Joline Dalton
Parkinson Research Foundation(US)Parkinson's Australia(AU)Parkinson's Foundation(US)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Muscle Physiology and Disorders, Parkinson's Disease Mechanisms and Treatments, Mitochondrial Function and Pathology, Genomics and Rare Diseases
Most-Cited Works
- → Myotonic dystrophy type 2(2003)457 cited
- → Spectrin mutations cause spinocerebellar ataxia type 5(2006)385 cited
- → Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort(2009)311 cited
- → Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation(2005)188 cited
- → Insulin Receptor Splicing Alteration in Myotonic Dystrophy Type 2(2004)162 cited
- → MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain(2015)152 cited
- → Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures