Structural basis of autoregulatory scaffolding by apoptosis signal-regulating kinase 1 von Weijman, Johannes F., Kumar, Abhishek, Jamieson, Sam A., King, Chontelle M., Caradoc-Davies, Tom T., Ledgerwood, Elizabeth C., Murphy, James M., Mace, Peter D.

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Developmental and epileptic encephalopathy: Personal utility of a genetic diagnosis for families von Jeffrey, Jennifer S., Leathem, Janet, King, Chontelle, Mefford, Heather C., Ross, Kirsty, Sadleir, Lynette G.

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Infantile‐onset myoclonic developmental and epileptic encephalopathy: A new RARS2 phenotype von de Valles‐Ibáñez, Guillem, Hildebrand, Michael S., Bahlo, Melanie, King, Chontelle, Coleman, Matthew, Green, Timothy E., Goldsmith, John, Davis, Suzanne, Gill, Deepak, Mandelstam, Simone, Scheffer, Ingrid E., Sadleir, Lynette G.

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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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Polygenic burden in focal and generalized epilepsies von Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy von Sadleir, Lynette G., de Valles‐Ibáñez, Guillem, King, Chontelle, Coleman, Matthew, Mossman, Stuart, Paterson, Sarah, Nguyen, John, Berkovic, Samuel F., Mullen, Saul, Bahlo, Melanie, Hildebrand, Michael S., Mefford, Heather C., Scheffer, Ingrid E.

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Levetiracetam efficacy in PCDH19 Girls Clustering Epilepsy von Sadleir, Lynette G., Kolc, Kristy L., King, Chontelle, Mefford, Heather C., Dale, Russell C., Gecz, Jozef, Scheffer, Ingrid E.

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Epilepsia Brief Communication: Inherited RORB pathogenic variants: overlap of photosensitive genetic generalized and occipital lobe epilepsy von Sadleir, Lynette G, de Valles-Ibáñez, Guillem, King, Chontelle, Coleman, Matthew, Mossman, Stuart, Paterson, Sarah, Nguyen, John, Berkovic, Samuel F, Mullen, Saul, Bahlo, Melanie, Hildebrand, Michael S., Mefford, Heather C, Scheffer, Ingrid E

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The epileptology of GNB5 encephalopathy von Poke, Gemma, King, Chontelle, Muir, Alison, Valles‐Ibáñez, Guillem, Germano, Michele, Moura de Souza, Carolina F., Fung, Jasmine, Chung, Brian, Fung, Cheuk Wing, Mignot, Cyril, Ilea, Adina, Keren, Boris, Vermersch, Anne‐Isabelle, Davis, Suzanne, Stanley, Thorsten, Moharir, Mahendranath, Kannu, Peter, Shao, Zhuo, Malerba, Natascia, Merla, Giuseppe, Mefford, Heather C., Scheffer, Ingrid E., Sadleir, Lynette G.

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Parental Mosaicism in "De Novo" Epileptic Encephalopathies: Letter 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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Double somatic mosaicism in a child with Dravet syndrome von Muir, Alison M, King, Chontelle, Schneider, Amy L, Buttar, Aman S, Scheffer, Ingrid E, Sadleir, Lynette G, Mefford, Heather C

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