Bernard Leroy
Paris, France
Last Updated: 09/26/2026
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Found 13 publications
Low-penetrance TP53 variants are mainly hypomorphic: an underestimated issue with high clinical significance.
Journal: NPJ genomic medicine
Published: September 20, 2025
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots.
The Broad Spectrum of TP53 Mutations in CLL: Evidence of Multiclonality and Novel Mutation Hotspots.
Journal: Human mutation
Published: December 20, 2022
TP53_PROF: a machine learning model to predict impact of missense mutations in TP53.
Journal: Briefings in bioinformatics
Published: September 06, 2021
Comprehensive assessment of TP53 loss of function using multiple combinatorial mutagenesis libraries.
Journal: Scientific reports
Published: April 15, 2020
Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.
Journal: Cell death and differentiation
Published: March 24, 2020
High prevalence of cancer-associated TP53 variants in the gnomAD database: A word of caution concerning the use of variant filtering.
Journal: Human mutation
Published: October 17, 2018
Seshat: A Web service for accurate annotation, validation, and analysis of TP53 variants generated by conventional and next-generation sequencing.
Journal: Human mutation
Published: January 12, 2018
Analysis of TP53 mutation status in human cancer cell lines: a reassessment.
Journal: Human mutation
Published: February 26, 2014
TP53 mutations in human cancer: database reassessment and prospects for the next decade.
Journal: Human mutation
Published: January 16, 2014
Recommendations for analyzing and reporting TP53 gene variants in the high-throughput sequencing era.
Journal: Human mutation
Published: December 10, 2013
The TP53 website: an integrative resource centre for the TP53 mutation database and TP53 mutant analysis.
Journal: Nucleic acids research
Published: November 20, 2012
Last Updated: 09/26/2026