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.