Graham, John M.

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

Finding of Rare Disease Genes (FORGE) Canada Consortium, Rivière, J.-B., Mirzaa, G. M., O'Roak, B. J., Beddaoui, M., Alcantara, D., Conway, R. L., St-Onge, J., Schwartzentruber, J. A., Gripp, K. W., et al. (2012) · Nature Genetics

Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases

Cited by 741

“Everybody in the world is my friend” hypersociability in young children with Williams syndrome

Doyle, T. F., Bellugi, U., Korenberg, J. R., & Graham, J. (2004) · American Journal of Medical Genetics Part A

Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders

Cited by 296

Coffin-Siris Syndrome and the BAF Complex: Genotype-Phenotype Study in 63 Patients

Santen, G. W. E., Aten, E., Vulto-van Silfhout, A. T., Pottinger, C., van Bon, B. W. M., van Minderhout, I. J. H. M., Snowdowne, R., van der Lans, C. A. C., Boogaard, M., Linssen, M. M. L., et al. (2013) · Human Mutation

Genomics and Rare DiseasesChromatin Remodeling and Cancer

Cited by 221

Fetal constraint as a potential risk factor for craniosynostosis

Sanchez‐Lara, P. A., Carmichael, S. L., Graham, J. M., Lammer, E. J., Shaw, G. M., Ma, C., & Rasmussen, S. A. (2010) · American Journal of Medical Genetics Part A

Craniofacial Disorders and TreatmentsCleft Lip and Palate Research

Cited by 106

Correction of Congenital Auricular Deformities by Splinting in the Neonatal Period

Brown, F. E., Colen, L. B., Addante, R. R., & Graham, J. M. (1986) · Pediatrics

Reconstructive Facial Surgery TechniquesCongenital Ear and Nasal Anomalies

Cited by 41