Cathryn S. Mellersh

Animal Health Trust — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

35h-index5.0kcitations136works0.32yr avg
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Research Topics

Retinal Development and Disorders(31), Neurological diseases and metabolism(25), Animal Genetics and Reproduction(17), Glaucoma and retinal disorders(12), Genomics and Phylogenetic Studies(11)

Publications136 total

Reproducibility of the evaluation of genetic variant pathogenicity based on the animal variant classification guidelines
2025Open Access
Autosomal dominant primary hyperparathyroidism in the Keeshond dog breed is strongly associated with a missense variant in <i>sirtuin‐6</i>
Animal Genetics·2025
Dogs help tease apart important differences in gene expression of brain tumours
Companion Animal Health and Genetics·2025Open Access
Common variants in the CPT1A gene are associated with cataracts in Northern breeds of domestic dog
PLoS ONE·2025Open Access
Genome-wide association study of idiopathic epilepsy in the Italian Spinone dog breed
PLoS ONE·2025Open Access
A <i>TTPA</i> deletion is associated with retinopathy with vitamin E deficiency in the English Cocker Spaniel dog
G3 Genes Genomes Genetics·2025Open Access
A preliminary genome‐wide association study of paroxysmal dyskinesia in the Norwich Terrier
Animal Genetics·2024· 1 citedOpen Access
Ocular melanosis in the adult Cairn Terrier population within the United Kingdom
Veterinary Ophthalmology·2024· 1 citedOpen Access
Exonic Short Interspersed Nuclear Element Insertion in FAM161A Is Associated with Autosomal Recessive Progressive Retinal Atrophy in the English Shepherd
Genes·2024· 1 citedOpen Access
Frequency of <i>RPGRIP1</i> and <i>MAP9</i> genetic modifiers of canine progressive retinal atrophy, in 132 breeds of dog
Animal Genetics·2024Open Access
Multiocular defect in the Old English Sheepdog: A canine form of Stickler syndrome type II associated with a missense variant in the collagen-type gene COL11A1
PLoS ONE·2023· 1 citedOpen Access
A <scp><i>TNR</i></scp> Frameshift Variant in Weimaraner Dogs with an Exercise‐Induced Paroxysmal Movement Disorder
Movement Disorders·2023· 4 citedOpen Access
Correction: Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog
PLoS ONE·2022Open Access
Investigation of the allele frequency of the G&gt;A intron 10 <i>ADAMTS17</i> mutation causing primary lens luxation in the Portuguese Podengo breed
Veterinary Ophthalmology·2021· 2 cited
A Missense Variant in the Bardet-Biedl Syndrome 2 Gene (BBS2) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog
Genes·2021· 7 citedOpen Access
Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel <i>RETREG1</i> variant
Journal of Veterinary Internal Medicine·2021· 9 citedOpen Access
Deafness in Australian Cattle Dogs associated to QTL on chromosome 20 in genome‐wide association study analyses
Animal Genetics·2021· 1 cited
Improving the resolution of canine genome‐wide association studies using genotype imputation: A study of two breeds
Animal Genetics·2021· 9 citedOpen Access
Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog
PLoS ONE·2021· 2 citedOpen Access
Deletion in the Bardet–Biedl Syndrome Gene TTC8 Results in a Syndromic Retinal Degeneration in Dogs
Genes·2020· 10 citedOpen Access
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Frequent Co-authors

Oliver P. Forman(14), Elaine A. Ostrander(12), Louise Pettitt(11), Gregory M. Acland(6), M. E. G. Boursnell(6), Hannes Lohi(6), Kunal Ray(5), Geoffrey K. Aguirre(5), Christopher A. Jenkins(5), David R. Sargan(5), Louise M Downs(5), Catherine André(4), Amelia Langston(4), Luisa De Risio(4), Saija Ahonen(4), Keith C. Barnett(4), Rebekkah J. Hitti‐Malin(4), Nigel G. Holmes(3), Francis Galibert(3), Jasper Rine(3)