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Mitsuhiro Kato

24PUBLICATIONS

136CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Clinical social work practiceNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)

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Publications (24)

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|Nov 06, 2025

Long-read genomic analyses to elucidate hidden structural variations associated with MECP2 duplication syndrome.

Qiaowei Liang, Yuri Uchiyama, Rie Seyama

|Jan 22, 2025

Clinical and genetic spectrum of patients with IRF2BPL syndrome.

Kazuhiro Iwama, Mitsuhiro Kato, Yuri Uchiyama

|May 28, 2024

Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A-related epilepsy and/or neurodevelopmental disorders.

Gabrielle Conecker, Maya Y Xia, JayEtta Hecker

|May 28, 2024

Global modified-Delphi consensus on comorbidities and prognosis of SCN8A-related epilepsy and/or neurodevelopmental disorders.

Gabrielle Conecker, Maya Y Xia, JayEtta Hecker

|Jan 12, 2024

Detection of hidden intronic DDC variant in aromatic L-amino acid decarboxylase deficiency by adaptive sampling.

Eriko Koshimizu, Mitsuhiro Kato, Kazuharu Misawa

|Mar 27, 2023

Molecular diagnosis of 405 individuals with autism spectrum disorder.

Noriko Miyake, Yoshinori Tsurusaki, Ryoko Fukai

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Frequent Collaborators

12 joint publications

Naomichi Matsumoto

11 joint publications

Hirotomo Saitsu

10 joint publications

Mitsuko Nakashima

7 joint publications

Takeshi Mizuguchi

5 joint publications

Satoko Miyatake

4 joint publications

Yuri Uchiyama

4 joint publications

Eriko Koshimizu

4 joint publications

Naomi Tsuchida

3 joint publications

Hitoshi Osaka

3 joint publications

Atsushi Takata

Frequent Collaborators

12 joint publications

Naomichi Matsumoto

11 joint publications

Hirotomo Saitsu

10 joint publications

Mitsuko Nakashima

7 joint publications

Takeshi Mizuguchi

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