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Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed

PloS one, 2013-05, Vol.8 (5), p.e64627-e64627

2013

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An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers

PloS one, 2014-04, Vol.9 (4), p.e93990

2014

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Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

PLoS genetics, 2020-01, Vol.16 (1), p.e1008527-e1008527

2020

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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, 2023-12, Vol.18 (12), p.e0295851-e0295851

2023

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Clinical, histopathological and genetic characterisation of oculoskeletal dysplasia in the Northern Inuit Dog

PloS one, 2019-08, Vol.14 (8), p.e0220761

2019

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DNA testing man's best friend: Roles and responsibilities

The veterinary journal (1997), 2016-01, Vol.207, p.10-12

Mellersh, Cathryn S.

2016

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An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs

PloS one, 2017-08, Vol.12 (8), p.e0183021-e0183021

2017

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Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation

BMC genetics, 2012-07, Vol.13, p.55

2012

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Correction: DNA Sequence Variants in the Five Prime Untranslated Region of the Cyclooxygenase-2 Gene Are Commonly Found in Healthy Dogs and Gray Wolves

PloS one, 2018-04, Vol.13 (4), p.e0195924-e0195924

2018

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A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations

PloS one, 2011-06, Vol.6 (6), p.e21452-e21452

2011

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Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species

Genome Biology, 2018-02, Vol.19 (1), p.22-22, Article 22

2018

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Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant

Journal of veterinary internal medicine, 2021-09, Vol.35 (5), p.2306-2314

2021

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Genome-wide association study identifies a novel canine glaucoma locus

PloS one, 2013-08, Vol.8 (8), p.e70903-e70903

2013

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Correction: Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog

PloS one, 2022-07, Vol.17 (7), p.e0272477-e0272477

2022

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A genome-wide association study of deafness in three canine breeds

PloS one, 2020-05, Vol.15 (5), p.e0232900-e0232900

2020

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Primary closed angle glaucoma in the Basset Hound: Genetic investigations using genome-wide association and RNA sequencing strategies

Molecular vision, 2019, Vol.25 (1), p.93-105

2019

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Correction: Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog

PloS one, 2016-05, Vol.11 (5), p.e0156192-e0156192

2016

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Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog

PloS one, 2021-05, Vol.16 (5), p.e0251071-e0251071

2021

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Investigation of the allele frequency of the G>A intron 10 ADAMTS17 mutation causing primary lens luxation in the Portuguese Podengo breed

Veterinary ophthalmology, 2022-01, Vol.25 (1), p.85-89

2022

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A Missense Variant in the Bardet-Biedl Syndrome 2 Gene ( BBS2 ) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog

Genes, 2021-11, Vol.12 (11), p.1771

2021

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Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy

PloS one, 2012-12, Vol.7 (12), p.e51598-e51598

2012

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DNA Sequence Variants in the Five Prime Untranslated Region of the Cyclooxygenase-2 Gene Are Commonly Found in Healthy Dogs and Gray Wolves

PloS one, 2015-08, Vol.10 (8), p.e0133127-e0133127

2015

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An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease

PLoS genetics, 2019-03, Vol.15 (3), p.e1007873-e1007873

2019

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Genetic screening for PRA‐associated mutations in multiple dog breeds shows that PRA is heterogeneous within and between breeds

Veterinary ophthalmology, 2014-03, Vol.17 (2), p.126-130

2014

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Missense mutation in CAPN1 is associated with spinocerebellar ataxia in the Parson Russell Terrier dog breed

A Deletion in the Canine POMC Gene Is Associated with Weight and Appetite in Obesity-Prone Labrador Retriever Dogs

An Intronic SINE insertion in FAM161A that causes exon-skipping is associated with progressive retinal atrophy in Tibetan Spaniels and Tibetan Terriers

Characterisation of canine KCNIP4: A novel gene for cerebellar ataxia identified by whole-genome sequencing two affected Norwegian Buhund dogs

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

Clinical, histopathological and genetic characterisation of oculoskeletal dysplasia in the Northern Inuit Dog

DNA testing man's best friend: Roles and responsibilities

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs

Genome-wide mRNA sequencing of a single canine cerebellar cortical degeneration case leads to the identification of a disease associated SPTBN2 mutation

Correction: DNA Sequence Variants in the Five Prime Untranslated Region of the Cyclooxygenase-2 Gene Are Commonly Found in Healthy Dogs and Gray Wolves

A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations

Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species

Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant

Genome-wide association study identifies a novel canine glaucoma locus

Correction: Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog

A genome-wide association study of deafness in three canine breeds

Primary closed angle glaucoma in the Basset Hound: Genetic investigations using genome-wide association and RNA sequencing strategies

Correction: Two Independent Mutations in ADAMTS17 Are Associated with Primary Open Angle Glaucoma in the Basset Hound and Basset Fauve de Bretagne Breeds of Dog

Identification of a variant in NDP associated with X-linked retinal dysplasia in the English cocker spaniel dog

Investigation of the allele frequency of the G>A intron 10 ADAMTS17 mutation causing primary lens luxation in the Portuguese Podengo breed

A Missense Variant in the Bardet-Biedl Syndrome 2 Gene ( BBS2 ) Leads to a Novel Syndromic Retinal Degeneration in the Shetland Sheepdog

Multiple mechanisms contribute to leakiness of a frameshift mutation in canine cone-rod dystrophy

DNA Sequence Variants in the Five Prime Untranslated Region of the Cyclooxygenase-2 Gene Are Commonly Found in Healthy Dogs and Gray Wolves

An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease

Genetic screening for PRA‐associated mutations in multiple dog breeds shows that PRA is heterogeneous within and between breeds

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