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A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs

PLoS genetics, 2007-05, Vol.3 (5), p.e79-e79

2007

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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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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, 2015-10, Vol.10 (10), p.e0140436-e0140436

2015

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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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Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed

PLoS genetics, 2012-01, Vol.8 (1), p.e1002462

2012

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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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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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A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17

PloS one, 2015-12, Vol.10 (12), p.e0143546-e0143546

2015

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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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NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

PLoS genetics, 2019-09, Vol.15 (9), p.e1008378-e1008378

2019

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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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A mutation in the myostatin gene increases muscle mass and enhances racing performance in heterozygote dogs

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

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

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

Parallel mapping and simultaneous sequencing reveals deletions in BCAN and FAM83H associated with discrete inherited disorders in a domestic dog breed

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

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

A Novel Genome-Wide Association Study Approach Using Genotyping by Exome Sequencing Leads to the Identification of a Primary Open Angle Glaucoma Associated Inversion Disrupting ADAMTS17

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

NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesia

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

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