Jill Madden

4PUBLICATIONS
48CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesPredictive and prognostic markers
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Publications (4)

|Jun 26, 2026
Multimodal Sequencing and Reanalysis Approaches to End the Diagnostic Odyssey of Individuals with Suspected Rare Monogenic Diseases.

|Jul 03, 2023
Loss-of-function variants in <i>CUL3</i> cause a syndromic neurodevelopmental disorder.

Patrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh

|Jul 07, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings.

Qifei Li, Michal Dibus, Alicia Casey

|Feb 08, 2021
Effect of the p53 P72R Polymorphism on Mutant TP53 Allele Selection in Human Cancer.

Cristabelle De Souza, Jill Madden, Devin C Koestler

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Frequent Collaborators

2 joint publications

Casie A Genetti

2 joint publications

Catherine A Brownstein

1 joint publications

Qifei Li

1 joint publications

Michal Dibus