Published in Vet Dermatol on December 01, 2002
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti. PLoS One (2013) 0.84
Congenital hypotrichosis and partial anodontia in a crossbred beef calf. Can Vet J (2007) 0.75
A mutation in hairless dogs implicates FOXI3 in ectodermal development. Science (2008) 2.06
Genome-wide analysis in German shepherd dogs reveals association of a locus on CFA 27 with atopic dermatitis. PLoS Genet (2013) 1.69
A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta. PLoS Genet (2009) 1.68
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
Candidate genes for physical performance in the horse. Vet J (2010) 1.44
Analysis of sequence variability of the bovine prion protein gene (PRNP) in German cattle breeds. Neurogenetics (2004) 1.43
Bovine prion protein gene (PRNP) promoter polymorphisms modulate PRNP expression and may be responsible for differences in bovine spongiform encephalopathy susceptibility. J Biol Chem (2005) 1.40
A genome-wide association study reveals loci influencing height and other conformation traits in horses. PLoS One (2012) 1.39
Genome-wide analysis reveals selection for important traits in domestic horse breeds. PLoS Genet (2013) 1.26
Fine mapping of the polled locus to a 1-Mb region on bovine chromosome 1q12. Mamm Genome (2005) 1.20
Genetic diversity in the modern horse illustrated from genome-wide SNP data. PLoS One (2013) 1.18
Spongiform encephalopathy in a miniature zebu. Emerg Infect Dis (2006) 1.17
Influence of priors in Bayesian estimation of genetic parameters for multivariate threshold models using Gibbs sampling. Genet Sel Evol (2007) 1.16
Proposal to reclassify Paenibacillus larvae subsp. pulvifaciens DSM 3615 (ATCC 49843) as Paenibacillus larvae subsp. larvae. Results of a comparative biochemical and genetic study. Vet Microbiol (2004) 1.16
Serial translocation by means of circular intermediates underlies colour sidedness in cattle. Nature (2012) 1.16
LUPA: a European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs. Vet J (2011) 1.15
LGI2 truncation causes a remitting focal epilepsy in dogs. PLoS Genet (2011) 1.14
Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development. PLoS Genet (2010) 1.13
PRNP promoter polymorphisms are associated with BSE susceptibility in Swiss and German cattle. BMC Genet (2007) 1.13
Mutations in MITF and PAX3 cause "splashed white" and other white spotting phenotypes in horses. PLoS Genet (2012) 1.11
Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Gastroenterology (2008) 1.07
Osteogenesis imperfecta in dachshunds. Vet Rec (2013) 1.07
Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4). BMC Genet (2007) 1.06
European domestic horses originated in two holocene refugia. PLoS One (2011) 1.06
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle. PLoS One (2011) 1.05
A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle. J Mol Med (Berl) (2002) 1.04
Mapping quantitative trait loci for canine hip dysplasia in German Shepherd dogs. Mamm Genome (2007) 1.04
Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition. Proc Natl Acad Sci U S A (2012) 1.04
Expression levels of LCORL are associated with body size in horses. PLoS One (2013) 1.03
German Francisella tularensis isolates from European brown hares (Lepus europaeus) reveal genetic and phenotypic diversity. BMC Microbiol (2013) 1.03
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier. PLoS Genet (2011) 1.02
A genome-wide association study to detect QTL for commercially important traits in Swiss Large White boars. PLoS One (2013) 1.02
Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Hum Mutat (2006) 1.01
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
High throughput detection of Coxiella burnetii by real-time PCR with internal control system and automated DNA preparation. BMC Microbiol (2008) 1.00
Single linkage group per chromosome genetic linkage map for the horse, based on two three-generation, full-sibling, crossbred horse reference families. Genomics (2005) 0.99
A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. PLoS One (2013) 0.99
The mutation causing the black-and-tan pigmentation phenotype of Mangalitza pigs maps to the porcine ASIP locus but does not affect its coding sequence. Mamm Genome (2006) 0.98
Unusual vascular ring anomaly associated with a persistent right aortic arch and an aberrant left subclavian artery in German pinschers. Vet J (2010) 0.98
Congenital sensorineural deafness in dogs: a molecular genetic approach toward unravelling the responsible genes. Vet J (2005) 0.98
Hereditary ataxia in the Jack Russell Terrier--clinical and genetic investigations. J Vet Intern Med (2004) 0.97
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease. Genomics (2008) 0.95
Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse. PLoS One (2013) 0.95
Biochemical typing of pathological prion protein in aging cattle with BSE. Virol J (2009) 0.94
A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogs. J Hered (2007) 0.93
Identification of quantitative trait loci (QTL) for canine hip dysplasia and canine elbow dysplasia in Bernese mountain dogs. PLoS One (2012) 0.93
Functional relevance of DNA polymorphisms within the promoter region of the prion protein gene and their association to BSE infection. FASEB J (2007) 0.92
A Single Nucleotide Polymorphism within the Interferon Gamma Receptor 2 Gene Perfectly Coincides with Polledness in Holstein Cattle. PLoS One (2013) 0.92
Two loci on chromosome 5 are associated with serum IgE levels in Labrador retrievers. PLoS One (2012) 0.92
A frameshift mutation within LAMC2 is responsible for Herlitz type junctional epidermolysis bullosa (HJEB) in black headed mutton sheep. PLoS One (2011) 0.91
Immunophenotyping of inflammatory cells associated with Schmallenberg virus infection of the central nervous system of ruminants. PLoS One (2013) 0.91
A MITF mutation associated with a dominant white phenotype and bilateral deafness in German Fleckvieh cattle. PLoS One (2011) 0.89
Analysis of copy number variants by three detection algorithms and their association with body size in horses. BMC Genomics (2013) 0.89
X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle. Genet Sel Evol (2003) 0.89
Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs. BMC Genet (2005) 0.89
[Review of literature and results from test matings of East Friesian milk sheep affected with brachygnathia inferior]. Berl Munch Tierarztl Wochenschr (2008) 0.89
[Congenital cardiac anomalies (pentalogy of Fallot) in a two year old ram with brachygnathia inferior]. Berl Munch Tierarztl Wochenschr (2013) 0.88
Arachnomelia in Brown Swiss cattle maps to chromosome 5. Mamm Genome (2008) 0.88
Expression of Foxi3 is regulated by ectodysplasin in skin appendage placodes. Dev Dyn (2013) 0.88
[Reproducibility of bovine neonatal pancytopenia (BNP) via the application of colostrum]. Berl Munch Tierarztl Wochenschr (2011) 0.87
Epidermolysis bullosa in German black headed mutton sheep. Berl Munch Tierarztl Wochenschr (2010) 0.87
Nontoxigenic tox-bearing Corynebacterium ulcerans infection among game animals, Germany. Emerg Infect Dis (2014) 0.87
A frameshift mutation in the cubilin gene (CUBN) in Border Collies with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). PLoS One (2013) 0.86
A 4 Mb high resolution BAC contig on bovine chromosome 1q12 and comparative analysis with human chromosome 21q22. Comp Funct Genomics (2005) 0.86
Genetic and phenotypic trends in canine hip dysplasia in the German population of German shepherd dogs. Berl Munch Tierarztl Wochenschr (2008) 0.86
Hare-to-human transmission of Francisella tularensis subsp. holarctica, Germany. Emerg Infect Dis (2015) 0.86
Multiple Loci are associated with dilated cardiomyopathy in Irish wolfhounds. PLoS One (2012) 0.85
A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. PLoS Genet (2013) 0.84
Further validation of the psychological injury risk indicator scale. J Occup Environ Med (2012) 0.84
Cloning and characterization of the mammalian-specific nicolin 1 gene (NICN1) encoding a nuclear 24 kDa protein. Eur J Biochem (2002) 0.84
A nonsense mutation in the IKBKG gene in mares with incontinentia pigmenti. PLoS One (2013) 0.84
Construction of a 1.2-Mb BAC/PAC contig of the porcine gene RYR1 region on SSC 6q1.2 and comparative analysis with HSA 19q13.13. Genomics (2002) 0.83
Schmallenberg virus in central nervous system of ruminants. Emerg Infect Dis (2013) 0.83
Multiple loci associated with canine hip dysplasia (CHD) in German shepherd dogs. Mamm Genome (2014) 0.83
Genetic correlations between conformation traits and radiographic findings in the limbs of German Warmblood riding horses. Genet Sel Evol (2006) 0.82
A massive reduction of the genetic diversity in the Lundehund. Anim Genet (2013) 0.82
Keel bone condition in laying hens: a histological evaluation of macroscopically assessed keel bones. Berl Munch Tierarztl Wochenschr (2008) 0.82
[Genetic-statistical analysis of environmental and genetic influences on the outcome of the juvenile and breeding performance tests for behaviour traits in Hovawart dogs]. Berl Munch Tierarztl Wochenschr (2006) 0.82
A duplication in the canine beta-galactosidase gene GLB1 causes exon skipping and GM1-gangliosidosis in Alaskan huskies. Genetics (2005) 0.82
A locus on chromosome 5 is associated with dilated cardiomyopathy in Doberman Pinschers. PLoS One (2011) 0.82
Genome-wide search for markers associated with osteochondrosis in Hanoverian warmblood horses. Mamm Genome (2007) 0.82
Evaluation of tafazzin as candidate for dilated cardiomyopathy in Irish wolfhounds. J Hered (2007) 0.82
A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption). Anim Genet (2013) 0.82
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion. Am J Med Genet A (2015) 0.82
A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. PLoS One (2013) 0.81
Analysis of relationships between German heavy horse breeds based on pedigree information. Berl Munch Tierarztl Wochenschr (2004) 0.81
Congenital infection with Anaplasma phagocytophilum in a calf in northern Germany. Acta Vet Scand (2013) 0.81
A high resolution physical and RH map of pig chromosome 6q1.2 and comparative analysis with human chromosome 19q13.1. BMC Genomics (2003) 0.81