Tsutomu Ogata

Professor

Hamamatsu University School of Medicine

Japan

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About

Professor Tsutomu Ogata is a faculty member at Hamamatsu University School of Medicine in Japan. His research areas include genetic factors related to height differences, epilepsy, Prader-Willi syndrome, and various genetic syndromes affecting reproduction and growth. He has contributed significantly to understanding the phenotypic variations in genetic disorders through numerous publications in these fields.

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Collaborators (4)

Hirotomo Saitsu

Hamamatsu University School of Medicine

JAPAN

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Takato Akiba

Juntendo University

JAPAN

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Tomohiro Ishii

Associate Professor

Keio University School of Medicine

JAPAN

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Kenichi Kashimada

Assistant Professor

Tokyo Medical and Dental University

JAPAN

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Tsutomu Ogata

Research Interests

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About

Articles (20)

Phenotypic variation in a family with GABRG2-related epilepsy caused by a novel missense variant

Why are men taller than women?: Genetic and hormonal factors involved in sex differences in human height

Temple Syndrome: Comprehensive Clinical Study in Genetically Confirmed 60 Japanese Patients

Homozygous FIGLA missense variant in two Japanese sisters with primary ovarian insufficiency: Case reports and literature review

<i>SHOX</i> and sex difference in height: a hypothesis

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

Congratulations on the 100<sup>th</sup> anniversary of the Japan Endocrine Society

Glutamic acid decarboxylase antibody-spectrum disorders and type 1 diabetes mellitus in a patient following allogenic hematopoietic cell transplantation with review of literature

Improvement in body composition of Japanese participants with Prader-Willi syndrome following somatropin treatment: an open-label, multi cohort Phase 3 study

Pathogenic sequence variant and microdeletion affecting HMGA2 in Silver–Russell syndrome: case reports and literature review

A deep intronic TCTN2 variant activating a cryptic exon predicted by SpliceRover in a patient with Joubert syndrome

PORCN‐related microphthalmia with limb anomalies: Case report and literature review

Correction to: Growth references for Japanese individuals with Noonan syndrome

Frequency and clinical characteristics of distinct etiologies in patients with Silver-Russell syndrome diagnosed based on the Netchine-Harbison clinical scoring system

ACAN biallelic variants in a girl with severe idiopathic short stature

Pathogenic Copy Number and Sequence Variants in Children Born SGA With Short Stature Without Imprinting Disorders

Genome sequencing and RNA sequencing of urinary cells reveal an intronic FBN1 variant causing aberrant splicing

SHOX far‐downstream deletion in a patient with nonsyndromic short stature

A novel intronic PORCN variant creating an alternative splice acceptor site in a mother and her daughter with focal dermal hypoplasia

Retrotransposition disrupting EBP in a girl and her mother with X-linked dominant chondrodysplasia punctata

Collaborators (4)

Hirotomo Saitsu

Takato Akiba

Tomohiro Ishii

Kenichi Kashimada

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