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As a pediatric epileptologist with a basic science background in the molecular control of neural development, I’m interested in revealing pathogenic mechanisms behind genetic epilepsies of childhood and using these findings to advance therapies for epilepsy. My laboratory uses human pluripotent stem cells derived into neural cultures to study why pathogenic variants in genes affect brain development and cause epilepsy. We focus on sodium channel genes that are related to Dravet Syndrome (SCN1A and SCN1B) as well as genes in the mechanistic target of rapamycin (mTOR) pathway, including STRADA.
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crossref(2023)
EPILEPSY CURRENTSno. 2 (2023): 130-132
Epilepsy Currentspp.153575972211492-153575972211492, (2023)
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AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2023)
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Christina Sloan-Heggen,Amanda Barone Pritchard,John Barks,Louis Dang,Karl Desch,Michael Quasney,Mark Russell,Jeffrey Innis
Genetics in Medicineno. 3 (2022): S158-S158
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Elizabeth Buttermore,Stormy Chamberlain,Jannine Cody,Gregory Costain,Louis Dang, Andrew DeWoody,Yssa DeWoody, Kira Dies,Evan Eichler,Santhosh Girirajan,Marie Gramm, Alycia Halladay,
AMERICAN JOURNAL OF HUMAN GENETICSno. 8 (2022): 1353-1365
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