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Jean Muller

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Chemicals & Drugs

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Bardet-Biedl Syndrome

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Oligonucleotide Array Sequence Analysis

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Publications

TOP 3
Elias El Inati; Jean Muller; Stéphane Viville
Autosomal mutations and human spermatogenic failure.
Claire Redin; Corinne Stoetzel; Marianne Till; Alain Verloes; Marie-Claire Vincent; Ines Ouertani; Florence Petit; Habiba Bouhamed Chaabouni; Pietro Chiurazzi; Hélène Dollfus; Véronique Geoffroy; Bernard Jost; Didier Lacombe; Stéphanie Le Gras; Jean-Louis Mandel; Oussema Mhamdi; Jean Muller
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.
Nasim Vasli; Serge Vicaire; Rafaelle Bernard; Valérie Biancalana; Johann Böhm; Jamel Chelly; Andoni Echaniz-Laguna; Bernard Jost; Vincent Laugel; Stéphanie Le Gras; Nicolas Levy; Jean-Louis Mandel; Jean Muller; Cécile Pizot; Frédéric Plewniak; Christine Tranchant; Jocelyn Laporte
Next generation sequencing for molecular diagnosis of neuromuscular diseases.

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All Publications

2012: Elias El Inati; Jean Muller; Stéphane Viville
Autosomal mutations and human spermatogenic failure.
Biochimica et biophysica acta 2012;1822(12):1873-9.
2012: Claire Redin; Corinne Stoetzel; Marianne Till; Alain Verloes; Marie-Claire Vincent; Ines Ouertani; Florence Petit; Habiba Bouhamed Chaabouni; Pietro Chiurazzi; Hélène Dollfus; Véronique Geoffroy; Bernard Jost; Didier Lacombe; Stéphanie Le Gras; Jean-Louis Mandel; Oussema Mhamdi; Jean Muller
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.
Journal of medical genetics 2012;49(8):502-12.
2012: Nasim Vasli; Serge Vicaire; Rafaelle Bernard; Valérie Biancalana; Johann Böhm; Jamel Chelly; Andoni Echaniz-Laguna; Bernard Jost; Vincent Laugel; Stéphanie Le Gras; Nicolas Levy; Jean-Louis Mandel; Jean Muller; Cécile Pizot; Frédéric Plewniak; Christine Tranchant; Jocelyn Laporte
Next generation sequencing for molecular diagnosis of neuromuscular diseases.
Acta neuropathologica 2012;124(2):273-83.
2012: Tien-Dao Luu; Luc Moulinier; Jean Muller; Odile Lecompte; Benjamin Linard; Olivier Poch; Laetitia Poidevin; Wolfgang Raffelsberger; Raymond Ripp; Alin Rusu; Julie D Thompson; Vincent Walter; Nicolas Wicker; Hoan Nguyen
KD4v: Comprehensible Knowledge Discovery System for Missense Variant.
Nucleic acids research 2012;40(Web Server issue):W71-5.
2012: Belinda Cowling; Jean Muller; Anne Toussaint; Jocelyn Laporte
Defective membrane remodeling in neuromuscular diseases: insights from animal models.
PLoS genetics 2012;8(4):e1002595.
2012: Tien-Dao Luu; Luc Moulinier; Jean Muller; Olivier Poch; Raymond Ripp; Alin-Mihai Rusu; Julie D Thompson; Thierry Toursel; Vincent Walter; Hoan Nguyen
MSV3d: database of human MisSense Variants mapped to 3D protein structure.
Database : the journal of biological databases and curation 2012;2012():bas018.
2012: Sean Powell; Thomas Rattei; Alexander Roth; Damian Szklarczyk; Kalliopi Trachana; Christian von Mering; Tobias Doerks; Lars Jensen; Michael Kuhn; Ivica Letunic; Jean Muller; Roland Arnold; Peer Bork
eggNOG v3.0: orthologous groups covering 1133 organisms at 41 different taxonomic ranges.
Nucleic acids research 2012;40(Database issue):D284-9.
2011: Agnès Bloch-Zupan; Christelle Etard; Véronique Geoffroy; Xavier Jamet; Virginie Laugel; Vincent Marion; Jean Muller; Valérie Pelletier; Olivier Poch; Corinne Stoetzel; Uwe Strahle; Jean-Pierre Strauss; Hélène Dollfus
Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects.
American journal of human genetics 2011;89(6):773-81.
2011: Kalliopi Trachana; Wei-Hua Chen; Tobias Doerks; Tomas A Larsson; Jean Muller; Sean Powell; Peer Bork
Orthology prediction methods: a quality assessment using curated protein families.
BioEssays : news and reviews in molecular, cellular and developmental biology 2011;33(10):769-80.
2010: Jean Muller; Corinne Stoetzel; M C Vincent; Carmen C Leitch; Virginie Laurier; Jean-Marc Danse; S Hellé; V Marion; V Bennouna-Greene; S Vicaire; A Megarbane; Josseline Kaplan; V Drouin-Garraud; M Hamdani; Sabine Sigaudy; C Francannet; J Roume; Pierre Bitoun; A Goldenberg; N Philip; S Odent; J Green; Mireille Cossée; Erica E Davis; Nicholas Katsanis; Dominique Bonneau; Alain Verloes; Olivier Poch; Jean-Louis Mandel; Hélène Dollfus
Identification of 28 novel mutations in the Bardet-Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease.
Human genetics 2010;127(5):583-93.
2010: Anne Friedrich; Nicolas Garnier; Nicolas Gagnière; Hoan Nguyen; Laurent-Philippe Albou; Valérie Biancalana; Emmanuel Bettler; Gilbert Deléage; Odile Lecompte; Jean Muller; Dino Moras; Jean-Louis Mandel; Thierry Toursel; Luc Moulinier; Olivier Poch
SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases.
Human mutation 2010;31(2):127-35.
2010: John H Werren; Stephen Richards; Christopher A Desjardins; Oliver Niehuis; Jürgen Gadau; John K Colbourne; John H Werren; Stephen Richards; Christopher A Desjardins; Oliver Niehuis; Jürgen Gadau; John K Colbourne; Leo W Beukeboom; Claude Desplan; Christine G Elsik; Cornelis J P Grimmelikhuijzen; Paul Kitts; Jeremy A Lynch; Terence Murphy; Deodoro C S G Oliveira; Christopher D Smith; Louis van de Zande; Kim C Worley; Evgeny M Zdobnov; Maarten Aerts; Stefan Albert; Victor H Anaya; Juan M Anzola; Angel R Barchuk; Susanta K Behura; Agata N Bera; May R Berenbaum; Rinaldo C Bertossa; Márcia M G Bitondi; Seth R Bordenstein; Peer Bork; Erich Bornberg-Bauer; Marleen Brunain; Giuseppe Cazzamali; Lesley Chaboub; Joseph Chacko; Dean Chavez; Christopher P Childers; Jeong-Hyeon Choi; Michael E Clark; Charles Claudianos; Rochelle A Clinton; Andrew G Cree; Alexandre S Cristino; Phat M Dang; Alistair C Darby; Dirk C de Graaf; Bart Devreese; Huyen H Dinh; Rachel Edwards; Navin Elango; Eran Elhaik; Olga Ermolaeva; Jay Evans; Sylvain Foret; Gerald R Fowler; Daniel Gerlach; Joshua D Gibson; Donald G Gilbert; Dan Graur; Stefan Gründer; Darren E Hagen; Yi Han; Frank Hauser; Da Hultmark; Henry C Hunter; Gregory D D Hurst; Shalini N Jhangian; Huaiyang Jiang; Reed McIntyre Johnson; Andrew Ken Jones; Thomas Junier; Tatsuhiko Kadowaki; Albert Kamping; Yuri Kapustin; Bobak Kechavarzi; Jaebum Kim; Jay Kim; Boris Kiryutin; Tosca Koevoets; Christie L Kovar; Evgenia V Kriventseva; Robert Kucharski; Heewook Lee; Sandra L Lee; Kristin Lees; Lora R Lewis; David W Loehlin; John M Logsdon; Jacqueline A Lopez; Ryan J Lozado; Donna Maglott; Ryszard Maleszka; Anoop Mayampurath; Danielle J Mazur; Marcella A McClure; Andrew D Moore; Margaret B Morgan; Jean Muller; Monica C Munoz-Torres; Donna M Muzny; Lynne V Nazareth; Susanne Neupert; Ngoc B Nguyen; Francis M F Nunes; John G Oakeshott; Geoffrey O Okwuonu; Bart A Pannebakker; Vikas R Pejaver; Zuogang Peng; Stephen C Pratt; Reinhard Predel; Ling-Ling Pu; Hilary Ranson; Rhitoban Raychoudhury; Andreas Rechtsteiner; Justin T Reese; Jeffrey G Reid; Megan Riddle; Hugh M Robertson; Jeanne Romero-Severson; Miriam Rosenberg; Timothy B Sackton; David B Sattelle; Helge Schlüns; Thomas Schmitt; Martina Schneider; Andreas Schüler; Andrew M Schurko; David M Shuker; Zilá L P Simões; Saurabh Sinha; Zachary Smith; Victor Solovyev; Alexandre Souvorov; Andreas Springauf; Elisabeth Stafflinger; Deborah E Stage; Mario Stanke; Yoshiaki Tanaka; Arndt Telschow; Carol Trent; Selina Vattathil; Eveline C Verhulst; Lumi Viljakainen; Kevin W Wanner; Robert Waterhouse; James B Whitfield; Timothy E Wilkes; Michael Williamson; Judith H Willis; Florian Wolschin; Stefan Wyder; Takuji Yamada; Soojin V Yi; Courtney N Zecher; Lan Zhang; Richard A Gibbs
Functional and evolutionary insights from the genomes of three parasitoid Nasonia species.
Science (New York, N.Y.) 2010;327(5963):343-8.
2010: Jean Muller; Christopher J Creevey; Julie D Thompson; Detlev Arendt; Peer Bork
AQUA: automated quality improvement for multiple sequence alignments.
Bioinformatics (Oxford, England) 2010;26(2):263-5.
2010: Jean Muller; D Szklarczyk; P Julien; Ivica Letunic; A Roth; M Kuhn; S Powell; Christian von Mering; Tobias Doerks; Lars Jensen; Peer Bork
eggNOG v2.0: extending the evolutionary genealogy of genes with enhanced non-supervised orthologous groups, species and functional annotations.
Nucleic acids research 2010;38(Database issue):D190-5.
2009: G Vetter; A Le Béchec; Jean Muller; A Muller; M Moes; M Yatskou; Z Al Tanoury; O Poch; L Vallar; E Friederich
Time-resolved analysis of transcriptional events during SNAI1-triggered epithelial to mesenchymal transition.
Biochemical and biophysical research communications 2009;385(4):485-91.
2009: Lars J Jensen; Michael Kuhn; Manuel Stark; Samuel Chaffron; Chris Creevey; Jean Muller; Tobias Doerks; Philippe Julien; Alexander Roth; Milan Simonovic; Peer Bork; Christian von Mering
STRING 8--a global view on proteins and their functional interactions in 630 organisms.
Nucleic acids research 2009;37(Database issue):D412-6.
2008: J A J Becker; Katia Befort; C Blad; Dominique Filliol; A Ghate; D Dembele; C Thibault; M Koch; Jean Muller; A Lardenois; Olivier Poch; Jerome Becker
Transcriptome analysis identifies genes with enriched expression in the mouse central extended amygdala.
Neuroscience 2008;156(4):950-65.
2008: K Befort; D Filliol; A Ghate; E Darcq; Audrey Matifas; Jean Muller; A Lardenois; C Thibault; D Dembele; Julie LE MERRER; J A J Becker; O Poch; Jerome Becker
Mu-opioid receptor activation induces transcriptional plasticity in the central extended amygdala.
The European journal of neuroscience 2008;27(11):2973-84.
2008: Konrad Foerstner; Tobias Doerks; Jean Muller; Jeroen Raes; Peer Bork
A nitrile hydratase in the eukaryote Monosiga brevicollis.
PloS one 2008;3(12):e3976.
2008: Katia Befort; Dominique Filliol; E Darcq; A Ghate; Audrey Matifas; A Lardenois; Jean Muller; Christelle Thibault; D Dembele; Olivier Poch; Brigitte L Kieffer
Gene expression is altered in the lateral hypothalamus upon activation of the mu opioid receptor.
Annals of the New York Academy of Sciences 2008;1129():175-84.
2008: Lars Jensen; Philippe Julien; Michael Kuhn; Christian von Mering; Jean Muller; Tobias Doerks; Peer Bork
eggNOG: automated construction and annotation of orthologous groups of genes.
Nucleic acids research 2008;36(Database issue):D250-4.
2007: Jean Muller; André Mehlen; Guillaume Vetter; Mikalai Yatskou; Arnaud Muller; Frédéric Chalmel; Olivier Poch; Evelyne Friederich; Laurent Vallar
Design and evaluation of Actichip, a thematic microarray for the study of the actin cytoskeleton.
BMC genomics 2007;8():294.
2007: Corinne Stoetzel; Jean Muller; Virginie Laurier; Erica E Davis; Norann Zaghloul; Serge Vicaire; Cecile Jacquelin; Frédéric Plewniak; Carmen C Leitch; Pierre Sarda; Christian Hamel; T J L de Ravel; Richard Alan Lewis; Evelyne Friederich; Christelle Thibault; Jean-Marc Danse; Alain Verloes; Dominique Bonneau; Nicholas Katsanis; Olivier Poch; Jean-Louis Mandel; Hélène Dollfus
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome.
American journal of human genetics 2007;80(1):1-11.
2006: Hélène Dollfus; Jean Muller; Corinne Stoetzel; Virginie Laurier; Dominique Bonneau; André Mégarbané; Olivier Poch; Jean-Louis Mandel
[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)].
Médecine sciences : M/S 2006;22(11):901-4.
2006: Virginie Laurier; Corinne Stoetzel; Jean Muller; Christelle Thibault; Sandra Corbani; Nadine Jalkh; Nabiha Salem; Eliane Chouery; Olivier Poch; Serge Licaire; Jean-Marc Danse; Patrizia Amati-Bonneau; Dominique Bonneau; André Mégarbané; Jean-Louis Mandel; Hélène Dollfus
Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism.
European journal of human genetics : EJHG 2006;14(11):1195-203.
2006: Corinne Stoetzel; Virginie Laurier; Erica E Davis; Jean Muller; Suzanne Rix; José L Badano; Carmen C Leitch; Nabiha Salem; Eliane Chouery; Sandra Corbani; Nadine Jalk; Serge Vicaire; Pierre Sarda; Christian Hamel; Didier Lacombe; Muriel Holder; Sylvie Odent; Susan Holder; Alice S Brooks; Nursel H Elcioglu; Eduardo D Silva; Eduardo Da Silva; Béatrice Rossillion; Sabine Sigaudy; Thomy J L de Ravel; Richard Alan Lewis; Bruno Leheup; Alain Verloes; Patrizia Amati-Bonneau; André Mégarbané; Olivier Poch; Dominique Bonneau; Philip L Beales; Jean-Louis Mandel; Nicholas Katsanis; Hélène Dollfus
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
Nature genetics 2006;38(5):521-4.
2006: Emmanuel Perrodou; Caroline Deshayes; Jean Muller; Christine Schaeffer; Alain Van Dorsselaer; Raymond Ripp; Olivier Poch; Reyrat Jean-Marc; Odile Lecompte
ICDS database: interrupted CoDing sequences in prokaryotic genomes.
Nucleic acids research 2006;34(Database issue):D338-43.
2005: Jean Muller; Yukako Oma; Laurent Vallar; Evelyne Friederich; Olivier Poch; Barbara Winsor
Sequence and comparative genomic analysis of actin-related proteins.
Molecular biology of the cell 2005;16(12):5736-48.
2005: Frédéric Chalmel; Aurélie Lardenois; julie thompson; Jean Muller; José-Alain Sahel; Thierry Léveillard; Olivier Poch
GOAnno: GO annotation based on multiple alignment.
Bioinformatics (Oxford, England) 2005;21(9):2095-6.
2003: Frédéric Plewniak; Laurent Bianchetti; Yann Brelivet; Annaïck Carles; Frédéric Chalmel; Odile Lecompte; Thiebaut Mochel; Luc Moulinier; Arnaud Muller; Jean Muller; Véronique Prigent; Raymond Ripp; Jean-Claude Thierry; julie thompson; Nicolas Wicker; Olivier Poch
PipeAlign: A new toolkit for protein family analysis.
Nucleic acids research 2003;31(13):3829-32.