• 1023 Citations
  • 20 h-Index
20062019
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Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 12 Similar Profiles
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Research Output 2006 2019

  • 1023 Citations
  • 20 h-Index
  • 46 Article
  • 5 Review article
  • 1 Comment/debate
  • 1 Short survey

A case of dihydropyrimidinase deficiency incidentally detected by urine metabolome analysis

Tsuchiya, H., Akiyama, T., Kuhara, T., Nakajima, Y., Ohse, M., Kurahashi, H., Kato, T., Maeda, Y., Yoshinaga, H. & Kobayashi, K., 01-03-2019, In : Brain and Development. 41, 3, p. 280-284 5 p.

Research output: Contribution to journalArticle

Metabolome
Urine
Mutation
Fluorouracil
Metabolomics
2 Citations (Scopus)

DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication

Tahara, S., Tahara, T., Horiguchi, N., Kato, T., Shinkai, Y., Yamashita, H., Yamada, H., Kawamura, T., Terada, T., Okubo, M., Nagasaka, M., Nakagawa, Y., Shibata, T., Yamada, S., Urano, M., Tsukamoto, T., Kurahashi, H., Kuroda, M. & Ohmiya, N., 01-01-2019, In : International Journal of Cancer. 144, 1, p. 80-88 9 p.

Research output: Contribution to journalArticle

DNA Methylation
Gastric Mucosa
Helicobacter pylori
Methylation
Stomach
1 Citation (Scopus)

Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders

Terasawa, S., Kato, A., Nishizawa, H., Kato, T., Yoshizawa, H., Noda, Y., Miyazaki, J., Ito, M., Sekiya, T., Fujii, T. & Kurahashi, H., 01-01-2019, In : Congenital Anomalies. 59, 1, p. 4-10 7 p.

Research output: Contribution to journalArticle

Thanatophoric Dysplasia
Achondroplasia
Multiplex Polymerase Chain Reaction
Prenatal Diagnosis
Mutation

Obstetric complication-associated ANXA5 promoter polymorphisms may affect gene expression via DNA secondary structures

Inagaki, H., Ota, S., Nishizawa, H., Miyamura, H., Nakahira, K., Suzuki, M., Nishiyama, S., Kato, T., Yanagihara, I. & Kurahashi, H., 01-05-2019, In : Journal of Human Genetics. 64, 5, p. 459-466 8 p.

Research output: Contribution to journalArticle

G-Quadruplexes
Annexin A5
Obstetrics
Gene Expression
DNA

FOXA2 gene mutation in a patient with congenital complex pituitary hormone deficiency

Boda, H., Miyata, M., Inagaki, H., Shinkai, Y., Kato, T., Yoshikawa, T. & Kurahashi, H., 01-01-2018, (Accepted/In press) In : European Journal of Medical Genetics.

Research output: Contribution to journalArticle

Pituitary Hormones
Missense Mutation
Intestinal Atresia
Imperforate Anus
Haploinsufficiency