Kenji Yamada

Dr. Kenji Yamada

Shimane University, Faculty of Medicine
orcid

Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2018 in Molecular Genetics and Metabolism Reports
Verified
Journal Article
Open access
NSNaoaki Shibata
Naoaki Shibata
YHYuki Hasegawa
Yuki Hasegawa
KYKenji Yamada
Kenji Yamada
HKHironori Kobayashi
Hironori Kobayashi
JPJamiyan Purevsuren
Jamiyan Purevsuren
SYSeiji Yamaguchi
Seiji Yamaguchi
Expanded newborn screening (ENBS) utilizing tandem mass spectrometry (MS/MS) for inborn metabolic diseases (IMDs), such as organic acidemias (OAs), fatty acid oxidation disorders, (FAODs), and amino acid disorders (AAs), is increasingly popular but has not yet been introduced in many Asian countries. This study aimed to determine the incidence rates of OAs, FAODs, and AAs in Asian countries and Germany using selective screening and ENBS records. Selective screening for IMDs using gas chromatography-mass spectrometry and MS/MS was performed among patients suspected to be afflicted in Asian countries (including Japan, Vietnam, China, and India) between 2000 and 2015, and the results from different countries were compared. Similarly, ENBS results from Japan, South Korea, Taiwan, and Germany were compared. Additionally, the results of selective screening and ENBS in Japan were compared. Among 39,270 patients who underwent selective screening, IMDs were detected in 1170. Methylmalonic acidemia was frequently identified in several countries, including Japan (81/377 diagnosed IMDs), China (94/216 IMDs), and India (72/293 IMDs). In Vietnam, however, β-ketothiolase deficiency was particularly frequent (33/250 IMDs). ENBS yielded differences in overall IMD rates by country: 1:8557 in Japan, 1:7030 in Taiwan, 1:13,205 in South Korea, and 1:2200 in Germany. Frequently discovered diseases included propionic acidemia (PPA) and phenylketonuria (PKU) in Japan, 3-methylcrotonyl-CoA carboxylase deficiency (MCCD) and PKU in Taiwan, MCCD and citrullinemia type I in South Korea, and PKU and medium-chain acyl-CoA dehydrogenase deficiency in Germany. Furthermore, in Japan, selective screening and ENBS yielded respective PPA frequencies of 14.7% and 49.4% among all organic acidemias. The incidence rates of IMDs vary by country. Moreover, the disease spectra of IMDs detected via selective screening differ from those detected via ENBS.

6 November 2018 in Journal of Human Genetics
Verified
Journal Article
Closed access
PDF file
KYKenji Yamada
Kenji Yamada
TTTakeshi Taketani
Takeshi Taketani

1 September 2012 in Molecular Genetics and Metabolism
Verified
Journal Article
Closed access
SYSeiji Yamaguchi
Seiji Yamaguchi
HLHong Li
Hong Li
JPJamiyan Purevsuren
Jamiyan Purevsuren
KYKenji Yamada
Kenji Yamada
MFMidori Furui
Midori Furui
SFSeiji Fukuda
Seiji Fukuda

1 May 2014 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
TYTetsuhiko Yasuno
Tetsuhiko Yasuno
KOKenji Osafune
Kenji Osafune
HSHidetoshi Sakurai
Hidetoshi Sakurai
IAIsao Asaka
Isao Asaka
ATAkihito Tanaka
Akihito Tanaka
HKHidetoshi Kaneoka
Hidetoshi Kaneoka

1 March 2016 in Brain and Development
Verified
Journal Article
Closed access
KYKenji Yamada
Kenji Yamada
HKHironori Kobayashi
Hironori Kobayashi
RBRyosuke Bo
Ryosuke Bo
TTTomoo Takahashi
Tomoo Takahashi
JPJamiyan Purevsuren
Jamiyan Purevsuren
SYSeiji Yamaguchi
Seiji Yamaguchi