Jean Muller

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Olivier POCHCSTB ICube UMR7357Email yang diverifikasi di unistra.fr
Peer BorkDirector of EMBL HeidelbergEmail yang diverifikasi di embl.de
Geoffroy VéroniqueU1112 INSERMEmail yang diverifikasi di inserm.fr
Michael Kuhnresearch staff scientist & research coordinator in the lab of Peer Bork, EMBLEmail yang diverifikasi di embl.de
Lars Juhl JensenUniversity of CopenhagenEmail yang diverifikasi di cpr.ku.dk
Christian von MeringProfessor of Computational Biology, University of Zurich and Swiss Institute of BioinformaticsEmail yang diverifikasi di imls.uzh.ch
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUEmail yang diverifikasi di igbmc.fr
Stéphane VivilleUniversité de StrasbourgEmail yang diverifikasi di unistra.fr
Alexander RothUniversity of ZurichEmail yang diverifikasi di uzh.ch
Claire RedinMedigenome, Swiss Institute of Genomic Medicine, Geneva, SwitzerlandEmail yang diverifikasi di medigenome.ch
Ozlem OkutmanPhDEmail yang diverifikasi di unistra.fr
Milan SimonovićScientific programmer, University of ZürichEmail yang diverifikasi di imls.uzh.ch
Amelie PITONMCU-PH Lab of Genetic diagnosis CHU Strasbourg, Researcher at IGBMCEmail yang diverifikasi di igbmc.fr
Damian SzklarczykSIB Swiss Institute of Bioinformatics / University of ZurichEmail yang diverifikasi di isb-sib.ch
Philippe JulienCenter for Genomic Regulation (CRG - Barcelona)Email yang diverifikasi di unil.ch
Chris CreeveyProfessor of Computational Biology, Queen’s University BelfastEmail yang diverifikasi di qub.ac.uk
Pablo MinguezResearcher & Head of Bioinformatics Unit - IIS Fundación Jiménez Díaz (Madrid, Spain)Email yang diverifikasi di quironsalud.es
Dominique BonneauProfesseur de Génétique Médicale, Université d'AngersEmail yang diverifikasi di chu-angers.fr
Sean PowellIMBAEmail yang diverifikasi di imba.oeaw.ac.at
Luc MoulinierIngénieur de Recherche CNRSEmail yang diverifikasi di unistra.fr

Ikuti

Jean Muller

Associate Professor of Genetics, Strasbourg University, Inserm, UMR_S 1112

Email yang diverifikasi di unistra.fr - Beranda

Human genetics HTS/NGS Bioinformatics Evolution Ciliopathy


Judul Urutkan menurut kutipan Urutkan menurut tahun Urutkan menurut judul	Dikutip oleh Dikutip oleh	Tahun
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	8784	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	3960	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	2965	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	1443	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	945	2010
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	635	2007
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	633	2012
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	350	2006
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	347	2018
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	303	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	300	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	296	2010
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	232	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	171	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	166	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	154	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	152	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	149	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	147	2003
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family O Okutman, J Muller, Y Baert, M Serdarogullari, M Gultomruk, A Piton, ... Human molecular genetics 24 (19), 5581-5588, 2015	141	2015

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