Published in Forensic Sci Int Genet on November 18, 2010
Analysis of 12 X-STRs in Greenlanders, Danes and Somalis using Argus X-12. Int J Legal Med (2011) 0.99
Development and population study of the 12 X-STR loci multiplexes PCR systems. Int J Legal Med (2012) 0.93
Genetic study of 12 X-STRs in Malay population living in and around Kuala Lumpur using Investigator Argus X-12 kit. Int J Legal Med (2012) 0.88
Population genetic study of six closely linked groups of X-STRs in a Japanese population. Int J Legal Med (2011) 0.79
Allele and haplotype diversity of X-chromosomal STRs in Ivory Coast. Int J Legal Med (2011) 0.77
Allele and Haplotype Diversity of 26 X-STR Loci in Four Nationality Populations from China. PLoS One (2013) 0.76
Genetic analysis of 19 X chromosome STR loci for forensic purposes in four Chinese ethnic groups. Sci Rep (2017) 0.75
Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population. Genet Test Mol Biomarkers (2014) 0.75
Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nat Genet (2011) 3.15
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics. Hum Mol Genet (2003) 2.01
Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis. PLoS Genet (2012) 1.69
Neuropsychiatric lupus syndromes: relationship with antiphospholipid antibodies. Neurology (2003) 1.65
A single-nucleotide polymorphism in the human beta-defensin 1 gene is associated with HIV-1 infection in Italian children. AIDS (2004) 1.59
The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease. Kidney Int (2011) 1.56
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene. Hum Mutat (2009) 1.55
Toward male individualization with rapidly mutating y-chromosomal short tandem repeats. Hum Mutat (2014) 1.53
Secreted protein acidic and rich in cysteine (SPARC) gene polymorphism association with hepatocellular carcinoma in Italian patients. J Gastroenterol Hepatol (2009) 1.42
Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci. Am J Hum Genet (2006) 1.41
Defective intracellular trafficking of uromodulin mutant isoforms. Traffic (2006) 1.31
Uromodulin storage diseases: clinical aspects and mechanisms. Am J Kidney Dis (2004) 1.23
Autosomal dominant Alport syndrome: molecular analysis of the COL4A4 gene and clinical outcome. Nephrol Dial Transplant (2009) 1.20
Antiphospholipid antibodies and renal involvement. Am J Nephrol (2009) 1.15
Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome. Eur J Hum Genet (2008) 1.13
Multicenter study on hepatitis C virus-related cryoglobulinemic glomerulonephritis. Am J Kidney Dis (2007) 1.08
MicroRNA/gene profiling unveils early molecular changes and nuclear factor erythroid related factor 2 (NRF2) activation in a rat model recapitulating human hepatocellular carcinoma (HCC). Hepatology (2013) 1.05
A rapid flow cytometry test based on histone H2AX phosphorylation for the sensitive and specific diagnosis of ataxia telangiectasia. Cytometry A (2008) 1.04
Thrombosis in systemic lupus erythematosus: congenital and acquired risk factors. Arthritis Rheum (2005) 1.02
Antimicrobial and immunoregulatory functions of lactoferrin and its potential therapeutic application. J Endotoxin Res (2002) 1.00
Thrombosis in nephrotic syndrome. Semin Thromb Hemost (2013) 1.00
Osteopontin gene haplotypes correlate with multiple sclerosis development and progression. J Neuroimmunol (2005) 0.99
Adipokines and systemic lupus erythematosus: relationship with metabolic syndrome and cardiovascular disease risk factors. J Rheumatol (2009) 0.98
Beta-defensin 1 gene variability among non-human primates. Immunogenetics (2002) 0.98
Anti-lactoferrin antibodies in systemic lupus erythematosus: isotypes and clinical correlates. Clin Rheumatol (2004) 0.97
Collaborative genetic mapping of 12 forensic short tandem repeat (STR) loci on the human X chromosome. Forensic Sci Int Genet (2012) 0.96
A study of host defence peptide beta-defensin 3 in primates. Biochem J (2003) 0.94
Frequency of the HFE gene mutations in five Italian populations. Blood Cells Mol Dis (2003) 0.93
Hypercoagulability and nephrotic syndrome. Curr Vasc Pharmacol (2014) 0.93
Effects of maturation on RNA transcription and protein expression of four MRP genes in human placenta and in BeWo cells. Biochem Biophys Res Commun (2003) 0.92
Structural and functional characterization of hBD-1(Ser35), a peptide deduced from a DEFB1 polymorphism. Biochem Biophys Res Commun (2002) 0.92
Local hypothyroidism favors the progression of preneoplastic lesions to hepatocellular carcinoma in rats. Hepatology (2014) 0.89
IgA nephropathy: the presence of familial disease does not confer an increased risk for progression. Am J Kidney Dis (2006) 0.89
Human mesenchymal stem cell-derived microvesicles modulate T cell response to islet antigen glutamic acid decarboxylase in patients with type 1 diabetes. Diabetologia (2014) 0.88
Role of interferon-gamma gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study. Eur J Hum Genet (2006) 0.88
OMiR: Identification of associations between OMIM diseases and microRNAs. Genomics (2010) 0.87
Primary hyperoxaluria: genotype-phenotype correlation. J Nephrol (2003) 0.87
Brake linings: a source of non-GSR particles containing lead, barium, and antimony. J Forensic Sci (2002) 0.87
Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy. J Nephrol (2009) 0.86
N-acetylcysteine infusion reduces the resistance index of renal artery in the early stage of systemic sclerosis. Acta Pharmacol Sin (2009) 0.85
Evaluation of Chronic Kidney Disease Epidemiology Collaboration equation to estimate glomerular filtration rate in scleroderma patients. Rheumatology (Oxford) (2012) 0.85
Validation of a large Italian Database of 15 STR loci. Forensic Sci Int (2005) 0.85
An in vitro model of T cell receptor revision in mature human CD8+ T cells. Mol Immunol (2007) 0.84
The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait. BMC Nephrol (2005) 0.84
Association of interferon-gamma +874A polymorphism with reduced long-term inflammatory response in haemodialysis patients. Nephrol Dial Transplant (2006) 0.83
A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome. Hum Genet (2006) 0.83
Genetic factors in mother-to-child transmission of HCV infection. Virology (2009) 0.83
Amplification failure of the amelogenin gene (AMELX) caused by a primer binding site mutation. Prenat Diagn (2009) 0.82
Role of L-selectin in the vascular homing of peripheral blood-derived endothelial progenitor cells. J Immunol (2004) 0.82
MBL2 polymorphisms are involved in HIV-1 infection in Brazilian perinatally infected children. AIDS (2003) 0.82
Prognostic value of the stromal cell-derived factor 1 3'A mutation in pediatric human immunodeficiency virus type 1 infection. J Infect Dis (2002) 0.82
Expression of lactoferrin on neutrophil granulocytes from synovial fluid and peripheral blood of patients with rheumatoid arthritis. J Rheumatol (2003) 0.82
Urinary secretion and extracellular aggregation of mutant uromodulin isoforms. Kidney Int (2012) 0.82
Variant mannose-binding lectin alleles are associated with celiac disease. Immunogenetics (2002) 0.82
Retroperitoneal fibrosis and ankylosing spondylitis: which links? Semin Arthritis Rheum (2005) 0.81
T2-T4 sympathectomy versus T3-T4 sympathicotomy for palmar and axillary hyperhidrosis. Clin Auton Res (2011) 0.81
Pathophysiology, diagnosis and clinical management of hepatorenal syndrome: from classic to new drugs. Curr Vasc Pharmacol (2014) 0.80
Estimation of human leukocyte antigen class I and class II high-resolution allele and haplotype frequencies in the Italian population and comparison with other European populations. Hum Immunol (2012) 0.80
Two-tier analysis of histone H2AX phosphorylation allows the identification of Ataxia Telangiectasia heterozygotes. Radiother Oncol (2009) 0.80
Analysis of 11 tetrameric STRs in wild boars for forensic purposes. Forensic Sci Int Genet (2010) 0.80
Human mesenchymal stem cells modulate cellular immune response to islet antigen glutamic acid decarboxylase in type 1 diabetes. J Clin Endocrinol Metab (2010) 0.80
Left ventricular mass correlates with lean body mass in patients with disease-associated wasting. J Cachexia Sarcopenia Muscle (2014) 0.80
Brief report: Why did two patients who type for HLA-B13 have antibodies that react with all Bw4 antigens except HLA-B13? Transpl Immunol (2011) 0.80
Search for genetic association between IgA nephropathy and candidate genes selected by function or by gene mapping at loci IGAN2 and IGAN3. Nephrol Dial Transplant (2011) 0.80
Intrarenal hemodynamic parameters correlate with glomerular filtration rate and digital microvascular damage in patients with systemic sclerosis. Semin Arthritis Rheum (2011) 0.80
IL-18 paradox in pancreatic carcinoma: elevated serum levels of free IL-18 are correlated with poor survival. J Immunother (2009) 0.79
Modeling the effect of 3 missense AGXT mutations on dimerization of the AGT enzyme in primary hyperoxaluria type 1. J Nephrol (2010) 0.79
Prostacyclin in liver disease: a potential therapeutic option. Expert Opin Biol Ther (2007) 0.79
Towards the identification of (a) gene(s) for autosomal dominant medullary cystic kidney disease. J Nephrol (2003) 0.79
Leptin, adiponectin and vascular stiffness parameters in women with systemic lupus erythematosus. Intern Emerg Med (2011) 0.78
Endothelial dysfunction and activation as an expression of disease: role of prostacyclin analogs. Int Immunopharmacol (2005) 0.78
Supernumerary ring chromosome 8: clinical and molecular cytogenetic characterization in a case report. Am J Med Genet A (2004) 0.78
Spotting expertise in the eyes: billiards knowledge as revealed by gaze shifts in a dynamic visual prediction task. J Vis (2012) 0.78
Analysis of 21 X-chromosomal STRs in an Algerian population sample. Int J Legal Med (2009) 0.78
Increased intrarenal arterial stiffness may predict the occurrence of new digital ulcers in systemic sclerosis. Arthritis Care Res (Hoboken) (2014) 0.78
An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation. Amyotroph Lateral Scler Other Motor Neuron Disord (2003) 0.77
Melusin gene (ITGB1BP2) nucleotide variations study in hypertensive and cardiopathic patients. BMC Med Genet (2009) 0.77
Evidence of a correlation between mannose binding lectin and celiac disease: a model for other autoimmune diseases. J Mol Med (Berl) (2005) 0.77
A novel defect in mitochondrial p53 accumulation following DNA damage confers apoptosis resistance in Ataxia Telangiectasia and Nijmegen Breakage Syndrome T-cells. DNA Repair (Amst) (2010) 0.77
Incestuous paternity detected by STR-typing of chorionic villi isolated from archival formalin-fixed paraffin-embedded abortion material using laser microdissection. J Forensic Sci (2006) 0.77
Cytokine gene polymorphisms in hepatitis C virus-related oral lichen planus. Exp Dermatol (2007) 0.77
Discordant evolution of nephrotic syndrome in mono- and dizygotic twins. Pediatr Nephrol (2005) 0.77
Gabexate mesylate as treatment in the course of ANCA-negative microscopic polyangiitis. Ren Fail (2013) 0.77
Allele and haplotype diversity of X-chromosomal STRs in Ivory Coast. Int J Legal Med (2011) 0.77
Conservative management of minor anastomotic leakage after open elective colorectal surgery. Ann Ital Chir (2012) 0.77
Gut Microbiota as a Target for Food Allergy. J Pediatr Gastroenterol Nutr (2016) 0.76
D-Lactic acidosis 25 years after bariatric surgery due to Salmonella enteritidis. Nutrition (2011) 0.76
The involvement of T regulatory lymphocytes in a cohort of lupus nephritis patients: a pilot study. Intern Emerg Med (2015) 0.76
Drugs and Rhabdomyolysis: From Liver to Kidney. Curr Vasc Pharmacol (2015) 0.76
NADPH oxidase (NOX2) activity is a modifier of survival in ALS. J Neurol (2014) 0.76
Diabetic Nephropathy: Focus on Current and Future Therapeutic Strategies. Curr Drug Metab (2016) 0.76
B cell positive cross-match not due to anti-HLA Class I antibodies and first kidney graft outcome. Transpl Immunol (2008) 0.76
Anomalous origin and aneurysm of the suprascapular artery: the first case observed. BMJ Case Rep (2009) 0.75
Evaluation of alloreactivity in responder-stimulator pairs by determination of gamma interferon-producing cells and cytotoxic-T-lymphocyte precursor frequencies. Clin Vaccine Immunol (2007) 0.75
Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12. J Nephrol (2003) 0.75