| SLC6A1 variants identified in epilepsy patients reduce γ‐aminobutyric acid transport KA Mattison, KM Butler, GAS Inglis, O Dayan, H Boussidan, V Bhambhani, ... Epilepsia 59 (9), e135-e141, 2018 | 58 | 2018 |
| ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy KA Mattison, G Tossing, F Mulroe, C Simmons, KM Butler, A Schreiber, ... Brain 146 (4), 1357-1372, 2023 | 8 | 2023 |
| Engaging young scholars in science through publication: A survey analysis of published middle and high school authors KA Mattison, AR Merchak, ST Wieman, S Zimmer, SC Fankhauser Learned Publishing 35 (3), 321-331, 2022 | 6 | 2022 |
| Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and … N Badshah, KA Mattison, S Ahmad, P Chopra, HR Johnston, S Ahmad, ... Frontiers in neurology 13, 918022, 2022 | 5 | 2022 |
| Pathogenic in-Frame Variants in SCN8A: Expanding the Genetic Landscape of SCN8A-Associated Disease JC Wong, KM Butler, L Shapiro, JT Thelin, KA Mattison, KB Garber, ... Frontiers in Pharmacology 12, 748415, 2021 | 4 | 2021 |
| The untapped potential of early career researchers in academic publishing: Lessons learned from the Journal of Emerging Investigators model CE Otero, V Osinski, KA Mattison Learned Publishing 35 (3), 393-399, 2022 | 3 | 2022 |
| 748.1 Characterizing the ATP6V0C epilepsy phenotype: a new gene associated with genetic epilepsy with febrile seizures plus spectrum R Morcos, P Macias-Sedas, R Obrocki, A Beltráan-Corbellini, ... Epilepsia 64 (S2), 387-387, 2023 | | 2023 |
| Towards a Better Understanding of the Genetic Contributions to Epilepsy KA Mattison Emory University, 2022 | | 2022 |
| Dent Disease GeneReview–Tables 4 and 5 JC Lieske, DS Milliner, L Beara-Lasic, P Harris, K Hopp, A Cogal, ... | | |
