Published in PLoS Genet on September 19, 2008
A high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studies. PLoS Genet (2012) 1.66
Analysis and update of the human solute carrier (SLC) gene superfamily. Hum Genomics (2009) 1.62
Genome-wide analysis reveals selection for important traits in domestic horse breeds. PLoS Genet (2013) 1.26
The SLC36 family of proton-coupled amino acid transporters and their potential role in drug transport. Br J Pharmacol (2011) 1.13
The genetic basis of divergent pigment patterns in juvenile threespine sticklebacks. Heredity (Edinb) (2011) 1.04
Whole-genome sequencing and genetic variant analysis of a Quarter Horse mare. BMC Genomics (2012) 0.99
Intracellular amino acid sensing and mTORC1-regulated growth: new ways to block an old target? Curr Opin Investig Drugs (2010) 0.96
Characterization of equine and other vertebrate TLR3, TLR7, and TLR8 genes. Immunogenetics (2009) 0.84
Next generation sequencing gives an insight into the characteristics of highly selected breeds versus non-breed horses in the course of domestication. BMC Genomics (2014) 0.83
Mapping of the domestic cat "SILVER" coat color locus identifies a unique genomic location for silver in mammals. J Hered (2009) 0.78
Whole genome sequence and analysis of the Marwari horse breed and its genetic origin. BMC Genomics (2014) 0.78
Two Variants in SLC24A5 Are Associated with "Tiger-Eye" Iris Pigmentation in Puerto Rican Paso Fino Horses. G3 (Bethesda) (2017) 0.75
The human genome browser at UCSC. Genome Res (2002) 168.23
Sequential tests for the detection of linkage. Am J Hum Genet (1955) 43.74
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science (2005) 12.02
Genetics, development and evolution of adaptive pigmentation in vertebrates. Heredity (Edinb) (2006) 2.83
Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation. Hum Mutat (2005) 2.15
A model for melanosome biogenesis based on the purification and analysis of early melanosomes. Proc Natl Acad Sci U S A (2001) 2.06
A missense mutation in PMEL17 is associated with the Silver coat color in the horse. BMC Genet (2006) 1.58
A mutation in the MATP gene causes the cream coat colour in the horse. Genet Sel Evol (2003) 1.39
Regulation of tyrosinase processing and trafficking by organellar pH and by proteasome activity. J Biol Chem (2003) 1.27
Structure, function and immunolocalization of a proton-coupled amino acid transporter (hPAT1) in the human intestinal cell line Caco-2. J Physiol (2003) 1.23
The H+-coupled electrogenic lysosomal amino acid transporter LYAAT1 localizes to the axon and plasma membrane of hippocampal neurons. J Neurosci (2003) 1.07
International Equine Gene Mapping Workshop Report: a comprehensive linkage map constructed with data from new markers and by merging four mapping resources. Cytogenet Genome Res (2005) 1.05
Inheritance of the palomino color in Icelandic horses. J Hered (1974) 0.97
Involvement of dynein and spectrin with early melanosome transport and melanosomal protein trafficking. J Invest Dermatol (2007) 0.96
A cluster of proton/amino acid transporter genes in the human and mouse genomes. Genomics (2003) 0.96
Organization and expression of the SLC36 cluster of amino acid transporter genes. Mamm Genome (2004) 0.94
The cream dilution gene, responsible for the palomino and buckskin coat colours, maps to horse chromosome 21. Anim Genet (2001) 0.94
Report of the International Equine Gene Mapping Workshop: male linkage map. Anim Genet (1999) 0.92
Characterization of equine microsatellites and microsatellite-linked repetitive elements (eMLREs) by efficient cloning and genotyping methods. DNA Res (2001) 0.86
The role of matricellular proteins thrombospondin-1 and osteonectin during RPE cell migration in proliferative vitreoretinopathy. Curr Eye Res (2002) 0.80
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 (2008) 2.15
Congenital ocular anomalies in purebred and crossbred Rocky and Kentucky Mountain horses in Canada. Can Vet J (2008) 1.73
Genotypes of predomestic horses match phenotypes painted in Paleolithic works of cave art. Proc Natl Acad Sci U S A (2011) 1.59
Neural correlates of body dissatisfaction in anorexia nervosa. Neuropsychologia (2010) 1.06
Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet (2007) 1.01
Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Brief Funct Genomics (2010) 1.00
The fat mass and obesity gene is linked to reduced verbal fluency in overweight and obese elderly men. Neurobiol Aging (2011) 0.95
Exon skipping in the KIT gene causes a Sabino spotting pattern in horses. Mamm Genome (2005) 0.94
Detailed analysis of variants in FTO in association with body composition in a cohort of 70-year-olds suggests a weakened effect among elderly. PLoS One (2011) 0.91
I'm not as slim as that girl: neural bases of body shape self-comparison to media images. Neuroimage (2007) 0.88
Rhodococcus equi and genetic susceptibility: assessing transferrin genotypes from paraffin-embedded tissues. J Vet Diagn Invest (2003) 0.86
Screening for foal immunodeficiency syndrome. Vet Rec (2011) 0.75