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Challenges in the management of operable triple-negative breast cancer in a survivor of the B-cell acute lymphoblastic leukemia: a case report

Frontiers in oncology, 2024-05, Vol.14, p.1404706

2024

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Genetic testing results in Slovenian male breast cancer cohort indicate the BRCA2 7806-2A > G founder variant could be associated with higher male breast cancer risk

Breast cancer research and treatment, 2021-08, Vol.188 (3), p.811-820

2021

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Bilateral Disease Common Among Slovenian CHEK2-Positive Breast Cancer Patients

Annals of surgical oncology, 2021-05, Vol.28 (5), p.2561-2570

2021

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Medullary Thyroid Carcinoma and Associated Endocrinopathies in Slovenia from 1995 to 2021

Life (Basel, Switzerland), 2022-07, Vol.12 (7), p.1091

2022

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Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation

Genetics in medicine, 2016-11, Vol.18 (11), p.1102-1110

2016

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Bilateral parotid glands aplasia: a case report and literature review

Oral radiology, 2022-07, Vol.38 (3), p.423-429

2022

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Identification of Spliceogenic Variants beyond Canonical GT-AG Splice Sites in Hereditary Cancer Genes

International journal of molecular sciences, 2022-07, Vol.23 (13), p.7446

2022

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Two Novel NF1 Pathogenic Variants Causing the Creation of a New Splice Site in Patients With Neurofibromatosis Type I

Frontiers in genetics, 2019-08, Vol.10, p.762

2019

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CDKN2A-positive melanoma patient treated with combination immunotherapy – A case report

Advances in cancer biology - metastasis, 2022-07, Vol.4, p.100028, Article 100028

2022

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A Novel Germline MLH1 In-Frame Deletion in a Slovenian Lynch Syndrome Family Associated with Uncommon Isolated PMS2 Loss in Tumor Tissue

Genes, 2020-03, Vol.11 (3), p.325

2020

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BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome

Breast cancer (Tokyo, Japan), 2022-09, Vol.29 (5), p.921-927

2022

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Real-World Data on Detection of Germline and Somatic Pathogenic/Likely Pathogenic Variants in BRCA1/2 and Other Susceptibility Genes in Ovarian Cancer Patients Using Next Generation Sequencing

Cancers, 2022-03, Vol.14 (6), p.1434

2022

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New Approach for Detection of Normal Alternative Splicing Events and Aberrant Spliceogenic Transcripts with Long-Range PCR and Deep RNA Sequencing

Biology (Basel, Switzerland), 2021-07, Vol.10 (8), p.706

2021

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The prevalence of occult ovarian cancer in the series of 155 consequently operated high risk asymptomatic patients – Slovenian population based study

Radiology and oncology, 2020-05, Vol.54 (2), p.180-186

2020

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Screening strategy modification based on personalized breast cancer risk stratification and its implementation in the national guidelines – pilot study

Zdravstveno varstvo, 2020-12, Vol.59 (4), p.211-218

2020

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Guidelines for the Li-Fraumeni and heritable TP53-related cancer syndromes

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1379-1386

2020

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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

Gynecologic oncology, 2024-11, Vol.190, p.104-112

2024

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BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome

Nature genetics, 2018-03, Vol.50 (3), p.329-332

2018

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Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

European journal of human genetics : EJHG, 2020-10, Vol.28 (10), p.1387-1393

2020

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Characteristics of breast cancer in Slovenian patients with germline CHEK2 c.444+1G>A mutation

Journal of clinical oncology, 2020-05, Vol.38 (15_suppl), p.e13536-e13536

2020

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A Population-Based Study of Patients With Small Cell Carcinoma of the Ovary, Hypercalcemic Type, Encompassing a 30-Year Period

Archives of pathology & laboratory medicine (1976), 2024-03, Vol.148 (3), p.299-309

2024

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Trends and timing of risk-reducing mastectomy uptake in unaffected BRCA1 and BRCA2 carriers in Slovenia

European journal of surgical oncology, 2021-08, Vol.47 (8), p.1900-1906

2021

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Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

European journal of human genetics : EJHG, 2023-11, Vol.31 (11), p.1261-1269

2023

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Challenges in the management of operable triple-negative breast cancer in a survivor of the B-cell acute lymphoblastic leukemia: a case report

Genetic testing results in Slovenian male breast cancer cohort indicate the BRCA2 7806-2A > G founder variant could be associated with higher male breast cancer risk

Bilateral Disease Common Among Slovenian CHEK2-Positive Breast Cancer Patients

Medullary Thyroid Carcinoma and Associated Endocrinopathies in Slovenia from 1995 to 2021

Phenotype-driven gene target definition in clinical genome-wide sequencing data interpretation

Bilateral parotid glands aplasia: a case report and literature review

Identification of Spliceogenic Variants beyond Canonical GT-AG Splice Sites in Hereditary Cancer Genes

Two Novel NF1 Pathogenic Variants Causing the Creation of a New Splice Site in Patients With Neurofibromatosis Type I

CDKN2A-positive melanoma patient treated with combination immunotherapy – A case report

A Novel Germline MLH1 In-Frame Deletion in a Slovenian Lynch Syndrome Family Associated with Uncommon Isolated PMS2 Loss in Tumor Tissue

BAP1-defficient breast cancer in a patient with BAP1 cancer syndrome

Real-World Data on Detection of Germline and Somatic Pathogenic/Likely Pathogenic Variants in BRCA1/2 and Other Susceptibility Genes in Ovarian Cancer Patients Using Next Generation Sequencing

New Approach for Detection of Normal Alternative Splicing Events and Aberrant Spliceogenic Transcripts with Long-Range PCR and Deep RNA Sequencing

The prevalence of occult ovarian cancer in the series of 155 consequently operated high risk asymptomatic patients – Slovenian population based study

Screening strategy modification based on personalized breast cancer risk stratification and its implementation in the national guidelines – pilot study

Recommendations for diagnosis, treatment and follow-up of patients with ovarian cancer, fallopian tube cancer and primary peritoneal cancer

Recommendations from the Institute of Oncology Ljubljana for the treatment of patients with gastric cancer

Guidelines for the Li-Fraumeni and heritable TP53-related cancer syndromes

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

BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome

Cancer Surveillance Guideline for individuals with PTEN hamartoma tumour syndrome

Characteristics of breast cancer in Slovenian patients with germline CHEK2 c.444+1G>A mutation

A Population-Based Study of Patients With Small Cell Carcinoma of the Ovary, Hypercalcemic Type, Encompassing a 30-Year Period

Trends and timing of risk-reducing mastectomy uptake in unaffected BRCA1 and BRCA2 carriers in Slovenia

Clinical practice guidelines for the diagnosis and surveillance of BAP1 tumour predisposition syndrome

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