[HTML][HTML] Genetic diversity in the modern horse illustrated from genome-wide SNP data

JL Petersen, JR Mickelson, EG Cothran, LS Andersson… - PloS one, 2013 - journals.plos.org
Horses were domesticated from the Eurasian steppes 5,000–6,000 years ago. Since then,
the use of horses for transportation, warfare, and agriculture, as well as selection for desired …

[HTML][HTML] Genome-wide analysis reveals selection for important traits in domestic horse breeds

JL Petersen, JR Mickelson, AK Rendahl… - PLoS …, 2013 - journals.plos.org
Intense selective pressures applied over short evolutionary time have resulted in
homogeneity within, but substantial variation among, horse breeds. Utilizing this population …

[HTML][HTML] A genome-wide association study reveals loci influencing height and other conformation traits in horses

H Signer-Hasler, C Flury, B Haase, D Burger… - PloS one, 2012 - journals.plos.org
The molecular analysis of genes influencing human height has been notoriously difficult.
Genome-wide association studies (GWAS) for height in humans based on tens of thousands …

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

R Hauswirth, B Haase, M Blatter, SA Brooks… - PLoS …, 2012 - journals.plos.org
During fetal development neural-crest-derived melanoblasts migrate across the entire body
surface and differentiate into melanocytes, the pigment-producing cells. Alterations in this …

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

B Haase, SA Brooks, A Schlumbaum, PJ Azor… - PLoS …, 2007 - journals.plos.org
White coat color has been a highly valued trait in horses for at least 2,000 years. Dominant
white (W) is one of several known depigmentation phenotypes in horses. It shows …

[HTML][HTML] A Missense Mutation in the SERPINH1 Gene in Dachshunds with Osteogenesis Imperfecta

C Drögemüller, D Becker, A Brunner, B Haase… - PLoS …, 2009 - journals.plos.org
Osteogenesis imperfecta (OI) is a hereditary disease occurring in humans and dogs. It is
characterized by extremely fragile bones and teeth. Most human and some canine OI cases …

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

RR Bellone, H Holl, V Setaluri, S Devi, N Maddodi… - PloS one, 2013 - journals.plos.org
Leopard complex spotting is a group of white spotting patterns in horses caused by an
incompletely dominant gene (LP) where homozygotes (LP/LP) are also affected with …

Seven novel KIT mutations in horses with white coat colour phenotypes

B Haase, SA Brooks, T Tozaki, D Burger… - Animal …, 2009 - Wiley Online Library
White coat colour in horses is inherited as a monogenic autosomal dominant trait showing a
variable expression of coat depigmentation. Mutations in the KIT gene have previously been …

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

RJ Schaefer, M Schubert, E Bailey, DL Bannasch… - BMC genomics, 2017 - Springer
Background To date, genome-scale analyses in the domestic horse have been limited by
suboptimal single nucleotide polymorphism (SNP) density and uneven genomic coverage of …

A Noncoding Melanophilin Gene (MLPH) SNP at the Splice Donor of Exon 1 Represents a Candidate Causal Mutation for Coat Color Dilution in Dogs

C Drögemüller, U Philipp, B Haase… - Journal of …, 2007 - academic.oup.com
Coat color dilution in several breeds of dog is characterized by a specific pigmentation
phenotype and sometimes accompanied by hair loss and recurrent skin inflammation, the so …