Kerry E. Kingham

2.2k citations
26 papers · 1.7k · 1 hit paper · h-index 17

Impact in

  • Genetics top 2%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Cancer Genomics and Diagnostics

Papers in

Kerry E. Kingham

26 papers receiving 1.6k citations

Kerry E. Kingham's Hit Papers

Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment 2014 · 405 citations
4050+4+8Years since publication100200300400

Peers

Kerry E. Kingham
Comparison fields: 5 of 84
  • Genetics 970
  • Cancer Research 353
  • Pathology and Forensic Medicine 410
  • Oncology 176
  • Molecular Biology 430
Replace Shan Yang with:
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Citations per year

Countries citing papers authored by Kerry E. Kingham

Since Specialization
Citations

This map shows the geographic impact of Kerry E. Kingham'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 Kerry E. Kingham with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kerry E. Kingham more than expected).

Fields of papers citing papers by Kerry E. Kingham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kerry E. Kingham. 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 Kerry E. Kingham. The network helps show where Kerry E. Kingham may publish in the future.

Co-authors

The 25 scholars most cited alongside Kerry E. Kingham, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kerry E. Kingham Line = papers co-authored together Kerry E. Kingham links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 26 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment
Hit paper breakdown →
2014405
2 2014351
3 2017153
4 2008116
5 201895
6 201174
7 200469
8 200854
9 201743
10 201940
11 201839
12 201437
13 202434
14 201434
15 202032
16 201226
17 200522
18 200715
19 201113
20 202012

About Kerry E. Kingham

Kerry E. Kingham is a scholar working on Genetics, Pathology and Forensic Medicine, Cancer Research, Oncology and Molecular Biology, having authored 26 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (6 papers), Genetic factors in colorectal cancer (5 papers), Wnt/β-catenin signaling in development and cancer (4 papers), Cancer Genomics and Diagnostics (2 papers), Neuroendocrine Tumor Research Advances (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (970 citations), Cancer Research (353 citations), Pathology and Forensic Medicine (410 citations), Oncology (176 citations) and Molecular Biology (430 citations). Kerry E. Kingham has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Allison W. Kurian, James M. Ford, Meredith A. Mills, Uri Ladabaum, Alice S. Whittemore, Lisa A. McPherson, Valerie McGuire, Emily E. Hare, Yuya Kobayashi and Stephen E. Lincoln. Their work appears in journals such as JCO Precision Oncology, Journal of Clinical Oncology, JAMA, Cancer and Familial Cancer.

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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