Anttonen, Anna-Kaisa
for the Polymicrogyria Genetics Research Network
3 papers on CoChatORCID 0000-0002-9749-7767
Most cited papers
- Verified
Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development
Smith, R. S., Kenny, C. J., Ganesh, V., Jang, A., Borges-Monroy, R., Partlow, J. N., Hill, R. S., Shin, T., Chen, A. Y., Doan, R. N., et al. (2018) · Neuron
Ion channel regulation and functionEpilepsy research and treatment
Cited by 160
- Verified
Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy
Muona, M., Ishimura, R., Laari, A., Ichimura, Y., Linnankivi, T., Keski-Filppula, R., Herva, R., Rantala, H., Paetau, A., Pöyhönen, M., et al. (2016) · The American Journal of Human Genetics
Ubiquitin and proteasome pathwaysGenetics and Neurodevelopmental Disorders
Cited by 119
- Verified
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria
Akula, S. K., Chen, A. Y., Neil, J. E., Shao, D. D., Mo, A., Hylton, N. K., DiTroia, S., Ganesh, V. S., Smith, R. S., O’Kane, K., et al. (2023) · JAMA Neurology
Fetal and Pediatric Neurological DisordersGenomics and Rare Diseases
Cited by 37
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