Samantha J. Turner
Murdoch Children's Research Institute(AU)Austin Health(AU)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Language Development and Disorders, Genomics and Rare Diseases, Epilepsy research and treatment, Congenital heart defects research
Most-Cited Works
- → X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment(2008)444 cited
- → GRIN2A mutations cause epilepsy-aphasia spectrum disorders(2013)372 cited
- → Epilepsy and mental retardation limited to females: an under-recognized disorder(2008)193 cited
- → Genetic Architecture of Idiopathic Generalized Epilepsy: Clinical Genetic Analysis of 55 Multiplex Families(2004)150 cited
- → Severe childhood speech disorder(2020)120 cited
- → Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families(2009)79 cited
- → GRIN2A(2015)77 cited
- → Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria(2013)75 cited
- → New Genes for Focal Epilepsies with Speech and Language Disorders(2015)70 cited
- → Shear Induces a Unique Series of Morphological Changes in Translocating Platelets(2005)66 cited