Kenichiro Yamada

InstitutionHiratsuka City Hospital
AddressKanagawa
Japan
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    Publication Timeline
    COVID-19 publications
    Bar chart showing 1 Covid-19 publications, with a maximum of 1 publications in April 2021
    All Publications
    Bar chart showing 31 publications over 15 distinct years, with a maximum of 6 publications in 2014
    These graphs show COVID-19 publications by month since August 2019 and all publications written by authors of COVID-19 publications over the past 30 years.

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    Publication Field Summary
    This graph shows the number and percent of publications by field. Fields are based on how the National Library of Medicine (NLM) classifies the publications' journals and might not represent the specific topics of the publications. Note that an individual publication can be assigned to more than one field. As a result, the publication counts in this graph might add up to more than the number of publications the person has written. To see the data as text, click here.
    Publication List
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Abe K, Shimura T, Takenouchi T, Iwasaki YW, Ishizu H, Uwamino Y, Uno S, Gotoh J, Tachikawa N, Takeuchi Y, Katayama J, Nozaki H, Fujii S, Seki S, Nakamura M, Uda K, Misumi T, Ishihara J, Yamada K, Kanai T, Murai S, Araki K, Ebihara T, Siomi H, Hasegawa N, Kitagawa Y, Amagai M, Suematsu M, Kosaki K. Identification of B.1.346 Lineage of SARS-CoV-2 in Japan: Genomic Evidence of Re-entry of Clade 20C. Keio J Med. 2021 Jun 25; 70(2):44-50. PMID: 33853975.
      Citations: Article has an altmetric score of 7    Fields:    Translation:Humans
    2. Higuchi Y, Okunushi R, Hara T, Hashiguchi A, Yuan J, Yoshimura A, Murayama K, Ohtake A, Ando M, Hiramatsu Y, Ishihara S, Tanabe H, Okamoto Y, Matsuura E, Ueda T, Toda T, Yamashita S, Yamada K, Koide T, Yaguchi H, Mitsui J, Ishiura H, Yoshimura J, Doi K, Morishita S, Sato K, Nakagawa M, Yamaguchi M, Tsuji S, Takashima H. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy. Brain. 2018 06 01; 141(6):1622-1636. PMID: 29718187.
      Citations: 9   Article has an altmetric score of 18    Fields:    Translation:HumansAnimalsCells
    3. Fukushi D, Yamada K, Suzuki K, Inaba M, Nomura N, Suzuki Y, Katoh K, Mizuno S, Wakamatsu N. Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation. Gene. 2018 May 20; 655:65-70. PMID: 29477873.
      Citations: 3   Article has an altmetric score of 3    Fields:    Translation:HumansCells
    4. Suzuki Y, Enokido Y, Yamada K, Inaba M, Kuwata K, Hanada N, Morishita T, Mizuno S, Wakamatsu N. The effect of rapamycin, NVP-BEZ235, aspirin, and metformin on PI3K/AKT/mTOR signaling pathway of PIK3CA-related overgrowth spectrum (PROS). Oncotarget. 2017 Jul 11; 8(28):45470-45483. PMID: 28525374.
      Citations: 6   Article has an altmetric score of 2    Fields:    Translation:HumansCells
    5. Suzuki K, Yamada K, Fukuhara Y, Tsuji A, Shibata K, Wakamatsu N. High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice. PLoS One. 2017; 12(6):e0180279. PMID: 28665968.
      Citations: 5   Article has an altmetric score of 4    Fields:    Translation:HumansAnimals
    6. Fukushi D, Kurosawa K, Suzuki Y, Suzuki K, Yamada K, Watanabe S, Yokochi K, Wakamatsu N. Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter. Am J Med Genet A. 2017 Aug; 173(8):2201-2209. PMID: 28599099.
      Citations: 1   Article has an altmetric score of 1    Translation:HumansCells
    7. Hosoda A, Gatayama R, Moriyama S, Ishii N, Yamada K, Matsuzaki Y, Shinjoh M. The first case of recurrent ultra late onset group B streptococcal sepsis in a 3-year-old child. IDCases. 2017; 7:16-18. PMID: 27920985.
      Citations: 1   
    8. Baba S, Saito T, Yamada Y, Takeshita E, Nomura N, Yamada K, Wakamatsu N, Sasaki M. Novel mutation in HPRT1 causing a splicing error with multiple variations. Nucleosides Nucleotides Nucleic Acids. 2017 Jan 02; 36(1):1-6. PMID: 27754763.
      Fields:    Translation:HumansCells
    9. Yamada K, Aiba K, Kitaura Y, Kondo Y, Nomura N, Nakamura Y, Fukushi D, Murayama K, Shimomura Y, Pitt J, Yamaguchi S, Yokochi K, Wakamatsu N. Clinical, biochemical and metabolic characterisation of a mild form of human short-chain enoyl-CoA hydratase deficiency: significance of increased N-acetyl-S-(2-carboxypropyl)cysteine excretion. J Med Genet. 2015 Oct; 52(10):691-8. PMID: 26251176.
      Citations: 24   Fields:    Translation:Humans
    10. Yamada K, Naiki M, Hoshino S, Kitaura Y, Kondo Y, Nomura N, Kimura R, Fukushi D, Yamada Y, Shimozawa N, Yamaguchi S, Shimomura Y, Miura K, Wakamatsu N. Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis. Mol Genet Metab Rep. 2014; 1:455-460. PMID: 27896122.
      Citations: 10   Article has an altmetric score of 3    
    11. Yamada Y, Nomura N, Yamada K, Matsuo M, Suzuki Y, Sameshima K, Kimura R, Yamamoto Y, Fukushi D, Fukuhara Y, Ishihara N, Nishi E, Imataka G, Suzumura H, Hamano S, Shimizu K, Iwakoshi M, Ohama K, Ohta A, Wakamoto H, Kajita M, Miura K, Yokochi K, Kosaki K, Kuroda T, Kosaki R, Hiraki Y, Saito K, Mizuno S, Kurosawa K, Okamoto N, Wakamatsu N. The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations. Am J Med Genet A. 2014 Aug; 164A(8):1899-908. PMID: 24715670.
      Citations: 11   Translation:HumansCells
    12. Naiki M, Ochi N, Kato YS, Purevsuren J, Yamada K, Kimura R, Fukushi D, Hara S, Yamada Y, Kumagai T, Yamaguchi S, Wakamatsu N. Mutations in HADHB, which encodes the ß-subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathy. Am J Med Genet A. 2014 May; 164A(5):1180-7. PMID: 24664533.
      Citations: 10   Translation:HumansCells
    13. Fukushi D, Yamada K, Nomura N, Naiki M, Kimura R, Yamada Y, Kumagai T, Yamaguchi K, Miyake Y, Wakamatsu N. Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2. Am J Med Genet A. 2014 Apr; 164A(4):924-33. PMID: 24478188.
      Citations: 6   Article has an altmetric score of 1    Translation:HumansCells
    14. Yoshimoto T, Himeno T, Takeshima S, Neshige S, Yamada K, Yamada Y, Kuriyama M. [Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase presenting seizure and psychomotor retardation: a case report]. Rinsho Shinkeigaku. 2014; 54(11):892-6. PMID: 25420563.
      Citations: Article has an altmetric score of 1    Fields:    Translation:Humans
    15. Yamada Y, Nomura N, Yamada K, Kimura R, Fukushi D, Wakamatsu N, Matsuda Y, Yamauchi T, Ueda T, Hasegawa H, Nakamura M, Ichida K, Kaneko K, Fujimori S. Hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiencies: HPRT1 mutations in new Japanese families and PRPP concentration. Nucleosides Nucleotides Nucleic Acids. 2014; 33(4-6):218-22. PMID: 24940672.
      Fields:    Translation:HumansCells
    16. Goto-Inoue N, Yamada K, Inagaki A, Furuichi Y, Ogino S, Manabe Y, Setou M, Fujii NL. Lipidomics analysis revealed the phospholipid compositional changes in muscle by chronic exercise and high-fat diet. Sci Rep. 2013 Nov 20; 3:3267. PMID: 24253370.
      Citations: 30   Article has an altmetric score of 1    Fields:    Translation:Animals
    17. Tsuchiya M, Manabe Y, Yamada K, Furuichi Y, Hosaka M, Fujii NL. Chronic exercise enhances insulin secretion ability of pancreatic islets without change in insulin content in non-diabetic rats. Biochem Biophys Res Commun. 2013 Jan 11; 430(2):676-82. PMID: 23211597.
      Citations: 3   Fields:    Translation:Animals
    18. Yamada K, Takado Y, Kato YS, Yamada Y, Ishiguro H, Wakamatsu N. Characterization of the mutant ß-subunit of ß-hexosaminidase for dimer formation responsible for the adult form of Sandhoff disease with the motor neuron disease phenotype. J Biochem. 2013 Jan; 153(1):111-9. PMID: 23127958.
      Citations: 4   Article has an altmetric score of 3    Fields:    Translation:HumansCells
    19. Yamada Y, Yamada K, Nomura N, Yamano A, Kimura R, Naiki M, Fukushi D, Wakamatsu N, Taniguchi A, Yamaoka N, Kaneko K, Fujimori S. Molecular analysis of X-linked inborn errors of purine metabolism: HPRT1 and PRPS1 mutations. Nucleosides Nucleotides Nucleic Acids. 2011 Dec; 30(12):1272-5. PMID: 22132986.
      Citations: 3   Fields:    Translation:Humans
    20. Naiki M, Mizuno S, Yamada K, Yamada Y, Kimura R, Oshiro M, Okamoto N, Makita Y, Seishima M, Wakamatsu N. MBTPS2 mutation causes BRESEK/BRESHECK syndrome. Am J Med Genet A. 2012 Jan; 158A(1):97-102. PMID: 22105905.
      Citations: 9   Article has an altmetric score of 3    Translation:Humans
    21. Yamada K, Nomura N, Yamano A, Yamada Y, Wakamatsu N. Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain development. Gene. 2012 Jan 15; 492(1):270-5. PMID: 22037487.
      Citations: 11   Article has an altmetric score of 3    Fields:    Translation:HumansAnimalsCells
    22. Mizuno S, Fukushi D, Kimura R, Yamada K, Yamada Y, Kumagai T, Wakamatsu N. Clinical and genomic characterization of siblings with a distal duplication of chromosome 9q (9q34.1-qter). Am J Med Genet A. 2011 Sep; 155A(9):2274-80. PMID: 21834029.
      Citations: 3   Translation:HumansCells
    23. Yamada K, Miura K, Hara K, Suzuki M, Nakanishi K, Kumagai T, Ishihara N, Yamada Y, Kuwano R, Tsuji S, Wakamatsu N. A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations. BMC Med Genet. 2010 Dec 22; 11:171. PMID: 21176162.
      Citations: 27   Fields:    Translation:Humans
    24. Yamada K, Fukushi D, Ono T, Kondo Y, Kimura R, Nomura N, Kosaki KJ, Yamada Y, Mizuno S, Wakamatsu N. Characterization of a de novo balanced t(4;20)(q33;q12) translocation in a patient with mental retardation. Am J Med Genet A. 2010 Dec; 152A(12):3057-67. PMID: 21086493.
      Citations: 7   Translation:HumansCells
    25. Niimura F, Kamei A, Tamame T, Yamada K, Komaki F, Okamoto S, Matsuda S, Oh Y, Endoh M. C1q nephropathy in a 2-year-old boy presenting with steroid resistant nephrotic syndrome. Tokai J Exp Clin Med. 2007 Sep 20; 32(3):95-8. PMID: 21318945.
      Fields:    Translation:Humans
    26. Yamada Y, Nomura N, Yamada K, Wakamatsu N. Molecular analysis of HPRT deficiencies: an update of the spectrum of Asian mutations with novel mutations. Mol Genet Metab. 2007 Jan; 90(1):70-6. PMID: 17027311.
      Citations: 2   Fields:    Translation:HumansCells
    27. Kondo Y, Mizuno S, Ohara K, Nakamura T, Yamada K, Yamamori S, Hayakawa C, Ishii T, Yamada Y, Wakamatsu N. Two cases of partial trisomy 21 (pter-q22.1) without the major features of Down syndrome. Am J Med Genet A. 2006 Feb 01; 140(3):227-32. PMID: 16411203.
      Citations: 3   Translation:HumansCells
    28. Mizuno S, Yamada Y, Yamada K, Nomura N, Wakamatsu N. Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation. Congenit Anom (Kyoto). 2005 Jun; 45(2):59-61. PMID: 15904433.
      Citations: 2   Fields:    Translation:Humans
    29. Mizunuma M, Yamada Y, Yamada K, Sonta S, Wakamatsu N, Kaneko K, Ogasawara N, Fujimori S. Disruption of the hypoxanthine-guanine phosphoribosyl-transferase gene caused by a translocation in a patient with Lesch-Nyhan syndrome. Nucleosides Nucleotides Nucleic Acids. 2004 Oct; 23(8-9):1173-6. PMID: 15571224.
      Citations: 2   Fields:    Translation:HumansCells
    30. Lescure A, Allmang C, Yamada K, Carbon P, Krol A. cDNA cloning, expression pattern and RNA binding analysis of human selenocysteine insertion sequence (SECIS) binding protein 2. Gene. 2002 May 29; 291(1-2):279-85. PMID: 12095701.
      Citations: 20   Article has an altmetric score of 3    Fields:    Translation:HumansCells
    31. Mutoh N, Nakagawa CW, Yamada K. Characterization of Cu, Zn-superoxide dismutase-deficient mutant of fission yeast Schizosaccharomyces pombe. Curr Genet. 2002 May; 41(2):82-8. PMID: 12073089.
      Citations: 2   Fields:    Translation:Animals