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Nature Neuroscience|July 16, 2020
Publisher Correction: Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.Nature|November 24, 2020
Author Correction: Innovations present in the primate interneuron repertoireFenna M Krienen, Melissa Goldman, Qiangge Zhang, et al.Autism Research : Official Journal of the International Society for Autism Research|May 14, 2014
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2Pauline Chaste, Stephan J Sanders, Kommu N Mohan, et al.Nature Genetics|March 3, 2017
Biallelic mutations in human DCC cause developmental split-brain syndromeSaumya S Jamuar, Klaus Schmitz-Abe, Alissa M D'Gama, et al.Plos Genetics|May 29, 2007
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defectsWeining Lu, Fabiola Quintero-Rivera, Yanli Fan, et al.Nature|October 1, 2020
Innovations present in the primate interneuron repertoireFenna M Krienen, Melissa Goldman, Qiangge Zhang, et al.American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.Scientific Data|November 20, 2023
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseasesMcKinzie A Garrison, Yeongjun Jang, Taejeong Bae, et al.Neuron|August 28, 2018
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor DevelopmentRichard S Smith, Connor J Kenny, Vijay Ganesh, et al.Pageof 41