Wyeth W. Wasserman
950 West 28th Avenue, V5Z 4H4
Vancouver, BC, Canada
Vancouver, BC, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 149 publications
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: Journal of human immunity
Published: April 15, 2026
Progranulin genetic variant rs5848 displays ancestry-specific associations with Alzheimer's disease.
Progranulin genetic variant rs5848 displays ancestry-specific associations with Alzheimer's disease.
Journal: Human genomics
Published: January 22, 2026
SCN3A-related neurodevelopmental disorder: Clinical case reports and biophysical characterization.
Journal: Channels (Austin, Tex.)
Published: October 30, 2025
CaseReportBench: An LLM Benchmark Dataset for Dense Information Extraction in Clinical Case Reports.
CaseReportBench: An LLM Benchmark Dataset for Dense Information Extraction in Clinical Case Reports.
Journal: Proceedings of machine learning research
Published: October 01, 2025
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: medRxiv : the preprint server for health sciences
Published: September 19, 2025
JASPAR 2026: expansion of transcription factor binding profiles and integration of deep learning models.
Journal: Nucleic acids research
Published: September 15, 2025
Pathway-Informed Machine Learning Identifies Genetic Predictors of High-Dose Methotrexate-Induced Mucositis in Pediatric Acute Lymphoblastic Leukemia.
Journal: Clinical pharmacology and therapeutics
Published: August 09, 2025
Caregiver experiences of an integrative patient-centered digital health application for pediatric type 1 diabetes care: Findings from a pilot clinical trial.
Journal: PLOS digital health
Published: April 21, 2025
The cost and cost trajectory of genome sequencing and bioinformatics analysis for Indigenous children with suspected rare diseases.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 28, 2025
Escape from X-chromosome inactivation at KDM5C is driven by promoter-proximal DNA elements and enhanced by domain context.
Journal: Human molecular genetics
Published: December 09, 2024
The Metabolic Treatabolome and Inborn Errors of Metabolism Knowledgebase therapy tool: Do not miss the opportunity to treat!
Journal: Journal of inherited metabolic disease
Published: July 10, 2024
Last Updated: 09/26/2026