Kazuhito Satou
Tokyo, Japan
Last Updated: 09/26/2026
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Found 42 publications
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.
Journal: Frontiers in genetics
Published: February 07, 2024
Biallelic CC2D2A variants, SNV and LINE-1 insertion simultaneously identified in siblings using long-read whole-genome sequencing and haplotype phasing.
Journal: Journal of human genetics
Published: October 19, 2022
Complete Genome Sequence of Lactococcus cremoris Strain 7-1, a Lactic Acid Bacterium Isolated from a Traditional Mongolian Milk Product Possessing Mucin-Adhesive Ability.
Journal: Microbiology resource announcements
Published: April 04, 2022
Additional findings of tibial dysplasia in a male with orofaciodigital syndrome type XVI.
Journal: Human genome variation
Published: January 19, 2022
Publisher Correction: Essential roles of plexin-B3+ oligodendrocyte precursor cells in the pathogenesis of Alzheimer's disease.
Journal: Communications biology
Published: December 03, 2021
Helicobacter pylori genomes reveal Paleolithic human migration to the east end of Asia.
Journal: iScience
Published: August 26, 2021
Online questionnaire on genetic testing for intractable diseases in Japan: response to and issues associated with the revised medical care act.
Journal: Journal of human genetics
Published: February 21, 2021
Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome.
Journal: Clinical epigenetics
Published: June 30, 2020
A novel stop-gain CUL3 mutation in a Japanese patient with autism spectrum disorder.
Journal: Brain & development
Published: June 11, 2020
A severe case of status dystonicus caused by a de novo KMT2B missense mutation.
Journal: European journal of medical genetics
Published: April 09, 2020
Last Updated: 09/26/2026