Kopanitsa, Maksym
UK Dementia Research Institute · Synome (United Kingdom) · Imperial College London
4 papers on CoChatORCID 0000-0001-8694-9644
Most cited papers
- Verified
Reciprocal effects on neurocognitive and metabolic phenotypes in mouse models of 16p11.2 deletion and duplication syndromes
Arbogast, T., Ouagazzal, A.-M., Chevalier, C., Kopanitsa, M., Afinowi, N., Migliavacca, E., Cowling, B. S., Birling, M.-C., Champy, M.-F., Reymond, A., et al. (2016) · PLOS Genetics
Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders
Cited by 151
- Verified
eEF2K/eEF2 Pathway Controls the Excitation/Inhibition Balance and Susceptibility to Epileptic Seizures
Heise, C., Taha, E., Murru, L., Ponzoni, L., Cattaneo, A., Guarnieri, F. C., Montani, C., Mossa, A., Vezzoli, E., Ippolito, G., et al. (2016) · Cerebral Cortex
Epilepsy research and treatmentNeuroscience and Neuropharmacology Research
Cited by 62
- Verified
The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal Sequences
McKay, S., Ryan, T. J., McQueen, J., Indersmitten, T., Marwick, K. F. M., Hasel, P., Kopanitsa, M. V., Baxter, P. S., Martel, M.-A., Kind, P. C., et al. (2018) · Cell Reports
Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental Disorders
Cited by 42
- Verified
Learning and reaction times in mouse touchscreen tests are differentially impacted by mutations in genes encoding postsynaptic interacting proteins SYNGAP1, NLGN3, DLGAP1, DLGAP2 and SHANK2
Horner, A. E., Norris, R. H., McLaren‐Jones, R., Alexander, L., Komiyama, N. H., Grant, S. G. N., Nithianantharajah, J., & Kopanitsa, M. V. (2021) · Genes, Brain and Behavior
Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research
Cited by 26
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