← all works
The contribution of de novo coding mutations to autism spectrum disorder
Why is this work in the frame?
A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.
No Canadian affiliation. An affiliation-only frame — the usual design — would never have seen this work. It is one of the works that make the case for inverting the frame.
Abstract
No abstract. This is not a gap in this database — OpenAlex has none either. 23.3% of the frame is in this state, and the screen finds HALF as much metaresearch here, so the absence is a measured bias rather than a missing field.
The record
- Venue
- Nature
- Topic
- Genomic variations and chromosomal abnormalities
- Field
- Biochemistry, Genetics and Molecular Biology
- Canadian institutions
- —
- Funders
- National Center for Advancing Translational SciencesNational Institute of Mental HealthNational Institute of General Medical SciencesNational Heart, Lung, and Blood InstituteCanadian Institutes of Health ResearchEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentHoward Hughes Medical Institute
- Keywords
- Missense mutationGeneticsAutismBiologyExome sequencingGeneExomeAutism spectrum disorderAlleleMutationMedicinePsychiatry
- Has abstract in OpenAlex
- no