Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders
Open Access
- 20 December 2018
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 21 (8), 1719-1725
- https://doi.org/10.1038/s41436-018-0404-y
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Advances in understanding – genetic basis of intellectual disabilityF1000Research, 2016
- Genetic studies in intellectual disability and related disordersNature Reviews Genetics, 2015
- Genome sequencing identifies major causes of severe intellectual disabilityNature, 2014
- Clinical Significance of De Novo and Inherited Copy-Number VariationHuman Mutation, 2013
- Genetic studies of craniofacial anomalies: clinical implications and applicationsOrthodontics & Craniofacial Research, 2009
- Impact of geometry and viewing angle on classification accuracy of 2D based analysis of dysmorphic facesEuropean Journal of Medical Genetics, 2008
- Morphometric analysis of face in dysmorphologyComputer Methods and Programs in Biomedicine, 2007
- Syndrome identification based on 2D analysis softwareEuropean Journal of Human Genetics, 2006
- Discriminating Power of Localized Three-Dimensional Facial MorphologyAmerican Journal of Human Genetics, 2005
- Computer-based recognition of dysmorphic facesEuropean Journal of Human Genetics, 2003