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Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

PLoS genetics, 2018-04, Vol.14 (4), p.e1007361-e1007361

2018

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Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs

PloS one, 2022-05, Vol.17 (5), p.e0267604-e0267604

2022

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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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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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Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs

PLoS genetics, 2023-02, Vol.19 (2), p.e1010651-e1010651

2023

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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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A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia

Human genetics, 2023-08, Vol.142 (8), p.1221-1230

2023

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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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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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A new Finnish flavor of feline coat coloration, "salmiak," is associated with a 95-kb deletion downstream of the KIT gene

Animal genetics, 2024-05

2024

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Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats

PLoS genetics, 2022-06, Vol.18 (6), p.e1009804-e1009804

2022

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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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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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Correction: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

PLoS genetics, 2019-01, Vol.15 (1), p.e1007938-e1007938

2019

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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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Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs

Genes, 2024-02, Vol.15 (2), p.198

2024

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Defining the ABC of gene essentiality in streptococci

BMC genomics, 2017-05, Vol.18 (1), p.426-426, Article 426

2017

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Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration

Mammalian genome, 2016-06, Vol.27 (5-6), p.237-245

2016

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Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1

Mammalian genome, 2015-02, Vol.26 (1-2), p.108-117

2015

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Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration

Genes, 2019-05, Vol.10 (5), p.385

2019

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Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus)

Animal genetics, 2021-06, Vol.52 (3), p.321-332

2021

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Environmental risk factors in puppies and kittens for developing chronic disorders in adulthood: A call for research on developmental programming

Frontiers in veterinary science, 2022-12, Vol.9, p.944821-944821

2022

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An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed

G3 : genes - genomes - genetics, 2016-09, Vol.6 (9), p.2687-2692

2016

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Investigating inherited diseases in dogs

Veterinary record, 2014-05, Vol.174 (20), p.512-512

2014

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Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed

BMC genetics, 2016-08, Vol.17 (1), p.123

2016

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Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs

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

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

Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs

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

A loss-of-function variant in canine GLRA1 associates with a neurological disorder resembling human hyperekplexia

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

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

A new Finnish flavor of feline coat coloration, "salmiak," is associated with a 95-kb deletion downstream of the KIT gene

Genetic epidemiology of blood type, disease and trait variants, and genome-wide genetic diversity in over 11,000 domestic cats

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

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

Correction: Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs

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

Association of FGF4L1 Retrogene Insertion with Prolapsed Gland of the Nictitans (Cherry Eye) in Dogs

Defining the ABC of gene essentiality in streptococci

Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1-associated canine retinal degeneration

Spinocerebellar ataxia in the Italian Spinone dog is associated with an intronic GAA repeat expansion in ITPR1

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration

Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus)

Environmental risk factors in puppies and kittens for developing chronic disorders in adulthood: A call for research on developmental programming

An Inversion Disrupting FAM134B Is Associated with Sensory Neuropathy in the Border Collie Dog Breed

Investigating inherited diseases in dogs

Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed

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