Alice Fievet

Villejuif, 94805, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 24 publications

RNA-seq Splicing Profile of the CDH1 Gene and Its Impact on the Clinical Pathogenicity Classification of CDH1 Variants: A Description of Alternative and Pathogenic Splicing Patterns.

RNA-seq Splicing Profile of the CDH1 Gene and Its Impact on the Clinical Pathogenicity Classification of CDH1 Variants: A Description of Alternative and Pathogenic Splicing Patterns.

Journal: Cancers

Published: May 23, 2025

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories.

Journal: International journal of cancer

Published: September 26, 2024

Genomic landscape of liquid biopsy mutations in TP53 and DNA damage genes in cancer patients.

Genomic landscape of liquid biopsy mutations in TP53 and DNA damage genes in cancer patients.

Journal: NPJ precision oncology

Published: June 11, 2023

The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.

The Frequency of Germline BRCA and Non-BRCA HR-Gene-Variants in a Cohort of Pancreatic Cancer Patients.

Journal: Digestive diseases and sciences

Published: May 06, 2022

Association of location of BRCA1 and BRCA2 mutations with benefit from olaparib and bevacizumab maintenance in high-grade ovarian cancer: phase III PAOLA-1/ENGOT-ov25 trial subgroup exploratory analysis.

Association of location of BRCA1 and BRCA2 mutations with benefit from olaparib and bevacizumab maintenance in high-grade ovarian cancer: phase III PAOLA-1/ENGOT-ov25 trial subgroup exploratory analysis.

Journal: Annals of oncology : official journal of the European Society for Medical Oncology

Published: April 19, 2022

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Journal: American journal of human genetics

Published: June 15, 2021

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder.

The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder.

Journal: Human mutation

Published: June 03, 2021

Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System.

Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System.

Journal: Cancer research

Published: March 31, 2020

DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility.

DNA repair functional analyses of NBN hypomorphic variants associated with NBN-related infertility.

Journal: Human mutation

Published: July 13, 2019

Role of MBD4 in hypermutator phenotype and malignant transformation

Role of MBD4 in hypermutator phenotype and malignant transformation

Journal: Medecine sciences : M/S

Published: December 12, 2018

Prevalence of Pathogenic Variants of FAN1 in More Than 5000 Patients Assessed for Genetic Predisposition to Colorectal, Breast, Ovarian, or Other Cancers.

Prevalence of Pathogenic Variants of FAN1 in More Than 5000 Patients Assessed for Genetic Predisposition to Colorectal, Breast, Ovarian, or Other Cancers.

Journal: Gastroenterology

Published: November 15, 2018

Three new cases of ataxia-telangiectasia-like disorder: No impairment of the ATM pathway, but S-phase checkpoint defect.

Three new cases of ataxia-telangiectasia-like disorder: No impairment of the ATM pathway, but S-phase checkpoint defect.

Journal: Human mutation

Published: September 07, 2018

Showing 1-12 of 24

Last Updated: 09/26/2026