Tatsuo Matsunaga


Ontology type: schema:Person     


Person Info

NAME

Tatsuo

SURNAME

Matsunaga

Publications in SciGraph latest 50 shown

  • 2018-12 Gene expression dataset for whole cochlea of Macaca fascicularis in SCIENTIFIC REPORTS
  • 2018-12 Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis in SCIENTIFIC REPORTS
  • 2018-12 A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX10 in BMC PEDIATRICS
  • 2018-12 IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis in SCIENTIFIC REPORTS
  • 2018-05 Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome in JOURNAL OF HUMAN GENETICS
  • 2017-12 Mitochondrial mutations in maternally inherited hearing loss in BMC MEDICAL GENETICS
  • 2017-12 Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss in ORPHANET JOURNAL OF RARE DISEASES
  • 2017 Genetics of Inner Ear Malformation and Cochlear Nerve Deficiency in COCHLEAR IMPLANTATION IN CHILDREN WITH INNER EAR MALFORMATION AND COCHLEAR NERVE DEFICIENCY
  • 2016-12 A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder in HUMAN GENOME VARIATION
  • 2016-11 Late onset and high-frequency dominant hearing loss in a family with MYH9 disorder in EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
  • 2015-12 High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss in ORPHANET JOURNAL OF RARE DISEASES
  • 2013-12 Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study in ORPHANET JOURNAL OF RARE DISEASES
  • 2012-12 In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss in BMC RESEARCH NOTES
  • 2011-12 Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation in BMC MEDICAL GENETICS
  • 2011-07 Acoustic overstimulation-induced apoptosis in fibrocytes of the cochlear spiral limbus of mice in EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
  • 2009 Trends in Genetic Research on Auditory Neuropathy in NEUROPATHIES OF THE AUDITORY AND VESTIBULAR EIGHTH CRANIAL NERVES
  • 2005-02 Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns in JOURNAL OF HUMAN GENETICS
  • 2000-09 Morphological evidence that impaired intraneural microcirculation is a possible mechanism of eighth nerve conduction block in acoustic neuromas in EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
  • 1994 Clinical Investigation of Hypoglossal-Facial Nerve Anastomosis in THE FACIAL NERVE
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