T. Kawabata

Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia

M. Ikeda, J. Egawa, T. Someya, 2020, Journal of Neurodevelopmental Disorders.

Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders

M. Ikeda, Y. Iwayama, T. Yoshikawa, 2017, Translational Psychiatry.

Gene expression and pathway analysis of CTNNB1 in cancer and stem cells

H. Yokozaki, Shihori Tanabe, K. Aoyagi, 2016, World journal of stem cells.

Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder

M. Ikeda, H. Bito, Shin-ichiro Horigane, 2022, Translational Psychiatry.

A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility

M. Ikeda, Y. Iwayama, T. Yoshikawa, 2017, Translational Psychiatry.