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JHG Young Scientist Award 2023

Journal of human genetics, 2024-01, Vol.69 (1), p.1-1

Tanaka, Toshihiro

2024

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JHG Young Scientist Award 2022

Journal of human genetics, 2023-04, Vol.68 (4), p.237-237

Tanaka, Toshihiro

2023

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JHG Young Scientist Award

Journal of human genetics, 2022-02, Vol.67 (2), p.69-69

Tanaka, Toshihiro

2022

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The 2019 JHG Young Scientist Award

Journal of human genetics, 2020-03, Vol.65 (3), p.207-207

Matsumoto, Naomichi

2020

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The 2018 JHG Young Scientist Award

Journal of human genetics, 2019-01, Vol.64 (1), p.1-1

Matsumoto, Naomichi

2019

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The 2017 JHG Young Scientist Award

Journal of human genetics, 2017-12, Vol.62 (12), p.1007-1007

Matsumoto, Naomichi

2017

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The 2016 JHG Young Scientist Award

Journal of human genetics, 2017-05, Vol.62 (5), p.521-521

Matsumoto, Naomichi

2017

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A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

Journal of human genetics, 2011-01, Vol.56 (1), p.34-40

2011

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Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders

Journal of human genetics, 2012-10, Vol.57 (10), p.621-632

2012

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Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet-Biedl syndrome

Journal of human genetics, 2016-05, Vol.61 (5), p.447-450

2016

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Mutation spectrum of the dystrophin gene in 442 Duchenne Becker muscular dystrophy cases from one Japanese referral center

Journal of human genetics, 2010-06, Vol.55 (6), p.379-388

2010

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Genetics and pathological mechanisms of Usher syndrome

Journal of human genetics, 2010-06, Vol.55 (6), p.327-335

2010

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Admixture and population structure in Mexican-Mestizos based on paternal lineages

Journal of human genetics, 2012-09, Vol.57 (9), p.568-574

2012

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The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations

Journal of human genetics, 2012-12, Vol.57 (12), p.787-795

2012

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Influence of CYP3A5 and drug transporter polymorphisms on imatinib trough concentration and clinical response among patients with chronic phase chronic myeloid leukemia

Journal of human genetics, 2010-11, Vol.55 (11), p.731-737

2010

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Implications of gene copy-number variation in health and diseases

Journal of human genetics, 2012-01, Vol.57 (1), p.6-13

2012

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Association of the oxytocin receptor ( ) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population

Journal of human genetics, 2010-03, Vol.55 (3), p.137-141

2010

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The Indonesian archipelago: an ancient genetic highway linking Asia and the Pacific

Journal of human genetics, 2013-03, Vol.58 (3), p.165-173

2013

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Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia

Journal of human genetics, 2013-02, Vol.58 (2), p.91-97

2013

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Tumor suppressive microRNAs (miR-222 and miR-31) regulate molecular pathways based on microRNA expression signature in prostate cancer

Journal of human genetics, 2012-11, Vol.57 (11), p.691-699

2012

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Tumor suppressive microRNA-133a regulates novel molecular networks in lung squamous cell carcinoma

Journal of human genetics, 2012-01, Vol.57 (1), p.38-45

2012

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The pursuit of genome-wide association studies: where are we now?

Journal of human genetics, 2010-04, Vol.55 (4), p.195-206

2010

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Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis

Journal of human genetics, 2012-06, Vol.57 (6), p.363-367

2012

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Tumor suppressive microRNA-375 regulates oncogene AEG-1/MTDH in head and neck squamous cell carcinoma (HNSCC)

Journal of human genetics, 2011-08, Vol.56 (8), p.595-601

2011

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JHG Young Scientist Award 2023

JHG Young Scientist Award 2022

JHG Young Scientist Award

The 2019 JHG Young Scientist Award

The 2018 JHG Young Scientist Award

The 2017 JHG Young Scientist Award

The 2016 JHG Young Scientist Award

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders

A genome-wide association study of a coronary artery disease risk variant

Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet-Biedl syndrome

Mutation spectrum of the dystrophin gene in 442 Duchenne Becker muscular dystrophy cases from one Japanese referral center

Genetics and pathological mechanisms of Usher syndrome

Admixture and population structure in Mexican-Mestizos based on paternal lineages

The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations

Influence of CYP3A5 and drug transporter polymorphisms on imatinib trough concentration and clinical response among patients with chronic phase chronic myeloid leukemia

Implications of gene copy-number variation in health and diseases

Association of the oxytocin receptor ( ) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population

The Indonesian archipelago: an ancient genetic highway linking Asia and the Pacific

Comprehensive DNA methylation analysis of peripheral blood cells derived from patients with first-episode schizophrenia

Tumor suppressive microRNAs (miR-222 and miR-31) regulate molecular pathways based on microRNA expression signature in prostate cancer

Tumor suppressive microRNA-133a regulates novel molecular networks in lung squamous cell carcinoma

The pursuit of genome-wide association studies: where are we now?

Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis

Tumor suppressive microRNA-375 regulates oncogene AEG-1/MTDH in head and neck squamous cell carcinoma (HNSCC)

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