Tara Newcomb

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 423 citations · Full text

Life Sciences, Genetics, Neurology +9

Population-Based Prevalence of Myotonic Dystrophy Type 1 Using Genetic Analysis of Statewide Blood Screening Program

Nicholas E. Johnson, Russell J. Butterfield, Katie Mayne et al. · Neurology · 2021 · 166 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Whole-genome analysis for effective clinical diagnosis and gene discovery in early infantile epileptic encephalopathy

Betsy Ostrander, Russell J. Butterfield, Brent S. Pedersen et al. · npj Genomic Medicine · 2018 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

Louis Viollet, Gustavo Glusman, Kelley J. Murphy et al. · PLoS ONE · 2015 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

A novel germline PIGA mutation in Ferro‐Cerebro‐Cutaneous syndrome: A neurodegenerative X‐linked epileptic encephalopathy with systemic iron‐overload

Kathryn J. Swoboda, Rebecca L. Margraf, John C. Carey et al. · American Journal of Medical Genetics Part A · 2013 · 70 citations

Life Sciences, Genetics, Molecular Genetics +17