J. Xing

发表

High-resolution copy number variation analysis of schizophrenia in Japan

M. Itokawa, T. Shimamura, T. Takahashi, 2017, Molecular Psychiatry.

Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders

B. Aleksic, I. Kushima, N. Ozaki, 2016, PloS one.

Common genetic risk factors in ASD and ADHD co-occurring families

Jinchuan Xing, S. Buyske, C. Bartlett, 2022, Human Genetics.

Identification of a rare variant in CHD8 that contributes to schizophrenia and autism spectrum disorder susceptibility

M. Ikeda, N. Iwata, B. Aleksic, 2016, Schizophrenia Research.

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

M. Owen, Jinchuan Xing, M. State, 2022, medRxiv.

Novel rare variants in F-box protein 45 (FBXO45) in schizophrenia

T. Iidaka, M. Ikeda, N. Iwata, 2014, Schizophrenia Research.

Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population

H. Kuwabara, M. Ikeda, Y. Iwayama, 2016, Scientific Reports.

Resequencing and Association Analysis of Six PSD-95-Related Genes as Possible Susceptibility Genes for Schizophrenia and Autism Spectrum Disorders

T. Iidaka, B. Aleksic, I. Kushima, 2016, Scientific Reports.

Association study of BCL9 gene polymorphism rs583583 with schizophrenia and negative symptoms in Japanese population

T. Iidaka, M. Ikeda, N. Iwata, 2015, Scientific Reports.

Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.

T. Iidaka, K. Kaibuchi, M. Ikeda, 2015, Schizophrenia bulletin.

Rare loss of function mutations in N-methyl-d-aspartate glutamate receptors and their contributions to schizophrenia susceptibility

K. Ohno, M. Ikeda, J. Egawa, 2018, Translational Psychiatry.

Resequencing and Association Analysis of CLN8 with Autism Spectrum Disorder in a Japanese Population

Shujiro Okuda, Yuichiro Watanabe, J. Egawa, 2015, PloS one.

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk

T. Shimamura, T. Nabeshima, K. Kaibuchi, 2020, Translational Psychiatry.

SET domain-containing protein 4: biological functions and role in genomic methylation profiles of bone marrow mesenchymal stem cells

Ru-jia Li, Junli Guo, Yanping Ha, 2020 .

Resequencing and Association Analysis of PTPRA, a Possible Susceptibility Gene for Schizophrenia and Autism Spectrum Disorders

M. Ikeda, N. Iwata, B. Aleksic, 2014, PloS one.