Jessica X Chong

18PUBLICATIONS
163CO-AUTHORS
Data qualityGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cardiology (incl. cardiovascular diseases)Neurogenetics
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Publications (18)

|Jun 04, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and Dataset.

|Nov 26, 2025
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions.

Yong-Han Hank Cheng, Adriana E Sedeño-Cortés, Jane E Ranchalis

|Nov 12, 2025
GREGoR: accelerating genomics for rare diseases.

Moez Dawood, Ben Heavner, Marsha M Wheeler

|Jun 04, 2025
Cell Modeling and Rescue of a Novel Non-coding Genetic Cause of Glycogen Storage Disease IX.

Apoorva K Iyengar, Xue Zou, Jian Dai

|Mar 17, 2025
GA4GH Phenopacket-Driven Characterization of Genotype-Phenotype Correlations in Mendelian Disorders.

Lauren Rekerle, Daniel Danis, Filip Rehburg

|Nov 28, 2024
The ClinGen Syndromic Disorders Gene Curation Expert Panel: Assessing the Clinical Validity of 111 Gene-Disease Relationships.

Eleanor Broeren, Vanessa Gitau, Alicia Byrne

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Frequent Collaborators

5 joint publications

Michael J Bamshad

4 joint publications

Anne O'Donnell-Luria

3 joint publications

Michael J Bamshad

3 joint publications

Chia-Lin Wei