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Clinical Calcium|February 5, 2008
[Genomic approaches to bone and joint diseases. A genome-wide approach for analysis of polygenic diseases]Hidenori Sato, Mitsuru Emi
Biological & Pharmaceutical Bulletin|March 1, 2023
Structural Variants of Midnolin, a Genetic Risk Factor for Parkinson's Disease, in a Yamagata CohortHidenori Sato, Kuniaki Ishii, Yutaro Obara
Cureus|July 14, 2025
Absence of KRAS Mutation as an Indicator of Pancreatic Metastasis Originating From Lung Cancer: A Case ReportShuhei Suzuki, Soshi Oyama, Takanobu Kabasawa, et al.
Annals of Clinical and Translational Neurology|October 8, 2019
Midnolin is a confirmed genetic risk factor for Parkinson's diseaseYutaro Obara, Hidenori Sato, Takahiro Nakayama, et al.
Emerging Infectious Diseases|January 20, 2018
Cerebral Syphilitic Gumma in Immunocompetent Man, JapanTatsuya Kodama, Hidenori Sato, Morichika Osa, et al.
BMC Medical Genetics|March 29, 2017
Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disordersShingo Koyama, Hidenori Sato, Manabu Wada, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 21, 2024
[A pedigree of myotonia congenita with a novel mutation p.F343C of the CLCN1 gene]Yoshitsugu Nakamura, Hidenori Sato, Kensuke Kakiuchi, et al.
ACS Omega|June 26, 2023
Direct Observation of Palladium Leaching from Pd/C by a Simple Method: X-ray Absorption Spectroscopy of Heterogeneous MixturesKenichi Uno, Takanori Itoh, Hidenori Sato, et al.
Scientific Reports|July 21, 2017
Midnolin is a novel regulator of parkin expression and is associated with Parkinson's DiseaseYutaro Obara, Toru Imai, Hidenori Sato, et al.
BMC Zoology|May 11, 2023
Complete mitochondrial genomes of three fairy shrimps from snowmelt pools in JapanTakashi Kitano, Hidenori Sato, Norihito Takahashi, et al.
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