Jacy L Wagnon

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 9

Top Topics

Escherichia Coli

Congenital Heart Disease

Top Venues

Epilepsy currents

This page only lists publications with an associated author ORCID identifier.

Publications

Jacy L Wagnon
Channeling the Future of Pathogenicity Prediction for Genetic Variants in Epilepsy. Epilepsy currents 23 (2) (2023)
Jacy L Wagnon
Neurons Are GIRKed in GNB1 Encephalopathy: Unraveling Pathogenic Mechanisms in a Complex Neurodevelopmental Disorder. Epilepsy currents 23 (6) (2023)
Jacy L Wagnon
Channeling the Future of Pathogenicity Prediction for Genetic Variants in Epilepsy. Epilepsy currents 23 (2) (2023)
Jacy L Wagnon
Neurons Are GIRKed in GNB1 Encephalopathy: Unraveling Pathogenic Mechanisms in a Complex Neurodevelopmental Disorder. Epilepsy currents 23 (6) (2023)
Jacy L Wagnon
Yo GABA GABA! Convergent Mechanisms Driven by Gain-of-Function GABRD and Loss-of-Function SLC6A1 Variants Implicate Elevated GABAergic Tone in Generalized Epilepsies. Epilepsy currents 22 (3) (2022)
Jacy L Wagnon
Back to Basics: A Role for Astrocyte Alkalization in Epileptogenesis. Epilepsy currents 21 (4) (2021)
Jacy L Wagnon
TANGO With SCN1A: Can This Molecular Dance Defeat Dravet Syndrome? Epilepsy currents 21 (1) (2020)
Ingo Helbig, Erin Rooney Riggs, Carrie-Anne Barry, Karl Martin Klein, David Dyment, Courtney Thaxton, Bekim Sadikovic, Tristan T Sands, Jacy L Wagnon, Khalida Liaquat, Maria Roberta Cilio, Ghayda Mirzaa, Kristen Park, Erika Axeen, Elizabeth Butler, Tanya M Bardakjian, Pasquale Striano, Annapurna Poduri, Rebecca K Siegert, Andrew R Grant, Katherine L Helbig, Heather C Mefford
The ClinGen Epilepsy Gene Curation Expert Panel-Bridging the divide between clinical domain knowledge and formal gene curation criteria. Human mutation 39 (11) (2019)
Jacy L Wagnon, Niccolò E Mencacci, Bryan S Barker, Eric R Wengert, Kailash P Bhatia, Bettina Balint, Miryam Carecchio, Nicholas W Wood, Manoj K Patel, Miriam H Meisler
Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus. Human mutation 39 (7) (2018)