Cara N. Inglese
Toronto, ON, Canada
Last Updated: 09/26/2026
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Found 8 publications
Timely and accurate RB1 genetic testing guides familial risk stratification in heritable retinoblastoma.
Journal: Ophthalmic genetics
Published: February 10, 2026
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 21, 2023
Exome sequencing identifies PD-L2 as a potential predisposition gene for lymphoma.
Journal: Hematological oncology
Published: May 25, 2022
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliability.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 05, 2021
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism.
Journal: American journal of human genetics
Published: February 13, 2020
Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patients.
Journal: Clinical genetics
Published: April 11, 2019
New developmental syndromes: Understanding the family experience.
Journal: Journal of genetic counseling
Published: June 22, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026