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Metastatic Site Location Influences the Diagnostic Accuracy of ctDNA EGFR- Mutation Testing in NSCLC Patients: a Pooled Analysis

Current cancer drug targets, 2018-01, Vol.18 (7), p.697-705

2018

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Universal testing for MSI/MMR status in colorectal and endometrial cancers to identify Lynch syndrome cases: state of the art in Italy and consensus recommendations from the Italian Association for the Study of Familial Gastrointestinal Tumors (A.I.F.E.G.)

European journal of cancer prevention, 2022-01, Vol.31 (1), p.44-49

2022

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Hereditary ovarian cancer

Critical reviews in oncology/hematology, 2009-01, Vol.69 (1), p.28-44

2009

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Role of tumor-infiltrating lymphocytes in patients with solid tumors: Can a drop dig a stone?

Cellular immunology, 2019-09, Vol.343, p.103753-103753, Article 103753

2019

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Absence of germline CDKN2A mutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?

Cancer biology & therapy, 2016-01, Vol.17 (1), p.83-90

2016

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Are Long Noncoding RNAs New Potential Biomarkers in Gastrointestinal Stromal Tumors (GISTs)? The Role of H19 and MALAT1

Journal of oncology, 2019, Vol.2019 (2019), p.1-7

2019

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Monitoring blood biomarkers to predict nivolumab effectiveness in NSCLC patients

Therapeutic advances in medical oncology, 2019, Vol.11, p.1758835919839928-1758835919839928

2019

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Detection of Germline Mutations in a Cohort of 139 Patients with Bilateral Breast Cancer by Multi-Gene Panel Testing: Impact of Pathogenic Variants in Other Genes beyond BRCA1/2

Cancers, 2020-08, Vol.12 (9), p.2415

2020

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SIUrO best practice recommendations to optimize BRCA 1/2 gene testing from DNA extracted from bone biopsy in mCRPC patients (BRCA Optimal Bone Biopsy Procedure: BOP)

Virchows Archiv : an international journal of pathology, 2023-11, Vol.483 (5), p.579-589

2023

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Hereditary Breast and Ovarian Cancer in Families from Southern Italy (Sicily)-Prevalence and Geographic Distribution of Pathogenic Variants in BRCA1/2 Genes

Cancers, 2020-05, Vol.12 (5), p.1158

2020

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BRCA1/2 pathogenic variants in triple-negative versus luminal-like breast cancers: genotype–phenotype correlation in a cohort of 531 patients

Therapeutic advances in medical oncology, 2020, Vol.12, p.1758835920975326

2020

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Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome

Frontiers in oncology, 2021-06, Vol.11, p.682445-682445

2021

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Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength

Frontiers in oncology, 2022-02, Vol.12, p.827822-827822

2022

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Janus kinase (JAK) 2 V617F mutation as the cause of primary thrombocythemia in acromegaly with severe visceromegaly and divergence between growth hormone and insulin-like growth factor-1 concentrations during the follow-up: causal or casual association?

Growth hormone & IGF research, 2012-04, Vol.22 (2), p.92-96

2012

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Stabilizing versus Destabilizing the Microtubules: A Double-Edge Sword for an Effective Cancer Treatment Option?

Analytical cellular pathology (Amsterdam), 2015-01, Vol.2015 (2015), p.1-19

2015

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STAT proteins: From normal control of cellular events to tumorigenesis

Journal of cellular physiology, 2003-11, Vol.197 (2), p.157-168

2003

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The diagnostic accuracy of PIK3CA mutations by circulating tumor DNA in breast cancer: an individual patient data meta-analysis

Therapeutic advances in medical oncology, 2022, Vol.14, p.17588359221110162

2022

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Analysis of tissue and circulating microRNA expression during metaplastic transformation of the esophagus

Oncotarget, 2016-07, Vol.7 (30), p.47821-47830

2016

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Prognostic and predictive biomarkers for targeted therapy in NSCLC: for whom the bell tolls?

Expert opinion on biological therapy, 2015-11, Vol.15 (11), p.1553-1566

2015

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"Back to a false normality": new intriguing mechanisms of resistance to PARP inhibitors

Oncotarget, 2017-04, Vol.8 (14), p.23891-23904

2017

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Non-Small Cell Lung Cancer Harboring Concurrent EGFR Genomic Alterations: A Systematic Review and Critical Appraisal of the Double Dilemma

Journal of Molecular Pathology, 2021-06, Vol.2 (2), p.173-196

2021

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How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis

Cancers, 2019-08, Vol.11 (8), p.1189

2019

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A headlight on liquid biopsies: a challenging tool for breast cancer management

Tumor biology, 2016-04, Vol.37 (4), p.4263-4273

2016

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BRCA1/BRCA2 rearrangements and CHEK2 common mutations are infrequent in Italian male breast cancer cases

Breast cancer research and treatment, 2008-07, Vol.110 (1), p.161-167

2008

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A new germline mutation in BRCA1 gene in a sicilian family with ovarian cancer

Breast cancer research and treatment, 2006-03, Vol.96 (1), p.97-100

2006

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Metastatic Site Location Influences the Diagnostic Accuracy of ctDNA EGFR- Mutation Testing in NSCLC Patients: a Pooled Analysis

Universal testing for MSI/MMR status in colorectal and endometrial cancers to identify Lynch syndrome cases: state of the art in Italy and consensus recommendations from the Italian Association for the Study of Familial Gastrointestinal Tumors (A.I.F.E.G.)

Hereditary ovarian cancer

Role of tumor-infiltrating lymphocytes in patients with solid tumors: Can a drop dig a stone?

Absence of germline CDKN2A mutation in Sicilian patients with familial malignant melanoma: Could it be a population-specific genetic signature?

Are Long Noncoding RNAs New Potential Biomarkers in Gastrointestinal Stromal Tumors (GISTs)? The Role of H19 and MALAT1

Monitoring blood biomarkers to predict nivolumab effectiveness in NSCLC patients

Detection of Germline Mutations in a Cohort of 139 Patients with Bilateral Breast Cancer by Multi-Gene Panel Testing: Impact of Pathogenic Variants in Other Genes beyond BRCA1/2

SIUrO best practice recommendations to optimize BRCA 1/2 gene testing from DNA extracted from bone biopsy in mCRPC patients (BRCA Optimal Bone Biopsy Procedure: BOP)

Hereditary Breast and Ovarian Cancer in Families from Southern Italy (Sicily)-Prevalence and Geographic Distribution of Pathogenic Variants in BRCA1/2 Genes

BRCA1/2 pathogenic variants in triple-negative versus luminal-like breast cancers: genotype–phenotype correlation in a cohort of 531 patients

Prevalence and Spectrum of Germline BRCA1 and BRCA2 Variants of Uncertain Significance in Breast/Ovarian Cancer: Mysterious Signals From the Genome

Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength

Janus kinase (JAK) 2 V617F mutation as the cause of primary thrombocythemia in acromegaly with severe visceromegaly and divergence between growth hormone and insulin-like growth factor-1 concentrations during the follow-up: causal or casual association?

Stabilizing versus Destabilizing the Microtubules: A Double-Edge Sword for an Effective Cancer Treatment Option?

STAT proteins: From normal control of cellular events to tumorigenesis

The diagnostic accuracy of PIK3CA mutations by circulating tumor DNA in breast cancer: an individual patient data meta-analysis

Analysis of tissue and circulating microRNA expression during metaplastic transformation of the esophagus

Prognostic and predictive biomarkers for targeted therapy in NSCLC: for whom the bell tolls?

"Back to a false normality": new intriguing mechanisms of resistance to PARP inhibitors

Non-Small Cell Lung Cancer Harboring Concurrent EGFR Genomic Alterations: A Systematic Review and Critical Appraisal of the Double Dilemma

How to Deal with Second Line Dilemma in Metastatic Colorectal Cancer? A Systematic Review and Meta-Analysis

A headlight on liquid biopsies: a challenging tool for breast cancer management

BRCA1/BRCA2 rearrangements and CHEK2 common mutations are infrequent in Italian male breast cancer cases

A new germline mutation in BRCA1 gene in a sicilian family with ovarian cancer

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