PubRank

Jean Muller

Author PubWeight™ 106.41‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Enterotypes of the human gut microbiome. Nature 2011 24.36
2 STRING 8--a global view on proteins and their functional interactions in 630 organisms. Nucleic Acids Res 2008 20.62
3 The STRING database in 2011: functional interaction networks of proteins, globally integrated and scored. Nucleic Acids Res 2010 18.73
4 The ecoresponsive genome of Daphnia pulex. Science 2011 6.55
5 Functional and evolutionary insights from the genomes of three parasitoid Nasonia species. Science 2010 5.56
6 eggNOG: automated construction and annotation of orthologous groups of genes. Nucleic Acids Res 2007 4.84
7 eggNOG v3.0: orthologous groups covering 1133 organisms at 41 different taxonomic ranges. Nucleic Acids Res 2011 3.94
8 BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus. Nat Genet 2006 2.68
9 Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome. Am J Hum Genet 2006 2.44
10 Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes. J Med Genet 2012 1.79
11 PipeAlign: A new toolkit for protein family analysis. Nucleic Acids Res 2003 1.78
12 Orthology prediction methods: a quality assessment using curated protein families. Bioessays 2011 1.56
13 Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18). J Med Genet 2013 1.32
14 DPY19L2 deletion as a major cause of globozoospermia. Am J Hum Genet 2011 1.20
15 Highly sensitive diagnosis of 43 monogenic forms of diabetes or obesity through one-step PCR-based enrichment in combination with next-generation sequencing. Diabetes Care 2013 1.18
16 Defective membrane remodeling in neuromuscular diseases: insights from animal models. PLoS Genet 2012 1.05
17 Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots. Hum Mol Genet 2012 1.05
18 ICDS database: interrupted CoDing sequences in prokaryotic genomes. Nucleic Acids Res 2006 1.04
19 Next generation sequencing for molecular diagnosis of neuromuscular diseases. Acta Neuropathol 2012 1.03
20 Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism. Eur J Hum Genet 2006 0.98
21 Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects. Am J Hum Genet 2011 0.93
22 MSV3d: database of human MisSense Variants mapped to 3D protein structure. Database (Oxford) 2012 0.92
23 Identifying single copy orthologs in Metazoa. PLoS Comput Biol 2011 0.89
24 A nitrile hydratase in the eukaryote Monosiga brevicollis. PLoS One 2008 0.87
25 SM2PH-db: an interactive system for the integrated analysis of phenotypic consequences of missense mutations in proteins involved in human genetic diseases. Hum Mutat 2010 0.85
26 KD4v: Comprehensible Knowledge Discovery System for Missense Variant. Nucleic Acids Res 2012 0.85
27 [Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]. Med Sci (Paris) 2006 0.79
28 The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey. J Hum Genet 2015 0.77
29 Autosomal mutations and human spermatogenic failure. Biochim Biophys Acta 2012 0.76