C. O'Leary

发表

Prevalence of congenital hereditary sensorineural deafness in Australian Cattle Dogs and associations with coat characteristics and sex

J. Morton, J. Seddon, M. Haile-Mariam, 2012, BMC Veterinary Research.

High‐throughput lectin magnetic bead array‐coupled tandem mass spectrometry for glycoprotein biomarker discovery

J. Dennis, M. Hill, Dorothy Loo, 2011, Electrophoresis.

Effect of dietary carbohydrate, fat, and protein on postprandial glycemia and energy intake in cats.

J. Morton, G. Sunvold, J. Rand, 2013, Journal of veterinary internal medicine.

An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

C. Mellersh, G. Johnson, P. Gharahkhani, 2010, Investigative ophthalmology & visual science.

Haplotype sharing excludes canine orthologous Filaggrin locus in atopy in West Highland White Terriers.

D. Duffy, M. Kyaw-Tanner, M. Shipstone, 2009, Animal genetics.

Associations between meal size, gastric emptying and post-prandial plasma glucose, insulin and lactate concentrations in meal-fed cats.

J. Morton, L. Filippich, J. Rand, 2015, Journal of animal physiology and animal nutrition.

PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers

D. Duffy, P. Gharahkhani, M. Kyaw-Tanner, 2011, BMC Research Notes.

Isolation and characterization of the canine NKX2-5 gene.

L. Lavulo, C. O'Leary, C. Hyun, 2006, Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie.

Molecular evidence supports the role of dogs as potential reservoirs for Rickettsia felis.

R. Traub, S. Hii, S. Kopp, 2011, Vector borne and zoonotic diseases.

No disease-associated mutations found in the coding sequence of the canine polycystic kidney disease gene 1 in Bull Terriers with polycystic kidney disease.

N. Laing, R. Atwell, C. O'Leary, 2003, Animal genetics.

Molecular evidence of Rickettsia felis infection in dogs from northern territory, Australia

R. Traub, S. Hii, S. Kopp, 2011, Parasites & Vectors.

IgE responsiveness to Dermatophagoides farinae in West Highland white terrier dogs is associated with region on CFA35.

D. Duffy, M. Kyaw-Tanner, M. Shipstone, 2011, The Journal of heredity.

ADAMTS17 mutation associated with primary lens luxation is widespread among breeds.

C. Mellersh, S. Ahonen, H. Lohi, 2011, Veterinary ophthalmology.

Atopic dermatitis in West Highland white terriers is associated with a 1.3-Mb region on CFA 17

D. Duffy, P. Gharahkhani, M. Kyaw-Tanner, 2012, Immunogenetics.

High allergen-specific serum immunoglobulin E levels in nonatopic West Highland white terriers.

D. Duffy, M. Kyaw-Tanner, M. Shipstone, 2011, Veterinary dermatology.

Congenital Sensorineural Deafness in Australian Stumpy-Tail Cattle Dogs Is an Autosomal Recessive Trait That Maps to CFA10

A. McRae, J. Seddon, L. Cuttell, 2010, PloS one.

Consequences of a screening programme on the prevalence of congenital hereditary sensorineural deafness in the Australian Cattle Dog.

J. Morton, J. Seddon, S. Sommerlad, 2014, Animal genetics.

Canine tick-borne pathogens and associated risk factors in dogs presenting with and without clinical signs consistent with tick-borne diseases in northern Australia.

R. Traub, S. Hii, A. Burleigh, 2015, Australian veterinary journal.

Canine vector-borne disease pathogens in dogs from south-east Queensland and north-east Northern Territory.

S. Hii, S. Kopp, C. O'Leary, 2012, Australian veterinary journal.

The inheritance of extra-hepatic portosystemic shunts and elevated bile acid concentrations in Maltese dogs.

D. Duffy, R. Malik, R. Hurford, 2014, The Journal of small animal practice.

Potential Modifying Loci Associated With Primary Lens Luxation, Pedal Hyperkeratosis, and Ocular Phenotypes in Miniature Bull Terriers.

D. Duffy, P. Gharahkhani, M. Kyaw-Tanner, 2015, Investigative ophthalmology & visual science.

Investigation of diabetes mellitus in Burmese cats as an inherited trait: a preliminary study

JS Rand, D. Duffy, C. O'Leary, 2013, New Zealand veterinary journal.

A Non-Synonymous Mutation in the Canine Pkd1 Gene Is Associated with Autosomal Dominant Polycystic Kidney Disease in Bull Terriers

Richard A. Sturm, D. Duffy, R. Sturm, 2011, PloS one.

A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breeds

G. Johnson, J. Coates, D. O'brien, 2015, Acta veterinaria Scandinavica.

Linkage confirms canine pkd1 orthologue as a candidate for bull terrier polycystic kidney disease.

D. Duffy, I. Biros, S. Corley, 2009, Animal genetics.

Expression profiling feline peripheral blood monocytes identifies a transcriptional signature associated with type two diabetes mellitus.

K. Irvine, C. O'Leary, Mamdouh A K Sedhom, 2017, Veterinary immunology and immunopathology.

Mapping of Diabetes Susceptibility Loci in a Domestic Cat Breed with an Unusually High Incidence of Diabetes Mellitus

L. Balmer, G. Morahan, M. Menotti-Raymond, 2020, Genes.

High‐throughput lectin magnetic bead array‐coupled tandem mass spectrometry for glycoprotein biomarker discovery

J. Dennis, M. Hill, Dorothy Loo, 2011, Electrophoresis.

Candidate Glycoprotein Biomarkers for Canine Visceral Hemangiosarcoma and Validation Using Semi-Quantitative Lectin/Immunohistochemical Assays

D. Duffy, Alok K. Shah, H. Bielefeldt-Ohmann, 2021, Veterinary sciences.

Cardiac Valvular and Vascular Disease in Bull Terriers

I. Wilkie, C. O'Leary, 2009, Veterinary pathology.

Haplotype sharing excludes orthologous COL4A3, COL4A4 or MYH9 loci in hereditary nephritis in bull terriers.

D. Duffy, G. Gobe, C. O'Leary, 2009, Animal genetics.