APC gene: database of germline and somatic mutations in human tumors and cell lines. - Christophe Béroud; Thierry Soussi (Nucleic Acids Res., 1996)

p53 gene mutation: software and database. - Christophe Béroud; Frédérique Verdier; Thierry Soussi (Nucleic Acids Res., 1996)

Software and database for the analysis of mutations in the human FBN1 gene. - Gwenaëlle Collod; Christophe Béroud; Thierry Soussi; Claudine Junien; Catherine Boileau (Nucleic Acids Res., 1996)

p53 and APC gene mutations: software and databases. - Christophe Béroud; Thierry Soussi (Nucleic Acids Res., 1997)

Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene. - Gwenaëlle Collod-Béroud; Christophe Béroud; Lesley Adès; Cheryl Black; Maureen Boxer; David J. H. Brock; Maurice Godfrey; Caroline Hayward; Leena Karttunen; Dianna Milewicz; Leena Peltonen; Robert I. Richards; et al. (Nucleic Acids Res., 1997)

Software and database for the analysis of mutations in the human LDL receptor gene. - Mathilde Varret; Jean-Pierre Rabès; Gwenaëlle Collod-Béroud; Claudine Junien; Catherine Boileau; Christophe Béroud (Nucleic Acids Res., 1997)

Software and database for the analysis of mutations in the VHL gene. - Christophe Béroud; Dominique Joly; Catherine Gallou; Frédéric Staroz; Marie Thérèse Orfanelli; Claudine Junien (Nucleic Acids Res., 1998)

p53 gene mutation: software and database. - Christophe Béroud; Thierry Soussi (Nucleic Acids Res., 1998)

Marfan Database (third edition): new mutations and new routines for the software. - Gwenaëlle Collod-Béroud; Christophe Béroud; Lesley Adès; Cheryl Black; Maureen Boxer; David J. H. Brock; Katherine J. Holman; Anne De Paepe; Uta Francke; Ulrich Grau; Caroline Hayward; Hanns-Georg Klein; et al. (Nucleic Acids Res., 1998)

Software and database for the analysis of mutations in the human WT1 gene. - Cécile Jeanpierre; Christophe Béroud; Patrick Niaudet; Claudine Junien (Nucleic Acids Res., 1998)

APC gene: database of germline and somatic mutations in human tumors and cell lines. - Pierre Laurent-Puig; Christophe Béroud; Thierry Soussi (Nucleic Acids Res., 1998)

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis. - Mathilde Varret; Jean-Pierre Rabès; Rochelle Thiart; Maritha J. Kotze; Heike Baron; Ana Cenarro; Olivier Descamps; Margit Ebhardt; Jean-Claude Hondelijn; Gert M. Kostner; Yasuko Miyake; Miguel Pocovi; et al. (Nucleic Acids Res., 1998)

Hydrophobic pulses predict transmembrane helix irregularities and channel transmembrane units. - Damien Paulet; Mireille Claustres; Christophe Béroud (BMC Bioinform., 2011)

VarioML framework for comprehensive variation data representation and exchange. - Myles Byrne; Ivo F. A. C. Fokkema; Owen Lancaster; Tomasz Adamusiak; Anni Ahonen-Bishopp; David Atlan; Christophe Béroud; Michael Cornell; Raymond Dalgleish; Andrew Devereau; George P. Patrinos; Morris A. Swertz; et al. (BMC Bioinform., 2012)

Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases. - Sandrine Caputo; Louisa Benboudjema; Olga Sinilnikova; Etienne Rouleau; Christophe Béroud; Rosette Lidereau (Nucleic Acids Res., 2012)

UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families. - Philippe Grandval; Aurélie J. Fabre; Pascaline Gaildrat; Stéphanie Baert-Desurmont; Marie-Pierre Buisine; Anthony Ferrari; Qing Wang; Christophe Béroud; Sylviane Olschwang (Database J. Biol. Databases Curation, 2013)

Dispelling myths about rare disease registry system development. - Matthew I. Bellgard; Christophe Béroud; Kay Parkinson; Tess Harris; Ségolène Aymé; Gareth Baynam; Tarun Weeramanthri; Hugh J. S. Dawkins; Adam Hunter (Source Code Biol. Medicine, 2013)

Correction: Dispelling myths about rare disease registry system development. - Matthew I. Bellgard; Christophe Béroud; Kay Parkinson; Tess Harris; Ségolène Aymé; Gareth Baynam; Tarun Weeramanthri; Hugh J. S. Dawkins; Adam Hunter (Source Code Biol. Medicine, 2014)

VarAFT: a variant annotation and filtration system for human next generation sequencing data. - Jean-Pierre Desvignes; Marc Bartoli; Valérie Delague; Martin Krahn; Morgane Miltgen; Christophe Béroud; David Salgado (Nucleic Acids Res., 2018)

The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. - David Salgado; Irina M. Armean; Michael Baudis; Sergi Beltran; Salvador Capella-Gutiérrez; Denise Carvalho-Silva; Victoria Dominguez Del Angel; Joaquín Dopazo; Laura I. Furlong; Bo Gao; Leyla Jael García Castro; Dietlind Gerloff; et al. (F1000Research, 2020)

Protein domains provide a new layer of information for classifying human variations in rare diseases. - Mélanie Corcuff; Marc Garibal; Jean-Pierre Desvignes; Céline Guien; Coralie Grattepanche; Gwenaëlle Collod-Béroud; Estelle Ménoret; David Salgado; Christophe Béroud (Frontiers Bioinform., 2023)