Carol Cremin

Vancouver, BC, Canada

Last Updated: 09/26/2026

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Found 8 publications

Improving Access to Hereditary Testing in Pancreatic Ductal Carcinoma.

Improving Access to Hereditary Testing in Pancreatic Ductal Carcinoma.

Journal: JCO precision oncology

Published: August 05, 2024

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation.

A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation.

Journal: Journal of genetic counseling

Published: October 01, 2022

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers.

Integrating Tumor Sequencing Into Clinical Practice for Patients With Mismatch Repair-Deficient Lynch Syndrome Spectrum Cancers.

Journal: Clinical and translational gastroenterology

Published: January 16, 2021

Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening.

Burden of hereditary cancer susceptibility in unselected patients with pancreatic ductal adenocarcinoma referred for germline screening.

Journal: Cancer medicine

Published: February 04, 2020

Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.

Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 07, 2020

Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis.

Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis.

Journal: Cold Spring Harbor molecular case studies

Published: November 15, 2018

CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome.

CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome.

Journal: Hereditary cancer in clinical practice

Published: November 15, 2017

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Thorough in silico and in vitro cDNA analysis of 21 putative BRCA1 and BRCA2 splice variants and a complex tandem duplication in BRCA2 allowing the identification of activated cryptic splice donor sites in BRCA2 exon 11.

Journal: Human mutation

Published: June 19, 2017

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Last Updated: 09/26/2026