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1. Rare FBXO18 variations and risk of schizophrenia: Whole‐exome sequencing in two parent‐affected offspring trios followed by resequencing and case–control studies. Issue 8 (10th May 2017)

2. Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole‐exome sequencing of a multiplex family and follow‐up study in a Japanese population. Issue 8 (17th February 2015)

3. Rare PDCD11 variations are not associated with risk of schizophrenia in Japan. Issue 11 (31st July 2017)

4. 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. (30th January 2016)

5. Rare UNC13B variations and risk of schizophrenia: Whole‐exome sequencing in a multiplex family and follow‐up resequencing and a case–control study. Issue 6 (14th March 2016)

6. Resequencing and association analysis of GAP43 with autism spectrum disorder and schizophrenia in a Japanese population. (April 2021)

7. Resequencing and association analysis of OXTR with autism spectrum disorder in a Japanese population. Issue 3 (7th July 2014)

9. Whole-exome sequencing in a family with a monozygotic twin pair concordant for autism spectrum disorder and a follow-up study. Issue 1 (30th September 2015)