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M. E. G. Boursnell

Animal Health Trust

29

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1498

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A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs

2020 BMC Genetics
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Defining the ABC of gene essentiality in streptococci

2017 BMC Genomics
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Canine genome assembly correction facilitates identification of a MAP9 deletion as a potential age of onset modifier for RPGRIP1 -associated canine retinal degeneration

2016 Mammalian Genome
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The global population diversity of Streptococcus equi highlights transmission across international boundaries

2016 Journal of Equine Veterinary Science
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Genome sequencing reveals a splice donor site mutation in the SNX14 gene associated with a novel cerebellar cortical degeneration in the Hungarian Vizsla dog breed

2016 BMC Genetics
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Copper toxicosis in non-COMMD1 Bedlington terriers is associated with metal transport gene ABCA12

2016 Journal of Trace Elements in Medicine and Biology
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Genome-wide association study in RPGRIP1(-/-) dogs identifies a modifier locus that determines the onset of retinal degeneration.

2012 Mammalian Genome
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A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations.

2011 PLOS ONE
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An ADAMTS17 splice donor site mutation in dogs with primary lens luxation.

2010 Investigative Ophthalmology & Visual Science
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Canine RPGRIP1 mutation establishes cone–rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis

2006 Genomics
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Citations (83)