Christophe Béroud

According to our database, Christophe Béroud authored at least 21 papers between 1996 and 2023.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2023

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., May, 2023

2020

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, Ivo Gut, Attila Gyenesei, Nina Habermann, John M. Hancock, Marc Hanauer, Eivind Hovig, Lennart F. Johansson, Thomas Keane, Jan Korbel, Katharina B. Lauer, Steve Laurie, Brane Leskosek, David Lloyd, Tomàs Marquès-Bonet, Hailiang Mei, Katalin Monostory, Janet Piñero, Krzysztof Poterlowicz, Ana Rath, Pubudu Samarakoon, Ferran Sanz, Gary Saunders, Daoud Sie, Morris A. Swertz, Kirill Tsukanov, Alfonso Valencia, Marko Vidak, Cristina Yenyxe González, Bauke Ylstra, Christophe Béroud

F1000Research, 2020

2018

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

2014

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

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

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

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

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, Peter E. M. Taschner, Gudmundur A. Thorisson, Mauno Vihinen, Anthony J. Brookes, Juha Muilu

BMC Bioinform., 2012

2011

Hydrophobic pulses predict transmembrane helix irregularities and channel transmembrane units.

Damien Paulet, Mireille Claustres, Christophe Béroud

BMC Bioinform., 2011

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, Hartmut Schmidt, Helena Schmidt, Herbert Schuster, Manfred Stuhrmann, Taku Yamamura, Claudine Junien, Christophe Béroud, Catherine Boileau

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

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

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, Wanguo Liu, Lieve Nuytinck, Leena Peltonen, Ana Beatriz Alvarez Perez, Terhi Rantamäki, Claudine Junien, Catherine Boileau

Nucleic Acids Res., 1998

p53 gene mutation: software and database.

Christophe Béroud, Thierry Soussi

Nucleic Acids Res., 1998

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

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

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, Mei Wang, Claudine Junien, Catherine Boileau

Nucleic Acids Res., 1997

p53 and APC gene mutations: software and databases.

Christophe Béroud, Thierry Soussi

Nucleic Acids Res., 1997

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 gene mutation: software and database.

Christophe Béroud, Frédérique Verdier, Thierry Soussi

Nucleic Acids Res., 1996

APC gene: database of germline and somatic mutations in human tumors and cell lines.

Christophe Béroud, Thierry Soussi

Nucleic Acids Res., 1996