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Alice Fiévet

Outlier response to anti-PD1 in uveal melanoma reveals germline MBD4 mutations in hypermutated tumors
2018 · Manuel Rodrigues, Lenha Mobuchon, et al. · Nature Communications · 153
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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
2022 · S.I. Labidi-Galy, M. Rodrigues, et al. · Annals of Oncology · 72
PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects
2018 · Aurélie Berland, Jérémie Rosain, et al. · Journal of Allergy and Clinical Immunology · 65
PFMG2025–integrating genomic medicine into the national healthcare system in France
2025 · Caroline Abadie, Aldja Abderrahmane, et al. · The Lancet Regional Health - Europe · 57
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Functional classification of ATM variants in ataxia‐telangiectasia patients
2019 · Alice Fiévet, Dorine Bellanger, et al. · Human Mutation · 44
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Genotype–phenotype correlations in ataxia telangiectasia patients with ATM c.3576G>A and c.8147T>C mutations
2019 · Nienke J H van Os, Luciana Chessa, et al. · Journal of Medical Genetics · 43
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Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
2021 · Sandrine M. Caputo, Lisa Golmard, et al. · The American Journal of Human Genetics · 33
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TCF2/HNF-1beta mutations: 3 cases of fetal severe pancreatic agenesis or hypoplasia and multicystic renal dysplasia
2013 · Delphine Body-Bechou, Philippe Loget, et al. · Prenatal Diagnosis · 33
Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System
2020 · Hélène Tubeuf, Sandrine M. Caputo, et al. · Cancer Research · 31
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Modulating BAP1 expression affects ROS homeostasis, cell motility and mitochondrial function
2017 · Lucie Hebert, Dorine Bellanger, et al. · Oncotarget · 30
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ART-DeCo: easy tool for detection and characterization of cross-contamination of DNA samples in diagnostic next-generation sequencing analysis
2019 · Alice Fiévet, Virginie Bernard, et al. · European Journal of Human Genetics · 29
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Three new cases of ataxia‐telangiectasia‐like disorder: No impairment of the ATM pathway, but S‐phase checkpoint defect
2019 · Alice Fiévet, Dorine Bellanger, et al. · Human Mutation · 21
Matrice poreuse et culture de cellules primaires : un même concept pour la reconstruction cutanée et cornéenne
2008 · C. Auxenfans, N. Builles, et al. · Pathologie Biologie · 21
The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder
2021 · Smitha Kumble, Amanda M. Levy, et al. · Human Mutation · 20
Involvement of germline DDX1–MYCN duplication in inherited nephroblastoma
2013 · Alice Fievet, Marc-Antoine Belaud-Rotureau, et al. · European Journal of Medical Genetics · 18
DNA repair functional analyses of NBN hypomorphic variants associated with NBN‐related infertility
2019 · Alice Fiévet, Dorine Bellanger, et al. · Human Mutation · 17
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Genomic landscape of liquid biopsy mutations in TP53 and DNA damage genes in cancer patients
2024 · Damien Vasseur, Ahmadreza Arbab, et al. · npj Precision Oncology · 16
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Mutational Landscape of DDR2 Gene in Lung Squamous Cell Carcinoma Using Next-generation Sequencing
2017 · Charles Ricordel, Alexandra Lespagnol, et al. · Clinical Lung Cancer · 15
Prevalence of Pathogenic Variants of FAN1 in More Than 5000 Patients Assessed for Genetic Predisposition to Colorectal, Breast, Ovarian, or Other Cancers
2019 · Alice Fievet, Emmanuelle Mouret-Fourme, et al. · Gastroenterology · 8
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Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutations
2017 · Bruno Buecher, Antoine De Pauw, et al. · Familial Cancer · 7
Efficacy of maintenance olaparib plus bevacizumab in patients with newly diagnosed advanced ovarian cancer according to BRCA mutation genotype in the phase III PAOLA-1/ENGOT-ov25 trial.
2022 · Sana Intidhar Labidi-Galy, Manuel Rodrigues, et al. · Journal of Clinical Oncology · 5
Deciphering dual clinical entities associated with TP53 pathogenic variants: Insights from 53,085 HBOC panel analyses in French laboratories
2025 · Edwige Kasper, Flavie Boulouard, et al. · International Journal of Cancer · 4
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Rôle du gène MBD4 dans un phénotype hypermutateur et dans la tumorigenèse
2018 · Manuel Rodrigues, Lenha Mobuchon, et al. · médecine/sciences · 2
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ATM Gene Mutation Detection Techniques and Functional Analysis
2017 · Guillaume Rieunier, Catherine Dubois D’Enghien, et al. · Methods in molecular biology · 2
Cancer risks for ATM variant heterozygotes
2026 · Yue Jiao, David E. Goldgar, et al. · Genetics in Medicine · 1
Works count: 48
Citation count: 747
H-index: 16
I10-index: 18
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