Naoto Nishimura

5PUBLICATIONS
17CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Medical devicesGene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|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 GRIN1 variant.

Naoto Nishimura, Tatsuro Kumaki, Hiroaki Murakami

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