Bryce A Mendelsohn

8PUBLICATIONS
68CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Quaternary environmentsGene mappingClinical nutrition
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Publications (8)

|Jun 18, 2026
USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes.

|Nov 24, 2025
Reclassifying IDUA c.250G>A (p.Gly84Ser): Evidence for a Possible Pseudodeficiency Allele.

Christopher Connolly, Rachel Fisher, Chen Yang

|Mar 05, 2025
ARID2-related disorder: further delineation of the clinical phenotype of 27 novel individuals and description of an epigenetic signature.

Clara Houdayer, Kathleen Rooney, Liselot van der Laan

|Oct 13, 2021
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders.

Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong

|Sep 24, 2021
Application of full-genome analysis to diagnose rare monogenic disorders.

Joseph T Shieh, Monica Penon-Portmann, Karen H Y Wong

|Aug 30, 2020
Defining the ATPome reveals cross-optimization of metabolic pathways.

Neal K Bennett, Mai K Nguyen, Maxwell A Darch

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Frequent Collaborators

2 joint publications

Michelle Verghese

2 joint publications

Pui-Yan Kwok

2 joint publications

Andrew G Sharo

2 joint publications

Anne Slavotinek