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Chelsea Barrows
Chelsea Barrows
UCSD Department of Neuroscience, Rady Children's Institute for Genomic Medicine
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Year
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
C Chung, X Yang, T Bae, KI Vong, S Mittal, C Donkels, H Westley Phillips, ...
Nature genetics 55 (2), 209-220, 2023
412023
TMEM161B modulates radial glial scaffolding in neocortical development
L Wang, C Heffner, K Vong, C Barrows, YJ Ha, S Lee, P Lara-Gonzalez, ...
Proceedings of the National Academy of Sciences 120 (4), e2209983120, 2023
52023
Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome
MM Beaman, L Guidugli, M Hammer, C Barrows, A Gregor, S Lee, ...
American Journal of Medical Genetics Part A 191 (11), 2757-2767, 2023
42023
Risk of meningomyelocele mediated by the common 22q11. 2 deletion
KI Vong, S Lee, KS Au, TB Crowley, V Capra, J Martino, M Haller, ...
Science 384 (6695), 584-590, 2024
2024
Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain
C Chung, X Yang, RF Hevner, K Kennedy, KI Vong, Y Liu, A Patel, ...
Nature, 1-9, 2024
2024
Cell-type-resolved somatic mosaicism reveals clonal dynamics of the human forebrain
C Chung, X Yang, RF Hevner, K Kennedy, KI Vong, Y Liu, A Patel, ...
bioRxiv, 2023
2023
UNDERSTANDING GENOTYPE PHENOTYPE CORRELATIONS IN MENINGOMYELOCELE
I Jhamb, Y Ha, S Kim, H Vong, C Barrows, S Lee, J Gleeson
JOURNAL OF INVESTIGATIVE MEDICINE 71 (1), NP403-NP403, 2023
2023
eP081: Dandy Walker malformation in three unrelated families with biallelic variants in CAPN15 expands the phenotypic spectrum of oculogastrointestinal neurodevelopmental disorder
MM Beaman, L Guidugli, M Hammer, C Barrows, A Gregor, M McDonald, ...
Genetics in Medicine 24 (3), S53-S54, 2022
2022
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