Jean Muller
Jean Muller
Associate Professor of Genetics, Strasbourg University, Inserm, UMR_S 1112
Bestätigte E-Mail-Adresse bei - Startseite
Zitiert von
Zitiert von
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
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
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
The ecoresponsive genome of Daphnia pulex
JK Colbourne, ME Pfrender, D Gilbert, WK Thomas, A Tucker, TH Oakley, ...
Science 331 (6017), 555-561, 2011
Functional and Evolutionary Insights from the Genomes of Three Parasitoid Nasonia Species
JH Werren, S Richards, CA Desjardins, O Niehuis, J Gadau, ...
Science 327 (5963), 343-348, 2010
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
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
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
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
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
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
AnnotSV: an integrated tool for structural variations annotation
V Geoffroy, Y Herenger, A Kress, C Stoetzel, A Piton, H Dollfus, J Muller
Bioinformatics 34 (20), 3572-3574, 2018
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
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
Alström Syndrome: Mutation Spectrum of ALMS1
JD Marshall, J Muller, GB Collin, G Milan, SF Kingsmore, D Dinwiddie, ...
Human mutation 36 (7), 660-668, 2015
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
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 Hellé, ...
Human genetics 127, 583-593, 2010
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
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
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
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