Ana Blatnik

Ljubljana, Slovenia

Last Updated: 09/26/2026

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Found 45 publications

Correction: Two recurrent pathogenic/likely pathogenic variants in PALB2 account for half of PALB2 positive families in Slovenia.

Correction: Two recurrent pathogenic/likely pathogenic variants in PALB2 account for half of PALB2 positive families in Slovenia.

Journal: Human genomics

Published: April 30, 2026

Correction: Cosegregation analysis following an excellent response to olaparib in a pancreatic cancer patient carrier of BRCA2:c.7892 T > C variant enables its reclassification from VUS to pathogenic.

Correction: Cosegregation analysis following an excellent response to olaparib in a pancreatic cancer patient carrier of BRCA2:c.7892 T > C variant enables its reclassification from VUS to pathogenic.

Journal: BJC reports

Published: April 02, 2026

ERN GENTURIS cancer surveillance guideline for individuals with PTEN hamartoma tumour syndrome (PHTS).

ERN GENTURIS cancer surveillance guideline for individuals with PTEN hamartoma tumour syndrome (PHTS).

Journal: European journal of human genetics : EJHG

Published: November 25, 2025

Secondary findings after multi-gene panel testing in 7,388 patients with suspected cancer predisposition syndrome.

Secondary findings after multi-gene panel testing in 7,388 patients with suspected cancer predisposition syndrome.

Journal: Scientific reports

Published: November 18, 2025

Cosegregation analysis following an excellent response to olaparib in a pancreatic cancer patient carrier of BRCA2:c.7892 T > C variant enables its reclassification from VUS to pathogenic.

Cosegregation analysis following an excellent response to olaparib in a pancreatic cancer patient carrier of BRCA2:c.7892 T > C variant enables its reclassification from VUS to pathogenic.

Journal: BJC reports

Published: November 14, 2025

Hereditary cancer: Germline testing practices across ERN GENTURIS member countries.

Hereditary cancer: Germline testing practices across ERN GENTURIS member countries.

Journal: European journal of human genetics : EJHG

Published: October 31, 2025

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Cancer prognosis and treatment results in patients with PTEN Hamartoma Tumour Syndrome (PHTS)-a European cohort study.

Journal: BJC reports

Published: February 13, 2025

Secondary findings in hereditary cancer genes after germline genetic testing - systematic review of literature.

Secondary findings in hereditary cancer genes after germline genetic testing - systematic review of literature.

Journal: Human genetics

Published: January 14, 2025

Analysis of informed consent forms of patients undergoing cancer genetic testing in the era of next-generation sequencing.

Analysis of informed consent forms of patients undergoing cancer genetic testing in the era of next-generation sequencing.

Journal: Hereditary cancer in clinical practice

Published: November 15, 2024

Multifocal vascular neoplasm with an EWSR1::NFATC2 gene fusion and progression to epithelioid angiosarcoma - a case report.

Multifocal vascular neoplasm with an EWSR1::NFATC2 gene fusion and progression to epithelioid angiosarcoma - a case report.

Journal: Virchows Archiv : an international journal of pathology

Published: September 04, 2024

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

The risk of a second primary cancer in PTEN Hamartoma Tumor Syndrome (PHTS).

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

Published: August 12, 2024

Exploring the impact of BRCA1 and BRCA2 mutation type and location on Olaparib maintenance therapy in platinum-sensitive relapsed ovarian Cancer patients: A single center report.

Exploring the impact of BRCA1 and BRCA2 mutation type and location on Olaparib maintenance therapy in platinum-sensitive relapsed ovarian Cancer patients: A single center report.

Journal: Gynecologic oncology

Published: July 08, 2024

Showing 1-12 of 45

Last Updated: 09/26/2026