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2020 – today
- 2023
[j20]Mélanie Corcuff, Marc Garibal, Jean-Pierre Desvignes, Céline Guien
, Coralie Grattepanche, Gwenaëlle Collod-Béroud, Estelle Ménoret, David Salgado, Christophe Béroud:
Protein domains provide a new layer of information for classifying human variations in rare diseases. Frontiers Bioinform. 3 (2023)- 2020
- [i1]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:
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research. F1000Research 9: 1229 (2020)
2010 – 2019
- 2018
- [j19]Jean-Pierre Desvignes, Marc Bartoli, Valérie Delague, Martin Krahn, Morgane Miltgen, Christophe Béroud, David Salgado:
VarAFT: a variant annotation and filtration system for human next generation sequencing data. Nucleic Acids Res. 46(Webserver-Issue): W545-W553 (2018) - 2014
- [j18]Matthew I. Bellgard, Christophe Béroud, Kay Parkinson, Tess Harris, Ségolène Aymé, Gareth Baynam, Tarun Weeramanthri, Hugh J. S. Dawkins, Adam Hunter:
Correction: Dispelling myths about rare disease registry system development. Source Code Biol. Medicine 9: 4 (2014) - 2013
- [j17]Philippe Grandval, Aurélie J. Fabre, Pascaline Gaildrat, Stéphanie Baert-Desurmont, Marie-Pierre Buisine, Anthony Ferrari, Qing Wang, Christophe Béroud, Sylviane Olschwang:
UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families. Database J. Biol. Databases Curation 2013 (2013) - [j16]Matthew I. Bellgard, Christophe Béroud, Kay Parkinson, Tess Harris, Ségolène Aymé, Gareth Baynam, Tarun Weeramanthri, Hugh J. S. Dawkins, Adam Hunter:
Dispelling myths about rare disease registry system development. Source Code Biol. Medicine 8: 21 (2013) - 2012
- [j15]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:
VarioML framework for comprehensive variation data representation and exchange. BMC Bioinform. 13: 254 (2012) - [j14]Sandrine Caputo, Louisa Benboudjema, Olga Sinilnikova, Etienne Rouleau, Christophe Béroud, Rosette Lidereau:
Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases. Nucleic Acids Res. 40(Database-Issue): 992-1002 (2012) - 2011
- [j13]Damien Paulet, Mireille Claustres, Christophe Béroud:
Hydrophobic pulses predict transmembrane helix irregularities and channel transmembrane units. BMC Bioinform. 12: 135 (2011)
1990 – 1999
- 1998
- [j12]Christophe Béroud, Thierry Soussi:
p53 gene mutation: software and database. Nucleic Acids Res. 26(1): 200-204 (1998) - [j11]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:
Marfan Database (third edition): new mutations and new routines for the software. Nucleic Acids Res. 26(1): 229-233 (1998) - [j10]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:
LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis. Nucleic Acids Res. 26(1): 248-252 (1998) - [j9]Christophe Béroud, Dominique Joly, Catherine Gallou, Frédéric Staroz, Marie Thérèse Orfanelli, Claudine Junien:
Software and database for the analysis of mutations in the VHL gene. Nucleic Acids Res. 26(1): 256-258 (1998) - [j8]Pierre Laurent-Puig, Christophe Béroud, Thierry Soussi:
APC gene: database of germline and somatic mutations in human tumors and cell lines. Nucleic Acids Res. 26(1): 269-270 (1998) - [j7]Cécile Jeanpierre, Christophe Béroud, Patrick Niaudet, Claudine Junien:
Software and database for the analysis of mutations in the human WT1 gene. Nucleic Acids Res. 26(1): 271-274 (1998) - 1997
- [j6]Christophe Béroud, Thierry Soussi:
p53 and APC gene mutations: software and databases. Nucleic Acids Res. 25(1): 138 (1997) - [j5]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:
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene. Nucleic Acids Res. 25(1): 147-150 (1997) - [j4]Mathilde Varret, Jean-Pierre Rabès, Gwenaëlle Collod-Béroud, Claudine Junien, Catherine Boileau, Christophe Béroud:
Software and database for the analysis of mutations in the human LDL receptor gene. Nucleic Acids Res. 25(1): 172-180 (1997) - 1996
- [j3]Christophe Béroud, Thierry Soussi:
APC gene: database of germline and somatic mutations in human tumors and cell lines. Nucleic Acids Res. 24(1): 121-124 (1996) - [j2]Gwenaëlle Collod, Christophe Béroud, Thierry Soussi, Claudine Junien, Catherine Boileau:
Software and database for the analysis of mutations in the human FBN1 gene. Nucleic Acids Res. 24(1): 137-140 (1996) - [j1]Christophe Béroud, Frédérique Verdier, Thierry Soussi:
p53 gene mutation: software and database. Nucleic Acids Res. 24(1): 147-150 (1996)
Coauthor Index
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