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American Journal of Medical Genetics. Part A|August 5, 2010
Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosisHeather C Mefford, Neil Shafer, Francesca Antonacci, et al.
Human Molecular Genetics|May 1, 2014
The genetic landscape of infantile spasmsJacques L Michaud, Mathieu Lachance, Fadi F Hamdan, et al.
Epilepsia|May 12, 2018
A population-based cost-effectiveness study of early genetic testing in severe epilepsies of infancyKatherine B Howell, Stefanie Eggers, Kim Dalziel, et al.
International Journal of Genomics|June 6, 2013
Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of OriginPhillip H Gallo, James J Cray, Emily L Durham, et al.
Genome Biology|September 6, 2007
Functional constraint and small insertions and deletions in the ENCODE regions of the human genomeTaane G Clark, Toby Andrew, Gregory M Cooper, et al.
Plastic and Reconstructive Surgery|June 3, 2010
Testing the critical size in calvarial bone defects: revisiting the concept of a critical-size defectGregory M Cooper, Mark P Mooney, Arun K Gosain, et al.
Neurology|February 13, 2015
CHD2 myoclonic encephalopathy is frequently associated with self-induced seizuresRhys H Thomas, Lin Mei Zhang, Gemma L Carvill, et al.
The Journal of Craniofacial Surgery|May 26, 2012
Tissue interactions between craniosynostotic dura mater and boneGregory M Cooper, Emily L Durham, James J Cray, et al.
The Journal of Craniofacial Surgery|January 18, 2011
Divided parietal bone in plagiocephalyRegina A Fenton, Christopher R Kinsella, James J Cray, et al.
The Journal of Craniofacial Surgery|September 25, 2008
BMP-2-based repair of large-scale calvarial defects in an experimental model: regenerative surgery in cranioplastyDarren M Smith, Ahmed M Afifi, Gregory M Cooper, et al.
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