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Shinichi Morishita

University of Tokyo

Japan

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Research Interests

Biostatistics

60%

Cell Biology

90%

Genomic

100%

Next-generation Sequencing

70%

Medical Science

50%

Neurodegenerative Disease

40%

Genetic

30%

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Articles20

A polygenic score method boosted by non-additive models

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Year:

2024

A whole-genome shotgun approach to human reference genome sequencing

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Year:

2024

A Japanese family with idiopathic basal ganglia calcification carrying a novel XPR1 variant

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Year:

2023

High-fat diet in early life triggers both reversible and persistent epigenetic changes in the medaka fish (Oryzias latipes)

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Year:

2023

JTK: targeted diploid genome assembler

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2023

A landscape of complex tandem repeats within individual human genomes.

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Year:

2023

Meningiomas in patients with neurofibromatosis type 2 predominantly comprise 'immunogenic subtype' tumours characterised by macrophage infiltration.

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Year:

2023

Phase-separated nuclear bodies of nucleoporin fusions promote condensation of MLL1/CRM1 and rearrangement of 3D genome structure.

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2023

Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1.

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Year:

2023

Decomposing mosaic tandem repeats accurately from long reads.

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Year:

2023

CTCF looping is established during gastrulation in medaka embryos

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2021

Hamster PIWI proteins bind to piRNAs with stage-specific size variations during oocyte maturation.

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2021

Finding long tandem repeats in long noisy reads

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2021

Investigating the mitochondrial genomic landscape of Arabidopsis thaliana by long-read sequencing

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2021

Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population

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2021

Splice-site mutations in KIF5A in the Japanese case series of amyotrophic lateral sclerosis

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Year:

2021

Targeted deep sequencing of DNA from multiple tissue types improves the diagnostic rate and reveals a highly diverse phenotype of mosaic neurofibromatosis type 2

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2021

The time is ripe to investigate human centromeres by long-read sequencing

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2021

A novel de novo KIF1A mutation in a patient with autism, hyperactivity, epilepsy, sensory disturbance, and spastic paraplegia

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Year:

2020

CNV analysis using whole exome sequencing identified biallelic CNVs of VPS13B in siblings with intellectual disability

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Year:

2020

Collaborators12

Yoichiro Nakatani

Osaka University

JAPAN

Manolis Kellis

Professor

Massachusetts Institute of Technology

UNITED STATES

Kuniaki Saito

Professor

National Institute of Genetics

JAPAN

Masahiro Oka

Associate Professor (Lecturer)

Osaka University

JAPAN

Ryohei Nakamura

University of Tokyo

JAPAN

Toshiyuki Kakumoto

University of Tokyo Hospital

JAPAN

Neva Durand

Broad Institute

UNITED STATES

Kiyotaka Nakamagoe

Assistant professor

University of Tsukuba

JAPAN

Yoichi Miyamoto

National Institutes of Biomedical Innovation, Health and Nutrition

JAPAN

Shin-ichi Arimura

Associate Professor

University of Tokyo

JAPAN

Hiroya Naruse

The Univeristy of Tokyo

JAPAN

Yuta Suzuki

Lecturer

University of Tokyo

JAPAN

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