S. Brooks

发表

Whole genome detection of sequence and structural polymorphism in six diverse horses

N. Sutter, M. Abri, H. Holl, 2019, bioRxiv.

The MC1R and ASIP Coat Color Loci May Impact Behavior in the Horse.

J. Albright, S. Brooks, L. N. Jacobs, 2016, The Journal of heredity.

Exon skipping in the KIT gene causes a Sabino spotting pattern in horses

S. Brooks, E. Bailey, 2005, Mammalian Genome.

STUDIES OF GENETIC VARIATION AT THE KIT LOCUS AND WHITE SPOTTING PATTERNS IN THE HORSE

S. Brooks, 2006 .

Impact of white-spotting alleles, including W20, on phenotype in the American Paint Horse.

S. Brooks, K. Palermo, A. Kahn, 2020, Animal genetics.

Impact of white spotting alleles, including W20, on phenotype in the American Paint Horse

S. Brooks, K. Palermo, A. Kahn, 2019, bioRxiv.

Loci impacting polymorphic gait in the Tennessee Walking Horse.

M. Abri, S. Brooks, E. Staiger, 2016, Journal of animal science.

Improved reference genome for the domestic horse increases assembly contiguity and composition

Ian T. Fiddes, Brendan L. O’Connell, B. Walenz, 2018, Communications Biology.

Metabogenomics reveals four candidate regions involved in the pathophysiology of Equine Metabolic Syndrome.

M. Mallicote, S. Brooks, M. Long, 2020, Molecular and cellular probes.

Insect bite hypersensitivity in horses

C. Wickens, S. Brooks, R. Marsella, 2020 .

Seven novel KIT mutations in horses with white coat colour phenotypes.

T. Leeb, B. Haase, S. Rieder, 2009, Animal genetics.

Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.

T. Leeb, B. Haase, M. Penedo, 2013, Animal genetics.

The evolutionary history of the DMRT3 ‘Gait keeper’ haplotype

E. G. Cothran, L. Andersson, M. S. Almén, 2017, Animal genetics.

Refining the Camelus dromedarius Myostatin Gene Polymorphism through Worldwide Whole-Genome Sequencing

K. S. Kim, A. Eggen, V. Landi, 2022, Animals : an open access journal from MDPI.

Genetics of Equine Behavioral Traits.

C. Wickens, S. Brooks, 2020, The Veterinary clinics of North America. Equine practice.

Preliminary Investigation of the Changes in Fecal Streptococcal Population due to Diet and Time of Day in Horses

S. Brooks, W. Staniar, L. Neuendorf, 2016 .

RT-qPCR comparison of mast cell populations in whole blood from healthy horses and those with laminitis.

S. Brooks, E. Bailey, 2010, Animal genetics.

Use of principle component analysis to quantitatively score the equine metabolic syndrome phenotype in an Arabian horse population

M. Mallicote, H. Holl, S. Brooks, 2018, PloS one.

Four Loci Explain 83% of Size Variation in the Horse

J. Mezey, N. Sutter, G. Hoffman, 2012, PloS one.

Morphological variation in the horse: defining complex traits of body size and shape.

N. Sutter, R. Bellone, S. Brooks, 2010, Animal genetics.

DMRT3 is associated with gait type in Mangalarga Marchador horses, but does not control gait ability.

S. Brooks, E. Staiger, L. Patterson, 2015, Animal genetics.

Genetics and Signaling Pathways of Laminitis.

H. Galantino-Homer, S. Brooks, 2020, The Veterinary clinics of North America. Equine practice.

Genomics in the Horse Industry: Discovering New Questions at Every Turn.

S. Brooks, 2021, Journal of equine veterinary science.

Genome-wide association study of equine herpesvirus type 1-induced myeloencephalopathy identifies a significant single nucleotide polymorphism in a platelet-related gene.

D. Antczak, N. Osterrieder, M. Brosnahan, 2019, Veterinary journal.

Whole-Genome SNP Association in the Horse: Identification of a Deletion in Myosin Va Responsible for Lavender Foal Syndrome

J. Mezey, Donald C. Miller, D. Antczak, 2010, PLoS genetics.

A non-synonymous SNP in exon 3 of the KIT gene is responsible for the classic grey phenotype in alpacas (Vicugna pacos).

M. Richardson, K. Munyard, S. Brooks, 2019, Animal genetics.

Y-Chromosomal Insights into Breeding History and Sire Line Genealogies of Arabian Horses

V. V. Kalashnikov, G. Cothran, M. Reissmann, 2022, Genes.

Genome Diversity and the Origin of the Arabian Horse

Elissa J. Cosgrove, S. R. Miraei-Ashtiani, A. Clark, 2020, Scientific Reports.

Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds

T. Kalbfleisch, C. Wade, J. MacLeod, 2017, BMC Genomics.

Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2012, PLoS Genetics.

Equine Neutrophils Respond to PGE2 by Activating Expression of CoreCircadian Clock Genes

R. F. Cook, D. Horohov, S. Brooks, 2008 .

A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses

D. Adelson, S. Brooks, E. Bailey, 2008, Cytogenetic and Genome Research.

Population genomics and morphometric assignment of western honey bees (Apis mellifera L.) in the Republic of South Africa

J. Ellis, A. Eimanifar, S. Brooks, 2018, BMC Genomics.

Assignment of the appaloosa coat colour gene (LP) to equine chromosome 1.

S. Brooks, S. Archer, E. Bailey, 2004, Animal genetics.

Molecular Detection of Severe Combined Immunodeficiency Disorder in Arabian Horses in Egypt

S. Brooks, K. El-Nesr, H. Ahmed, 2018, Journal of equine veterinary science.

Short Communication Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes

T. Leeb, V. Jagannathan, H. Holl, 2022 .

A Frameshift Mutation in KIT is Associated with White Spotting in the Arabian Camel

D. Antczak, Y. Mohamoud, F. Almathen, 2017, Genes.

Genomewide association study reveals a risk locus for equine metabolic syndrome in the Arabian horse.

M. Mallicote, N. Place, H. Holl, 2017, Journal of animal science.

Cytogenetics

S. Brooks, E. Bailey, 1983, Horse genetics.

Construction of two whole genome radiation hybrid panels for dromedary (Camelus dromedarius): 5000RAD and 15000RAD

D. Larkin, P. Perelman, T. Raudsepp, 2018, Scientific Reports.

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

T. Kalbfleisch, J. MacLeod, L. Orlando, 2021, Frontiers in Genetics.

An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.

T. Leeb, B. Haase, S. Brooks, 2008, Animal genetics.

Allelic Heterogeneity at the Equine KIT Locus in Dominant White (W) Horses

T. Leeb, B. Haase, S. Rieder, 2007, PLoS genetics.

A candidate gene approach identifies variants in SLC45A2 that explain dilute phenotypes, pearl and sunshine, in compound heterozygote horses.

H. Holl, S. Brooks, D. Cook, 2019, Animal genetics.

Missense Mutation in Exon 2 of SLC36A1 Responsible for Champagne Dilution in Horses

R. Bellone, S. Brooks, E. Bailey, 2008, PLoS genetics.

Identification of a novel missense variant in SLC45A2 associated with dilute snowdrop phenotype in Gypsy horses.

M. Carpenter, S. Brooks, C. Lafayette, 2020, Animal genetics.

Identification of a novel missense variant in SLC45A2 associated with dilute snowdrop phenotype in Gypsy horses

M. Carpenter, S. Brooks, C. Lafayette, 2019, bioRxiv.

Phylogeography and population genetic structure of an exotic invasive brine shrimp, Artemia Leach, 1819 (Crustacea : Anostraca), in Australia

M. Wink, A. Eimanifar, S. Brooks, 2018 .

An Independent Locus Upstream of ASIP Controls Variation in the Shade of the Bay Coat Colour in Horses

Donald C. Miller, D. Antczak, L. Corbin, 2020, Genes.

Coat Color Genomics

R. Bellone, S. Brooks, 2013 .

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

R. Bellone, S. Brooks, G. Forsyth, 2008, Genetics.

De novo mutation of KIT discovered as a result of a non-hereditary white coat colour pattern

H. Holl, S. Brooks, E. Bailey, 2010 .

Non-frameshift deletion on MITF is associated with a novel splashed white spotting pattern in horses (Equus caballus).

S. Brooks, L. Patterson Rosa, K. Martin, 2022, Animal genetics.

De novo mutation of KIT causes extensive coat white patterning in a family of Berber horses.

S. Brooks, L. Patterson Rosa, K. Martin, 2020, Animal genetics.

Whole-genome sequencing reveals a large deletion in the MITF gene in horses with white spotted coat colour and increased risk of deafness.

T. Leeb, V. Jagannathan, S. Brooks, 2019, Animal genetics.

A novel splice mutation within equine KIT and the W15 allele in the homozygous state lead to all white coat color phenotypes.

C. Bustamante, M. Carpenter, H. Holl, 2017, Animal genetics.

A PCR-RFLP for KIT associated with tobiano spotting pattern in horses.

S. Brooks, E. Bailey, R. B. Terry, 2002, Animal genetics.

Genome‐Wide Scans Reveal a Quantitative Trait Locus for Withers Height in Horses Near the ANKRD1 Gene

N. Sutter, G. Hoffman, S. Brooks, 2018 .

Evidence for a Retroviral Insertion in TRPM1 as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse

Arne Ludwig, David L. Adelson, Padmanabhan Mahadevan, 2013, PloS one.

Polymorphism at expressed DQ and DR loci in five common equine MHC haplotypes

B. Zhu, Donald C. Miller, D. Antczak, 2017, Immunogenetics.

Equine clinical genomics: A clinician's primer.

D. Antczak, M. Brosnahan, S. Brooks, 2010, Equine Veterinary Journal.

Identification of loci affecting sexually dimorphic patterns for height and recurrent laryngeal neuropathy risk in American Belgian Draft Horses.

S. Brooks, D. Ainsworth, J. Stick, 2018, Physiological genomics.

Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds

Kyle C. Oliveira, A. Boyko, R. Todhunter, 2014, BMC Genomics.

Single nucleotide polymorphisms for DNA typing in the domestic horse

C. Bustamante, R. E. Everts, M. Carpenter, 2017, Animal genetics.

Population genomics and morphometric assignment of western honey bees (Apis mellifera L.) in the Republic of South Africa

J. Ellis, A. Eimanifar, S. Brooks, 2018, BMC genomics.

Generation of a de novo transcriptome from equine lamellar tissue

Z. Fei, Shan Gao, C. Andrews, 2015, BMC Genomics.

Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting.

M. Penedo, R. Bellone, H. Holl, 2016, Animal genetics.

Skeletal variation in Tennessee Walking Horses maps to the LCORL/NCAPG gene region.

N. Sutter, T. Raudsepp, S. E. Kalla, 2016, Physiological genomics.

Morphological Variation in Gaited Horse Breeds

N. Sutter, R. Bellone, S. Brooks, 2016 .

Improved reference genome for the domestic horse increases assembly contiguity and composition

Ian T. Fiddes, Brendan L. O’Connell, B. Walenz, 2018, Communications Biology.

EquCab3, an Updated Reference Genome for the Domestic Horse

Ian T. Fiddes, Brendan L. O’Connell, B. Walenz, 2018 .

A Nonsynonymous Change in Adhesion G Protein–Coupled Receptor L3 Associated With Risk for Equine Degenerative Myeloencephalopathy in the Caspian Horse

G. Pollott, T. Southard, T. Divers, 2018, Journal of Equine Veterinary Science.

Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2012, PLoS genetics.

TBX3 and ASIP genotypes reveal discrepancies in officially recorded coat colors of Hucul horses.

M. Maćkowski, S. Brooks, J. Cieslak, 2019, Animal : an international journal of animal bioscience.

Detection of two equine trisomies using SNP-CGH

H. Holl, S. Brooks, T. Lear, 2013, Mammalian Genome.

Application of Genomic Estimation Methods of Inbreeding and Population Structure in an Arabian Horse Herd

U. König von Borstel, S. Brooks, M. A. Al Abri, 2017, The Journal of heredity.

Development of a high-density, 2M SNP genotyping array and 670k SNP imputation array for the domestic horse

T. Kalbfleisch, C. Wade, L. Orlando, 2017 .

Genomic analysis establishes correlation between growth and laryngeal neuropathy in Thoroughbreds

Kyle C. Oliveira, A. Boyko, R. Todhunter, 2014, BMC Genomics.

Correction: Mutations in MITF and PAX3 Cause “Splashed White” and Other White Spotting Phenotypes in Horses

J. Matthews, C. Drögemüller, T. Leeb, 2019, PLoS Genetics.

Generation of a de novo transcriptome from equine lamellar tissue

Z. Fei, Shan Gao, C. Andrews, 2015, BMC Genomics.

Genomic Association of Chronic Idiopathic Anhidrosis to a Potassium Channel Subunit in a Large Animal Model.

R. MacKay, M. Mallicote, S. Brooks, 2021, The Journal of investigative dermatology.

Mapping of Lavender Foal Syndrome using the EquineSNP50 Chip

Donald C. Miller, S. Brooks, N. Gabreski, 2009 .

Investigation of allele frequencies for Lavender foal syndrome in the horse.

O. Distl, B. Haase, S. Brooks, 2012, Animal genetics.

Variant in the RFWD3 gene associated with PATN1, a modifier of leopard complex spotting.

M. Penedo, R. Bellone, H. Holl, 2016, Animal genetics.

Genome Diversity and the Origin of the Arabian Horse

Elissa J. Cosgrove, S. R. Miraei-Ashtiani, J. Malek, 2020, Scientific Reports.

Genomewide association study reveals a risk locus for equine metabolic syndrome in the Arabian horse.

M. Mallicote, N. Place, H. Holl, 2017, Journal of animal science.