Julie S Cohen

8PUBLICATIONS
114CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Predictive and prognostic markersNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
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Publications (8)

|Aug 01, 2026
Genetic Counselor Utilization Across Non-Genetics Departments for Neurodevelopmental Disorders.

|Jul 10, 2026
Disease Outcomes in Boys with ABCD1 Variants Identified by Newborn Screening for X-ALD.

|Apr 16, 2025
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.

Eric N Anderson, Stephan Drukewitz, Sukhleen Kour

|Sep 25, 2023
Clinical actionability of genetic findings in cerebral palsy.

Sara A Lewis, Maya Chopra, Julie S Cohen

|May 12, 2021
Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotype.

Marija Kojic, Tomasz Gawda, Monika Gaik

|Jan 12, 2021
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari

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Frequent Collaborators

4 joint publications

Ali Fatemi

3 joint publications

Michael C Fahey

3 joint publications

Michael C Kruer

3 joint publications

Sara A Lewis