Published in Medicine (Baltimore) on July 01, 2015
Estrogen-related receptor β (ERRβ) - renaissance receptor or receptor renaissance? Nucl Recept Signal (2016) 0.79
Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction. Proc Natl Acad Sci U S A (2017) 0.78
Genetic variants in the peripheral auditory system significantly affect adult cochlear implant performance. Hear Res (2017) 0.76
Long-Term Cochlear Implant Outcomes in Children with GJB2 and SLC26A4 Mutations. PLoS One (2015) 0.75
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss. Sci Rep (2017) 0.75
A method and server for predicting damaging missense mutations. Nat Methods (2010) 78.53
An integrated map of genetic variation from 1,092 human genomes. Nature (2012) 59.82
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc (2009) 38.62
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells. Nature (2007) 4.87
Sensorineural hearing loss in children. Lancet (2005) 4.05
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. Sci Transl Med (2012) 4.02
Forty-six genes causing nonsyndromic hearing impairment: which ones should be analyzed in DNA diagnostics? Mutat Res (2008) 3.76
Hearing loss. N Engl J Med (1993) 3.49
Spoken language development in children following cochlear implantation. JAMA (2010) 3.35
Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness. Science (1999) 2.25
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. Proc Natl Acad Sci U S A (2002) 2.17
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum Mol Genet (2003) 2.14
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci (2007) 1.90
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet (2008) 1.78
The societal costs of severe to profound hearing loss in the United States. Int J Technol Assess Health Care (2000) 1.76
Advancing genetic testing for deafness with genomic technology. J Med Genet (2013) 1.66
Clinical findings for a group of infants and young children with auditory neuropathy. Ear Hear (1999) 1.60
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet (2006) 1.51
The varieties of auditory neuropathy. J Basic Clin Physiol Pharmacol (2000) 1.48
Cochlear implantation in children with anomalous cochleovestibular anatomy. Laryngoscope (2005) 1.46
Age at implantation: its importance in pediatric cochlear implantation. Laryngoscope (1999) 1.39
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction. Hum Mutat (2007) 1.38
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. Am J Hum Genet (2009) 1.37
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1. Am J Hum Genet (1999) 1.37
Cochlear implantation in children younger than 12 months. Pediatrics (2005) 1.25
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35. Am J Hum Genet (2008) 1.24
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS. PLoS One (2013) 1.17
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochem Cell Biol (2003) 1.17
Reliability of a rating scale for measuring speech intelligibility after pediatric cochlear implantation. Otol Neurotol (2001) 1.14
Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings. J Med Genet (2007) 1.10
Predicting cochlear implant outcomes in children with auditory neuropathy. Otol Neurotol (2008) 1.06
Next generation sequencing for molecular diagnosis of neuromuscular diseases. Acta Neuropathol (2012) 1.03
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment. Hum Mutat (2007) 1.03
Cochlear implantation in individuals with Usher type 1 syndrome. Int J Pediatr Otorhinolaryngol (2008) 1.03
Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss. Otol Neurotol (2004) 0.99
Role for a novel Usher protein complex in hair cell synaptic maturation. PLoS One (2012) 0.98
Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment. Hum Mol Genet (2001) 0.98
Cochlear implantation in auditory neuropathy. Laryngoscope (1999) 0.98
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders. Orphanet J Rare Dis (2014) 0.97
Cochlear implantation in patients with substantial residual hearing. Laryngoscope (2004) 0.97
Results of cochlear implantation in two children with mutations in the OTOF gene. Int J Pediatr Otorhinolaryngol (2005) 0.96
Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations. J Assoc Res Otolaryngol (2011) 0.96
Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation. Am J Otol (1998) 0.95
Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children. Arch Pediatr Adolesc Med (2008) 0.94
Long-term use of cochlear implant systems in paediatric recipients and factors contributing to non-use. Cochlear Implants Int (2009) 0.94
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis. Hear Res (2012) 0.94
Categories of auditory performance: inter-user reliability. Br J Audiol (1998) 0.93
Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1. Mol Vis (2010) 0.92
Good speech recognition and quality-of-life scores after cochlear implantation in patients with DFNA9. Otol Neurotol (2006) 0.90
Cochlear implantation in children with congenital X-linked deafness due to novel mutations in POU3F4 gene. Ann Otol Rhinol Laryngol (2010) 0.89
Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss. Biochim Biophys Acta (2012) 0.89
Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants. Clin Genet (2009) 0.88
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. Clin Genet (2007) 0.88
The cost and analysis of nonuse of cochlear implants. Otol Neurotol (2008) 0.88
Genetic characteristics in children with cochlear implants and the corresponding auditory performance. Laryngoscope (2011) 0.88
Genetic diagnosis of familial hypercholesterolaemia by targeted next-generation sequencing. J Intern Med (2014) 0.87
Characterization of a new allele of Ames waltzer generated by ENU mutagenesis. Hear Res (2005) 0.86
Auditory performance and speech intelligibility of Mandarin-speaking children implanted before age 5. Int J Pediatr Otorhinolaryngol (2014) 0.85
Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities. Audiol Neurootol (2007) 0.85
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing. Mutat Res (2014) 0.85
The effectiveness of the promotion of newborn hearing screening in Taiwan. Int J Pediatr Otorhinolaryngol (2013) 0.84
Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment. PLoS One (2013) 0.84
Auditory dyssynchrony or auditory neuropathy: understanding the pathophysiology and exploring methods of treatment. Int J Pediatr Otorhinolaryngol (2013) 0.83
Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutations. Audiol Neurootol (2003) 0.83
Audiologic performance and benefit of cochlear implantation in Usher syndrome type I. Laryngoscope (2006) 0.82
A sensitive period for cochlear implantation in deaf children. J Matern Fetal Neonatal Med (2011) 0.78
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis. Lancet Neurol (2008) 5.33
Relationship between androgen levels and blood pressure in young women with polycystic ovary syndrome. Hypertension (2007) 3.15
Metabolic factors and risk of hepatocellular carcinoma by chronic hepatitis B/C infection: a follow-up study in Taiwan. Gastroenterology (2008) 2.46
Insulin-like growth factor-1 mediates stretch-induced upregulation of myostatin expression in neonatal rat cardiomyocytes. Cardiovasc Res (2005) 2.33
Clinical features of sudden sensorineural hearing loss in diabetic patients. Laryngoscope (2005) 2.12
Opposite association between diabetes, dyslipidemia, and hepatocellular carcinoma mortality in the middle-aged and elderly. Hepatology (2014) 2.09
Determinants of bilateral audiometric notches in noise-induced hearing loss. Laryngoscope (2013) 2.04
The effects of 3-month atorvastatin therapy on arterial inflammation, calcification, abdominal adipose tissue and circulating biomarkers. Eur J Nucl Med Mol Imaging (2011) 1.80
Deep neck infection: analysis of 185 cases. Head Neck (2004) 1.72
Serum myostatin levels and grip strength in normal subjects and patients on maintenance haemodialysis. Clin Endocrinol (Oxf) (2011) 1.68
Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germline. Dev Biol (2006) 1.66
A common variant in the PNPLA3 gene is a risk factor for non-alcoholic fatty liver disease in obese Taiwanese children. J Pediatr (2010) 1.60
Impaired exercise capacity in diabetic patients after coronary bypass surgery: effects of diastolic and endothelial function. Cardiology (2007) 1.46
Microdebrider-assisted versus radiofrequency-assisted inferior turbinoplasty. Laryngoscope (2009) 1.41
Mutational spectrum of multiple endocrine neoplasia type 2 and sporadic medullary thyroid carcinoma in taiwan. J Formos Med Assoc (2009) 1.40
Effects of speech processing strategy on Chinese tone recognition by nucleus-24 cochlear implant users. Ear Hear (2004) 1.38
Sex differences in high-fat diet-induced obesity, metabolic alterations and learning, and synaptic plasticity deficits in mice. Obesity (Silver Spring) (2009) 1.36
Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness. Genet Med (2003) 1.34
Factors affecting the bacteriology of deep neck infection: a retrospective study of 128 patients. Acta Otolaryngol (2006) 1.21
Deep neck infection in diabetic patients: comparison of clinical picture and outcomes with nondiabetic patients. Otolaryngol Head Neck Surg (2005) 1.18
Association of central obesity with the severity and audiometric configurations of age-related hearing impairment. Obesity (Silver Spring) (2009) 1.12
The relationship between anti-Mullerian hormone, androgen and insulin resistance on the number of antral follicles in women with polycystic ovary syndrome. Hum Reprod (2008) 1.09
Videostrobolaryngoscopy of mucus layer during vocal fold vibration in patients with laryngeal tension-fatigue syndrome. Ann Otol Rhinol Laryngol (2002) 1.06
Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: a unique spectrum of mutations in Taiwan, including a frequent founder mutation. Laryngoscope (2005) 1.04
Adiponectin: a biomarker of obesity-induced insulin resistance in adipose tissue and beyond. J Biomed Sci (2008) 1.02
Familiality of novel factorial dimensions of schizophrenia. Arch Gen Psychiatry (2009) 1.02
Adiponectin as a potential differential marker to distinguish pancreatic cancer and chronic pancreatitis. Pancreas (2007) 1.02
Characterization of plaques using 18F-FDG PET/CT in patients with carotid atherosclerosis and correlation with matrix metalloproteinase-1. J Nucl Med (2007) 1.00
Clinical Implication of the C Allele of the ITPKC Gene SNP rs28493229 in Kawasaki Disease: Association With Disease Susceptibility and BCG Scar Reactivation. Pediatr Infect Dis J (2011) 1.00
Association of plasma adiponectin levels with hearing thresholds in adults. Clin Endocrinol (Oxf) (2011) 1.00
Serum adipocyte fatty acid-binding protein levels in patients with critical illness are associated with insulin resistance and predict mortality. Crit Care (2013) 0.99
The clinical implications of blood adiponectin in cardiometabolic disorders. J Formos Med Assoc (2009) 0.98
Common clinical features of children with enlarged vestibular aqueduct and Mondini dysplasia. Laryngoscope (2005) 0.97
Outcomes of malignant external otitis: survival vs mortality. Acta Otolaryngol (2010) 0.97
Prognostic factors of sudden sensorineural hearing loss in diabetic patients. Diabetes Care (2004) 0.97
Serum adiponectin correlates with viral characteristics but not histologic features in patients with chronic hepatitis C. J Hepatol (2005) 0.96
Lack of independent relationship between plasma adiponectin, leptin levels and bone density in nondiabetic female adolescents. Clin Endocrinol (Oxf) (2004) 0.96
Metabolic syndrome components worsen lower urinary tract symptoms in women with type 2 diabetes. J Clin Endocrinol Metab (2010) 0.96
Diet-induced obesity exacerbates auditory degeneration via hypoxia, inflammation, and apoptosis signaling pathways in CD/1 mice. PLoS One (2013) 0.96
Newborn genetic screening for hearing impairment: a preliminary study at a tertiary center. PLoS One (2011) 0.96
Community-acquired methicillin-resistant Staphylococcus aureus infections in discharging ears. Acta Otolaryngol (2002) 0.95
Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. PLoS One (2011) 0.95
Concurrent-vowel and tone recognition by Mandarin-speaking cochlear implant users. Hear Res (2009) 0.94
Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children. Arch Pediatr Adolesc Med (2008) 0.94
Optimal graft thickness for different sizes of tympanic membrane perforation in cartilage myringoplasty: a finite element analysis. Laryngoscope (2007) 0.93
Plasma adiponectin levels and blood pressures in nondiabetic adolescent females. J Clin Endocrinol Metab (2003) 0.93
Association of diabetes and HbA1c levels with gastrointestinal manifestations. Diabetes Care (2012) 0.93
Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy. Audiol Neurootol (2010) 0.91
Plasma adiponectin levels and metabolic factors in nondiabetic adolescents. Obes Res (2004) 0.91
Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome. Audiol Neurootol (2009) 0.90
Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology. PLoS One (2011) 0.89
Bright liver and alanine aminotransferase are associated with metabolic syndrome in adults. Obes Res (2005) 0.89
Neurotoxicological mechanism of methylmercury induced by low-dose and long-term exposure in mice: oxidative stress and down-regulated Na+/K(+)-ATPase involved. Toxicol Lett (2007) 0.89
Brain activation in patients with idiopathic hyperacusis. Am J Otolaryngol (2009) 0.88
Surgical management of first branchial cleft anomaly presenting as infected retroauricular mass using a microscopic dissection technique. Am J Otolaryngol (2011) 0.88
Genetic characteristics in children with cochlear implants and the corresponding auditory performance. Laryngoscope (2011) 0.88
Intratympanic steroid injections as a salvage treatment for sudden sensorineural hearing loss: a randomized, double-blind, placebo-controlled study. Otol Neurotol (2011) 0.87
Changes in bacteriology of discharging ears. J Laryngol Otol (2002) 0.87
Association of circulating matrix metalloproteinase-1, but not adiponectin, with advanced coronary artery disease. Atherosclerosis (2008) 0.87
Aging effects on the activation of the auditory cortex during binaural speech listening in white noise: an fMRI study. Audiol Neurootol (2007) 0.86
Measurement of hearing aid outcome in the elderly: comparison between young and old elderly. Otolaryngol Head Neck Surg (2008) 0.86
Functional role of soluble receptor for advanced glycation end products in stroke. Arterioscler Thromb Vasc Biol (2013) 0.86
Sphenopalatine ganglion block before removal of nasal packing. Laryngoscope (2003) 0.86
Biomechanical modeling and design optimization of cartilage myringoplasty using finite element analysis. Audiol Neurootol (2006) 0.86
Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations. Audiol Neurootol (2005) 0.86
Long-term language levels and reading skills in mandarin-speaking prelingually deaf children with cochlear implants. Audiol Neurootol (2010) 0.86
Association of obstructive sleep apnea and auditory dysfunctions in older subjects. Otolaryngol Head Neck Surg (2011) 0.85
Association between serum adipocyte fatty-acid binding protein concentrations, left ventricular function and myocardial perfusion abnormalities in patients with coronary artery disease. Cardiovasc Diabetol (2013) 0.85
Correlation of increased activities of Na+, K+-ATPase and Ca2+-ATPase with the reversal of cisplatin ototoxicity induced by D-methionine in guinea pigs. Hear Res (2005) 0.85
Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities. Audiol Neurootol (2007) 0.85
Pathophysiology of neuropathic pain in type 2 diabetes: skin denervation and contact heat-evoked potentials. Diabetes Care (2010) 0.85
Linkage and association on 8p21.2-p21.1 in schizophrenia. Am J Med Genet B Neuropsychiatr Genet (2010) 0.85
Adiponectin levels among patients with chronic hepatitis B and C infections and in response to IFN-alpha therapy. Liver Int (2005) 0.84
The application of infrared thermography in evaluation of patients at high risk for lower extremity peripheral arterial disease. J Vasc Surg (2011) 0.84
Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment. Laryngoscope (2009) 0.84
Hyperandrogenemia is independently associated with elevated alanine aminotransferase activity in young women with polycystic ovary syndrome. J Clin Endocrinol Metab (2010) 0.84
Expression of COX-2 and NMDA receptor genes at the cochlea and midbrain in salicylate-induced tinnitus. Laryngoscope (2011) 0.84
Application of massively parallel sequencing to genetic diagnosis in multiplex families with idiopathic sensorineural hearing impairment. PLoS One (2013) 0.84
A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease. Transl Res (2013) 0.83
Neurotoxicological effects of low-dose methylmercury and mercuric chloride in developing offspring mice. Toxicol Lett (2010) 0.83
Myostatin and insulin-like growth factor I: potential therapeutic biomarkers for pompe disease. PLoS One (2013) 0.83
Outcomes of facial palsy in children. Acta Otolaryngol (2009) 0.83
Hypoadiponectinemia: a useful marker of dyslipidemia in women with polycystic ovary syndrome. Taiwan J Obstet Gynecol (2012) 0.83