Clinical genetic study of the epilepsy‐aphasia spectrum von Tsai, Meng‐Han, Vears, Danya F., Turner, Samantha J., Smith, Robert L., Berkovic, Samuel F., Sadleir, Lynette G., Scheffer, Ingrid E.

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Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of Speech von Turner, Samantha J., Vogel, Adam P., Parry-Fielder, Bronwyn, Campbell, Rhonda, Scheffer, Ingrid E., Morgan, Angela T.

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GRIN2A mutations cause epilepsy-aphasia spectrum disorders von Carvill, Gemma L, Regan, Brigid M, Yendle, Simone C, O'Roak, Brian J, Lozovaya, Natalia, Bruneau, Nadine, Burnashev, Nail, Khan, Adiba, Cook, Joseph, Geraghty, Eileen, Sadleir, Lynette G, Turner, Samantha J, Tsai, Meng-Han, Webster, Richard, Ouvrier, Robert, Damiano, John A, Berkovic, Samuel F, Shendure, Jay, Hildebrand, Michael S, Szepetowski, Pierre, Scheffer, Ingrid E, Mefford, Heather C

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Dysarthria and broader motor speech deficits in Dravet syndrome von Turner, Samantha J, Brown, Amy, Arpone, Marta, Anderson, Vicki, Morgan, Angela T, Scheffer, Ingrid E

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Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families von Marini, Carla, Scheffer, Ingrid E., Crossland, Kathryn M., Grinton, Bronwyn E., Phillips, Fiona L., McMahon, Jacinta M., Turner, Samantha J., Dean, Joanne T., Kivity, Sara, Mazarib, Aziz, Neufeld, Miriam Y., Korczyn, Amos D., Harkin, Louise A., Dibbens, Leanne M., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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GRIN2A: An aptly named gene for speech dysfunction von Turner, Samantha J, Mayes, Angela K, Verhoeven, Andrea, Mandelstam, Simone A, Morgan, Angela T, Scheffer, Ingrid E

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Atypical development of Broca's area in a large family with inherited stuttering von Thompson-Lake, Daisy G Y, Scerri, Thomas S, Block, Susan, Turner, Samantha J, Reilly, Sheena, Kefalianos, Elaina, Bonthrone, Alexandra F, Helbig, Ingo, Bahlo, Melanie, Scheffer, Ingrid E, Hildebrand, Michael S, Liégeois, Frédérique J, Morgan, Angela T

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Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40 von Morgan, Angela T, Scerri, Thomas S, Vogel, Adam P, Reid, Christopher A, Quach, Mara, Jackson, Victoria E, McKenzie, Chaseley, Burrows, Emma L, Bennett, Mark F, Turner, Samantha J, Reilly, Sheena, Horton, Sarah E, Block, Susan, Kefalianos, Elaina, Frigerio-Domingues, Carlos, Sainz, Eduardo, Rigbye, Kristin A, Featherby, Travis J, Richards, Kay L, Kueh, Andrew, Herold, Marco J, Corbett, Mark A, Gecz, Jozef, Helbig, Ingo, Thompson-Lake, Daisy G Y, Liégeois, Frédérique J, Morell, Robert J, Hung, Andrew, Drayna, Dennis, Scheffer, Ingrid E, Wright, David K, Bahlo, Melanie, Hildebrand, Michael S

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Dorsal language stream anomalies in an inherited speech disorder von Liégeois, Frédérique J, Turner, Samantha J, Mayes, Angela, Bonthrone, Alexandra F, Boys, Amber, Smith, Libby, Parry-Fielder, Bronwyn, Mandelstam, Simone, Spencer-Smith, Megan, Bahlo, Melanie, Scerri, Tom S, Hildebrand, Michael S, Scheffer, Ingrid E, Connelly, Alan, Morgan, Angela T

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Early neuroimaging markers of FOXP2 intragenic deletion von Liégeois, Frédérique J., Hildebrand, Michael S., Bonthrone, Alexandra, Turner, Samantha J., Scheffer, Ingrid E., Bahlo, Melanie, Connelly, Alan, Morgan, Angela T.

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Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria von Turner, Samantha J, Hildebrand, Michael S., Block, Susan, Damiano, John, Fahey, Michael, Reilly, Sheena, Bahlo, Melanie, Scheffer, Ingrid E., Morgan, Angela T.

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Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations von Scheffer, Ingrid E., Harkin, Louise A., Grinton, Bronwyn E., Dibbens, Leanne M., Turner, Samantha J., Zielinski, Marta A., Xu, Ruwei, Jackson, Graeme, Adams, Judith, Connellan, Mary, Petrou, Steven, Wellard, R. Mark, Briellmann, Regula S., Wallace, Robyn H., Mulley, John C., Berkovic, Samuel F.

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New Genes for Focal Epilepsies with Speech and Language Disorders von Turner, Samantha J., Morgan, Angela T., Perez, Eliane Roulet, Scheffer, Ingrid E.

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Epilepsy and mental retardation limited to females: an under-recognized disorder von Scheffer, Ingrid E., Turner, Samantha J., Dibbens, Leanne M., Bayly, Marta A., Friend, Kathryn, Hodgson, Bree, Burrows, Linda, Shaw, Marie, Wei, Chen, Ullmann, Reinhard, Ropers, Hans-Hilger, Szepetowski, Pierre, Haan, Eric, Mazarib, Aziz, Afawi, Zaid, Neufeld, Miriam Y., Andrews, P. Ian, Wallace, Geoffrey, Kivity, Sara, Lev, Dorit, Lerman-Sagie, Tally, Derry, Christopher P., Korczyn, Amos D., Gecz, Jozef, Mulley, John C., Berkovic, Samuel F.

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Perisylvian and Hippocampal Anomalies in Individuals With Pathogenic GRIN2A Variants von Thompson-Lake, Daisy G Y, Liegeois, Frederique J, Braden, Ruth O, Jackson, Graeme D, Turner, Samantha J, Morison, Lottie, Hildebrand, Michael, Scheffer, Ingrid E, Morgan, Angela T

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Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families von Hynes, Kim, Tarpey, Patrick, Dibbens, Leanne M, Bayly, Marta A, Berkovic, Samuel F, Smith, Raffaella, Raisi, Zahyia Al, Turner, Samantha J, Brown, Natasha J, Desai, Tarishi D, Haan, Eric, Turner, Gillian, Christodoulou, John, Leonard, Helen, Gill, Deepak, Stratton, Michael R, Gecz, Jozef, Scheffer, Ingrid E

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Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations von Corbett, Mark A, Turner, Samantha J, Gardner, Alison, Silver, Jeremy, Stankovich, Jim, Leventer, Richard J, Derry, Christopher P, Carroll, Renée, Ha, Thuong, Scheffer, Ingrid E, Bahlo, Melanie, Jackson, Graeme D, Mackey, David A, Berkovic, Samuel F, Gecz, Jozef

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Shear Induces a Unique Series of Morphological Changes in Translocating Platelets: Effects of Morphology on Translocation Dynamics von Maxwell, Mhairi J, Dopheide, Sacha M, Turner, Samantha J, Jackson, Shaun P

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Erratum to: New Genes for Focal Epilepsies with Speech and Language Disorders von Turner, Samantha J., Morgan, Angela T., Perez, Eliane Roulet, Scheffer, Ingrid E.

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X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment von Jenkinson, Andrew, Varian, Jennifer, Shoubridge, Cheryl, Vandeleur, Lucianne, Shepherd, Rebecca, Hynes, Kim, Shaw, Marie, Gusella, James F, Teague, John, Edkins, Sarah, Dicks, Ed, Dibbens, Leanne M, Haan, Eric, Gécz, Jozef, Halliday, Kelly, Lerman-Sagie, Tally, Sutton, Edwina, Corbett, Mark, Wray, Paul, Bomar, Jamee, Stevens, Claire, Scheffer, Ingrid E, Barthorpe, Syd, Butler, Adam, Tarpey, Patrick S, Jones, David, Bayly, Marta A, Madison, Mark, West, Sofie, Lev, Dorit, Stratton, Michael R, Neufeld, Miriam Y, Korczyn, Amos D, Tofts, Calli, Futreal, P Andrew, Turner, Samantha J, Kim, Hyung-Goo, Berkovic, Samuel F, Buck, Gemma, O'Meara, Sarah, Friend, Kathryn, Kivity, Sara, Afawi, Zaid, Mironenko, Tatiana, McKee, Shane, Cole, Jennifer, Lee, Rebecca, Geschwind, Daniel H, Widaa, Sara, Ryan, Stephen, Smith, Raffaella, Sutherland, Grant R, Menzies, Andrew, Mulley, John C, Mazarib, Aziz, Derry, Christopher P, Thomas, Paul

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