PubRank

Gian Marco Ghiggeri

Author PubWeight™ 113.72‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis. Electrophoresis 2004 6.97
2 Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet 2011 3.15
3 Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int 2009 3.13
4 Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study. J Am Soc Nephrol 2006 2.89
5 COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. J Am Soc Nephrol 2007 2.52
6 SIX2 and BMP4 mutations associate with anomalous kidney development. J Am Soc Nephrol 2008 2.30
7 Autoimmunity in membranous nephropathy targets aldose reductase and SOD2. J Am Soc Nephrol 2010 2.22
8 MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003 2.05
9 Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. Hum Mol Genet 2003 2.01
10 AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis. Nat Genet 2010 1.89
11 Rituximab in children with resistant idiopathic nephrotic syndrome. J Am Soc Nephrol 2012 1.83
12 New insights into the pathogenesis and the therapy of recurrent focal glomerulosclerosis. Am J Transplant 2005 1.79
13 New insights into membranous glomerulonephritis: from bench to bedside. Nephrol Dial Transplant 2011 1.64
14 Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet 2012 1.63
15 Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial. Clin J Am Soc Nephrol 2011 1.62
16 Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy. Clin J Am Soc Nephrol 2012 1.51
17 Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome. J Am Soc Nephrol 2006 1.37
18 Broadening the spectrum of diseases related to podocin mutations. J Am Soc Nephrol 2003 1.33
19 Defective intracellular trafficking of uromodulin mutant isoforms. Traffic 2006 1.31
20 Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens. J Proteomics 2011 1.28
21 Non-muscle myosin heavy chain IIA and IIB interact and co-localize in living cells: relevance for MYH9-related disease. Int J Mol Med 2006 1.26
22 Uromodulin storage diseases: clinical aspects and mechanisms. Am J Kidney Dis 2004 1.23
23 Genetic screening in adolescents with steroid-resistant nephrotic syndrome. Kidney Int 2013 1.21
24 CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS). Nephrol Dial Transplant 2009 1.21
25 WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes. Pediatr Nephrol 2006 1.16
26 Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene. Hum Genet 2001 1.15
27 Oxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy. Clin J Am Soc Nephrol 2011 1.14
28 Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin. Am J Kidney Dis 2003 1.13
29 NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms. Pediatr Res 2005 1.13
30 Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic association. Medicine (Baltimore) 2009 1.09
31 Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds. J Am Soc Nephrol 2005 1.08
32 Wolfram syndrome: new mutations, different phenotype. PLoS One 2012 1.08
33 Genetic approaches to human renal agenesis/hypoplasia and dysplasia. Pediatr Nephrol 2007 1.07
34 Phenotypic and genetic heterogeneity in Dent's disease--the results of an Italian collaborative study. Nephrol Dial Transplant 2006 1.07
35 A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. J Am Soc Nephrol 2009 1.04
36 Immature renal structures associated with a novel UMOD sequence variant. Am J Kidney Dis 2008 1.03
37 Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome. J Am Soc Nephrol 2002 1.00
38 Familial forms of nephrotic syndrome. Pediatr Nephrol 2008 0.98
39 Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood. Kidney Int 2003 0.98
40 Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract. Hum Mutat 2010 0.97
41 Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin. J Am Soc Nephrol 2007 0.97
42 Collapsing glomerulopathy associated with inherited mitochondrial injury. Kidney Int 2008 0.97
43 TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype. Clin J Am Soc Nephrol 2011 0.97
44 Recurrent focal glomerulosclerosis in the era of genetics of podocyte proteins: theory and therapy. Nephrol Dial Transplant 2004 0.96
45 A computational platform for MALDI-TOF mass spectrometry data: application to serum and plasma samples. J Proteomics 2009 0.95
46 Soft immobilized pH gradient gels in proteome analysis: a follow-up. Proteomics 2003 0.94
47 Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy. Clin Transplant 2014 0.94
48 Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations. Clin J Am Soc Nephrol 2009 0.92
49 Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33. Am J Hum Genet 2007 0.90
50 Genetic risk factors in typical haemolytic uraemic syndrome. Nephrol Dial Transplant 2008 0.90
51 The oxido-redox potential of albumin methodological approach and relevance to human diseases. J Proteomics 2009 0.89
52 IgA nephropathy: the presence of familial disease does not confer an increased risk for progression. Am J Kidney Dis 2006 0.89
53 Lupus nephritis in children and adolescents: results of the Italian Collaborative Study. Nephrol Dial Transplant 2013 0.88
54 Characterization of oxidation end product of plasma albumin 'in vivo'. Biochem Biophys Res Commun 2006 0.88
55 Mesenchymal stem cells protective effect in adriamycin model of nephropathy. Cell Transplant 2008 0.87
56 Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders. Br J Haematol 2002 0.87
57 Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy. J Nephrol 2009 0.86
58 DQ molecules are the principal stimulators of de novo donor-specific antibodies in nonsensitized pediatric recipients receiving a first kidney transplant. Transpl Int 2014 0.86
59 A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis. Clin J Am Soc Nephrol 2010 0.86
60 Two-dimensional maps in soft immobilized pH gradient gels: a new approach to the proteome of the Third Millennium. Electrophoresis 2002 0.85
61 Two cases of swine H1N1 influenza presenting with hematuria as prodrome. Pediatr Nephrol 2009 0.85
62 Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations. Pediatr Nephrol 2009 0.84
63 2D-electrophoresis and the urine proteome map: where do we stand? J Proteomics 2009 0.84
64 Cyclosporin and organ specific toxicity: clinical aspects, pharmacogenetics and perspectives. Curr Clin Pharmacol 2008 0.84
65 New iodo-acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido-redox status. Proteomics 2009 0.84
66 Direct effect of plasma permeability factors from patients with idiopatic FSGS on nephrin and podocin expression in human podocytes. Int J Mol Med 2005 0.84
67 In vivo characterization of renal auto-antigens involved in human auto-immune diseases: the case of membranous glomerulonephritis. Proteomics Clin Appl 2011 0.83
68 Characterization of plasma factors that alter the permeability to albumin within isolated glomeruli. Proteomics 2002 0.83
69 Combinatorial peptide ligand libraries for urine proteome analysis: investigation of different elution systems. Electrophoresis 2009 0.83
70 "Cheek-to-cheek" urinary proteome profiling via combinatorial peptide ligand libraries: A novel, unexpected elution system. J Proteomics 2011 0.82
71 Urinary secretion and extracellular aggregation of mutant uromodulin isoforms. Kidney Int 2012 0.82
72 Immunity to Polyomavirus BK Infection: Immune Monitoring to Regulate the Balance between Risk of BKV Nephropathy and Induction of Alloimmunity. Clin Dev Immunol 2013 0.82
73 Glomerulocystic kidney disease in a family. Nephrol Dial Transplant 2002 0.81
74 Hyponatremic-hypertensive syndrome with extensive and reversible renal defects. Pediatr Nephrol 2004 0.81
75 Association of the macrophage migration inhibitory factor -173*C allele with childhood nephrotic syndrome. Pediatr Nephrol 2008 0.81
76 'Congenital solitary functioning kidneys: which ones warrant follow-up into adult life?'. Nephrol Dial Transplant 2011 0.81
77 Oxidized albumin. The long way of a protein of uncertain function. Biochim Biophys Acta 2013 0.80
78 Determination of the oxido-redox status of plasma albumin in hemodialysis patients. J Chromatogr B Analyt Technol Biomed Life Sci 2008 0.80
79 Lack of cardiac anomalies in children with NPHS2 mutations. Nephrol Dial Transplant 2007 0.80
80 Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia. Nephron 2016 0.80
81 Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome. Gene Expr 2006 0.79
82 Proteins and protein fragments in nephrotic syndrome: Clusters, specificity and mechanisms. Proteomics Clin Appl 2008 0.79
83 The effect of proteinase inhibitors on glomerular albumin permeability induced in vitro by serum from patients with idiopathic focal segmental glomerulosclerosis. Nephrol Dial Transplant 2004 0.79
84 Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin. Am J Kidney Dis 2004 0.79
85 Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy. Nephrol Dial Transplant 2006 0.79
86 Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis. Kidney Int 2003 0.79
87 Angiotensin-converting enzyme (ACE) haplotypes and cyclosporine A (CsA) response: a model of the complex relationship between ACE quantitative trait locus and pathological phenotypes. Hum Mol Genet 2005 0.79
88 Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney disease. J Nephrol 2003 0.79
89 Urinary proteome in a snapshot: normal urine and glomerulonephritis. J Nephrol 2012 0.78
90 Nephronophthisis-medullary cystic kidney disease: from bedside to bench and back again. Saudi J Kidney Dis Transpl 2007 0.78
91 Posttransplant soluble B-cell activating factor kinetics in pediatric recipients of first kidney allograft. Transplantation 2015 0.78
92 Albumin heterogeneity in low-abundance fluids. The case of urine and cerebro-spinal fluid. Biochim Biophys Acta 2013 0.78
93 Nephrectomy for multicystic dysplastic kidney and renal hypodysplasia in children: where do we stand? Pediatr Surg Int 2010 0.78
94 Analysis of the oxido-redox status of plasma proteins. Technology advances for clinical applications. J Chromatogr B Analyt Technol Biomed Life Sci 2010 0.77
95 Urinary proteomics and drug discovery in chronic kidney disease: a new perspective. J Proteome Res 2010 0.77
96 Proteome profile of peritoneal effluents in children on glucose- or icodextrin-based peritoneal dialysis. Nephrol Dial Transplant 2010 0.77
97 mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis. Saudi J Kidney Dis Transpl 2014 0.76
98 Nephrotic urine prevents increased rat glomerular albumin permeability induced by serum from the same patient with idiopathic nephrotic syndrome. Nephrol Dial Transplant 2003 0.76
99 Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible trait. Pediatr Nephrol 2009 0.76
100 Focal and segmental glomerulosclerosis (FSGS). Clinical, morphological and genetic features. J Nephrol 2004 0.76
101 Combinatorial ligand libraries as a two-dimensional method for proteome analysis. J Chromatogr A 2013 0.76
102 Teaching molecular genetics: chapter 4-positional cloning of genetic disorders. Pediatr Nephrol 2007 0.76
103 Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria. Kidney Int 2004 0.75
104 Protein-protein interaction heterogeneity of plasma apolipoprotein A1 in nephrotic syndrome. Mol Biosyst 2011 0.75
105 Glomerulocystic kidney disease in hypomelanosis of Ito. Pediatr Nephrol 2008 0.75
106 Intraureteral injection of NASHA/Dx gel under direct ureteroscopic visualization for the treatment of primary high-grade vesicoureteral reflux. J Laparoendosc Adv Surg Tech A 2012 0.75
107 Circulating antipodocyte antibodies in membranous nephropathy: new findings. Am J Kidney Dis 2013 0.75
108 Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations. Am J Hum Genet 2017 0.75
109 Proteomics of plasma and urine in primary nephrotic syndrome in children. Contrib Nephrol 2008 0.75
110 The latest advancements in proteomic two-dimensional gel electrophoresis analysis applied to biological samples. Methods Mol Biol 2015 0.75
111 [Familial Focal Segmental Glomerulosclerosis, a vademecum for clinical nephrologist]. G Ital Nefrol 2015 0.75
112 2DE maps in the discovery of human autoimmune kidney diseases: the case of membranous glomerulonephritis. Methods Mol Biol 2015 0.75
113 [Mutant uromodulin is secreted in the urine of patients with familial hyperuricemic nephropathy and induces the formation of extracellular aggregates]. G Ital Nefrol 2012 0.75
114 Transitions of serum albumin in patients with glomerulosclerosis 'in vivo' characterization by electrophoretic titration curves. Electrophoresis 2006 0.75
115 [TRPC6 mutations in children with steroid-resistant nephrotic syndrome]. G Ital Nefrol 2011 0.75
116 The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults. Nephrol Dial Transplant 2009 0.75
117 Images in vascular medicine. A challenging case of renovascular hypertension. Vasc Med 2013 0.75