Is CRT Optimization Obsolete? A Referral Center’s Experience by Saleem-Talib, Shmaila, Duineveld, Mirjam D., Schipper, Jurjan C., Hauer, Arnaud D., Ramanna, Hemanth, de Groot, Natasja M.S., Scheffer, Michael G.

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Non-bacterial thrombotic (marantic) endocarditis associated with giant-cell arteritis by Hesselink, Dennis A, van der Klooster, Johan M, Schelfhout, Lodewijk J.D.M, Scheffer, Michael G

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Dietary nitrate attenuates oxidative stress, prevents cardiac and renal injuries, and reduces blood pressure in salt-induced hypertension by Carlström, Mattias, Persson, A Erik G, Larsson, Erik, Hezel, Michael, Scheffer, Peter G, Teerlink, Tom, Weitzberg, Eddie, Lundberg, Jon O

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Fenfluramine in the treatment of Dravet syndrome: Results of a third randomized, placebo-controlled clinical trial by Sullivan, Joseph, Lagae, Lieven, Cross, J Helen, Devinsky, Orrin, Guerrini, Renzo, Knupp, Kelly G, Laux, Linda, Nikanorova, Marina, Polster, Tilman, Talwar, Dinesh, Ceulemans, Berten, Nabbout, Rima, Farfel, Gail M, Galer, Bradley S, Gammaitoni, Arnold R, Lock, Michael, Agarwal, Anupam, Scheffer, Ingrid E

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Quantifying resilience of humans and other animals by Scheffer, Marten, Bolhuis, J. Elizabeth, Borsboom, Denny, Buchman, Timothy G., Gijzel, Sanne M. W., Goulson, Dave, Kammenga, Jan E., Kemp, Bas, van de Leemput, Ingrid A., Levin, Simon, Martin, Carmel Mary, Melis, René J. F., van Nes, Egbert H., Romero, L. Michael, Rikkert, Marcel G. M. Olde

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures by Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy by Ricos, Michael G., Hodgson, Bree L., Pippucci, Tommaso, Saidin, Akzam, Ong, Yeh Sze, Heron, Sarah E., Licchetta, Laura, Bisulli, Francesca, Bayly, Marta A., Hughes, James, Baldassari, Sara, Palombo, Flavia, Santucci, Margherita, Meletti, Stefano, Berkovic, Samuel F., Rubboli, Guido, Thomas, Paul Q., Scheffer, Ingrid E., Tinuper, Paolo, Geoghegan, Joel, Schreiber, Andreas W., Dibbens, Leanne M.

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Overexpression of Glyoxalase-I Reduces Hyperglycemia-induced Levels of Advanced Glycation End Products and Oxidative Stress in Diabetic Rats by Brouwers, Olaf, Niessen, Petra M., Ferreira, Isabel, Miyata, Toshio, Scheffer, Peter G., Teerlink, Tom, Schrauwen, Patrick, Brownlee, Michael, Stehouwer, Coen D., Schalkwijk, Casper G.

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Self‐reported impact of developmental stuttering across the lifespan by Boyce, Jessica O., Jackson, Victoria E., Reyk, Olivia, Parker, Richard, Vogel, Adam P., Eising, Else, Horton, Sarah E., Gillespie, Nathan A., Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Fisher, Simon E., Martin, Nicholas G., Reilly, Sheena, Bahlo, Melanie, Morgan, Angela T.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies by Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study by Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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Mutations of the Sonic Hedgehog Pathway Underlie Hypothalamic Hamartoma with Gelastic Epilepsy by Hildebrand, Michael S., Griffin, Nicole G., Damiano, John A., Cops, Elisa J., Burgess, Rosemary, Ozturk, Ezgi, Jones, Nigel C., Leventer, Richard J., Freeman, Jeremy L., Harvey, A. Simon, Sadleir, Lynette G., Scheffer, Ingrid E., Major, Heather, Darbro, Benjamin W., Allen, Andrew S., Goldstein, David B., Kerrigan, John F., Berkovic, Samuel F., Heinzen, Erin L.

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Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations by Scheffer, Ingrid E., Heron, Sarah E., Regan, Brigid M., Mandelstam, Simone, Crompton, Douglas E., Hodgson, Bree L., Licchetta, Laura, Provini, Federica, Bisulli, Francesca, Vadlamudi, Lata, Gecz, Jozef, Connelly, Alan, Tinuper, Paolo, Ricos, Michael G., Berkovic, Samuel F., Dibbens, Leanne M.

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Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders by Pfundt, Rolph, Del Rosario, Marisol, Vissers, Lisenka E L M, Kwint, Michael P, Janssen, Irene M, de Leeuw, Nicole, Yntema, Helger G, Nelen, Marcel R, Lugtenberg, Dorien, Kamsteeg, Erik-Jan, Wieskamp, Nienke, Stegmann, Alexander P A, Stevens, Servi J C, Rodenburg, Richard J T, Simons, Annet, Mensenkamp, Arjen R, Rinne, Tuula, Gilissen, Christian, Scheffer, Hans, Veltman, Prof Dr, Joris A, Hehir-Kwa, Jayne Y

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Mutations in KCNT1 cause a spectrum of focal epilepsies by Møller, Rikke S., Heron, Sarah E., Larsen, Line H. G., Lim, Chiao Xin, Ricos, Michael G., Bayly, Marta A., Kempen, Marjan J. A., Klinkenberg, Sylvia, Andrews, Ian, Kelley, Kent, Ronen, Gabriel M., Callen, David, McMahon, Jacinta M., Yendle, Simone C., Carvill, Gemma L., Mefford, Heather C., Nabbout, Rima, Poduri, Annapurna, Striano, Pasquale, Baglietto, Maria G., Zara, Federico, Smith, Nicholas J., Pridmore, Clair, Gardella, Elena, Nikanorova, Marina, Dahl, Hans Atli, Gellert, Pia, Scheffer, Ingrid E., Gunning, Boudewijn, Kragh‐Olsen, Bente, Dibbens, Leanne M.

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The spectrum of SCN1A-related infantile epileptic encephalopathies by Harkin, Louise A., McMahon, Jacinta M., Iona, Xenia, Dibbens, Leanne, Pelekanos, James T., Zuberi, Sameer M., Sadleir, Lynette G., Andermann, Eva, Gill, Deepak, Farrell, Kevin, Connolly, Mary, Stanley, Thorsten, Harbord, Michael, Andermann, Frederick, Wang, Jing, Batish, Sat Dev, Jones, Jeffrey G., Seltzer, William K., Gardner, Alison, Sutherland, Grant, Berkovic, Samuel F., Mulley, John C., Scheffer, Ingrid E.

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Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response by Johnson, Jennifer L., Stoica, Loredana, Liu, Yuwei, Zhu, Ping Jun, Bhattacharya, Abhisek, Buffington, Shelly A., Huq, Redwan, Eissa, N. Tony, Larsson, Ola, Porse, Bo T., Domingo, Deepti, Nawaz, Urwah, Carroll, Renee, Jolly, Lachlan, Scerri, Tom S., Kim, Hyung-Goo, Brignell, Amanda, Coleman, Matthew J., Braden, Ruth, Kini, Usha, Jackson, Victoria, Baxter, Anne, Bahlo, Melanie, Scheffer, Ingrid E., Amor, David J., Hildebrand, Michael S., Bonnen, Penelope E., Beeton, Christine, Gecz, Jozef, Morgan, Angela T., Costa-Mattioli, Mauro

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Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice by Scheffer, Ingrid E., Bennett, Caitlin A., Gill, Deepak, Silva, Michelle G., Boggs, Kirsten, Marum, Justine, Baker, Naomi, Palmer, Elizabeth E., Howell, Katherine B., Andrews, Ian, Antony, Jayne, Ardern‐Holmes, Simone, Bye, Ann M, Cardamone, Michael, Chelakkadan, Shabeed, Clark, Damian, Curnow, Sarah R, Dabscheck, Gabriel, Fahey, Michael C, Freeman, Jeremy L, Gupta, Sachin, Harvey, A Simon, Hildebrand, Michael S, Inder, Marie, Kanhangad, Manoj, Kornberg, Andrew J, Kothur, Kavitha, Lawson, John A, Leventer, Richard J, Malone, Stephen, Menezes, Manoj P, Mohammad, Shekeeb, Nagarajan, Lakshmi, Pillai, Sekhar, Pridmore, Clair, Procopis, Peter G, Sampaio, Hugo, Silberstein, Jonathon, Sinclair, Adriane, Smith, Nicholas, Subramanian, Gopinath, Troedson, Christopher, Ware, Tyson, White, Susan M

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Damaging de novo missense variants in EEF1A2 lead to a developmental and degenerative epileptic‐dyskinetic encephalopathy by Carvill, Gemma L., Helbig, Katherine L., Myers, Candace T., Scala, Marcello, Huether, Robert, Lewis, Sara, Kruer, Tyler N., Guida, Brandon S., Bakhtiari, Somayeh, Sebe, Joy, Tang, Sha, Stickney, Heather, Oktay, Sehribani Ulusoy, Bhandiwad, Ashwin A., Ramsey, Keri, Narayanan, Vinodh, Feyma, Timothy, Rohena, Luis O., Accogli, Andrea, Severino, Mariasavina, Hollingsworth, Georgina, Gill, Deepak, Depienne, Christel, Nava, Caroline, Sadleir, Lynette G., Caruso, Paul A., Lin, Angela E., Jansen, Floor E., Koeleman, Bobby, Brilstra, Eva, Willemsen, Marjolein H., Kleefstra, Tjitske, Sa, Joaquim, Mathieu, Marie‐Laure, Perrin, Laurine, Lesca, Gaetan, Striano, Pasquale, Casari, Giorgio, Scheffer, Ingrid E., Raible, David, Sattlegger, Evelyn, Capra, Valeria, Padilla‐Lopez, Sergio, Mefford, Heather C., Kruer, Michael C.

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Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike–Wave Activation in Sleep (D/EE‐SWAS ) by Viswanathan, Sindhu, Oliver, Karen L., Regan, Brigid M., Schneider, Amy L., Myers, Candace T., Mehaffey, Michele G., LaCroix, Amy J., Antony, Jayne, Webster, Richard, Cardamone, Michael, Subramanian, Gopinath M., Chiu, Annie T.G., Roza, Eugenia, Teleanu, Raluca I., Malone, Stephen, Leventer, Richard J., Gill, Deepak, Berkovic, Samuel F., Hildebrand, Michael S., Goad, Beatrice S., Howell, Katherine B., Symonds, Joseph D., Brunklaus, Andreas, Sadleir, Lynette G., Zuberi, Sameer M., Mefford, Heather C., Scheffer, Ingrid E.

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