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Mad Cow Methodology
Publication Date: August 2003
Citing URL: http://esi-topics.com/madcow

Mad Cow & Other Prion Diseases
& Other Prion Diseases

The baseline time span for this database is 1993-2003. The resulting database contained 1,282 papers; 2,394 authors; 46 countries; 487 journals; and 799 institutions. Read the methodology used to create this special topic.
M
Top Papers
Top 20 papers overall
1993 - 2003
Top Authors
Top 20 overall
1993 - 2003
Top Institutions
Top 20 overall
1993 - 2003
Top Nations
Top 20 overall
1993 - 2003
Top Journals
Top 20 overall
1993 - 2003
Time Series
1 year
5 year
Field Distribution
Field representation
1993 - 2003
Editorial
Read interviews and first-person essays about people in a wide variety of fields, and information on journals in the topic of Mad Cow.
February 2004
Journal of Molecular Biology
September 2003
Annals of Neurology
August 2003
The Institute of Animal Health
E
N
U

Overview

Bovine spongiform encephalopathy, colloquially known as mad cow disease, is a neurodegenerative disease that was first documented in the UK in 1986. Its spread is thought to be linked to cannibalistic practices in the livestock feed industry, in which the meat and bone meal of infected animals were used as a protein source in feed for healthy animals. According to the USDA’s Animal and Planet Health Inspection Service, there have been upwards of 180,000 cases to date. Over 95% of these cases were reported in the UK, but infected cattle have also been diagnosed in various other European and Asian countries. Mad cow is part of a family of transmissible spongiform encephalopathies, which include scrapie of sheep, Creutzfeldt-Jakob disease (CJD), kuru, and Gerstmann-Straussler-Scheinker syndrome in humans. In 1996, a new form of CJD known as variant CJD began to crop up in humans. Evidence for a link between mad cow disease and variant CJD was published by various research groups. Many of the papers in our Special Topic on Mad Cow and Other Prion Diseases discuss the possible causal relationship between mad cow and variant CJD. Several other papers in the top 20 explore the molecular biology of prions and their role as a causative agent in these pathologies. Diagnostic methods, patterns of incidence, molecular analyses, and species barrier studies round out the top articles in our analysis.

Methodology

To construct this database, papers were extracted based on a TOPIC search for Mad Cow. The keywords used were as follows: 

  • mad cow
  • bovine spongiform encephalopathy

The baseline time span for this database is 1993-2003. The resulting database contained 1,282 papers; 2,394 authors; 46 countries; 487 journals; and 799 institutions.

Rankings

Once the database was in place, it was used to generate the lists of top 20 papers, authors, journals, institutions, and nations, covering a time span of 1993-2003.

The top 20 papers are ranked according to total cites. Rankings for author, journal, institution, and country are listed in three ways: according to total cites, total papers, and total cites/paper. The paper thresholds used to determine scientist, institution, country, and journal rankings according to total cites/paper were as follows: 14, 15, 4, and 7, respectively.

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