Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental RetardationLars Riff Jensen, Steffen Lenzner, M Amende et al.|The American Journal of Human Genetics|2005Cited by 376
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardationReinhard Ullmann, Hans‐Hilger Ropers, Gillian Turner et al.|Human Mutation|2007Cited by 288
SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman SyndromeGregor D. Gilfillan, Petter Strømme, Hans Sjöholm et al.|The American Journal of Human Genetics|2008Cited by 236
Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and TremorPatrick Tarpey, Jozef Gécz, F. Lucy Raymond et al.|The American Journal of Human Genetics|2007Cited by 228
Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental RetardationGuy Froyen, Jozef Gécz, Mark Corbett et al.|The American Journal of Human Genetics|2008Cited by 220