John Kidd

2.2k total citations · 2 hit papers
28 papers, 1.4k citations indexed

About

John Kidd is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, John Kidd has authored 28 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 13 papers in Cancer Research and 8 papers in Pathology and Forensic Medicine. Recurrent topics in John Kidd's work include BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (13 papers) and Genetic factors in colorectal cancer (8 papers). John Kidd is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Cancer Genomics and Diagnostics (13 papers) and Genetic factors in colorectal cancer (8 papers). John Kidd collaborates with scholars based in United States, Cayman Islands and Germany. John Kidd's co-authors include Richard Wenstrup, Brian Allen, Nanda Singh, Anne‐Renee Hartman, Krystal Brown, Judy E. Garber, Nadine Tung, Nancy U. Lin, Eric P. Winer and Johnathan M. Lancaster and has published in prestigious journals such as Journal of Clinical Oncology, JNCI Journal of the National Cancer Institute and Cancer.

In The Last Decade

John Kidd

28 papers receiving 1.3k citations

Hit Papers

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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.

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer

2016 364 citations John Kidd, Brian Allen et al. Journal of Clinical Oncology profile →
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer

2017 344 citations Matthew B. Yurgelun, Matthew H. Kulke et al. Journal of Clinical Oncology profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
John Kidd	780	575	541	509	471	28	1.4k
Jenna Lilyquist	645 0.8×	559 1.0×	545 1.0×	297 0.6×	434 0.9×	19	1.2k
Raymond M. Moore	590 0.8×	482 0.8×	511 0.9×	279 0.5×	476 1.0×	22	1.2k
Shan Yang	745 1.0×	276 0.5×	382 0.7×	294 0.6×	377 0.8×	37	1.2k
Catherine Walsh Vockley	546 0.7×	667 1.2×	494 0.9×	794 1.6×	220 0.5×	13	1.3k
H. T. Lynch	545 0.7×	885 1.5×	572 1.1×	911 1.8×	281 0.6×	11	1.5k
Elisha Hughes	498 0.6×	524 0.9×	375 0.7×	164 0.3×	521 1.1×	38	1.1k
Sarah M. Nielsen	329 0.4×	273 0.5×	340 0.6×	146 0.3×	255 0.5×	75	882
Erin Salo‐Mullen	265 0.3×	886 1.5×	588 1.1×	355 0.7×	331 0.7×	44	1.3k
Angela George	596 0.8×	564 1.0×	307 0.6×	144 0.3×	412 0.9×	60	1.2k
DF Easton	724 0.9×	238 0.4×	291 0.5×	283 0.6×	318 0.7×	16	940

Countries citing papers authored by John Kidd

Since Specialization

Citations

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

Fields of papers citing papers by John Kidd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John Kidd. 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 John Kidd. The network helps show where John Kidd may publish in the future.

Co-authorship network of co-authors of John Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of John Kidd. A scholar is included among the top collaborators of John Kidd 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 John Kidd. John Kidd is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Culver, Julie O., Charité Ricker, Kerry Kingham, et al.. (2025). Breast Cancer MRI Screening of Patients After Multiplex Gene Panel Testing. JAMA Network Open. 8(1). e2454447–e2454447. 1 indexed citations

Daly, Mary B., Eric T. Rosenthal, Shelly Cummings, et al.. (2023). The association between age at breast cancer diagnosis and prevalence of pathogenic variants. Breast Cancer Research and Treatment. 199(3). 617–626. 5 indexed citations

Kidd, John & D. Y. Lin. (2023). Improving the Power to Detect Indirect Effects in Mediation Analysis. Statistics in Biosciences. 16(1). 129–141. 1 indexed citations

Kidd, John, Chelsea K. Raulerson, Karen L. Mohlke, & D. Y. Lin. (2022). Mediation analysis of multiple mediators with incomplete omics data. Genetic Epidemiology. 47(1). 61–77. 2 indexed citations

Weitzel, Jeffrey N., John Kidd, Ryan Bernhisel, et al.. (2021). Multigene assessment of genetic risk for women for two or more breast cancers. Breast Cancer Research and Treatment. 188(3). 759–768. 5 indexed citations

Calip, Gregory S., John Kidd, Ryan Bernhisel, et al.. (2020). Family history of breast cancer in men with non-BRCA male breast cancer: implications for cancer risk counseling. Breast Cancer Research and Treatment. 185(1). 195–204. 9 indexed citations

Mancini‐DiNardo, Debora, Thaddeus Judkins, John Kidd, et al.. (2019). Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing. BMC Medical Genomics. 12(1). 138–138. 16 indexed citations

Idos, Gregory, Allison W. Kurian, Charité Ricker, et al.. (2019). Preventive surgery after multiplex genetic panel testing (MGPT).. Journal of Clinical Oncology. 37(15_suppl). 1525–1525. 1 indexed citations

Kidd, John. (2019). Web-based mapping: an evaluation of free mapping applications and Web GIS for library reference services. Carolina Digital Repository (University of North Carolina at Chapel Hill). 1 indexed citations

10.

Chaffee, Kari G., Ann L. Oberg, Robert R. McWilliams, et al.. (2017). Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history. Genetics in Medicine. 20(1). 119–127. 97 indexed citations

11.

Coffee, Bradford, Hannah C. Cox, John Kidd, et al.. (2017). Detection of somatic variants in peripheral blood lymphocytes using a next generation sequencing multigene pan cancer panel. Cancer Genetics. 211. 5–8. 39 indexed citations

12.

Rosenthal, Eric T., Ryan Bernhisel, Krystal Brown, John Kidd, & Susan Manley. (2017). Clinical testing with a panel of 25 genes associated with increased cancer risk results in a significant increase in clinically significant findings across a broad range of cancer histories. Cancer Genetics. 218-219. 58–68. 58 indexed citations

13.

Yurgelun, Matthew B., Matthew H. Kulke, Charles S. Fuchs, et al.. (2017). Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer. Journal of Clinical Oncology. 35(10). 1086–1095. 344 indexed citations breakdown →

14.

Whitworth, Pat W., Peter D. Beitsch, Christopher Arnell, et al.. (2017). Impact of Payer Constraints on Access to Genetic Testing. Journal of Oncology Practice. 13(1). e47–e56. 42 indexed citations

15.

Rosenthal, Eric T., et al.. (2016). Increased Identification of Candidates for High-Risk Breast Cancer Screening Through Expanded Genetic Testing. Journal of the American College of Radiology. 14(4). 561–568. 22 indexed citations

16.

Cockerell, Clay J., Jaime A. Tschen, Brent Evans, et al.. (2016). The influence of a gene expression signature on the diagnosis and recommended treatment of melanocytic tumors by dermatopathologists. Medicine. 95(40). e4887–e4887. 20 indexed citations

17.

Petersen, Gloria M., Kari G. Chaffee, Robert R. McWilliams, et al.. (2016). Genetic heterogeneity and survival among pancreatic adenocarcinoma (PDAC) patients with positive family history.. Journal of Clinical Oncology. 34(15_suppl). 4108–4108. 9 indexed citations

18.

Eguchi, Takashi, Kyuichi Kadota, Jamie E. Chaft, et al.. (2016). Cell cycle progression score is a marker for five-year lung cancer-specific mortality risk in patients with resected stage I lung adenocarcinoma. Oncotarget. 7(23). 35241–35256. 16 indexed citations

19.

Kurian, Allison W., Gregory Idos, Julie O. Culver, et al.. (2016). Safety of multiplex gene testing for inherited cancer risk: Interim analysis of a clinical trial.. Journal of Clinical Oncology. 34(15_suppl). 1503–1503. 3 indexed citations

20.

Kidd, John, et al.. (2016). Hereditary cancer testing in patients with ovarian cancer using a 25-gene panel. The Journal of Community and Supportive Oncology. 14(7). 314–319. 9 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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