PubRank

Willy Morelle

Author PubWeight™ 30.55‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Oligosaccharyltransferase-subunit mutations in nonsyndromic mental retardation. Am J Hum Genet 2008 1.82
2 Both IgA nephropathy and alcoholic cirrhosis feature abnormally glycosylated IgA1 and soluble CD89-IgA and IgG-IgA complexes: common mechanisms for distinct diseases. Kidney Int 2011 1.64
3 A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation. Hum Mol Genet 2007 1.40
4 Deletion of GEL2 encoding for a beta(1-3)glucanosyltransferase affects morphogenesis and virulence in Aspergillus fumigatus. Mol Microbiol 2005 1.33
5 Golgi function and dysfunction in the first COG4-deficient CDG type II patient. Hum Mol Genet 2009 1.32
6 Does O-GlcNAc play a role in neurodegenerative diseases? Expert Rev Proteomics 2005 1.30
7 TMEM165 deficiency causes a congenital disorder of glycosylation. Am J Hum Genet 2012 1.20
8 Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice. Hum Mol Genet 2008 1.20
9 Conserved oligomeric Golgi complex specifically regulates the maintenance of Golgi glycosylation machinery. Glycobiology 2011 1.15
10 O-GlcNAc glycosylation: a signal for the nuclear transport of cytosolic proteins? Int J Biochem Cell Biol 2005 1.13
11 Proteomics and glycomics analyses of N-glycosylated structures involved in Toxoplasma gondii--host cell interactions. Mol Cell Proteomics 2008 1.09
12 Galectin-4-regulated delivery of glycoproteins to the brush border membrane of enterocyte-like cells. Traffic 2009 1.05
13 Rhamnogalacturonan II structure shows variation in the side chains monosaccharide composition and methylation status within and across different plant species. Plant J 2013 1.00
14 A rapid mass spectrometric strategy for the characterization of N- and O-glycan chains in the diagnosis of defects in glycan biosynthesis. Proteomics 2007 1.00
15 Sialylation levels of anti-proteinase 3 antibodies are associated with the activity of granulomatosis with polyangiitis (Wegener's). Arthritis Rheum 2011 0.94
16 Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis. Mol Cell Biol 2010 0.87
17 Mapping of O-linked beta-N-acetylglucosamine modification sites in key contractile proteins of rat skeletal muscle. Proteomics 2009 0.87
18 Both core and terminal glycosylation alter epitope expression in thyrotropin and introduce discordances in hormone measurements. Clin Chem Lab Med 2005 0.87
19 Unusual N-glycan structures required for trafficking Toxoplasma gondii GAP50 to the inner membrane complex regulate host cell entry through parasite motility. Mol Cell Proteomics 2011 0.86
20 Nucleolin undergoes partial N- and O-glycosylations in the extranuclear cell compartment. Biochemistry 2005 0.85
21 Modifications of human total serum N-glycome during liver fibrosis-cirrhosis, is it all about immunoglobulins? Proteomics Clin Appl 2010 0.84
22 Semen clusterin is a novel DC-SIGN ligand. J Immunol 2011 0.84
23 Site-specific glycosylation analysis of the bovine lysosomal alpha-mannosidase. Glycobiology 2006 0.83
24 Localization of the O-glycosylated sites in peptides by fixed-charge derivatization with a phosphonium group. Anal Chem 2004 0.81
25 Overexpression of Man2C1 leads to protein underglycosylation and upregulation of endoplasmic reticulum-associated degradation pathway. Glycobiology 2010 0.81
26 Immunoglobulins are the major glycoproteins involved in the modifications of total serum N-glycome in cirrhotic patients. Proteomics Clin Appl 2010 0.80
27 Gammopathy with IgA mesangial deposition provides a monoclonal model of IgA nephritogenicity and offers new insights into its molecular mechanisms. Nephrol Dial Transplant 2011 0.78
28 Glycosylation status of the membrane protein CD9P-1. Proteomics 2007 0.78
29 PUGNAc treatment leads to an unusual accumulation of free oligosaccharides in CHO cells. J Biochem 2012 0.77
30 A mass spectrometric strategy for profiling glycoproteinoses, Pompe disease, and sialic acid storage diseases. Proteomics Clin Appl 2008 0.77