Rachel Wevrick
Edmonton, AB T6G2H7, Canada
Last Updated: 09/26/2026
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Found 32 publications
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental Disorders.
Journal: bioRxiv : the preprint server for biology
Published: June 26, 2025
Hypothalamic AAV-BDNF gene therapy improves metabolic function and behavior in the Magel2-null mouse model of Prader-Willi syndrome.
Journal: Molecular therapy. Methods & clinical development
Published: July 08, 2022
The N-terminal domain of the Schaaf-Yang syndrome protein MAGEL2 likely has a role in RNA metabolism.
Journal: The Journal of biological chemistry
Published: March 26, 2021
The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry.
Journal: Human genetics
Published: February 21, 2020
Disentangling ingestive behavior-related phenotypes in Prader-Willi syndrome: Integrating information from nonclinical studies and clinical trials to better understand the pathophysiology of hyperphagia and obesity.
Journal: Physiology & behavior
Published: November 14, 2019
A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1.
Journal: PloS one
Published: September 25, 2019
Regulation of autism-relevant behaviors by cerebellar-prefrontal cortical circuits.
Journal: Nature neuroscience
Published: July 30, 2019
Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis.
Journal: Molecular therapy. Methods & clinical development
Published: April 17, 2019
Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder.
Journal: Journal of psychiatric research
Published: July 31, 2018
Chronic diazoxide treatment decreases fat mass and improves endurance capacity in an obese mouse model of Prader-Willi syndrome.
Journal: Molecular genetics and metabolism
Published: December 14, 2017
ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison.
Journal: Orphanet journal of rare diseases
Published: November 27, 2017
Genetic analysis of very obese children with autism spectrum disorder.
Journal: Molecular genetics and genomics : MGG
Published: November 23, 2017
Last Updated: 09/26/2026