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)

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|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

Michael J Bamshad

Anne O'Donnell-Luria

Michael J Bamshad

Chia-Lin Wei

Danny E Miller

Seth I Berger

Peter N Robinson

Melissa A Haendel

James R Lupski

Richard A Gibbs

Frequent Collaborators

Michael J Bamshad

Anne O'Donnell-Luria

Michael J Bamshad

Chia-Lin Wei