Paula Bray
University of Sydney(AU)The University of Sydney(AU)UNSW Sydney(AU)Sydney Children’s Hospitals Network(AU)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Cerebral Palsy and Movement Disorders, Neurogenetic and Muscular Disorders Research, Botulinum Toxin and Related Neurological Disorders, Family and Disability Support Research
Most-Cited Works
- → Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes(2020)172 cited
- → Genomic instability in the type II TGF-beta1 receptor gene in atherosclerotic and restenotic vascular cells.(1997)168 cited
- → Variations of the human glucocorticoid receptor gene (NR3C1): Pathological and in vitro mutations and polymorphisms(2003)167 cited
- → Toll‐like receptors in the brain and their potential roles in neuropathology(2007)118 cited
- → Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease(2016)95 cited
- → Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study(2020)88 cited