Georgina E. Hollway
QIMR Berghofer Medical Research Institute(AU)
Publications by Year
Research Areas
MicroRNA in disease regulation, Genomics and Rare Diseases, Cancer Genomics and Diagnostics, Developmental Biology and Gene Regulation, Congenital heart defects research
Most-Cited Works
- A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome.(1997)
- → Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2(1995)323 cited
- → Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation(2003)296 cited
- → Whole-Somite Rotation Generates Muscle Progenitor Cell Compartments in the Developing Zebrafish Embryo(2007)182 cited
- → The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congenital muscular dystrophy(2007)175 cited
- A novel method for development of species and strain-specific DNA probes and PCR primers for identifying Burkholderia solanacearum (formerly Pseudomonas solanacearum)(1997)
- → Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1(2014)157 cited
- → miR-139-5p Modulates Radiotherapy Resistance in Breast Cancer by Repressing Multiple Gene Networks of DNA Repair and ROS Defense(2017)129 cited
- → Scube2 mediates Hedgehog signalling in the zebrafish embryo(2006)117 cited
- → Cadherin-Mediated Differential Cell Adhesion Controls Slow Muscle Cell Migration in the Developing Zebrafish Myotome(2003)98 cited