Marco Marino

Modena, Italy

Last Updated: 09/26/2026

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Found 21 publications

Characterization of Copy Number Variants in Hereditary Cancer Patients Through NGS Shows a Distinctive PALB2 Contribution to the Diagnostic Yield.

Characterization of Copy Number Variants in Hereditary Cancer Patients Through NGS Shows a Distinctive PALB2 Contribution to the Diagnostic Yield.

Journal: Human mutation

Published: May 13, 2025

Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study.

Diagnostic Yield and Clinical Impact of a Small Genetic Panel for Kidney Disease: A Multicenter, Retrospective European Study.

Journal: Clinical genetics

Published: January 07, 2025

Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk.

Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk.

Journal: JCO precision oncology

Published: September 08, 2022

Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions.

Detection of Germline Variants in 450 Breast/Ovarian Cancer Families with a Multi-Gene Panel Including Coding and Regulatory Regions.

Journal: International journal of molecular sciences

Published: June 12, 2021

Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework.

Automated capture-based NGS workflow: one thousand patients experience in a clinical routine framework.

Journal: Diagnosis (Berlin, Germany)

Published: April 09, 2021

Characterization of New ATM Deletion Associated with Hereditary Breast Cancer.

Characterization of New ATM Deletion Associated with Hereditary Breast Cancer.

Journal: Genes

Published: December 22, 2020

iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification.

iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification.

Journal: Genes

Published: December 14, 2020

Real-life use of BRAF-V600E mutation analysis in thyroid nodule fine needle aspiration: consequences on clinical decision-making.

Real-life use of BRAF-V600E mutation analysis in thyroid nodule fine needle aspiration: consequences on clinical decision-making.

Journal: Endocrine

Published: September 17, 2020

Altered methylation pattern of the SRD5A2 gene in the cerebrospinal fluid of post-finasteride patients: a pilot study.

Altered methylation pattern of the SRD5A2 gene in the cerebrospinal fluid of post-finasteride patients: a pilot study.

Journal: Endocrine connections

Published: June 10, 2019

Hereditary Pancreatic Cancer: A Retrospective Single-Center Study of 5143 Italian Families with History of BRCA-Related Malignancies.

Hereditary Pancreatic Cancer: A Retrospective Single-Center Study of 5143 Italian Families with History of BRCA-Related Malignancies.

Journal: Cancers

Published: December 29, 2018

Estrogen Modulates Specific Life and Death Signals Induced by LH and hCG in Human Primary Granulosa Cells In Vitro.

Estrogen Modulates Specific Life and Death Signals Induced by LH and hCG in Human Primary Granulosa Cells In Vitro.

Journal: International journal of molecular sciences

Published: February 28, 2017

Human LH and hCG stimulate differently the early signalling pathways but result in equal testosterone synthesis in mouse Leydig cells in vitro.

Human LH and hCG stimulate differently the early signalling pathways but result in equal testosterone synthesis in mouse Leydig cells in vitro.

Journal: Reproductive biology and endocrinology : RB&E

Published: September 23, 2016

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Last Updated: 09/26/2026