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Nature|November 11, 2016
Evolution of Osteocrin as an activity-regulated factor in the primate brainBulent Ataman, Gabriella L Boulting, David A Harmin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 28, 2020
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survivalMichael E Coulter, Damir Musaev, Ellen M DeGennaro, et al.
American Journal of Human Genetics|September 11, 2012
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndromeM Chiara Manzini, Dimira E Tambunan, R Sean Hill, et al.
Nature|October 28, 2011
Spatio-temporal transcriptome of the human brainHyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 18, 2018
MAFA missense mutation causes familial insulinomatosis and diabetes mellitusDonato Iacovazzo, Sarah E Flanagan, Emily Walker, et al.
Cell|May 15, 2012
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortexKenneth Y Kwan, Mandy M S Lam, Matthew B Johnson, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Variants in ADD1 cause intellectual disability, corpus callosum dysgenesis, and ventriculomegaly in humansCai Qi, Irena Feng, Ana Rita Costa, et al.
Science (New York, N.Y.)|July 16, 2008
Identifying autism loci and genes by tracing recent shared ancestryEric M Morrow, Seung-Yun Yoo, Steven W Flavell, et al.
Human Molecular Genetics|February 7, 2014
METTL23, a transcriptional partner of GABPA, is essential for human cognitionRachel E Reiff, Bassam R Ali, Byron Baron, et al.
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