D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 78 Citations 22,855 276 World Ranking 12821 National Ranking 6675

Best Publications

Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability

Julie M. Cunningham;Eric R. Christensen;David J. Tester;Cheong Yong Kim.
Cancer Research (1998)

1209 Citations

Compendium of Cardiac Channel Mutations in 541 Consecutive Unrelated Patients Referred for Long QT Syndrome Genetic Testing

David J. Tester;Melissa L. Will;Carla M. Haglund;Michael J. Ackerman.
Heart Rhythm (2005)

767 Citations

Microsatellite instability in colorectal cancer: different mutator phenotypes and the principal involvement of hMLH1.

Stephen N. Thibodeau;Amy J. French;Julie M. Cunningham;David Tester.
Cancer Research (1998)

746 Citations

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

Jamie D. Kapplinger;David J. Tester;Marielle Alders;Begoña Benito.
Heart Rhythm (2010)

706 Citations

Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome

Matteo Vatta;Michael J. Ackerman;Bin Ye;Jonathan C. Makielski.
Circulation (2006)

695 Citations

Altered Expression of hMSH2 and hMLH1 in Tumors with Microsatellite Instability and Genetic Alterations in Mismatch Repair Genes

Stephen N. Thibodeau;Amy J. French;Patrick C. Roche;Julie M. Cunningham.
Cancer Research (1996)

682 Citations

Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.

Michael J. Ackerman;Benjamin L. Siu;William Q. Sturner;David J. Tester.
JAMA (2001)

619 Citations

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.

David J. Tester;Michael J. Ackerman.
Journal of the American College of Cardiology (2007)

480 Citations

Most LQT2 Mutations Reduce Kv11.1 (hERG) Current by a Class 2 (Trafficking-Deficient) Mechanism

Corey L. Anderson;Brian P. Delisle;Blake D. Anson;Jennifer A. Kilby.
Circulation (2006)

449 Citations

Syntrophin mutation associated with long QT syndrome through activation of the nNOS–SCN5A macromolecular complex

Kazuo Ueda;Carmen Valdivia;Argelia Medeiros-Domingo;David J. Tester.
Proceedings of the National Academy of Sciences of the United States of America (2008)

444 Citations

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