Maya Chopra
10PUBLICATIONS
39CO-AUTHORS

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Publications (10)
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|Jul 14, 2025
Finding buried genetic test results in the electronic health record is inefficient and variable across institutions.Olivia J Veatch, Jomol Mathew, Shira Rockowitz
|Dec 02, 2024
Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes.Courtney E French, Nancy C Andrews, Alan H Beggs
|Apr 27, 2024
Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder.Ineke Cordova, Alyssa Blesson, Juliann M Savatt
|Sep 25, 2023
Clinical actionability of genetic findings in cerebral palsy.Sara A Lewis, Maya Chopra, Julie S Cohen
|Aug 25, 2023
Toward representative genomic research: the children's rare disease cohorts experience.Zoë J Frazier, Eurnestine Brown, Shira Rockowitz
|May 19, 2022
Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1.Maya Chopra, Richard Caswell, Giulia Barcia
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Frequent Collaborators
2 joint publications
Guilia Barcia
2 joint publications
Mustafa Sahin
2 joint publications
Annapurna Poduri
2 joint publications
Siddharth Srivastava
1 joint publications
Christopher T Gordon
1 joint publications
Allan Bayat
1 joint publications
Sumaiya Iqbal
1 joint publications
Claudio DeGusmao
1 joint publications
Darius Ebrahimi-Fakhari
1 joint publications
Richard Caswell