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Connor J Kenny
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Sodium channel SCN3A (NaV1. 3) regulation of human cerebral cortical folding and oral motor development
RS Smith, CJ Kenny, V Ganesh, A Jang, R Borges-Monroy, JN Partlow, ...
Neuron 99 (5), 905-913. e7, 2018
1392018
Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions
KM Girskis, AB Stergachis, EM DeGennaro, RN Doan, X Qian, ...
Neuron 109 (20), 3239-3251. e7, 2021
872021
Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain
AY Huang, P Li, RE Rodin, SN Kim, Y Dou, CJ Kenny, SK Akula, ...
Proceedings of the National Academy of Sciences 117 (25), 13886-13895, 2020
362020
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features
R Khalil, C Kenny, RS Hill, GH Mochida, R Nasir, JN Partlow, BJ Barry, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018
302018
Rates and patterns of clonal oncogenic mutations in the normal human brain
J Ganz, EA Maury, B Becerra, S Bizzotto, RN Doan, CJ Kenny, T Shin, ...
Cancer discovery 12 (1), 172-185, 2022
262022
Posterior neocortex-specific regulation of neuronal migration by CEP85L identifies maternal centriole-dependent activation of CDK5
A Kodani, C Kenny, A Lai, DM Gonzalez, E Stronge, GM Sejourne, ...
Neuron 106 (2), 246-255. e6, 2020
222020
A rare autism-associated MINT2/APBA2 mutation disrupts neurexin trafficking and synaptic function
AY Lin, S Henry, C Reissner, C Neupert, C Kenny, M Missler, U Beffert, ...
Scientific Reports 9 (1), 6024, 2019
142019
MEK and TAK1 regulate apoptosis in colon cancer cells with KRAS-dependent activation of proinflammatory signaling
KL McNew, WJ Whipple, AK Mehta, TJ Grant, L Ray, C Kenny, A Singh
Molecular cancer research 14 (12), 1204-1216, 2016
122016
Exome sequencing and the identification of new genes and shared mechanisms in polymicrogyria
SK Akula, AY Chen, JE Neil, DD Shao, A Mo, NK Hylton, S DiTroia, ...
JAMA neurology 80 (9), 980-988, 2023
42023
Human LUC7 proteins impact splicing of two major subclasses of 5’splice sites
CJ Kenny, MP McGurk, CB Burge
bioRxiv, 2022.12. 07.519539, 2022
42022
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder risk
T Shin, JHT Song, M Kosicki, C Kenny, SG Beck, L Kelley, X Qian, ...
medRxiv, 2023
32023
Somatic Mosaicism in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Reveals Widespread Degeneration from Focal Mutations
Z Zhou, J Kim, AY Huang, M Nolan, J Park, R Doan, T Shin, MB Miller, ...
Biorxiv, 2023.11. 30.569436, 2023
2023
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