Phenotypic analysis of 303 multiplex families with common epilepsies
B Abou-Khalil, Z Afawi, AS Allen, JF Bautista, ST Bellows, SF Berkovic, J Bluvstein, R Burgess, G Cascino, EJ Cops, P Cossette, S Cristofaro, DE Crompton, N Delanty, O Devinsky, D Dlugos, MP Epstein, NB Fountain, C Freyer, SI Garry, EB Geller, T Glauser, Simon Glynn, H Goldberg-Stern, DB Goldstein, M Gravel, K Haas, S Haut, EL Heinzen, HE Kirsch, S Kivity, R Knowlton, AD Korczyn, E Kossoff, R Kuzniecky, R Loeb, DH Lowenstein, AG Marson, M McCormack, K McKenna, HC Mefford, P Motika, . Mullen, TJ O'Brien, R Ottman, J Paolicchi, Jack Parent, S Paterson, S Petrovski, WO Pickrell, A Poduri, MI Rees, LG Sadleir, IE Scheffer, J Shih, R Singh, J Sirven, PEM Smith, LL Thio, RH Thomas, A Venkat, E Vining, G Von Allmen, J Weisenberg, P Widdess-Walsh, . Winawer
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data
AS Allen, SF Berkovic, J Bridgers, P Cossette, D Dlugos, MP Epstein, T Glauser, DB Goldstein, EL Heinzen, Y Jiang, . Johnson, R Kuzniecky, DH Lowenstein, AG Marson, HC Mefford, TJ O'Brien, R Ottman, S Petrou, S Petrovski, A Poduri, Z Ren, IE Scheffer, E Sherr, Q Wang, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, P De Jonghe, C Depienne, R Guerrini, I Helbig, H Hjalgrim, D Hoffman-Zacharska, J Jähn, KM Klein, B Koeleman, V Komarek, R Krause, E Leguern, AE Lehesjoki, . Lemke, H Lerche, T Linnankivi, C Marini, P May, RS Møller, H Muhle, D Pal, A Palotie, F Rosenow, K Selmer, JM Serratosa, S Sisodiya, U Stephani, K Sterbova, P Striano, A Suls, T Talvik, S Von Spiczak, Y Weber, S Weckhuysen, F Zara, B Abou-Khalil, BK Alldredge, D Amrom, F Andermann, JF Bautista, J Bluvstein, GD Cascino, D Consalvo, P Crumrine, O Devinsky, ME Fiol, NB Fountain, J French, D Friedman, K Haas, . Haut, J Hayward, Sucheta Joshi, A Kanner, HE Kirsch, EH Kossoff, R Kuperman, SM McGuire, PV Motika, EJ Novotny, JM Paolicchi, Jack Parent, K Park, Renee Shellhaas, J Sirven, MC Smith, J Sullivan, LL Thio, A Venkat, EPG Vining
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
AS Allen, ST Bellows, SF Berkovic, J Bridgers, R Burgess, G Cavalleri, SK Chung, P Cossette, N Delanty, D Dlugos, MP Epstein, C Freyer, DB Goldstein, EL Heinzen, . Hildebrand, . Johnson, R Kuzniecky, DH Lowenstein, AG Marson, R Mayeux, C Mebane, HC Mefford, TJ O'Brien, R Ottman, S Petrou, S Petrovski, WO Pickrell, RA Radtke, MI Rees, BM Regan, Z Ren, IE Scheffer, GJ Sills, RH Thomas, Q Wang, B Abou-Khalil, BK Alldredge, D Amrom, F Andermann, JF Bautista, J Bluvstein, A Boro, GD Cascino, D Consalvo, P Crumrine, O Devinsky, M Fiol, NB Fountain, J French, D Friedman, EB Geller, T Glauser, Simon Glynn, K Haas, . Haut, J Hayward, SL Helmers, Sucheta Joshi, A Kanner, HE Kirsch, RC Knowlton, EH Kossoff, R Kuperman, PV Motika, EJ Novotny, JM Paolicchi, Jack Parent, K Park, A Poduri, LG Sadleir, Renee Shellhaas, EH Sherr, JJ Shih, S Shinnar, RK Singh, J Sirven, MC Smith, J Sullivan, LL Thio, A Venkat, EPG Vining, GK Von Allmen, JL Weisenberg, P Widdess-Walsh, . Winawer
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))
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, P De Jonghe, C Depienne, P Dimova, T Djémié, P Gormley, R Guerrini, I Helbig, H Hjalgrim, D Hoffman-Zacharska, J Jähn, KM Klein, B Koeleman, V Komarek, R Krause, G Kuhlenbäumer, E Leguern, AE Lehesjoki, . Lemke, H Lerche, T Linnankivi, C Marini, P May, RS Møller, H Muhle, D Pal, A Palotie, M Pendziwiat, A Robbiano, F Roelens, F Rosenow, K Selmer, JM Serratosa, S Sisodiya, U Stephani, K Sterbova, P Striano, A Suls, T Talvik, S von Spiczak, Y Weber, S Weckhuysen, F Zara, B Abou-Khalil, BK Alldredge, F Andermann, D Amrom, JF Bautista, SF Berkovic, J Bluvstein, A Boro, G Cascino, D Consalvo, P Crumrine, O Devinsky, D Dlugos, MP Epstein, M Fiol, NB Fountain, J French, D Friedman, EB Geller, T Glauser, Simon Glynn, K Haas, . Haut, J Hayward, SL Helmers, Sucheta Joshi, A Kanner, HE Kirsch, RC Knowlton, EH Kossoff, R Kuperman, R Kuzniecky, DH Lowenstein, SM McGuire, PV Motika, EJ Novotny, R Ottman, JM Paolicchi, Jack Parent, K Park, A Poduri, L Sadleir, IE Scheffer, Renee Shellhaas, E Sherr, JJ Shih, R Singh, J Sirven, MC Smith, J Sullivan, LL Thio
SCN8A encephalopathy: Research progress and prospects
Miriam Meisler, G Helman, MF Hammer, BE Fureman, WD Gaillard, AL Goldin, S Hirose, A Ishii, BL Kroner, C Lossin, HC Mefford, Jack Parent, M Patel, J Schreiber, R Stewart, V Whittemore, K Wilcox, Jacy Wagnon, PL Pearl, A Vanderver, IE Scheffer
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