Paul Motika

Associate Professor

  • 1070 Citations
  • 5 h-Index
20132018
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Fingerprint Dive into the research topics where Paul Motika is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Epilepsy Medicine & Life Sciences
Brain Diseases Medicine & Life Sciences
Seizures Medicine & Life Sciences
Genes Medicine & Life Sciences
Synaptic Transmission Medicine & Life Sciences
Mutation Medicine & Life Sciences
Periventricular Nodular Heterotopia Medicine & Life Sciences
Stroke Medicine & Life Sciences

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Research Output 2013 2018

  • 1070 Citations
  • 5 h-Index
  • 9 Article
  • 1 Comment/debate
  • 1 Review article
2 Citations (Scopus)

Emergency department neuroimaging for epileptic seizures

Salinsky, M., Wong, V., Motika, P., Meuse, J. & Nguyen, J., Jan 1 2018, (Accepted/In press) In : Epilepsia.

Research output: Contribution to journalArticle

Neuroimaging
Hospital Emergency Service
Epilepsy
Seizures
Neurologic Examination
3 Citations (Scopus)

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 journalArticle

Brain Diseases
Infantile Spasms
Genes
Recessive Genes
Ion Channels
1 Citation (Scopus)

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Appenzeller, S., Balling, R., Barisic, N., Baulac, S., Caglayan, H., Craiu, D., De Jonghe, P., Depienne, C., Dimova, P., Djémié, T., Gormley, P., Guerrini, R., Helbig, I., Hjalgrim, H., Hoffman-Zacharska, D., Jähn, J., Klein, K. M., Koeleman, B., Komarek, V., Krause, R. & 111 others, Kuhlenbäumer, G., Leguern, E., Lehesjoki, A. E., Lemke, J. R., Lerche, H., Linnankivi, T., Marini, C., May, P., Møller, R. S., Muhle, H., Pal, D., Palotie, A., Pendziwiat, M., Robbiano, A., Roelens, F., Rosenow, F., Selmer, K., Serratosa, J. M., Sisodiya, S., Stephani, U., Sterbova, K., Striano, P., Suls, A., Talvik, T., von Spiczak, S., Weber, Y., Weckhuysen, S., Zara, F., Abou-Khalil, B., Alldredge, B. K., Andermann, E., Andermann, F., Amrom, D., Bautista, J. F., Berkovic, S. F., Bluvstein, J., Boro, A., Cascino, G., Consalvo, D., Crumrine, P., Devinsky, O., Dlugos, D., Epstein, M. P., 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., Kuzniecky, R., Lowenstein, D. H., McGuire, S. M., Motika, P., Novotny, E. J., Ottman, R., Paolicchi, J. M., Parent, J., Park, K., Poduri, A., Sadleir, L., Scheffer, I. E., Shellhaas, R. A., Sherr, E., Shih, J. J., Singh, R., 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., 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., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Marson, A. G., Mefford, H. C., Nieh, S. E., O'Brien, T. J., Ottman, R., Petrou, S., Petrovski, S., Poduri, A., Ruzzo, E. K., Scheffer, I. E. & Sherr, E., Jan 5 2017, In : American Journal of Human Genetics. 100, 1, p. 179 1 p.

Research output: Contribution to journalComment/debate

Medical Genetics
Brain Diseases
Synaptic Transmission
Names
Epilepsy
8 Citations (Scopus)

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 journalArticle

Epilepsy
Partial Epilepsy
Generalized Epilepsy
Pedigree
Seizures
69 Citations (Scopus)

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 others, Mebane, 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., 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 journalArticle

Case-Control Studies
Epilepsy
Partial Epilepsy
Generalized Epilepsy
Genes