Sherman, Maxwell A; Barton, Alison R; Lodato, Michael A et al. (2018) PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Res 46:e20
|
Rodin, Rachel E; Walsh, Christopher A (2018) Somatic Mutation in Pediatric Neurological Diseases. Pediatr Neurol 87:20-22
|
Walsh, Christopher A (2018) Rainer W. Guillery and the genetic analysis of brain development. Eur J Neurosci :
|
Dou, Yanmei; Gold, Heather D; Luquette, Lovelace J et al. (2018) Detecting Somatic Mutations in Normal Cells. Trends Genet 34:545-557
|
Johnson, Matthew B; Sun, Xingshen; Kodani, Andrew et al. (2018) Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size. Nature 556:370-375
|
Lodato, Michael A; Rodin, Rachel E; Bohrson, Craig L et al. (2018) Aging and neurodegeneration are associated with increased mutations in single human neurons. Science 359:555-559
|
Smith, Richard S; Kenny, Connor J; Ganesh, Vijay et al. (2018) Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development. Neuron 99:905-913.e7
|
Woodworth, Mollie B; Girskis, Kelly M; Walsh, Christopher A (2017) Building a lineage from single cells: genetic techniques for cell lineage tracking. Nat Rev Genet 18:230-244
|
Jamuar, Saumya S; Schmitz-Abe, Klaus; D'Gama, Alissa M et al. (2017) Biallelic mutations in human DCC cause developmental split-brain syndrome. Nat Genet 49:606-612
|
Oaks, Adam W; Zamarbide, Marta; Tambunan, Dimira E et al. (2017) Cc2d1a Loss of Function Disrupts Functional and Morphological Development in Forebrain Neurons Leading to Cognitive and Social Deficits. Cereb Cortex 27:1670-1685
|
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