Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing
Our data suggest that these identified variants are essential for the genetic architecture of HFA.
Authors
- Shigeru Yokoyama (ORCID: https://orcid.org/0000-0001-5044-1400)
- Chiaki Hasegawa (ORCID: https://orcid.org/0000-0001-8730-8769)
- Yuka Shiota
- Yuko Yoshimura (ORCID: https://orcid.org/0000-0001-9226-4561)
- Tomoaki Nishiyama (ORCID: https://orcid.org/0000-0003-1279-7806)
- Sanae Tanaka (ORCID: https://orcid.org/0000-0003-4960-7965)
- Mitsuru Kikuchi (ORCID: https://orcid.org/0000-0003-3013-7844)
- Sumie Iwasaki (ORCID: https://orcid.org/0000-0002-6083-5902)
Institutions
- Kanazawa University (JP)
- University of Fukui (JP)
- Chiba University (JP)
- Japan Society for the Promotion of Science (JP)
- Hamamatsu University School of Medicine (JP)
- The University of Osaka (JP)
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2024-08-30
- DOI
- https://doi.org/10.3389/fgene.2024.1352480
- Citations
- 6
- Primary Topic
- Autism Spectrum Disorder Research
- Type
- article
- Field-Weighted Citation Impact
- 2.06
Funders
- Kawano Masanori Memorial Public Interest Incorporated Foundation
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- Moonshot Research and Development Program