Published in Cancer Biomark on September 07, 2011
FOXE1 association with differentiated thyroid cancer and its progression. Thyroid (2014) 0.91
Quantitative assessment of common genetic variants on FOXE1 and differentiated thyroid cancer risk. PLoS One (2014) 0.85
Patterns of FOXE1 expression in papillary thyroid carcinoma by immunohistochemistry. Thyroid (2013) 0.83
A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1. Hum Mol Genet (2015) 0.82
Polyalanine expansions drive a shift into α-helical clusters without amyloid-fibril formation. Nat Struct Mol Biol (2015) 0.81
Replication and Meta-Analysis of Common Gene Mutations in TTF1 and TTF2 with Papillary Thyroid Cancer. Medicine (Baltimore) (2015) 0.79
Selected single-nucleotide polymorphisms in FOXE1, SERPINA5, FTO, EVPL, TICAM1 and SCARB1 are associated with papillary and follicular thyroid cancer risk: replication study in a German population. Carcinogenesis (2016) 0.77
Thyroid transcription factor FOXE1 interacts with ETS factor ELK1 to co-regulate TERT. Oncotarget (2016) 0.75
rs965513 polymorphism as a common risk marker is associated with papillary thyroid cancer. Oncotarget (2016) 0.75
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum Mol Genet (2003) 2.37
Enhanced magnetic field sensitivity of spin-dependent transport in cluster-assembled metallic nanostructures. Nat Mater (2006) 2.29
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet (2008) 1.78
Bladder cancer and exposure to water disinfection by-products through ingestion, bathing, showering, and swimming in pools. Am J Epidemiol (2006) 1.73
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability. EMBO J (2007) 1.65
Proteomic approaches for discovering biomarkers of diabetic nephropathy. Nephrol Dial Transplant (2010) 1.64
Tag STS in the AZF region associated with azoospermia in a Tunisian population. J Androl (2007) 1.38
What's in the pool? A comprehensive identification of disinfection by-products and assessment of mutagenicity of chlorinated and brominated swimming pool water. Environ Health Perspect (2010) 1.32
Short-term changes in respiratory biomarkers after swimming in a chlorinated pool. Environ Health Perspect (2010) 1.30
Genotoxic effects in swimmers exposed to disinfection by-products in indoor swimming pools. Environ Health Perspect (2010) 1.29
TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families. Audiol Neurootol (2008) 1.16
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family. Eur J Hum Genet (2008) 1.11
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. Eur J Hum Genet (2003) 1.10
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice. Nat Genet (2011) 1.10
Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia. Hum Mol Genet (2002) 1.10
Genetic variations associated with interindividual sensitivity in the response to arsenic exposure. Pharmacogenomics (2008) 1.09
Ganglioneuroma of adrenal gland in a patient with Turner syndrome. Ann Diagn Pathol (2009) 1.06
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus. Genet Test Mol Biomarkers (2009) 1.06
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain. Blood (2004) 1.05
Genome-wide association study on differentiated thyroid cancer. J Clin Endocrinol Metab (2013) 1.03
[Complications of Meckel's diverticulum. Report of 42 cases]. Tunis Med (2009) 1.02
Strong association of chromosome 1p12 loci with thyroid cancer susceptibility. Cancer Epidemiol Biomarkers Prev (2008) 1.02
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss. Hum Mutat (2005) 0.98
Clusters of transcription-coupled repair in the human genome. Proc Natl Acad Sci U S A (2002) 0.97
Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations. J Hum Genet (2003) 0.97
Biomonitoring of four European populations occupationally exposed to pesticides: use of micronuclei as biomarkers. Mutagenesis (2003) 0.97
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families. Neurogenetics (2003) 0.96
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects. Genet Test Mol Biomarkers (2010) 0.96
Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases. Arthritis Res Ther (2009) 0.95
Probing one antiferromagnetic antiphase boundary and single magnetite domain using nanogap contacts. Nano Lett (2010) 0.94
Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness. Genet Epidemiol (2004) 0.92
A comparative study of the oxidative profile in Graves' disease, Hashimoto's thyroiditis, and papillary thyroid cancer. Biol Trace Elem Res (2010) 0.92
DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects. Rheumatol Int (2009) 0.92
Long-term outcome of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Am J Med Sci (2012) 0.91
Relationship between genetic polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase as risk factors for type 2 diabetes in Tunisian patients. Clin Biochem (2009) 0.90
Common variants of the thyroglobulin gene are associated with differentiated thyroid cancer risk. Thyroid (2011) 0.89
Myeloperoxidase-antineutrophil cytoplasmic antibody-positive crescentic glomerulonephritis associated with benzylthiouracil therapy: report of the first case. Nephrol Dial Transplant (2003) 0.88
Polycarbonate microchannel network with carpet of gold nanowires as SERS-active device. Lab Chip (2009) 0.88
Mutation in gap and tight junctions in patients with non-syndromic hearing loss. Biochem Biophys Res Commun (2009) 0.88
Hypermethylation of tumor-related genes in Tunisian patients with gastric carcinoma: clinical and biological significance. J Surg Oncol (2011) 0.88
Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies. J Clin Immunol (2007) 0.88
Gene and protein markers of diabetic nephropathy. Nephrol Dial Transplant (2007) 0.87
Micronuclei and pesticide exposure. Mutagenesis (2011) 0.86
Association studies of OGG1, XRCC1, XRCC2 and XRCC3 polymorphisms with differentiated thyroid cancer. Mutat Res (2011) 0.86
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study. J Clin Endocrinol Metab (2003) 0.86
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family. Hum Hered (2005) 0.86
Leydig Cell Tumor Associated with Testicular Adrenal Rest Tumors in a Patient with Congenital Adrenal Hyperplasia due to 11β-Hydroxylase Deficiency. Case Rep Urol (2012) 0.86
Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk. J Clin Endocrinol Metab (2014) 0.86
Polymorphism of glutathione transferase Omega 1 in a population exposed to a high environmental arsenic burden. Pharmacogenet Genomics (2008) 0.85
Mutagenic stress modulates the dynamics of CTG repeat instability associated with myotonic dystrophy type 1. Nucleic Acids Res (2003) 0.85
Microalbuminuria: a useful marker of cardiovascular disease. Iran J Kidney Dis (2013) 0.85
Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia. Genet Test Mol Biomarkers (2011) 0.85
Genotypic interactions of renin-angiotensin system genes with diabetes type 2 in a Tunisian population. Life Sci (2010) 0.85
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1. Hum Genet (2009) 0.85
The heteroplasmic m.14709T>C mutation in the tRNA(Glu) gene in two Tunisian families with mitochondrial diabetes. J Diabetes Complications (2010) 0.84
Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness. Mol Vis (2010) 0.84
Brain magnetic resonance imaging findings in adult patients with congenital adrenal hyperplasia: Increased frequency of white matter impairment and temporal lobe structures dysgenesis. Indian J Endocrinol Metab (2013) 0.84
Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphism. J Autoimmun (2004) 0.83
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population. Ann Hum Genet (2011) 0.83
[Carcinoid tumors of the appendix. A report of 46 cases]. Tunis Med (2004) 0.82
Complicated urinary tract infections associated with diabetes mellitus: Pathogenesis, diagnosis and management. Indian J Endocrinol Metab (2013) 0.82
Micronuclei assessment in the urothelial cells of women using hair dyes and its modulation by genetic polymorphisms. Cancer Lett (2008) 0.82
Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1. Eur J Hum Genet (2008) 0.82
WDR3 gene haplotype is associated with thyroid cancer risk in a Spanish population. Thyroid (2010) 0.82
Metabolism of arsenic in Drosophila melanogaster and the genotoxicity of dimethylarsinic acid in the Drosophila wing spot test. Environ Mol Mutagen (2006) 0.82
Non-HLA autoimmunity genetic factors contributing to Autoimmune Polyglandular Syndrome type II in Tunisian patients. Hum Immunol (2012) 0.82
Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population. Eur Cytokine Netw (2007) 0.82
[Gastric sarcoma]. Presse Med (2007) 0.82
The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population. Ann Hum Biol (2009) 0.82
Polymorphism analysis of Epstein-Barr virus isolates of nasopharyngeal carcinoma biopsies from Tunisian patients. Virus Genes (2007) 0.82
Identification of candidate regions for a novel Usher syndrome type II locus. Mol Vis (2008) 0.81
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy. Biochem Biophys Res Commun (2011) 0.81
Comparative genotoxic evaluation of 2-furylethylenes and 5-nitrofurans by using the comet assay in TK6 cells. Mutagenesis (2005) 0.81
Oxidative DNA damage in chronic renal failure patients. Nephrol Dial Transplant (2009) 0.81
[Kinetics, diagnostic and prognostic value of procalcitonin after cardiac surgery]. Ann Biol Clin (Paris) (2012) 0.81
Genetic structure of Kuwaiti population revealed by Y-STR diversity. Ann Hum Biol (2010) 0.81
Ogg1 genetic background determines the genotoxic potential of environmentally relevant arsenic exposures. Arch Toxicol (2013) 0.81
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions. Biochem Biophys Res Commun (2013) 0.81
Congenital adrenal hyperplasia: Treatment and outcomes. Indian J Endocrinol Metab (2013) 0.81