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Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease

Overview of attention for article published in BMC Medical Genomics, September 2013
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Title
Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease
Published in
BMC Medical Genomics, September 2013
DOI 10.1186/1471-2350-14-91
Pubmed ID
Authors

Matthew T Bishop, Pascual Sanchez-Juan, Richard SG Knight

Abstract

Variant Creutzfeldt-Jakob disease is an infectious, neurodegenerative, protein-misfolding disease, of the prion disease family, originally acquired through ingestion of meat products contaminated with bovine spongiform encephalopathy (BSE). Public health concern was increased by the discovery of human-to-human transmission via blood transfusion. This study has verified a novel genetic marker linked to disease risk.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 34 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 8 24%
Student > Ph. D. Student 6 18%
Researcher 4 12%
Student > Postgraduate 4 12%
Student > Master 2 6%
Other 4 12%
Unknown 6 18%
Readers by discipline Count As %
Medicine and Dentistry 8 24%
Agricultural and Biological Sciences 7 21%
Biochemistry, Genetics and Molecular Biology 6 18%
Neuroscience 3 9%
Business, Management and Accounting 1 3%
Other 2 6%
Unknown 7 21%