Kenichi Kashimada

Assistant Professor

Tokyo Medical and Dental University

Japan

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About

Kenichi Kashimada is an Assistant Professor at Tokyo Medical and Dental University in Japan. His research focuses on developmental biology, genetic disorders, and endocrine conditions, as evidenced by his recent publications on transcriptional regulatory mechanisms, hyperphagia in Prader-Willi syndrome, and novel case reports related to genetic anomalies. His contributions to the field enhance the understanding of both common and rare medical conditions.

Articles (14)

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2025

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2025

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2025

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2021

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2021

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2020

Collaborators (6)

Tomohiro Morio

Professor and Chairman

Tokyo Medical and Dental University

JAPAN

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Kei Takasawa

JAPAN

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Shizuka Kirino

Tokyo Medical and Dental University

JAPAN

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Masatoshi Takagi

Tokyo Medical and Dental University

JAPAN

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Tomohiro Ishii

Associate Professor

Keio University School of Medicine

JAPAN

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Tsutomu Ogata

Professor

Hamamatsu University School of Medicine

JAPAN

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Kenichi Kashimada

Research Interests

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About

Articles (14)

A questionnaire-based survey on hyperphagia in individuals with Prader–Willi syndrome in Japan

Analysis of Functional Cis-regulatory Elements Reveals Novel Transcriptional Regulatory Mechanisms in Gonadal Development

Classic 21‐hydroxylase deficiency in opposite‐sex twins

RMRP-related short stature: A report of six additional Japanese individuals with cartilage hair hypoplasia and literature review.

Monitoring hypoparathyroidism in long QT syndrome detected by electrocardiogram screening

Neonatal alloimmune thrombocytopenia associated with fetomaternal hemorrhage

Transient immune deficiency accompanied with homozygous CBL rare variant

A suspected case of heterotopic glia in an MM‐twin discordant for anencephaly

Autonomously functioning thyroid nodule due to a somatic TSHR mutation

PAX3/7-FOXO1 fusion-negative alveolar rhabdomyosarcoma in Schuurs-Hoeijmakers syndrome

When to eat and sleep matters to children's health

Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation

The flash glucose monitoring system is useful but has some limitations

Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited

Collaborators (6)

Tomohiro Morio

Kei Takasawa

Shizuka Kirino

Masatoshi Takagi

Tomohiro Ishii

Tsutomu Ogata

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