Resultats de la cerca - Ellis, Colin A.

Authors’ Reply to Drs Bourque and Breiner, Re: Cerebrospinal Fluid in Posterior Reversible Encephalopathy Syndrome per Ellis, Colin A., Balu, Ramani

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Early-onset genetic epilepsies reaching adult clinics per Lewis-Smith, David, Ellis, Colin A, Helbig, Ingo, Thomas, Rhys H

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The “Maternal Effect” on Epilepsy Risk: Analysis of Familial Epilepsies and Reassessment of Prior Evidence per Ellis, Colin A., Berkovic, Samuel F., Epstein, Michael P., Ottman, Ruth

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Generalized, Focal, and Combined Epilepsies in Families: New Evidence for Distinct Genetic Factors per Ellis, Colin A., Ottman, Ruth, Epstein, Michael P., Berkovic, Samuel F.

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Epilepsy risk in offspring of affected parents; a cohort study of the “maternal effect” in epilepsy per Dreier, Julie W., Ellis, Colin A., Berkovic, Samuel F., Cotsapas, Chris, Ottman, Ruth, Christensen, Jakob

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Unilateral thalamic lesion mimicking genetic generalized epilepsy per Kulick-Soper, Catherine V., Stein, Joel M., Chen, Isaac H., Ellis, Colin A., Davis, Kathryn A.

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Seizure Detection in Continuous Inpatient EEG: A Comparison of Human vs Automated Review per Ganguly, Taneeta Mindy, Ellis, Colin A., Tu, Danni, Shinohara, Russell T., Davis, Kathryn A., Litt, Brian, Pathmanathan, Jay

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Epilepsy in Families: Age at onset is a familial trait, independent of syndrome per Ellis, Colin A., Churilov, Leonid, Epstein, Michael P., Xie, Sharon X., Bellows, Susannah T., Ottman, Ruth, Berkovic, Samuel F.

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Cerebrospinal Fluid in Posterior Reversible Encephalopathy Syndrome: Implications of Elevated Protein and Pleocytosis per Ellis, Colin A., McClelland, Andrew C., Mohan, Suyash, Kuo, Emory, Kasner, Scott E., Zhang, Cen, Khankhanian, Pouya, Balu, Ramani

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A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation per Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Gonzalez, Alexander K., Felmeister, Alex S., Khankhanian, Pouya, Ellis, Colin A., Helbig, Ingo

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Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation per Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Gonzalez, Alexander K., Felmeister, Alex S., Khankhanian, Pouya, Ellis, Colin A., Helbig, Ingo

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Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable per Lewis-Smith, David, Galer, Peter D., Balagura, Ganna, Kearney, Hugh, Ganesan, Shiva, Cosico, Mahgenn, O’Brien, Margaret, Vaidiswaran, Priya, Krause, Roland, Ellis, Colin A., Thomas, Rhys H., Robinson, Peter N., Helbig, Ingo

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Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data per Lewis-Smith, David, Ganesan, Shiva, Galer, Peter D., Helbig, Katherine L., McKeown, Sarah E., O’Brien, Margaret, Khankhanian, Pouya, Kaufman, Michael C., Gonzalez, Alexander K., Felmeister, Alex S., Krause, Roland, Ellis, Colin A., Helbig, Ingo

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Using Generalized Polyspike Train to Predict Drug-Resistant Idiopathic Generalized Epilepsy per Conrad, Erin C., Chugh, Nanak, Ganguly, Taneeta M., Gugger, James J., Tizazu, Etsegenet F., Shinohara, Russell T., Raghupathi, Ramya, Becker, Danielle A., Gelfand, Michael A., Omole, Armina T., Decker, Barbara M., Pathmanathan, Jay S., Davis, Kathryn A., Ellis, Colin A.

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Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders per Crawford, Katherine, Xian, Julie, Helbig, Katherine L., Galer, Peter D., Parthasarathy, Shridhar, Lewis-Smith, David, Kaufman, Michael C., Fitch, Eryn, Ganesan, Shiva, O’Brien, Margaret, Codoni, Veronica, Ellis, Colin A., Conway, Laura J., Taylor, Deanne, Krause, Roland, Helbig, Ingo

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Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies per Galer, Peter D., Ganesan, Shiva, Lewis-Smith, David, McKeown, Sarah E., Pendziwiat, Manuela, Helbig, Katherine L., Ellis, Colin A., Rademacher, Annika, Smith, Lacey, Poduri, Annapurna, Seiffert, Simone, von Spiczak, Sarah, Muhle, Hiltrud, van Baalen, Andreas, Thomas, Rhys H., Krause, Roland, Weber, Yvonne, Helbig, Ingo

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Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery per Oliver, Karen L., Ellis, Colin A., Scheffer, Ingrid E., Ganesan, Shiva, Leu, Costin, Sadleir, Lynette G., Heinzen, Erin L., Mefford, Heather C., Bass, Andrew J., Curtis, Sarah W., Harris, Rebekah V., Whiteman, David C., Helbig, Ingo, Ottman, Ruth, Epstein, Michael P., Bahlo, Melanie, Berkovic, Samuel F.

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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy per Helbig, Ingo, Lopez-Hernandez, Tania, Shor, Oded, Galer, Peter, Ganesan, Shiva, Pendziwiat, Manuela, Rademacher, Annika, Ellis, Colin A., Hümpfer, Nadja, Schwarz, Niklas, Seiffert, Simone, Peeden, Joseph, Shen, Joseph, Štěrbová, Katalin, Hammer, Trine Bjørg, Møller, Rikke S., Shinde, Deepali N., Tang, Sha, Smith, Lacey, Poduri, Annapurna, Krause, Roland, Benninger, Felix, Helbig, Katherine L., Haucke, Volker, Weber, Yvonne G.

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Extracting seizure frequency from epilepsy clinic notes: a machine reading approach to natural language processing per Xie, Kevin, Gallagher, Ryan S, Conrad, Erin C, Garrick, Chadric O, Baldassano, Steven N, Bernabei, John M, Galer, Peter D, Ghosn, Nina J, Greenblatt, Adam S, Jennings, Tara, Kornspun, Alana, Kulick-Soper, Catherine V, Panchal, Jal M, Pattnaik, Akash R, Scheid, Brittany H, Wei, Danmeng, Weitzman, Micah, Muthukrishnan, Ramya, Kim, Joongwon, Litt, Brian, Ellis, Colin A, Roth, Dan

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Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into Adulthood per Stamberger, Hannah, Crosiers, David, Balagura, Ganna, Bonardi, Claudia M., Basu, Anna, Cantalupo, Gaetano, Chiesa, Valentina, Christensen, Jakob, Dalla Bernardina, Bernardo, Ellis, Colin A., Furia, Francesca, Gardiner, Fiona, Giron, Camille, Guerrini, Renzo, Klein, Karl Martin, Korff, Christian, Krijtova, Hana, Leffner, Melanie, Lerche, Holger, Lesca, Gaetan, Lewis-Smith, David, Marini, Carla, Marjanovic, Dragan, Mazzola, Laure, McKeown Ruggiero, Sarah, Mochel, Fanny, Ramond, Francis, Reif, Philipp S., Richard-Mornas, Aurélie, Rosenow, Felix, Schropp, Christian, Thomas, Rhys H., Vignoli, Aglaia, Weber, Yvonne, Palmer, Elizabeth, Helbig, Ingo, Scheffer, Ingrid E., Striano, Pasquale, Møller, Rikke S., Gardella, Elena, Weckhuysen, Sarah

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