Monogenic defects in Russian children with autism spectrum disorders
These data confirm a tremendous diversity of genetic causes of ASD. Clinical exome sequencing may serve as a reasonable alternative to whole-exome sequencing.
Authors
- S. A. Laptiev (ORCID: https://orcid.org/0009-0004-0163-0271)
- Евгений Наумович Имянитов (ORCID: https://orcid.org/0000-0003-4529-7891)
- Yuliy A. Gorgul
- Evgeny N. Suspitsin (ORCID: https://orcid.org/0000-0001-9764-2090)
- Т. В. Мелашенко (ORCID: https://orcid.org/0000-0001-6693-8710)
- Maria V. Syomina (ORCID: https://orcid.org/0009-0003-3206-2871)
- Anastasiya S Abuzova (ORCID: https://orcid.org/0009-0006-0170-6963)
- Polina R. Korzun
- Jeyla O. Binnatova
- Olga S Sharonova
- Oksana V Efremova
- Kristina S Malysheva
- Anastasiya A Kuznitsyna
Institutions
- Leningrad Regional Cancer Center (RU)
- Institute of Oncology NN Petrov (RU)
- Saint Petersburg State Pediatric Medical University (RU)
Publication Details
- Journal
- World Journal of Clinical Pediatrics
- Published
- 2025-10-31
- DOI
- https://doi.org/10.5409/wjcp.v14.i4.108733
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Russian Science Foundation
- Intellectual and Developmental Disabilities Research Center