Search filters

List of works by Carol Cremin

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

scientific article published on 01 April 2019

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

scientific article published on 07 April 2020

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

scientific article published on 7 March 2018

Genetics: Alzheimer disease

scientific article published on June 2009

Genetics: Codeine metabolism.

scientific article published on February 2009

Genetics: Hypertrophic cardiomyopathy

scientific article published on November 2009

Genetics: Newborn screening for sickle cell anemia

scientific article published on October 2009

Genetics: Preimplantation genetic diagnosis

scientific article

Genetics: factor V Leiden.

scientific article published on April 2010

Genetics: familial melanoma.

scientific article published on January 2010

Genetics: hereditary hemochromatosis

scientific article published on January 2009

Genetics: newborn screening for MCAD deficiency.

scientific article published on May 2009

Genetics: prostate cancer

scientific article published on July 2009

Genetics: schizophrenia

scientific article published on December 2009

Genetics: type 2 diabetes

scientific article published on September 2009

Hereditary breast and ovarian cancers

scientific article published on December 2008

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

scientific article published on 06 July 2020

Lynch syndrome-chasing a better ascertainment rate in British Columbia

scientific article published on 25 May 2010

Nonovarian Pelvic Cancers in BRCA1/2 Mutation Carriers and the BRCAPRO Statistical Model

article

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

scientific article published on 12 March 2011

The identification of Lynch syndrome in British Columbia

scientific article

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.

scientific article

Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer

scientific article published in February 2010

Paulina is supported by:

About Paulina

Help