Search

Search Constraints

You searched for: Author/Creator Igeta, Hirofumi

Search Results

3. Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis. (April 2022)

4. 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)

5. 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)

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

7. 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)

8. 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)

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