| meta-analysis | Q815382 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/MP.2012.148 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/mp.2012.148 |
| P698 | PubMed publication ID | 23147383 |
| P50 | author | Sagiv Shifman | Q37374201 |
| Eyal Ben-David | Q52280691 | ||
| P2860 | cites work | Patterns and rates of exonic de novo mutations in autism spectrum disorders | Q28264242 |
| Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations | Q29030218 | ||
| De Novo Gene Disruptions in Children on the Autistic Spectrum | Q29394534 | ||
| De novo mutations revealed by whole-exome sequencing are strongly associated with autism | Q29547269 | ||
| Spatio-temporal transcriptome of the human brain | Q29614572 | ||
| Evolution and functional impact of rare coding variation from deep sequencing of human exomes | Q29617587 | ||
| Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability | Q34283663 | ||
| ATP-dependent chromatin remodeling in neural development. | Q37482388 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | autism | Q38404 |
| P304 | page(s) | 1054-1056 | |
| P577 | publication date | 2012-11-13 | |
| P1433 | published in | Molecular Psychiatry | Q6895973 |
| P1476 | title | Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism | |
| P478 | volume | 18 |
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| Q28069757 | Advancing the understanding of autism disease mechanisms through genetics |
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