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EB

Eliane Beauregard-Lacroix

Medical Genetics / Medical Biochemical Genetics

Credentials: ·

Research

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
The American Journal of Human Genetics · 2019 · 46 citations
UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism
The American Journal of Human Genetics · 2021 · 20 citations
Exploring the phenotypic spectrum and osteopenia mechanisms in Yunis-Varón syndrome
Genetics in Medicine Open · 2024 · First of 12 authors · 2 citations