The widespread use of elite sires by means of artificial insemination in livestock breeding leads to the frequent emergence of recessive genetic defects, which cause significant economic and animal welfare concerns. Here we show that the availability of genome-wide, high-density SNP panels, combined with the typical structure of livestock populations, markedly accelerates the positional identification of genes and mutations that cause inherited defects. We report the fine-scale mapping of five recessive disorders in cattle and the molecular basis for three of these: congenital muscular dystony (CMD) types 1 and 2 in Belgian Blue cattle and ichthyosis fetalis in Italian Chianina cattle. Identification of these causative mutations has an imme...
Mammalian species carry ~100 loss-of-function variants per individual, where ~1-5 of these impact es...
The Belgian Blue beef cattle is well known for its double muscling phenotype resulting from fixation...
In the last decade, five different genetic recessive disorders with known molecular causes were repo...
The widespread use of elite sires by means of artificial insemination in livestock breeding leads to...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
Background For decades, identifying genes and mutations underlying inherited diseases and economica...
Abstract We present a data-mining framework designed to detect recessive defects in livestock that h...
peer reviewedMammalian species carry ~100 loss-of-function variants per individual(1,2), where ~1-5 ...
Dystocia and stillbirth are significant causes of female and neonatal death in many species and ther...
Abstract Background Genome-wide association studies (GWAS) have been successfully implemented in cat...
Twelve animals affected with syndactyly or mulefoot were sampled in the Dutch black-and-white cattle...
Background: Copy number variation (CNV) represents another important source of genetic variation com...
Over the past few years, several genetic defects have reached substantial frequencies in major breed...
Mammalian species carry ~100 loss-of-function variants per individual, where ~1-5 of these impact es...
The Belgian Blue beef cattle is well known for its double muscling phenotype resulting from fixation...
In the last decade, five different genetic recessive disorders with known molecular causes were repo...
The widespread use of elite sires by means of artificial insemination in livestock breeding leads to...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
In humans, the clinical and molecular characterization of sporadic syndromes is often hindered by th...
Background For decades, identifying genes and mutations underlying inherited diseases and economica...
Abstract We present a data-mining framework designed to detect recessive defects in livestock that h...
peer reviewedMammalian species carry ~100 loss-of-function variants per individual(1,2), where ~1-5 ...
Dystocia and stillbirth are significant causes of female and neonatal death in many species and ther...
Abstract Background Genome-wide association studies (GWAS) have been successfully implemented in cat...
Twelve animals affected with syndactyly or mulefoot were sampled in the Dutch black-and-white cattle...
Background: Copy number variation (CNV) represents another important source of genetic variation com...
Over the past few years, several genetic defects have reached substantial frequencies in major breed...
Mammalian species carry ~100 loss-of-function variants per individual, where ~1-5 of these impact es...
The Belgian Blue beef cattle is well known for its double muscling phenotype resulting from fixation...
In the last decade, five different genetic recessive disorders with known molecular causes were repo...