Susan J. Hayflick
Oregon Health & Science University(US)
Publications by Year
Research Areas
Neurological diseases and metabolism, Metabolism and Genetic Disorders, Porphyrin Metabolism and Disorders, RNA regulation and disease, Hereditary Neurological Disorders
Most-Cited Works
- → A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome(2001)757 cited
- → Genetic, Clinical, and Radiographic Delineation of Hallervorden–Spatz Syndrome(2003)717 cited
- → PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron(2006)537 cited
- → Clinical and genetic delineation of neurodegeneration with brain iron accumulation(2008)367 cited
- → Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA(2012)358 cited
- → Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia(2016)314 cited
- → Neurodegeneration with brain iron accumulation