Harris, Catharine J.
University of Missouri Health System · University of Missouri
2 papers on CoChatORCID 0009-0005-5798-6055
Most cited papers
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MEF2C Haploinsufficiency features consistent hyperkinesis, variable epilepsy, and has a role in dorsal and ventral neuronal developmental pathways
Paciorkowski, A. R., Traylor, R. N., Rosenfeld, J. A., Hoover, J. M., Harris, C. J., Winter, S., Lacassie, Y., Bialer, M., Lamb, A. N., Schultz, R. A., et al. (2013) · neurogenetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 109
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Phenotypic and genetic spectrum of ATP6V1A encephalopathy: a disorder of lysosomal homeostasis
Guerrini, R., Mei, D., Kerti-Szigeti, K., Pepe, S., Koenig, M. K., Von Allmen, G., Cho, M. T., McDonald, K., Baker, J., Bhambhani, V., et al. (2022) · Brain
ATP Synthase and ATPases ResearchGenetics and Neurodevelopmental Disorders
Cited by 34
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