Tracy S. Gertler

Lurie Children's Hospital — United States

Neuroscience · Life Sciences

18h-index2.4kcitations35works1.02yr avg
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Research Topics

Neuroscience and Neuropharmacology Research(12), Neurological disorders and treatments(9), Genetics and Neurodevelopmental Disorders(7), Parkinson's Disease Mechanisms and Treatments(6), Epilepsy research and treatment(5)

Publications35 total

Bringing nutritional ketosis to the table as an option for healing the pediatric brain
Frontiers in Nutrition·2024· 1 citedOpen Access
19. Excitatory Dysfunction Drives Synchrony Deficits in a Schizophrenia 16p11.2 Duplication iPSC Derived Neuron Model
Biological Psychiatry·2023
Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons
Biological Psychiatry·2022· 24 citedOpen Access
Monoallelic and biallelic mutations in<i>RELN</i>underlie a graded series of neurodevelopmental disorders
Brain·2022· 20 citedOpen Access
KNa1.1 gain-of-function preferentially dampens excitability of murine parvalbumin-positive interneurons
Neurobiology of Disease·2022· 37 citedOpen Access
Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures
The American Journal of Human Genetics·2022· 39 citedOpen Access
DLG4-related synaptopathy: a new rare brain disorder
Genetics in Medicine·2021· 48 citedOpen Access
Hypoglycemia in Infants and Effect on Neurodevelopment
Pediatric Neurology Briefs·2020Open Access
Pearls &amp; Oy-sters: When Genetic Generalized Epilepsy Becomes Progressive
Neurology·2020Open Access
Corrigendum to “A single-center, retrospective analysis of genotype–phenotype correlations in children with Dravet syndrome” [Seizure: Eur. J. Epilepsy 75 (2020) 1–6]
Seizure·2020Open Access
A single-center, retrospective analysis of genotype-phenotype correlations in children with Dravet syndrome
Seizure·2019· 18 citedOpen Access
Functional consequences of a <i>KCNT1</i> variant associated with status dystonicus and early‐onset infantile encephalopathy
Annals of Clinical and Translational Neurology·2019· 36 citedOpen Access
<i>SCN8A</i>: When Neurons Are So Excited, They Just Can’t Hide It
Epiliepsy currents/Epilepsy currents·2019· 11 citedOpen Access
Treatment Responsiveness in KCNT1-Related Epilepsy
Neurotherapeutics·2019· 97 citedOpen Access
Case Series: Expansion of MT-ATP6 Pathogenic Variant Phenotype (P1.6-040)
Neurology·2019
Figure 1. [Pathogenic variants identified in KCNT1-related...].
2018
KCNT1-Related Epilepsy
Europe PMC (PubMed Central)·2018· 7 cited
Screening of conventional anticonvulsants in a genetic mouse model of epilepsy
Annals of Clinical and Translational Neurology·2017· 122 citedOpen Access
Imaging of Glutamate Concentration in Sturge-Weber Syndrome
Pediatric Neurology Briefs·2017· 3 citedOpen Access
Visual Processing in Infants with Tuberous Sclerosis Complex
Pediatric Neurology Briefs·2016· 1 citedOpen Access
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Frequent Co-authors

C. Savio Chan(12), D. James Surmeier(12), Michelle Day(5), Paul Greengard(4), Joshua L. Plotkin(4), Linda Laux(4), Weixing Shen(4), M. Angela Cenci(3), Alfred L. George(3), David Bearden(3), Gemma L. Carvill(3), Cynthia V. Stack(3), Tim Fieblinger(2), Steven M. Graves(2), Luke E. Sebel(2), Cristina Alcacer(2), Myriam Heiman(2), Hitoshi Kita(2), Jennifer A. Kearney(2), William B. Dobyns(2)