Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus by Danielle deCampo, Danielle deCampo, Danielle deCampo, Julie Xian, Julie Xian, Julie Xian, Alexis Karlin, Alexis Karlin, Alexis Karlin, Katie R. Sullivan, Katie R. Sullivan, Katie R. Sullivan, Sarah M. Ruggiero, Sarah M. Ruggiero, Sarah M. Ruggiero, Peter Galer, Peter Galer, Peter Galer, Mark Ramos, Nicholas S. Abend, Nicholas S. Abend, Nicholas S. Abend, Alex Gonzalez, Ingo Helbig, Ingo Helbig, Ingo Helbig, Ingo Helbig, Ingo Helbig

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals by Ludovica Montanucci, David Lewis-Smith, Ryan L. Collins, Lisa-Marie Niestroj, Shridhar Parthasarathy, Julie Xian, Shiva Ganesan, Marie Macnee, Tobias Brünger, Rhys H. Thomas, Michael Talkowski, Epi25 Collaborative, Ingo Helbig, Costin Leu, Dennis Lal

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A disease concept model for STXBP1‐related disorders by Katie R. Sullivan, Sarah M. Ruggiero, Julie Xian, Kim M. Thalwitzer, Rahma Ali, Sydni Stewart, Mahgenn Cosico, Jackie Steinberg, James Goss, Anna C. Pfalzer, Kyle J. Horning, Nicole Weitzel, Sydney Corey, Laura Conway, Charlene Son Rigby, Terry Jo Bichell, Ingo Helbig

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Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome by Ingo Helbig, Giulia Barcia, Manuela Pendziwiat, Shiva Ganesan, Stefanie H. Mueller, Katherine L. Helbig, Priya Vaidiswaran, Julie Xian, Peter D. Galer, Zaid Afawi, Nicola Specchio, Gerhard Kluger, Gregor Kuhlenbäumer, Silke Appenzeller, Michael Wittig, Uri Kramer, Andreas vanBaalen, Rima Nabbout, FIRES Genetics Study Group

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