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Hereditary Breast Cancer: The Era of New Susceptibility Genes

BioMed research international, 2013-01, Vol.2013 (2013), p.1-11

2013

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Breast-Cancer Risk in Families with Mutations in PALB2

The New England journal of medicine, 2014-08, Vol.371 (6), p.497-506

2014

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Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing

JNCI : Journal of the National Cancer Institute, 2018-08, Vol.110 (8), p.855-862

2018

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Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

Journal of clinical oncology, 2015-02, Vol.33 (4), p.304-311

2015

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Neoadjuvant treatment in ovarian cancer: New perspectives, new challenges

Frontiers in oncology, 2022-07, Vol.12, p.820128-820128

2022

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PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk

Journal of human genetics, 2019-08, Vol.64 (8), p.767-773

2019

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MARGINAL: An Automatic Classification of Variants in BRCA1 and BRCA2 Genes Using a Machine Learning Model

Biomolecules (Basel, Switzerland), 2022-10, Vol.12 (11), p.1552

2022

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Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece

Scientific reports, 2017-12, Vol.7 (1), p.16697-9, Article 16697

2017

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Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece

Journal of human genetics, 2018-11, Vol.63 (11), p.1149-1158

2018

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Lung cancer as a predominant feature in a patient with Peutz–Jeghers syndrome: Case report

Thoracic cancer, 2022-06, Vol.13 (12), p.1862-1865

2022

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Abstract 1755: The fate of germline BRCA related mutations in breast tumor tissues

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.1755-1755

2017

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Follow-up of tissue genomics in BRCA1/2 carriers who underwent prophylactic surgeries

Breast cancer (Tokyo, Japan), 2021-11, Vol.28 (6), p.1367-1382

2021

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Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients

Journal of human genetics, 2018-07, Vol.63 (8), p.877-886

2018

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Tumor Genotyping and Homologous Recombination Repair Gene Variants in Patients With Epithelial Ovarian Cancer: Is Pathogenic Enough?

Frontiers in oncology, 2021-06, Vol.11, p.683057-683057

2021

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Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients

BMC cancer, 2010-07, Vol.10 (1), p.389-389, Article 389

2010

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A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation

Case reports in oncological medicine, 2019-01, Vol.2019 (2019), p.1-2

2019

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Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women

JAMA : the journal of the American Medical Association, 2020-07, Vol.324 (4), p.397

2020

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Variant Interpretation in Patients With Metastatic Breast Cancer

JAMA oncology, 2020-04, Vol.6 (4), p.581

2020

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Asymptomatic Gastric Giant Polyp in a Boy with Peutz-Jeghers Syndrome Presented with Multiple Café Au Lait Traits

Case reports in surgery, 2018-01, Vol.2018 (2018), p.1-3

2018

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Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio

Genomics (San Diego, Calif.), 2021-01, Vol.113 (1), p.748-754

2021

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CLINICAL CHARACTERIZATION AND MUTATION SPECTRUM IN CRETAN PATIENTS WITH HEREDITARY POLYPOSIS SYNDROMES

Gastrointestinal endoscopy, 2022-06, Vol.95 (6), p.AB142-AB142

2022

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Current practices on genetic testing in ovarian cancer

Annals of translational medicine, 2020-12, Vol.8 (24), p.1703-1703

2020

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Breast cancer in very young (≤35 years) women: clinicopathological and genetic features of the disease from a breast surgical oncology department

European journal of surgical oncology, 2023-02, Vol.49 (2), p.e91-e92

2023

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Male Breast Carcinoma: A single-institution experience in surgical treatment and clinical outcomes

European journal of surgical oncology, 2023-02, Vol.49 (2), p.e92-e92

2023

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Hereditary Breast Cancer: The Era of New Susceptibility Genes

Breast-Cancer Risk in Families with Mutations in PALB2

Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

Neoadjuvant treatment in ovarian cancer: New perspectives, new challenges

PALB2 c.2257C>T truncating variant is a Greek founder and is associated with high breast cancer risk

MARGINAL: An Automatic Classification of Variants in BRCA1 and BRCA2 Genes Using a Machine Learning Model

Mutational analysis of TSC1 and TSC2 genes in Tuberous Sclerosis Complex patients from Greece

Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece

Lung cancer as a predominant feature in a patient with Peutz–Jeghers syndrome: Case report

Abstract 1755: The fate of germline BRCA related mutations in breast tumor tissues

Follow-up of tissue genomics in BRCA1/2 carriers who underwent prophylactic surgeries

Characterization and prevalence of two novel CHEK2 large deletions in Greek breast cancer patients

Tumor Genotyping and Homologous Recombination Repair Gene Variants in Patients With Epithelial Ovarian Cancer: Is Pathogenic Enough?

Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients

Prevalence of BRCA1 mutations in familial and sporadic greek ovarian cancer cases

A Patient Affected with Serous Ovarian/Peritoneal Carcinoma Carrying the FANCM Mutation

Pathogenic Variants in Breast Cancer Susceptibility Genes in Older Women

Variant Interpretation in Patients With Metastatic Breast Cancer

Asymptomatic Gastric Giant Polyp in a Boy with Peutz-Jeghers Syndrome Presented with Multiple Café Au Lait Traits

Pitfalls in variant annotation for hereditary cancer diagnostics: The example of Illumina® VariantStudio

CLINICAL CHARACTERIZATION AND MUTATION SPECTRUM IN CRETAN PATIENTS WITH HEREDITARY POLYPOSIS SYNDROMES

Current practices on genetic testing in ovarian cancer

Breast cancer in very young (≤35 years) women: clinicopathological and genetic features of the disease from a breast surgical oncology department

Male Breast Carcinoma: A single-institution experience in surgical treatment and clinical outcomes

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