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Naoto Nishimura

5PUBLICATIONS

17CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)Medical devicesGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Cancer genetics

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Publications (5)

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|May 02, 2025

Hemizygous SMARCA1 variants cause X-linked intellectual disability.

Naoto Nishimura, Takeshi Mizuguchi, Keisuke Hamada

|Dec 23, 2022

Complex congenital cardiovascular anomaly in a patient with AGO1-associated disorder.

Minako Takagi, Shin Ono, Tatsuro Kumaki

|Oct 16, 2020

Arthrogryposis multiplex congenita with polymicrogyria and infantile encephalopathy caused by a novel <i>GRIN1</i> variant.

Naoto Nishimura, Tatsuro Kumaki, Hiroaki Murakami

|Apr 12, 2020

Multiple craniosynostosis and facial dysmorphisms with homozygous IL11RA variant caused by maternal uniparental isodisomy of chromosome 9.

Naoto Nishimura, Hiroaki Murakami, Tomoko Hayashi

|Oct 10, 2019

Tumor predisposition in an individual with chromosomal rearrangements of 1q31.2-q41 encompassing cell division cycle protein 73.

Naoto Nishimura, Hiroaki Murakami, Toshiyuki Saito

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Frequent Collaborators

4 joint publications

Kenji Kurosawa

3 joint publications

Hiroaki Murakami

1 joint publications

Takeshi Mizuguchi

1 joint publications

Keisuke Hamada

1 joint publications

Kotaro Yuge

1 joint publications

Masamune Sakamoto

1 joint publications

Naomi Tsuchida

1 joint publications

Yuri Uchiyama

1 joint publications

Atsushi Fujita

1 joint publications

Eriko Koshimizu

Frequent Collaborators

4 joint publications

Kenji Kurosawa

3 joint publications

Hiroaki Murakami

1 joint publications

Takeshi Mizuguchi

1 joint publications

Keisuke Hamada

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