₂Isamu Yuge

Summary for 2002 [at-glance overview of Isamu Yuge work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Isamu Yuge. According to available data, in 2002 Isamu Yuge published at least 2 articles. This work was completed in collaboration with several authors including Usami, Shin-ichi and Abe, Satoko. Several other authors have collaborated with Isamu Yuge as well. There is no information about the funding or the grants awarded to support this work.

Analysis of the article abstracts and the titles suggests that Isamu Yuge professional interests are focused around "gjb2 mutation japanese", "identification 605ins46 novel" and "deafness impact gene". These might also be referred to as "gjb2 mutation", "deafness impact" or "diagnosis deafness". Statistical analysis shows that Isamu Yuge's writing is likely to contains terms "mutation", "gjb2", "identification", "deafness", "novel" and "gene".

The majority of Isamu Yuge articles are affiliated with Department of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan. Luckily, one email address is on file.

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Alternative names (0) [other authors with names similar to Isamu Yuge]

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Year 2002 Charts [Isamu Yuge frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Isamu Yuge publication and funding history for the range of years]

Emails (1) [email addresses extracted from Isamu Yuge affiliations]

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Isamu Yuge Coauthors (7) [all coauthors with the number of joint publications]

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Affiliations (1) [condensed summary of the Isamu Yuge affiliations, the leading number and the color conveys importance]

₂Department of Otorhinolaryngology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan.

Key Opinion Leader In [Isamu Yuge is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

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Keywords (17) [keywords assigned to Isamu Yuge articles by PubMed, the leading number and the color conveys importance]

₂Connexins | ₂Point Mutation | ₂Humans | ₂Deafness | ₁Child | ₁Gene Expression | ₁Pedigree | ₁Severity of Illness Index | ₁Male | ₁Polymerase Chain Reaction | ₁DNA Mutational Analysis | ₁Molecular Biology | ₁Magnetic Resonance Imaging | ₁Endolymphatic Sac | ₁Membrane Transport Proteins | ₁Carrier Proteins | ₁Tomography, X-Ray Computed

Isamu Yuge Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Isamu Yuge might be a good expert witness on these terms]

₅mutation | ₅gjb2 | ₄identification | ₃deafness | ₃novel | ₃gene | ₃mutations | ₂605ins46 | ₂nucleotide | ₂known | ₂molecular | ₂japanese | ₂family | ₂impact | ₂diagnosis | ₂recessive | ₁variable | ₁heterozygotes | ₁group | ₁sensorineural | ₁phenotype-genotype | ₁sequence | ₁aminoglycoside | ₁high-risk | ₁screening | ₁point | ₁relationship | ₁rapid | ₁severity | ₁profound | ₁responsible | ₁may
₃gjb2 mutation | ₂deafness impact | ₂diagnosis deafness | ₂novel gjb2 | ₂mutation japanese | ₂identification 605ins46 | ₂impact gene | ₂gene identification | ₂japanese family | ₂605ins46 novel | ₂molecular diagnosis | ₁may considerably | ₁screening system | ₁deafness recessive | ₁phenotype-genotype relationship | ₁mutation consisting | ₁congenital severe | ₁identification | ₁group rapid | ₁nucleotide sequence | ₁avoid possible | ₁report novel | ₁hearing loss | ₁235delc express | ₁connexin gene | ₁high-risk population | ₁may | ₁consist point | ₁recessive congenital | ₁30-80 autosomal | ₁responsible significant | ₁gjb2 reported
₂gjb2 mutation japanese | ₂identification 605ins46 novel | ₂deafness impact gene | ₂mutation japanese family | ₂molecular diagnosis deafness | ₂diagnosis deafness impact | ₂605ins46 novel gjb2 | ₂impact gene identification | ₂novel gjb2 mutation | ₁may considerably | ₁mutation consisting repetitive | ₁counseling recommended molecular | ₁known associated susceptibility | ₁reported consist point | ₁consisting repetitive nucleotide | ₁profound deafness recessive | ₁possible side effects | ₁identification | ₁associated susceptibility aminoglycoside | ₁235delc express sensorineural | ₁mutations known responsible | ₁large high-risk population | ₁phenotype-genotype relationship required | ₁significant portion 30-80 | ₁group rapid mass | ₁avoid possible side | ₁gjb2 reported consist | ₁hearing loss variable | ₁population avoid possible | ₁known responsible significant | ₁required identification 605ins46 | ₁may

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