Shinichi Morishita

University of Tokyo

Japan

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Articles (20)

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2023

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2021

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2021

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2021

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2021

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2021

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2021

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2021

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2021

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2020

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2020

Collaborators (12)

Yoichiro Nakatani

Osaka University

JAPAN

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Manolis Kellis

Professor

Massachusetts Institute of Technology

UNITED STATES

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Kuniaki Saito

Professor

National Institute of Genetics

JAPAN

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Masahiro Oka

Associate Professor (Lecturer)

Osaka University

JAPAN

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Ryohei Nakamura

University of Tokyo

JAPAN

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Toshiyuki Kakumoto

University of Tokyo Hospital

JAPAN

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Neva Durand

Broad Institute

UNITED STATES

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Kiyotaka Nakamagoe

Assistant professor

University of Tsukuba

JAPAN

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Yoichi Miyamoto

National Institutes of Biomedical Innovation, Health and Nutrition

JAPAN

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Shin-ichi Arimura

Associate Professor

University of Tokyo

JAPAN

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Hiroya Naruse

The Univeristy of Tokyo

JAPAN

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Yuta Suzuki

Lecturer

University of Tokyo

JAPAN

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Shinichi Morishita

Research Interests

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Articles (20)

A polygenic score method boosted by non-additive models

A whole-genome shotgun approach to human reference genome sequencing

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

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

JTK: targeted diploid genome assembler

A landscape of complex tandem repeats within individual human genomes.

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

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

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

Decomposing mosaic tandem repeats accurately from long reads.

CTCF looping is established during gastrulation in medaka embryos

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

Finding long tandem repeats in long noisy reads

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

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

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

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

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

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

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

Collaborators (12)

Yoichiro Nakatani

Manolis Kellis

Kuniaki Saito

Masahiro Oka

Ryohei Nakamura

Toshiyuki Kakumoto

Neva Durand

Kiyotaka Nakamagoe

Yoichi Miyamoto

Shin-ichi Arimura

Hiroya Naruse

Yuta Suzuki

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