| Accession |
PRJCA001606 |
| Title |
Targeted Sequencing of Autism Risk Genes |
| Relevance |
Medical |
| Data types |
Targeted Locus (Loci)
|
| Organisms |
Homo sapiens
|
| Description |
This project aims to understand the prevalence, inheritance, and genotype-phenotype correlations of mutations for autism candidate genes by massively parallel targeted-sequencing approach. |
| Sample scope |
Multispecies |
| Release date |
2019-08-08 |
| Publication |
| PubMed ID |
Article title |
Journal name |
DOI |
Year |
| 27824329
|
De novo genic mutations among a Chinese autism spectrum disorder cohort
|
Nature Communications
|
10.1038/ncomms13316
|
2016
|
| 30564305
|
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model
|
Molecular Autism
|
10.1186/s13229-018-0247-z
|
2018
|
| 31300657
|
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
|
Nature Communications
|
10.1038/s41467-019-10910-w
|
2019
|
|
|
| Grants |
| Agency |
program |
Grant ID |
Grant title |
| National Natural Science Foundation of China (NSFC)
|
National Science Funds for Distinguished Young Scholars
|
81525007
|
|
| National Natural Science Foundation of China (NSFC)
|
General Program
|
81871079
|
|
|
|
| Submitter |
Hui
Guo (guohui@sklmg.edu.cn)
|
| Organization |
Central South University |
| Submission date |
2019-07-24 |
