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Evolution and diversity of the 2–oxoglutarate‐dependent dioxygenase superfamily in plants

The Plant journal : for cell and molecular biology, 2014-04, Vol.78 (2), p.328-343

2014

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Practical guide for managing large-scale human genome data in research

Journal of human genetics, 2021-01, Vol.66 (1), p.39-52

2021

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A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing

Journal of human genetics, 2019-05, Vol.64 (5), p.359-368

2019

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Comprehensive analysis of microsatellite polymorphisms in human populations

Human genetics, 2023-01, Vol.142 (1), p.45-57

2023

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A conserved strategy of chalcone isomerase-like protein to rectify promiscuous chalcone synthase specificity

Nature communications, 2020-02, Vol.11 (1), p.870-870, Article 870

2020

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GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion

Scientific reports, 2022-01, Vol.12 (1), p.1332-1332, Article 1332

2022

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Exploring models of human migration to the Japanese archipelago using genome-wide genetic data

Anthropological Science, 2021, Vol.129(1), pp.45-58

2021

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Late Jomon male and female genome sequences from the Funadomari site in Hokkaido, Japan

Anthropological Science, 2019, Vol.127(2), pp.83-108

2019

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House mouse Mus musculus dispersal in East Eurasia inferred from 98 newly determined complete mitochondrial genome sequences

Heredity, 2021-01, Vol.126 (1), p.132-147

2021

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Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals

Journal of human genetics, 2015-10, Vol.60 (10), p.581-587

2015

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Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19

Scientific reports, 2022-03, Vol.12 (1), p.3854-3854, Article 3854

2022

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Identification of a Highly Specific Isoflavone 7-O-glucosyltransferase in the soybean (Glycine max (L.) Merr.)

Plant and cell physiology, 2015-08, Vol.56 (8), p.1512-1520

2015

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Time-Series Filtering for Replicated Observations via a Kernel Approximate Bayesian Computation

IEEE transactions on signal processing, 2018-12, Vol.66 (23), p.6148-6161

2018

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Bone Regeneration Using Dentin Matrix Depends on the Degree of Demineralization and Particle Size

PloS one, 2016-01, Vol.11 (1), p.e0147235-e0147235

2016

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Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people

Journal of human genetics, 2021-07, Vol.66 (7), p.681-687

2021

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rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis

Scientific reports, 2021-02, Vol.11 (1), p.4557-4557, Article 4557

2021

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Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels

Genetics (Austin), 2020-04, Vol.214 (4), p.1079-1090

2020

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Proton Transfer Reaction Mass Spectrometry

Journal of the Mass Spectrometry Society of Japan, 2022/03/01, Vol.70(1), pp.70-71

Kawai, Yosuke

2022

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Bcl2l1 Deficiency in Osteoblasts Reduces the Trabecular Bone Due to Enhanced Osteoclastogenesis Likely through Osteoblast Apoptosis

International journal of molecular sciences, 2023-12, Vol.24 (24), p.17319

2023

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HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data

BMC genomics, 2015-01, Vol.16 Suppl 2 (S2), p.S7-S7, Article S7

2015

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Dlx5 and Mef2 Regulate a Novel Runx2 Enhancer for Osteoblast‐Specific Expression

Journal of bone and mineral research, 2014-09, Vol.29 (9), p.1960-1969

2014

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Phasing analysis of lung cancer genomes using a long read sequencer

Nature communications, 2022-06, Vol.13 (1), p.3464-3464, Article 3464

2022

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NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study

Journal of gastroenterology, 2018-09, Vol.53 (9), p.1065-1078

2018

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A novel NODAL variant in a young embolic stroke patient with visceral heterotaxy

BMC neurology, 2024-04, Vol.24 (1), p.119-119

2024

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Evolution and diversity of the 2–oxoglutarate‐dependent dioxygenase superfamily in plants

Practical guide for managing large-scale human genome data in research

A 12-kb structural variation in progressive myoclonic epilepsy was newly identified by long-read whole-genome sequencing

Comprehensive analysis of microsatellite polymorphisms in human populations

A conserved strategy of chalcone isomerase-like protein to rectify promiscuous chalcone synthase specificity

GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion

Exploring models of human migration to the Japanese archipelago using genome-wide genetic data

Late Jomon male and female genome sequences from the Funadomari site in Hokkaido, Japan

House mouse Mus musculus dispersal in East Eurasia inferred from 98 newly determined complete mitochondrial genome sequences

Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals

Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19

Identification of a Highly Specific Isoflavone 7-O-glucosyltransferase in the soybean (Glycine max (L.) Merr.)

Time-Series Filtering for Replicated Observations via a Kernel Approximate Bayesian Computation

Bone Regeneration Using Dentin Matrix Depends on the Degree of Demineralization and Particle Size

Genome-wide SNP data of Izumo and Makurazaki populations support inner-dual structure model for origin of Yamato people

rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis

Contribution of Rare Variants of the SLC22A12 Gene to the Missing Heritability of Serum Urate Levels

Proton Transfer Reaction Mass Spectrometry

Bcl2l1 Deficiency in Osteoblasts Reduces the Trabecular Bone Due to Enhanced Osteoclastogenesis Likely through Osteoblast Apoptosis

HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data

Dlx5 and Mef2 Regulate a Novel Runx2 Enhancer for Osteoblast‐Specific Expression

Phasing analysis of lung cancer genomes using a long read sequencer

NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study

A novel NODAL variant in a young embolic stroke patient with visceral heterotaxy

Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis

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