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Prediction of histone post-translational modification patterns based on nascent transcription data

Nature genetics, 2022-03, Vol.54 (3), p.295-305

2022

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DNA methylation aging and transcriptomic studies in horses

Nature communications, 2022-01, Vol.13 (1), p.40-13, Article 40

2022

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Four loci explain 83% of size variation in the horse

PloS one, 2012-07, Vol.7 (7), p.e39929-e39929

2012

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Functional annotation of the animal genomes: An integrated annotation resource for the horse

PLoS genetics, 2023-03, Vol.19 (3), p.e1010468-e1010468

2023

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Novel genetic variant associated with globoid cell leukodystrophy in a family of mixed breed dogs

Journal of veterinary internal medicine, 2023-09, Vol.37 (5), p.1710-1715

2023

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Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse‐related breeds with the MYH1E321G mutation

Journal of veterinary internal medicine, 2022-05, Vol.36 (3), p.1152-1159

2022

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Preliminary investigation of potential links between pigmentation variants and opioid analgesic effectiveness in horses during cerebrospinal fluid centesis

BMC veterinary research, 2024-07, Vol.20 (1), p.1-13, Article 311

2024

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Identification of W13 in the American Miniature Horse and Shetland Pony Populations

Genes, 2021-12, Vol.12 (12), p.1985

2021

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Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)

Genetics (Austin), 2008-08, Vol.179 (4), p.1861-1870

2008

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Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses

PloS one, 2013-09, Vol.8 (9), p.e75071-e75071

2013

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Breed Distribution and Allele Frequencies of Base Coat Color, Dilution, and White Patterning Variants across 28 Horse Breeds

Genes, 2022-09, Vol.13 (9), p.1641

2022

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DDB2 Genetic Risk Factor for Ocular Squamous Cell Carcinoma Identified in Three Additional Horse Breeds

Genes, 2020-12, Vol.11 (12), p.1460

2020

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"Adopt-a-Tissue" Initiative Advances Efforts to Identify Tissue-Specific Histone Marks in the Mare

Frontiers in genetics, 2021-03, Vol.12, p.649959

2021

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Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms

The Journal of heredity, 2022-07, Vol.113 (3), p.238-247

2022

Volltextzugriff (PDF)

Decoding the Equine Genome: Lessons from ENCODE

Genes, 2021-10, Vol.12 (11), p.1707

2021

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GO-FAANG meeting: a Gathering On Functional Annotation of Animal Genomes

Animal genetics, 2016-10, Vol.47 (5), p.528-533

2016

Volltextzugriff (PDF)

Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States

Genes, 2020-12, Vol.11 (12), p.1518

2020

Volltextzugriff (PDF)

Generation of a Biobank From Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative

Frontiers in genetics, 2021-03, Vol.12, p.650305

2021

Volltextzugriff (PDF)

Genetics of Equine Ocular Disease

The Veterinary clinics of North America. Equine practice, 2020-08, Vol.36 (2), p.303-322

Bellone, Rebecca R.

2020

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The localization of centromere protein A is conserved among tissues

Communications biology, 2023-09, Vol.6 (1), p.963-963, Article 963

2023

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Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies

Genes, 2019-10, Vol.10 (10), p.826

2019

Volltextzugriff (PDF)

Response to comments on ‘Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’

Equine veterinary journal, 2021-11, Vol.53 (6), p.1297-1297

2021

Volltextzugriff (PDF)

A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse

Animal genetics, 2022-08, Vol.53 (4), p.534-537

2022

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Evidence supports white spotting in donkeys as a homozygous lethal condition

Animal genetics, 2020-10, Vol.51 (5), p.840-842

2020

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Prediction of histone post-translational modification patterns based on nascent transcription data

DNA methylation aging and transcriptomic studies in horses

Four loci explain 83% of size variation in the horse

Functional annotation of the animal genomes: An integrated annotation resource for the horse

Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse

Novel genetic variant associated with globoid cell leukodystrophy in a family of mixed breed dogs

Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse‐related breeds with the MYH1E321G mutation

Preliminary investigation of potential links between pigmentation variants and opioid analgesic effectiveness in horses during cerebrospinal fluid centesis

Identification of W13 in the American Miniature Horse and Shetland Pony Populations

Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)

Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses

Breed Distribution and Allele Frequencies of Base Coat Color, Dilution, and White Patterning Variants across 28 Horse Breeds

DDB2 Genetic Risk Factor for Ocular Squamous Cell Carcinoma Identified in Three Additional Horse Breeds

"Adopt-a-Tissue" Initiative Advances Efforts to Identify Tissue-Specific Histone Marks in the Mare

Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms

Decoding the Equine Genome: Lessons from ENCODE

GO-FAANG meeting: a Gathering On Functional Annotation of Animal Genomes

Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States

Generation of a Biobank From Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative

Genetics of Equine Ocular Disease

The localization of centromere protein A is conserved among tissues

Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies

Response to comments on ‘Whole‐genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’

A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse

Evidence supports white spotting in donkeys as a homozygous lethal condition

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