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Journal of Human Genetics (1)
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Advanced filters: Author: Yoshinori Ozono Clear advanced filters

Mice with Calr mutations homologous to human CALR mutations only exhibit mild thrombocytosis

Kotaro Shide
Takuro Kameda
Kazuya Shimoda
ResearchOpen Access29 Mar 2019
Blood Cancer Journal

Volume: 9, P: 1-9
De novo WDR45 mutation in a patient showing clinically Rett syndrome with childhood iron deposition in brain

Chihiro Ohba
Shin Nabatame
Naomichi Matsumoto
Research13 Mar 2014
Journal of Human Genetics

Volume: 59, P: 292-295
Neoplastic fibrocytes play an essential role in bone marrow fibrosis in Jak2V617F-induced primary myelofibrosis mice

Yoshinori Ozono
Kotaro Shide
Kazuya Shimoda
ResearchOpen Access29 May 2020
Leukemia

Volume: 35, P: 454-467
Genetic and phenotypic landscape of the mitochondrial genome in the Japanese population

Kenichi Yamamoto et al. report a genetic analysis of mitochondrial DNA (mtDNA) and a phenome-wide association study in Japanese individuals from the BioBank Japan Project. They describe the genetic landscape of the mitochondria and identify pleiotropic mtDNA variants associated with 5 late-onset complex traits.

Kenichi Yamamoto
Saori Sakaue
Yukinori Okada
ResearchOpen Access05 Mar 2020
Communications Biology

Volume: 3, P: 1-11

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