Dr. Rachel Burt
Honorary
Paediatrics Royal Children's Hospital
25 Scholarly works
0 Projects
HIGHLIGHTS
2020
Journal article
In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness.
DOI: 10.1126/scitranslmed.aay91012020
Journal article
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
DOI: 10.1038/s41431-019-0553-82020
Journal article
Intravenously delivered aminoglycoside antibiotics, tobramycin and amikacin, are not ototoxic in mice
DOI: 10.1016/j.heares.2019.1078702019
Journal article
Data Resource Profile: The Victorian Childhood Hearing Impairment Longitudinal Databank (VicCHILD)
DOI: 10.1093/ije/dyz1682019
Journal article
Prevalence of Childhood Hearing Loss and Secular Trends: A Systematic Review and Meta-Analysis
DOI: 10.1016/j.acap.2019.01.0102019
Journal article
Effect of a pneumococcal whole cell vaccine on influenza A-induced pneumococcal otitis media in infant mice
DOI: 10.1016/j.vaccine.2019.03.0132019
Journal article
Organotypic Culture of Neonatal Murine Inner Ear Explants
DOI: 10.3389/fncel.2019.00170
RECENT SCHOLARLY WORKS
2019
Journal article
High prevalence of slight and mild hearing loss across mid-life: a cross-sectional national Australian study
DOI: 10.1016/j.puhe.2018.11.0172018
Journal article
Cross-sectional epidemiology of hearing loss in Australian children aged 11-12 years old and 25-year secular trends
DOI: 10.1136/archdischild-2017-3135052018
Journal article
An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome
DOI: 10.1038/s41598-018-23856-82017
Journal article
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort.
DOI: 10.1136/bmjpo-2017-0001192015
Journal article
Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome
DOI: 10.1016/j.ajpath.2015.03.0262014
Journal article
A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination
DOI: 10.1242/dmm.0146052014
Journal article
CHD7 Deficiency in "Looper", a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment
DOI: 10.1371/journal.pone.00975592013
Journal article
Two ENU-Induced Alleles of Atp2b2 Cause Deafness in Mice
DOI: 10.1371/journal.pone.0067479