Fuyuki Miya

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Associate Professor

Keio University

Japan

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About

Fuyuki Miya serves as an Associate Professor at Keio University in Japan. His research focuses on the intersection of genomics and clinical diagnosis, particularly in relation to cancer immunotherapy and rare diseases. Recent articles authored by Professor Miya explore topics such as cost-effectiveness in whole-exome sequencing, tumor microenvironment diversity, and the genetic underpinnings of various conditions, including chronic thromboembolic pulmonary hypertension and neurodevelopmental disorders.

Recent Grants

Grant: Close

Multi-faceted approach to break the stagnation of the disease-causing mutations identified rates in Ekusomu analysis

Open Date: 2016-04-01

Close Date: 2019-03-31

Grant: Close

Study of responsible genes for cochlea and cochlear nerve dysplasia

Open Date: 2012-04-01

Close Date: 2014-03-31

Grant: Close

Elucidation of novel genes causing auditory neuropathy

Open Date: 2012-04-01

Close Date: 2015-03-31

Grant: Close

Attenuation of Progressive Hearing Loss in DBA/2J Mice by Epigenetic-Modifying Reagents

Open Date: 2012-04-01

Close Date: 2015-03-31

Grant: Close

Analysis of niche involved with survival, proliferation, and maintenance of undifferentiated state of glioma stem cell

Open Date: 2012-04-01

Close Date: 2015-03-31

Articles (15)

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2021

Collaborators (9)

Shinichi Goto

Tokai University School of Medicine

JAPAN

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Hiroki Hoshino

Tohoku University Hospital

JAPAN

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Hideaki Kanemura

JAPAN

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Kenjiro Kosaki

Professor

Keio University

JAPAN

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Jun-ichi Takanashi

Prof.

Tokyo Women’s Medical University Yachiyo Medical Center

JAPAN

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Mitsuhiro Kato

Professor

Showa University

JAPAN

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Atsuko Noguchi

Akita University Graduate School of Medicine

JAPAN

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Hiroyuki Adachi

Akita University Graduate School of Medicine

JAPAN

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Jun Hosoe

Assistant Professor

Graduate School of Medicine, The University of Tokyo

JAPAN

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Fuyuki Miya

Research Interests

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About

Recent Grants

Articles (15)

Augmenting cost-effectiveness in clinical diagnosis using extended whole-exome sequencing: SNVs, SVs, and beyond

Clonal diversity shapes the tumour microenvironment leading to distinct immunotherapy responses in metastatic urothelial carcinoma

An organoid library of human esophageal squamous cell carcinomas (ESCCs) uncovers the chemotherapy-resistant ESCC features

Japanese Public Health Insurance System’s new genomic strategic action to shorten the “diagnostic odyssey” for patients with rare and intractable diseases

Clonal Hematopoiesis in Chronic Thromboembolic Pulmonary Hypertension

A case of infantile epileptic spasms syndrome and autism spectrum disorder with an RFX3 mutation

Neurochemistry evaluated by magnetic resonance spectroscopy in a patient with FBXO28-related developmental and epileptic encephalopathy

Diagnosis of SLC25A46-related pontocerebellar hypoplasia in two siblings with fulminant neonatal course: role of postmortem CT and whole genomic analysis: a case report

Efficacy of ethosuximide on atonic seizures with KCNB1 mutation

Landscape of prognostic signatures and immunogenomics of the AXL/GAS6 axis in renal cell carcinoma

Four pedigrees with aminoacyl-tRNA synthetase abnormalities.

Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy.

Structural basis of ethnic-specific variants of PAX4 associated with type 2 diabetes.

Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants.

Two cases of DYNC1H1 mutations with intractable epilepsy.

Collaborators (9)

Shinichi Goto

Hiroki Hoshino

Hideaki Kanemura

Kenjiro Kosaki

Jun-ichi Takanashi

Mitsuhiro Kato

Atsuko Noguchi

Hiroyuki Adachi

Jun Hosoe

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