Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials von Li, Wenhui, Schneider, Amy L., Scheffer, Ingrid E.

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Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic Encephalopathies von Donnan, Alice M., Schneider, Amy L., Russ-Hall, Sophie, Churilov, Leonid, Scheffer, Ingrid E.

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Development and Validation of a Prediction Model for Early Diagnosis of SCN1A-Related Epilepsies von Brunklaus, Andreas, Pérez-Palma, Eduardo, Ghanty, Ismael, Xinge, Ji, Brilstra, Eva, Ceulemans, Berten, Chemaly, Nicole, de Lange, Iris, Depienne, Christel, Guerrini, Renzo, Mei, Davide, Møller, Rikke S., Nabbout, Rima, Regan, Brigid M., Schneider, Amy L., Scheffer, Ingrid E., Schoonjans, An-Sofie, Symonds, Joseph D., Weckhuysen, Sarah, Kattan, Michael W., Zuberi, Sameer M., Lal, Dennis

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Parental Mosaicism in “De Novo” Epileptic Encephalopathies von Myers, Candace T, Hollingsworth, Georgina, Muir, Alison M, Schneider, Amy L, Thuesmunn, Zoe, Knupp, Allison, King, Chontelle, Lacroix, Amy, Mehaffey, Michele G, Berkovic, Samuel F, Carvill, Gemma L, Sadleir, Lynette G, Scheffer, Ingrid E, Mefford, Heather C

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Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures von Petrovski, Slavé, Küry, Sébastien, Myers, Candace T., Anyane-Yeboa, Kwame, Cogné, Benjamin, Bialer, Martin, Xia, Fan, Hemati, Parisa, Riviello, James, Mehaffey, Michele, Besnard, Thomas, Becraft, Emily, Wadley, Alexandrea, Politi, Anya Revah, Colombo, Sophie, Zhu, Xiaolin, Ren, Zhong, Andrews, Ian, Dudding-Byth, Tracy, Schneider, Amy L., Wallace, Geoffrey, Rosen, Aaron B.I., Schelley, Susan, Enns, Gregory M., Corre, Pierre, Dalton, Joline, Mercier, Sandra, Latypova, Xénia, Schmitt, Sébastien, Guzman, Edwin, Moore, Christine, Bier, Louise, Heinzen, Erin L., Karachunski, Peter, Shur, Natasha, Grebe, Theresa, Basinger, Alice, Nguyen, Joanne M., Bézieau, Stéphane, Wierenga, Klaas, Bernstein, Jonathan A., Scheffer, Ingrid E., Rosenfeld, Jill A., Mefford, Heather C., Isidor, Bertrand, Goldstein, David B.

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Silver carp experience metabolic and behavioral changes when exposed to water from the Chicago Area Waterway von Schneider, Amy E., Esbaugh, A. J., Cupp, Aaron R., Suski, C. D.

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Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizures von Nabbout, Rima, Auvin, Stephane, Chiron, Catherine, Thiele, Elizabeth, Cross, Helen, Scheffer, Ingrid E, Schneider, Amy L, Guerrini, Renzo, Williamson, Nicola, Irwin, John, Mistry, Arun, Grimes, Rebecca, Bennett, Bryan

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Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome von Brown, Amy, Arpone, Marta, Schneider, Amy L., Micallef, Silvana, Anderson, Vicki A., Scheffer, Ingrid E.

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Sleep problems in Dravet syndrome: a modifiable comorbidity von Licheni, Shane H, Mcmahon, Jacinta M, Schneider, Amy L, Davey, Margot J, Scheffer, Ingrid E

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Determination of quality of life-related health utilities for surgical complications in ovarian cancer von Suidan, Rudy S., Sun, Charlotte C., Schneider, Amy K., Lu, Karen H., Giordano, Sharon H., Meyer, Larissa A.

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A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy von Howell, Katherine B., Eggers, Stefanie, Dalziel, Kim, Riseley, Jessica, Mandelstam, Simone, Myers, Candace T., McMahon, Jacinta M., Schneider, Amy, Carvill, Gemma L., Mefford, Heather C., Scheffer, Ingrid E., Harvey, A. Simon

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Predicting 180-day mortality for women with ovarian cancer using machine learning and patient-reported outcome data von Sidey-Gibbons, Chris J., Sun, Charlotte, Schneider, Amy, Lu, Sheng-Chieh, Lu, Karen, Wright, Alexi, Meyer, Larissa

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The severe epilepsy syndromes of infancy: A population‐based study von Howell, Katherine B., Freeman, Jeremy L., Mackay, Mark T., Fahey, Michael C., Archer, John, Berkovic, Samuel F., Chan, Eunice, Dabscheck, Gabriel, Eggers, Stefanie, Hayman, Michael, Holberton, James, Hunt, Rodney W., Jacobs, Susan E., Kornberg, Andrew J., Leventer, Richard J., Mandelstam, Simone, McMahon, Jacinta M., Mefford, Heather C., Panetta, Julie, Riseley, Jessica, Rodriguez‐Casero, Victoria, Ryan, Monique M., Schneider, Amy L., Smith, Lindsay J., Stark, Zornitza, Wong, Flora, Yiu, Eppie M., Scheffer, Ingrid E., Harvey, A. Simon

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The epilepsy phenotypic spectrum associated with a recurrent CUX2 variant von Chatron, Nicolas, Møller, Rikke S., Champaigne, Neena L., Schneider, Amy L., Kuechler, Alma, Labalme, Audrey, Simonet, Thomas, Baggett, Lauren, Bardel, Claire, Kamsteeg, Erik‐Jan, Pfundt, Rolph, Romano, Corrado, Aronsson, Johan, Alberti, Antonino, Vinci, Mirella, Miranda, Maria J., Lacroix, Amy, Marjanovic, Dragan, des Portes, Vincent, Edery, Patrick, Wieczorek, Dagmar, Gardella, Elena, Scheffer, Ingrid E., Mefford, Heather, Sanlaville, Damien, Carvill, Gemma L., Lesca, Gaetan

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Solving the Etiology of Developmental and Epileptic Encephalopathy with Spike-Wave Activation in Sleep (D/EE-SWAS) von 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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CHD2 variants are a risk factor for photosensitivity in epilepsy von Galizia, Elizabeth C, Myers, Candace T, Leu, Costin, de Kovel, Carolien G F, Afrikanova, Tatiana, Cordero-Maldonado, Maria Lorena, Martins, Teresa G, Jacmin, Maxime, Drury, Suzanne, Krishna Chinthapalli, V, Muhle, Hiltrud, Pendziwiat, Manuela, Sander, Thomas, Ruppert, Ann-Kathrin, Møller, Rikke S, Thiele, Holger, Krause, Roland, Schubert, Julian, Lehesjoki, Anna-Elina, Nürnberg, Peter, Lerche, Holger, Palotie, Aarno, Coppola, Antonietta, Striano, Salvatore, Gaudio, Luigi Del, Boustred, Christopher, Schneider, Amy L, Lench, Nicholas, Jocic-Jakubi, Bosanka, Covanis, Athanasios, Capovilla, Giuseppe, Veggiotti, Pierangelo, Piccioli, Marta, Parisi, Pasquale, Cantonetti, Laura, Sadleir, Lynette G, Mullen, Saul A, Berkovic, Samuel F, Stephani, Ulrich, Helbig, Ingo, Crawford, Alexander D, Esguerra, Camila V, Kasteleijn-Nolst Trenité, Dorothee G A, Koeleman, Bobby P C, Mefford, Heather C, Scheffer, Ingrid E, Sisodiya, Sanjay M

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Complications of Influenza A or B Virus Infection in Individuals With SCN1A -Positive Dravet Syndrome von Howell, Katherine B., Butcher, Sophie, Schneider, Amy L., Russ-Hall, Sophie, Muzariri, Pearl R., Kerr, Rachel, Overmars, Isabella, Hayman, Michael, Kornberg, Andrew J., Danchin, Margie, Crawford, Nigel W., Scheffer, Ingrid E.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von 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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Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome von Palencia-Campos, Adrian, Aoto, Phillip C., Machal, Erik M.F., Rivera-Barahona, Ana, Soto-Bielicka, Patricia, Bertinetti, Daniela, Baker, Blaine, Vu, Lily, Piceci-Sparascio, Francesca, Torrente, Isabella, Boudin, Eveline, Peeters, Silke, Van Hul, Wim, Huber, Celine, Bonneau, Dominique, Hildebrand, Michael S., Coleman, Matthew, Bahlo, Melanie, Bennett, Mark F., Schneider, Amy L., Scheffer, Ingrid E., Kibæk, Maria, Kristiansen, Britta S., Issa, Mahmoud Y., Mehrez, Mennat I., Ismail, Samira, Tenorio, Jair, Li, Gaoyang, Skålhegg, Bjørn Steen, Otaify, Ghada A., Temtamy, Samia, Aglan, Mona, Jønch, Aia E., De Luca, Alessandro, Mortier, Geert, Cormier-Daire, Valérie, Ziegler, Alban, Wallis, Mathew, Lapunzina, Pablo, Herberg, Friedrich W., Taylor, Susan S., Ruiz-Perez, Victor L.

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BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures von Scheffer, Ingrid E, Boysen, Katja E, Schneider, Amy L, Myers, Candace T, Mehaffey, Michele G, Rochtus, Anne M, Yuen, Yuet‐Ping, Ronen, Gabriel M, Chak, Wai Km, Gill, Deepak, Poduri, Annapurna, Mefford, Heather C

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