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Martina Bebin

Epilepsy Foundation ·
Area of research
Psychiatry and Mental health · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Epilepsy research and treatment, Tuberous Sclerosis Complex Research, Pharmacological Effects and Toxicity Studies, and Genetics and Neurodevelopmental Disorders.
h-index
22
citations
2,312
works
49
NIH funding
primary concept
email

Recent publications

Treatment Response to Antiseizure Medications in People With Newly Diagnosed Focal Epilepsy
JAMA Neurology 2025cited by 10position: middledoi
Mood and Anxiety Disorders and Suicidality in Patients With Newly Diagnosed Focal Epilepsy
Neurology 2022cited by 47position: middledoi
Antiepileptogenesis and disease modification: Clinical and regulatory issues
Epilepsia Open 2021cited by 38position: middledoi
Profile of Autism Spectrum Disorder in Tuberous Sclerosis Complex: Results from a Longitudinal, Prospective, Multisite Study
Annals of Neurology 2021cited by 35position: middledoi
Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex
Pediatric Neurology 2020cited by 23position: middledoi
Tuberous Sclerosis Complex Genotypes and Developmental Phenotype
Pediatric Neurology 2019cited by 40position: middledoi
Modifying genetic epilepsies – Results from studies on tuberous sclerosis complex
Neuropharmacology 2019cited by 37position: lastdoi
Language predictors of autism spectrum disorder in young children with tuberous sclerosis complex
Epilepsy & Behavior 2019cited by 21position: middledoi
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
The American Journal of Human Genetics 2017cited by 454position: middledoi
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus
PLoS Genetics 2017cited by 91position: middledoi
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism
The American Journal of Human Genetics 2016cited by 87position: middledoi
<i>UBQLN2</i> mutation causing heterogeneous X‐linked dominant neurodegeneration
Annals of Neurology 2014cited by 63position: middledoi
Functional Assessment of<i>TSC2</i>Variants Identified in Individuals with Tuberous Sclerosis Complex
Human Mutation 2013cited by 52position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Jamie K. Capal · University of Rochester Medical Center2 papers (2019–2021) · 2 papers (2019–2021)Paul S. Horn · University of Rochester Medical Center2 papers (2019–2021)Darcy A. Krueger · Tufts University2 papers (2019–2021) · 2 papers (2019–2021)Hope Northrup · Memorial Hermann2 papers (2019–2021) · 2 papers (2019–2021)Mustafa Şahin · Ankara Bilkent City Hospital2 papers (2019–2021)Deborah A. Pearson · The University of Texas at Austin2 papers (2019–2021)Joyce Y. Wu · Northwestern University2 papers (2019–2021) · 1 papers (2013–2013)Eric Glasgow · Georgetown University1 papers (2017–2017)Michelle L. Thompson · Albert Einstein College of Medicine1 papers (2017–2017) · 1 papers (2017–2017)Kira A. Dies · The University of Texas Health Science Center at Houston1 papers (2013–2013) · 1 papers (2017–2017)Christine E. Seidman · Harvard University1 papers (2014–2014) · 1 papers (2021–2021)Steven Sparagana · Southwestern Medical Center1 papers (2013–2013)Charu Deshpande · St Thomas' Hospital1 papers (2017–2017)