Using Whole-Exome Sequencing to Identify Inherited Causes of AutismTimothy W. Yu, Christopher A. Walsh, Maria H. Chahrour et al.|Neuron|2013Cited by 459
Somatic Mutations in Cerebral Cortical MalformationsSaumya Shekhar Jamuar, Christopher A. Walsh, Anh-Thu N. Lam et al.|New England Journal of Medicine|2014Cited by 394
Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg SyndromeM. Chiara Manzini, Christopher A. Walsh, Dimira Tambunan et al.|The American Journal of Human Genetics|2012Cited by 184
Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and DystroglycanopathyDaniel P. S. Osborn, M. Chiara Manzini, Heather L. Pond et al.|The American Journal of Human Genetics|2017Cited by 71
Loss of PCLO function underlies pontocerebellar hypoplasia type IIIGaneshwaran H. Mochida, Kyriacos Markianos, Christopher A. Walsh et al.|Neurology|2015Cited by 67