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Nature Neuroscience|December 3, 2024
Applying single-cell and single-nucleus genomics to studies of cellular heterogeneity and cell fate transitions in the nervous systemIgor Adameyko, Trygve Bakken, Aparna Bhaduri, et al.Biorxiv : the Preprint Server for Biology|November 21, 2023
Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortexSonia Nan Kim, Vinayak V Viswanadham, Ryan N Doan, et al.Neuron|February 26, 2020
Posterior Neocortex-Specific Regulation of Neuronal Migration by CEP85L Identifies Maternal Centriole-Dependent Activation of CDK5Andrew Kodani, Connor Kenny, Abbe Lai, et al.Proceedings of the National Academy of Sciences of the United States of America|June 23, 2021
Early role for a Na+,K+-ATPase (ATP1A3) in brain developmentRichard S Smith, Marta Florio, Shyam K Akula, et al.Nature|April 21, 2022
Somatic genomic changes in single Alzheimer's disease neuronsMichael B Miller, August Yue Huang, Junho Kim, et al.American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.Neuron|December 19, 2014
Katanin p80 regulates human cortical development by limiting centriole and cilia numberWen F Hu, Oz Pomp, Tawfeg Ben-Omran, et al.Science (New York, N.Y.)|July 28, 2022
Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutabilityTaejeong Bae, Liana Fasching, Yifan Wang, et al.American Journal of Human Genetics|March 5, 2013
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanElizabeth Stevens, Keren J Carss, Sebahattin Cirak, et al.Nature Genetics|October 2, 2012
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar developmentGaneshwaran H Mochida, Vijay S Ganesh, Maria I de Michelena, et al.Pageof 34