Ayako Nunokawa

Whole-exome sequencing in a family with a monozygotic twin pair concordant for schizophrenia and a follow-up case-control study of identified de-novo variants.

Journal: Psychiatric genetics

Published: February 28, 2020

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.

Journal: Cell reports

Published: January 17, 2018

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.

Journal: Psychiatry and clinical neurosciences

Published: March 21, 2017

Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.

Journal: Psychiatry and clinical neurosciences

Published: January 18, 2017

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: December 18, 2015

Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.

Journal: Psychiatry research

Published: October 01, 2015

High-resolution copy number variation analysis of schizophrenia in Japan.

Journal: Molecular psychiatry

Published: September 20, 2015

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

Journal: PloS one

Published: June 21, 2015

Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population.

Journal: Neuropsychiatric disease and treatment

Published: June 18, 2015

Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study.

Journal: Psychiatry research

Published: March 17, 2015

Association analysis of the HLA-DRB101 and HLA-DRB104 with schizophrenia by tag SNP genotyping in the Japanese population.

Journal: Psychiatry research

Published: February 22, 2015

Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese population.

Journal: PloS one

Published: November 14, 2014

Whole-exome sequencing in a family with a monozygotic twin pair concordant for schizophrenia and a follow-up case-control study of identified de-novo variants.

Whole-exome sequencing in a family with a monozygotic twin pair concordant for schizophrenia and a follow-up case-control study of identified de-novo variants.

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.

Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.

Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.

Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.

Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.

Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.

Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population.

High-resolution copy number variation analysis of schizophrenia in Japan.

High-resolution copy number variation analysis of schizophrenia in Japan.

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

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

Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population.

Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population.

Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study.

Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study.

Association analysis of the HLA-DRB1*01 and HLA-DRB1*04 with schizophrenia by tag SNP genotyping in the Japanese population.

Association analysis of the HLA-DRB1*01 and HLA-DRB1*04 with schizophrenia by tag SNP genotyping in the Japanese population.

Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese population.

Novel rare missense variations and risk of autism spectrum disorder: whole-exome sequencing in two families with affected siblings and a two-stage follow-up study in a Japanese population.

Association analysis of the HLA-DRB101 and HLA-DRB104 with schizophrenia by tag SNP genotyping in the Japanese population.

Association analysis of the HLA-DRB101 and HLA-DRB104 with schizophrenia by tag SNP genotyping in the Japanese population.