Carole Harris‐Kerr

2.7k total citations · 1 hit paper
10 papers, 1.4k citations indexed

About

Carole Harris‐Kerr is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Carole Harris‐Kerr has authored 10 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 2 papers in Genetics. Recurrent topics in Carole Harris‐Kerr's work include Cardiac electrophysiology and arrhythmias (4 papers), Genetic Associations and Epidemiology (2 papers) and Ion channel regulation and function (2 papers). Carole Harris‐Kerr is often cited by papers focused on Cardiac electrophysiology and arrhythmias (4 papers), Genetic Associations and Epidemiology (2 papers) and Ion channel regulation and function (2 papers). Carole Harris‐Kerr collaborates with scholars based in United States, Netherlands and Ireland. Carole Harris‐Kerr's co-authors include David J. Tester, Arthur A.M. Wilde, Benjamin A. Salisbury, Michael J. Ackerman, Yunlong Ma, Richard E. Straub, Kenneth S. Kendler, Charles J. MacLean, Bradley T. Webb and F. Anthony O’Neill and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and The American Journal of Human Genetics.

In The Last Decade

Carole Harris‐Kerr

10 papers receiving 1.4k citations

Hit Papers

Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Or... 2002 2026 2010 2018 2002 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia
    2002 619 citations Richard E. Straub, Yuxin Jiang et al. The American Journal of Human Genetics profile →

Peers

Carole Harris‐Kerr
Maura T. Walker United Kingdom
Mirna Kvajo United States
Huijun Zhong Canada
Tianlan Lu China
Emi Mazaki Japan
Ikuo Ogiwara Japan
R. Dayne Mayfield United States
Elaine C. Budreck United States
Nanda A. Singh United States
Hisako Ohba Japan
Maura T. Walker United Kingdom
Carole Harris‐Kerr
Citations per year, relative to Carole Harris‐Kerr Carole Harris‐Kerr (= 1×) peers Maura T. Walker

Countries citing papers authored by Carole Harris‐Kerr

Since Specialization
Citations

This map shows the geographic impact of Carole Harris‐Kerr's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Carole Harris‐Kerr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carole Harris‐Kerr more than expected).

Fields of papers citing papers by Carole Harris‐Kerr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carole Harris‐Kerr. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Carole Harris‐Kerr. The network helps show where Carole Harris‐Kerr may publish in the future.

Co-authorship network of co-authors of Carole Harris‐Kerr

This figure shows the co-authorship network connecting the top 25 collaborators of Carole Harris‐Kerr. A scholar is included among the top collaborators of Carole Harris‐Kerr based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Carole Harris‐Kerr. Carole Harris‐Kerr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
1.
Tester, David J., Carmen R. Valdivia, Carole Harris‐Kerr, et al.. (2010). Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation. Heart Rhythm. 7(7). 912–919. 30 indexed citations
2.
Kapplinger, Jamie D., David J. Tester, Benjamin A. Salisbury, et al.. (2009). Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test. Heart Rhythm. 6(9). 1297–1303. 329 indexed citations
3.
Kapa, Suraj, David J. Tester, Benjamin A. Salisbury, et al.. (2009). Genetic Testing for Long-QT Syndrome. Circulation. 120(18). 1752–1760. 237 indexed citations
4.
Tester, David J., Benjamin A. Salisbury, Janet L. Carr, et al.. (2007). Abstract 2966: Should a Minimum Corrected QT Interval (QTc) be a Prerequisite for Long QT Syndrome Genetic Testing?. Circulation. 116(suppl_16). 1 indexed citations
5.
Salisbury, Benjamin A., Manish Pungliya, Carole Harris‐Kerr, et al.. (2006). P1-81. Heart Rhythm. 3(5). S134–S134. 2 indexed citations
6.
Straub, Richard E., Yuxin Jiang, Charles J. MacLean, et al.. (2002). Genetic Variation in the 6p22.3 Gene DTNBP1, the Human Ortholog of the Mouse Dysbindin Gene, Is Associated with Schizophrenia. The American Journal of Human Genetics. 71(2). 337–348. 619 indexed citations breakdown →
7.
Silverman, Michael A., Michael C. Neale, Patrick F. Sullivan, et al.. (2000). Haplotypes of four novel single nucleotide polymorphisms in the nicotinic acetylcholine receptor β2‐subunit (CHRNB2) gene show no association with smoking initiation or nicotine dependence. American Journal of Medical Genetics. 96(5). 646–653. 1 indexed citations
8.
Silverman, Michael A., Michael C. Neale, Patrick F. Sullivan, et al.. (2000). Haplotypes of four novel single nucleotide polymorphisms in the nicotinic acetylcholine receptor ?2-subunit (CHRNB2) gene show no association with smoking initiation or nicotine dependence. American Journal of Medical Genetics. 96(5). 646–653. 67 indexed citations
9.
Straub, Richard E., Charles J. MacLean, Rory Martin, et al.. (1998). A schizophrenia locus may be located in region 10p15-p11. American Journal of Medical Genetics. 81(4). 296–301. 111 indexed citations
10.
Harris‐Kerr, Carole, et al.. (1993). The phylogenetically predicted base-pairing interaction between alpha and alpha' is required for group II splicing in vitro.. Proceedings of the National Academy of Sciences. 90(22). 10658–10662. 33 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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