Gerard D Schellenberg

9PUBLICATIONS
104CO-AUTHORS
Forensic epidemiologyEpigenetics (incl. genome methylation and epigenomics)Computational neuroscience (incl. mathematical neuroscience and theoretical neuroscience)Gene expression (incl. microarray and other genome-wide approaches)Atmospheric aerosols
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Publications (9)

|Mar 08, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.

Hui Wang, Timothy S Chang, Beth A Dombroski

|Sep 04, 2024
Variant-to-function mapping of late-onset Alzheimer's disease GWAS signals in human microglial cell models implicates <i>RTFDC1</i> at the <i>CASS4</i> locus.

Elizabeth A Burton, Mariana Argenziano, Kieona Cook

|Aug 07, 2024
A Specialized Reference Panel with Structural Variants Integration for Improving Genotype Imputation in Alzheimer's Disease and Related Dementias (ADRD).

Po-Liang Cheng, Hui Wang, Beth A Dombroski

|Feb 28, 2024
A comparative study of structural variant calling in WGS from Alzheimer's disease families.

John S Malamon, John J Farrell, Li Charlie Xia

|Jul 05, 2022
A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry.

Farid Rajabli, Gary W Beecham, Hugh C Hendrie

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