R. Burt

发表

Exome sequencing in infants with congenital hearing impairment: a population-based cohort study

H. Rehm, M. Wake, D. Phelan, 2019, European Journal of Human Genetics.

ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death

P. Lockhart, D. Paterson, B. Nayagam, 2022, Journal of Molecular Medicine.

An NZW-Derived Interval on Chromosome 7 Moderates Sialadenitis, But Not Insulitis in Congenic Nonobese Diabetic Mice

G. Morahan, S. Berzins, Jian‐guo Zhang, 2009, The Journal of Immunology.

Congenic Nonobese Diabetic Mice Moderates Sialadenitis, But Not Insulitis in An NZW-Derived Interval on Chromosome 7

G. Morahan, Christopher M Thomas, S. Berzins, 2009 .

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

M. G. Manning, A. Voss, B. Kile, 2014, Disease Models & Mechanisms.

Temporal expression of an H2-linked locus in host response to mouse malaria

T. Baldwin, S. Foote, R. Burt, 1999, Immunogenetics.

Anti-apoptotic gene Bcl2 is required for stapes development and hearing

M. G. Manning, A. Wise, P. Bouillet, 2012, Cell Death and Disease.

Genetic Modifier Screens in Mice

B. Kile, M. Carpinelli, R. Burt, 2012, Current protocols in mouse biology.

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

M. Bahlo, W. Alexander, D. Hilton, 2002, The American journal of pathology.

High prevalence of slight and mild hearing loss across mid-life: a cross-sectional national Australian study.

M. Wake, F. Mensah, L. Gold, 2019, Public health.

Effect of a pneumococcal whole cell vaccine on influenza A-induced pneumococcal otitis media in infant mice.

E. Mulholland, R. Malley, R. Robins-Browne, 2019, Vaccine.

Organotypic Culture of Neonatal Murine Inner Ear Explants

B. Nayagam, R. Lim, R. Burt, 2019, Front. Cell. Neurosci..

Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues.

M. Karayiorgou, K. Stark, J. Gogos, 2009, The international journal of neuropsychopharmacology.

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome.

Elizabeth A. Kruse, E. Kruse, B. Kile, 2015, The American journal of pathology.

Intravenously delivered aminoglycoside antibiotics, tobramycin and amikacin, are not ototoxic in mice

P. Lockhart, R. Burt, Jacqueline M. Ogier, 2019, Hearing Research.

Antibodies against Merozoite Surface Protein (Msp)-119 Are a Major Component of the Invasion-Inhibitory Response in Individuals Immune to Malaria

A. Cowman, B. Crabb, T. D. de Koning-Ward, 2001, The Journal of experimental medicine.

Mouse loci for malaria-induced mortality and the control of parasitaemia

T. Baldwin, S. Foote, A. Roberts, 1997, Nature Genetics.

Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia

M. Morel-Kopp, C. Ward, B. Kile, 2018, Platelets.

Description of a novel mutation leading to MYH9-related disease.

B. Kile, J. Collinge, J. Joseph, 2008, Thrombosis research.

Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1.

Gonçalo R Abecasis, Maria Karayiorgou, Kimberly F Doheny, 2004, American journal of human genetics.

Genetics of host response to malaria.

R. Burt, 1999, International journal for parasitology.

Data Resource Profile: The Victorian Childhood Hearing Impairment Longitudinal Databank (VicCHILD).

M. Wake, Z. Poulakis, S. Tobin, 2019, International journal of epidemiology.

A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohort

H. Rehm, M. Wake, D. Amor, 2017, BMJ Paediatrics Open.

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

Maria Karayiorgou, M. Karayiorgou, J. Gogos, 2004, Nature Genetics.

CHD7 Deficiency in “Looper”, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment

B. Kile, B. Arhatari, R. C. Symons, 2014, PloS one.

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

B. Arhatari, M. Carpinelli, Michael A. Wilson, 2018, Scientific Reports.

Prevalence of Childhood Hearing Loss and Secular Trends: A Systematic Review and Meta-Analysis.

M. Wake, Mengjiao Liu, Jing Wang, 2019, Academic pediatrics.

Vitamin D-deficient diet rescues hearing loss in Klotho mice

A. Wise, M. Carpinelli, R. Burt, 2011, Hearing Research.

Cross-sectional epidemiology of hearing loss in Australian children aged 11–12 years old and 25-year secular trends

M. Wake, F. Mensah, L. Gold, 2018, Archives of Disease in Childhood.

Mice That Are Congenic for the char2 Locus Are Susceptible to Malaria

T. Baldwin, S. Foote, R. Burt, 2002, Infection and Immunity.

In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness

David R. Liu, J. R. Holt, Gregory A. Newby, 2020, Science Translational Medicine.

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

B. Arhatari, M. Carpinelli, Michael A. Wilson, 2018, Scientific Reports.

Correction: Two ENU-Induced Alleles of Atp2b2 Cause Deafness in Mice

M. G. Manning, B. Kile, M. Carpinelli, 2013, PLoS ONE.