Gerard D. Schellenberg, PhD
Affiliations: | Pathology and Laboratory Medicine | University of Pennsylvania, Philadelphia, PA, United States | |
1978 | University of California, Riverside, Riverside, CA, United States |
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=57Website:
http://www.med.upenn.edu/apps/faculty/index.php/g275/p8214136Google:
"Gerard Schellenberg"Mean distance: 106866
Cross-listing: Alzheimer's Tree
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Publications
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Abu-Amara H, Zhao W, Li Z, et al. (2024) Region-based analysis with functional annotation identifies genes associated with cognitive function in South Asians from India. Medrxiv : the Preprint Server For Health Sciences |
Ho PC, Yu WH, Tee BL, et al. (2024) Asian Cohort for Alzheimer's Disease (ACAD) pilot study on genetic and non-genetic risk factors for Alzheimer's disease among Asian Americans and Canadians. Alzheimer's & Dementia : the Journal of the Alzheimer's Association |
Vance JM, Farrer LA, Huang Y, et al. (2024) Report of the APOE4 National Institute on Aging/Alzheimer Disease Sequencing Project Consortium Working Group: Reducing APOE4 in Carriers is a Therapeutic Goal for Alzheimer's Disease. Annals of Neurology |
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 |
Guo MH, Lee WP, Vardarajan B, et al. (2023) Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease. Medrxiv : the Preprint Server For Health Sciences |
Lee WP, Wang H, Dombroski B, et al. (2023) Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Research Square |
Greenfest-Allen E, Valladares O, Kuksa PP, et al. (2023) NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge. Alzheimer's & Dementia : the Journal of the Alzheimer's Association |
Wang H, Dombroski BA, Cheng PL, et al. (2023) Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Medrxiv : the Preprint Server For Health Sciences |
Ray NR, Kunkle BW, Hamilton-Nelson K, et al. (2023) Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer's Disease in individuals of African ancestry. 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 |