Paul Motika

Associate Professor

Calculated based on number of publications stored in Pure and citations from Scopus
20102022

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  • 2013

    De novo mutations in epileptic encephalopathies

    Allen, A. S., Berkovic, S. F., Cossette, P., Delanty, N., Dlugos, D., Eichler, E. E., Epstein, M. P., Glauser, T., Goldstein, D. B., Han, Y., Heinzen, E. L., Hitomi, Y., Howell, K. B., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Lu, Y. F., Madou, M. R. Z., Marson, A. G., Mefford, H. C., & 51 othersEsmaeeli Nieh, S., O'Brien, T. J., Ottman, R., Petrovski, S., Poduri, A., Ruzzo, E. K., Scheffer, I. E., Sherr, E. H., Yuskaitis, C. J., Abou-Khalil, B., Alldredge, B. K., Bautista, J. F., Boro, A., Cascino, G. D., Consalvo, D., Crumrine, P., Devinsky, O., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glynn, S., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., McGuire, S. M., Motika, P. V., Novotny, E. J., Paolicchi, J. M., Parent, J. M., Park, K., Shellhaas, R. A., Shih, J. J., Singh, R., Sirven, J., Smith, M. C., Sullivan, J., Lin Thio, L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P. & Winawer, M. R., 2013, In: Nature. 501, 7466, p. 217-221 5 p.

    Research output: Contribution to journalArticlepeer-review

    1031 Scopus citations
  • 2014

    De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies

    EuroEPINOMICS-RES Consortium, Epilepsy Phenome/Genome Project & Epi4K Consortium, 2014, In: American Journal of Human Genetics. 95, 4, p. 360-370 11 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    297 Scopus citations
  • 2015

    About stroke and seizures

    Motika, P., Aug 25 2015, In: Neurology. 85, 8, p. e68

    Research output: Contribution to journalArticlepeer-review

  • Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy

    for the EPGP Investigators, Oct 1 2015, In: Epilepsy and Behavior. 51, p. 321-327 7 p.

    Research output: Contribution to journalArticlepeer-review

    9 Scopus citations
  • 2017

    Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data

    Epi4K Consortium, Epilepsy Phenome Genome Project & EuroEPINOMICS-RES Consortium, Jun 1 2017, In: European Journal of Human Genetics. 25, 7, p. 894-899 6 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    5 Scopus citations
  • Phenotypic analysis of 303 multiplex families with common epilepsies

    The Epi4K Consortium, Aug 1 2017, In: Brain. 140, 8, p. 2144-2156 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    19 Scopus citations
  • Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

    Allen, A. S., Bellows, S. T., Berkovic, S. F., Bridgers, J., Burgess, R., Cavalleri, G., Chung, S. K., Cossette, P., Delanty, N., Dlugos, D., Epstein, M. P., Freyer, C., Goldstein, D. B., Heinzen, E. L., Hildebrand, M. S., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Marson, A. G., Mayeux, R., & 66 othersMebane, C., Mefford, H. C., O'Brien, T. J., Ottman, R., Petrou, S., Petrovski, S., Pickrell, W. O., Radtke, R. A., Rees, M. I., Regan, B. M., Ren, Z., Scheffer, I. E., Sills, G. J., Thomas, R. H., Wang, Q., Abou-Khalil, B., Alldredge, B. K., Amrom, D., Andermann, E., Andermann, F., Bautista, J. F., Bluvstein, J., Boro, A., Cascino, G. D., Consalvo, D., Crumrine, P., Devinsky, O., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glauser, T., Glynn, S., Haas, K., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., Motika, P. V., Novotny, E. J., Paolicchi, J. M., Parent, J. M., Park, K., Poduri, A., Sadleir, L. G., Shellhaas, R. A., Sherr, E. H., Shih, J. J., Shinnar, S., Singh, R. K., Sirven, J., Smith, M. C., Sullivan, J., Thio, L. L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P. & Winawer, M. R., Feb 1 2017, In: The Lancet Neurology. 16, 2, p. 135-143 9 p.

    Research output: Contribution to journalArticlepeer-review

    132 Scopus citations
  • 2018

    Emergency department neuroimaging for epileptic seizures

    Salinsky, M., Wong, V. S. S., Motika, P., Meuse, J. & Nguyen, J., Sep 2018, In: Epilepsia. 59, 9, p. 1676-1683 8 p.

    Research output: Contribution to journalArticlepeer-review

    13 Scopus citations
  • 2019

    Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies

    Epi4K Consortium, Nov 1 2019, In: Epilepsia. 60, 11, p. 2194-2203 10 p.

    Research output: Contribution to journalArticlepeer-review

  • 2021

    Diverse genetic causes of polymicrogyria with epilepsy

    Epilepsy Phenome/Genome Project, Epi4K Consortium, Apr 2021, In: Epilepsia. 62, 4, p. 973-983 11 p.

    Research output: Contribution to journalArticlepeer-review

    7 Scopus citations
  • 2022

    Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

    Canadian Epilepsy Network, Epi4K Consortium, Epilepsy Phenome/Genome Project, EpiPGX Consortium & EuroEPINOMICS-CoGIE Consortium, Mar 2022, In: Epilepsia. 63, 3, p. 723-735 13 p.

    Research output: Contribution to journalArticlepeer-review

    Open Access
    1 Scopus citations