Olivia M. Moran
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 10 publications
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B.
Journal: American journal of human genetics
Published: February 12, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.
Journal: Journal of genetic counseling
Published: July 11, 2025
A cardiovascular, craniofacial, and neurodevelopmental disorder caused by loss-of-function variants in the eIF3 complex component genes EIF3A and EIF3B.
Journal: American journal of human genetics
Published: April 07, 2025
Clinical applications of and molecular insights from RNA sequencing in a rare disease cohort.
Journal: Genome medicine
Published: December 21, 2024
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease.
Journal: European journal of human genetics : EJHG
Published: January 06, 2024
Drug-resistant focal epilepsy in a girl with SETD5-related intellectual disability.
Journal: Seizure
Published: July 10, 2023
Challenges experienced by genetic counselors while they provided counseling about mosaic embryos.
Journal: F&S reports
Published: December 14, 2022
Predictors of mammographic density among women with a strong family history of breast cancer.
Journal: BMC cancer
Published: November 21, 2018
Serum osteoprotegerin levels and mammographic density among high-risk women.
Journal: Cancer causes & control : CCC
Published: January 02, 2018
Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.
Journal: Breast cancer research and treatment
Published: October 18, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026