ColinEllisMD

PubMed

• 1 citations
  Disparities in Genetic Testing for Neurologic Disorders.
  Aaron Baldwin, Juliette Copeland, Meron Azage, Laynie Dratch, Kelsey Johnson, Rachel A Paul, Defne A Amado, Michael Baer, Andres Deik, Lauren B Elman, Michael Guo, Ali...> ;Neurology. 2024 Mar 26
• Disparities in seizure outcomes revealed by large language models.
  Kevin Xie, William K S Ojemann, Ryan S Gallagher, Russell T Shinohara, Alfredo Lucas, Chloé E Hill, Roy H Hamilton, Kevin B Johnson, Dan Roth, Brian Litt, Colin A Ellis> ;Journal of the American Medical Informatics Association. 2024 Mar 13
• Alcohol for seizure induction in the epilepsy monitoring unit.
  Emmert, B., Xie, K., Conrad, E., Ghosn, N., Bauman, K., Korzun, J., Kulick-Soper, C., Naveed, O., Hartmann, N., LaRocque, J., Mindy Ganguly, T., Gugger, J., Raghupathi...> ;Epilepsy & Behavior. 2024 Jan 1
• 1 citations
  Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts.
  Laynie Dratch, Meron Azage, Aaron Baldwin, Kelsey Johnson, Rachel A Paul, Tanya M Bardakjian, Sara-Claude Michon, Defne A Amado, Michael Baer, Andres F Deik, Lauren B ...> ;Journal of Neurology. 2024 Feb 1
• Macrocephaly and developmental delay caused by missense variants in RAB5C.
  Koop, K., Yuan, W., Tessadori, F., Rodriguez-Polanco, W., Grubbs, J., Zhang, B., Osmond, M., Graham, G., Sawyer, S., Conboy, E., Vetrini, F., Treat, K., Płoski, R., Pi...> ;Human Molecular Genetics. 2023 Oct 17
• Generalization of finetuned transformer language models to new clinical contexts.
  Kevin Xie, Samuel W Terman, Ryan S Gallagher, Chloe E Hill, Kathryn A Davis, Brian Litt, Dan Roth, Colin A Ellis> ;JAMIA Open. 2023 Oct 1
• Disparities in seizure outcomes revealed by large language models.
  Kevin Xie, William K S Ojemann, Ryan S Gallagher, Alfredo Lucas, Chloé E Hill, Roy H Hamilton, Kevin B Johnson, Dan Roth, Brian Litt, Colin A Ellis> ;Medrxiv. 2023 Sep 22
• 1 citations
  ILAE Genetics Literacy series: Progressive myoclonus epilepsies.
  Jillian M Cameron, Colin A Ellis, Samuel F Berkovic, > ;Epileptic Disorders. 2023 Oct 1
• Characterizing the treatment gap in the United States among adult patients with a new diagnosis of epilepsy.
  Barbara M Decker, Colin A Ellis, Emily Schriver, Kelly Fischbein, Debbie Smith, Jason T Moyer, Catherine V Kulick-Soper, Danielle Mowery, Brian Litt, Chloe E Hill> ;Epilepsia. 2023 Jul 1
• 5 citations
  Long-term epilepsy outcome dynamics revealed by natural language processing of clinic notes.
  Kevin Xie, Ryan S Gallagher, Russell T Shinohara, Sharon X Xie, Chloe E Hill, Erin C Conrad, Kathryn A Davis, Dan Roth, Brian Litt, Colin A Ellis> ;Epilepsia. 2023 Jul 1
• 3 citations
  A pharmacokinetic model of antiseizure medication load to guide care in the epilepsy monitoring unit.
  Nina J Ghosn, Kevin Xie, Akash R Pattnaik, James J Gugger, Colin A Ellis, Elizabeth Sweeney, Emily Fox, John M Bernabei, Jenaye Johnson, Jacqueline Boccanfuso, Brian L...> ;Epilepsia. 2023 May 1
• 1 citations
  Quantitative artifact reduction and pharmacologic paralysis improve detection of EEG epileptiform activity in critically ill patients.
  Catherine V Kulick-Soper, Russell T Shinohara, Colin A Ellis, Taneeta M Ganguly, Ramya Raghupathi, Jay S Pathmanathan, Erin C Conrad> ;Clinical Neurophysiology. 2023 Jan 1
• Inherited bone marrow failure with macrothrombocytopenia due to germline tubulin beta class I (TUBB) variant.
  Yash B Shah, Ping Lin, Stone Chen, Alan Zheng, Wendy Alcaraz, Meghan C Towne, Courtney Gabriel, Elizabeth J Bhoj, Michele P Lambert, Timothy S Olson, Dale M Frank, Col...> ;British Journal of Haematology. 2023 Jan 1
• 7 citations
  Development of a natural language processing algorithm to extract seizure types and frequencies from the electronic health record.
  Barbara M Decker, Alexandra Turco, Jian Xu, Samuel W Terman, Nikitha Kosaraju, Alisha Jamil, Kathryn A Davis, Brian Litt, Colin A Ellis, Pouya Khankhanian, Chloe E Hill> ;Seizure. 2022 Oct 1
• 8 citations
  Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery.
  Karen L Oliver, Colin A Ellis, Ingrid E Scheffer, Shiva Ganesan, Costin Leu, Lynette G Sadleir, Erin L Heinzen, Heather C Mefford, Andrew J Bass, Sarah W Curtis, Rebek...> ;Ebiomedicine. 2022 Jul 1
• 12 citations
  The role of common genetic variation in presumed monogenic epilepsies.
  Ciarán Campbell, Costin Leu, Yen-Chen Anne Feng, Stefan Wolking, Claudia Moreau, Colin Ellis, Shiva Ganesan, Helena Martins, Karen Oliver, Isabelle Boothman, Katherine...> ;Ebiomedicine. 2022 Jul 1
• 23 citations
  Assessing the landscape of STXBP1-related disorders in 534 individuals.
  Julie Xian, Shridhar Parthasarathy, Sarah M Ruggiero, Ganna Balagura, Eryn Fitch, Katherine Helbig, Jing Gan, Shiva Ganesan, Michael C Kaufman, Colin A Ellis, David Le...> ;Brain. 2022 Jun 3
• 5 citations
  Seizure Detection in Continuous Inpatient EEG: A Comparison of Human vs Automated Review.
  Taneeta Mindy Ganguly, Colin A Ellis, Danni Tu, Russell T Shinohara, Kathryn A Davis, Brian Litt, Jay Pathmanathan> ;Neurology. 2022 May 31
• 8 citations
  Extracting seizure frequency from epilepsy clinic notes: a machine reading approach to natural language processing.
  Kevin Xie, Ryan S Gallagher, Erin C Conrad, Chadric O Garrick, Steven N Baldassano, John M Bernabei, Peter D Galer, Nina J Ghosn, Adam S Greenblatt, Tara Jennings, Ala...> ;Journal of the American Medical Informatics Association. 2022 Apr 13
• 10 citations
  De novo DHDDS variants cause a neurodevelopmental and neurodegenerative disorder with myoclonus
  Serena Galosi, Ban H Edani, Simone Martinelli, Hana Hansikova, Erik A. Eklund, Caterina Caputi, Laura Masuelli, Nicole Corsten-Janssen, Myriam Srour, Renske Oegema, Da...> ;Brain. 2021 Aug 11
• 12 citations
  Assessing seizure burden in pediatric epilepsy using an electronic medical record-based tool through a common data element approach.
  Mark Fitzgerald, Michael C. Kaufman, Shavonne L. Massey, Sara E. Fridinger, Marisa S. Prelack, Colin A Ellis, Xilma R. Ortiz-Gonzalez, Lawrence E. Fried, Marissa DiGio...> ;Epilepsia. 2021 Jun 2
• 10 citations
  Temporal trends and yield of clinical diagnostic genetic testing in adult neurology.
  Michael H. Guo, Tanya Bardakjian, Morgan R Brzozowski, Steven S. Scherer, Colin Quinn, Lauren Elman, Jennifer L. Orthmann-Murphy, Thomas F. Tropea, Colin A Ellis, Pedr...> ;American Journal of Medical Genetics. Part A. 2021 Jun 2
• 5 citations
  Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data
  David Lewis-Smith, Shiva Ganesan, Peter D. Galer, Katherine L. Helbig, Sarah E McKeown, Margaret O'Brien, Pouya Khankhanian, Michael C. Kaufman, Alexander K. Gonzalez,...> ;European Journal of Human Genetics. 2021 May 24
• 10 citations
  Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable
  David Lewis-Smith, Peter D. Galer, Ganna Balagura, Hugh Kearney, Shiva Ganesan, Mahgenn Cosico, Margaret O'Brien, Priya Vaidiswaran, Roland Krause, Colin A Ellis, Rhys...> ;Epilepsia. 2021 May 5
• 27 citations
  Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.
  Katherine Crawford, Julie Xian, Katherine L. Helbig, Peter D. Galer, Shridhar Parthasarathy, David Lewis-Smith, Michael C. Kaufman, Eryn Fitch, Shiva Ganesan, Margaret...> ;Genetics in Medicine. 2021 Mar 17
• Join now to see all