Adam C. Naj, Ph.D.
Affiliations: | 2008 | Johns Hopkins University, Baltimore, MD |
Area:
Epidemiology, Public Health, GeneticsGoogle:
"Adam Naj"Cross-listing: Epi Tree
Parents
Sign in to add mentorW.-H L. Kao | grad student | 2008 | Johns Hopkins | |
(Genetic determinants of type 2 diabetes mellitus and related endophenotypes in the Old Order Amish.) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Farrell K, Humphrey J, Chang T, et al. (2024) Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes. Nature Communications. 15: 7880 |
Wang H, Chang TS, Dombroski BA, et al. (2024) Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy. Molecular Neurodegeneration. 19: 61 |
Cruchaga C, Bradley J, Western D, et al. (2024) Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracell signaling pathways. Research Square |
Yan D, Hu B, Darst BF, et al. (2024) Biobank-wide association scan identifies risk factors for late-onset Alzheimer's disease and endophenotypes. Elife. 12 |
Mews MA, Naj AC, Griswold AJ, et al. (2024) Brain and Blood Transcriptome-Wide Association Studies Identify Five Novel Genes Associated with Alzheimer's Disease. Medrxiv : the Preprint Server For Health Sciences |
Zhang X, Gomez L, Below JE, et al. (2024) An X Chromosome Transcriptome Wide Association Study Implicates ARMCX6 in Alzheimer's Disease. Journal of Alzheimer's Disease : Jad |
Leung YY, Naj AC, Chou YF, et al. (2024) Human whole-exome genotype data for Alzheimer's disease. Nature Communications. 15: 684 |
Wang H, Chang TS, Dombroski BA, et al. (2023) Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy. Medrxiv : the Preprint Server For Health Sciences |
Lee WP, Choi SH, Shea MG, et al. (2023) 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. Medrxiv : the Preprint Server For Health Sciences |
Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |