Jaroslav Kotlas

Prague, PR 12800, Czech Republic

Last Updated: 09/26/2026

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Found 8 publications

Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance.

Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition - Mutation Types and their Biological and Clinical Relevance.

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: August 15, 2019

Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.

Contribution of Massive Parallel Sequencing to Diagnosis of Hereditary Ovarian Cancer in the Czech Republic.

Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti

Published: August 15, 2019

Estrogen Receptor Status Oppositely Modifies Breast Cancer Prognosis in BRCA1/BRCA2 Mutation Carriers Versus Non-Carriers.

Estrogen Receptor Status Oppositely Modifies Breast Cancer Prognosis in BRCA1/BRCA2 Mutation Carriers Versus Non-Carriers.

Journal: Cancers

Published: March 28, 2019

Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.

Identification of deleterious germline CHEK2 mutations and their association with breast and ovarian cancer.

Journal: International journal of cancer

Published: February 06, 2019

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene.

Two Czech patients with familial adenomatous polyposis presenting mosaicism in APC gene.

Journal: Neoplasma

Published: July 31, 2018

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.

Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.

Journal: BMC nephrology

Published: May 22, 2017

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele.

Journal: BMC nephrology

Published: October 10, 2012

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Journal: Familial cancer

Published: September 19, 2012

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Last Updated: 09/26/2026