Jean Muller
Jean Muller
Laboratoire de Génétique Médicale U1112
Adresse e-mail validée de unistra.fr - Page d'accueil
Titre
Citée par
Citée par
Année
Enterotypes of the human gut microbiome
M Arumugam, J Raes, E Pelletier, D Le Paslier, T Yamada, DR Mende, ...
nature 473 (7346), 174-180, 2011
52202011
The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored
D Szklarczyk, A Franceschini, M Kuhn, M Simonovic, A Roth, P Minguez, ...
Nucleic acids research 39 (suppl_1), D561-D568, 2010
31332010
STRING 8—a global view on proteins and their functional interactions in 630 organisms
LJ Jensen, M Kuhn, M Stark, S Chaffron, C Creevey, J Muller, T Doerks, ...
Nucleic acids research 37 (suppl_1), D412-D416, 2009
23282009
The ecoresponsive genome of Daphnia pulex
JK Colbourne, ME Pfrender, D Gilbert, WK Thomas, A Tucker, TH Oakley, ...
Science 331 (6017), 555-561, 2011
11112011
eggNOG v3. 0: orthologous groups covering 1133 organisms at 41 different taxonomic ranges
S Powell, D Szklarczyk, K Trachana, A Roth, M Kuhn, J Muller, R Arnold, ...
Nucleic acids research 40 (D1), D284-D289, 2012
4912012
eggNOG: automated construction and annotation of orthologous groups of genes
LJ Jensen, P Julien, M Kuhn, C von Mering, J Muller, T Doerks, P Bork
Nucleic acids research 36 (suppl_1), D250-D254, 2007
3632007
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus
C Stoetzel, V Laurier, EE Davis, J Muller, S Rix, JL Badano, CC Leitch, ...
Nature genetics 38 (5), 521-524, 2006
2942006
Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome
C Stoetzel, J Muller, V Laurier, EE Davis, NA Zaghloul, S Vicaire, ...
The American Journal of Human Genetics 80 (1), 1-11, 2007
2612007
eggNOG v2. 0: extending the evolutionary genealogy of genes with enhanced non-supervised orthologous groups, species and functional annotations
J Muller, D Szklarczyk, P Julien, I Letunic, A Roth, M Kuhn, S Powell, ...
Nucleic acids research 38 (suppl_1), D190-D195, 2010
2482010
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing
C Redin, B Gérard, J Lauer, Y Herenger, J Muller, A Quartier, ...
Journal of medical genetics 51 (11), 724-736, 2014
1952014
DPY19L2 deletion as a major cause of globozoospermia
I Koscinski, E ElInati, C Fossard, C Redin, J Muller, JV de la Calle, ...
The American Journal of Human Genetics 88 (3), 344-350, 2011
1552011
PipeAlign: A new toolkit for protein family analysis
F Plewniak, L Bianchetti, Y Brelivet, A Carles, F Chalmel, O Lecompte, ...
Nucleic acids research 31 (13), 3829-3832, 2003
1382003
Orthology prediction methods: a quality assessment using curated protein families
K Trachana, TA Larsson, S Powell, WH Chen, T Doerks, J Muller, P Bork
Bioessays 33 (10), 769-780, 2011
1252011
Exome sequencing of Bardet–Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
S Scheidecker, C Etard, NW Pierce, V Geoffroy, E Schaefer, J Muller, ...
Journal of medical genetics 51 (2), 132-136, 2014
1222014
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes
C Redin, S Le Gras, O Mhamdi, V Geoffroy, C Stoetzel, MC Vincent, ...
Journal of medical genetics 49 (8), 502-512, 2012
1172012
Sequence and comparative genomic analysis of actin-related proteins
J Muller, Y Oma, L Vallar, E Friederich, O Poch, B Winsor
Molecular biology of the cell 16 (12), 5736-5748, 2005
1152005
Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease
J Muller, C Stoetzel, MC Vincent, CC Leitch, V Laurier, JM Danse, S Helle, ...
Human genetics 127 (5), 583-593, 2010
1042010
Next generation sequencing for molecular diagnosis of neuromuscular diseases
N Vasli, J Böhm, S Le Gras, J Muller, C Pizot, B Jost, A Echaniz-Laguna, ...
Acta neuropathologica 124 (2), 273-283, 2012
962012
Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects
A Bloch-Zupan, X Jamet, C Etard, V Laugel, J Muller, V Geoffroy, ...
The American Journal of Human Genetics 89 (6), 773-781, 2011
862011
Mutations in SDCCAG8/NPHP10 cause Bardet-Biedl syndrome and are associated with penetrant renal disease and absent polydactyly
E Schaefer, A Zaloszyc, J Lauer, M Durand, F Stutzmann, ...
Molecular syndromology 1 (6), 273-281, 2010
842010
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20