Tracy Graham

981 total citations
8 papers, 164 citations indexed

About

Tracy Graham is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Tracy Graham has authored 8 papers receiving a total of 164 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Cancer Research and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Tracy Graham's work include BRCA gene mutations in cancer (7 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Tracy Graham is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Genomics and Rare Diseases (3 papers) and Cancer Genomics and Diagnostics (3 papers). Tracy Graham collaborates with scholars based in Canada, United States and Japan. Tracy Graham's co-authors include Ellen Warner, Andrea Eisen, Alex Kiss, Steven A. Narod, Aletta Poll, Ping Sun, Kimberley Hill, Debora B. Farber, Nancy Hamel and Victoria Marcus and has published in prestigious journals such as SHILAP Revista de lepidopterología, Cancer Research and British Journal of Cancer.

In The Last Decade

Tracy Graham

7 papers receiving 161 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tracy Graham Canada 5 133 65 49 48 34 8 164
Christina Rybak United States 6 119 0.9× 34 0.5× 36 0.7× 66 1.4× 37 1.1× 11 164
Adrià López‐Fernández Spain 7 116 0.9× 47 0.7× 112 2.3× 53 1.1× 33 1.0× 18 199
Mónica Salinas Spain 8 87 0.7× 41 0.6× 85 1.7× 51 1.1× 37 1.1× 15 163
Judit Sanz Spain 7 146 1.1× 41 0.6× 86 1.8× 59 1.2× 28 0.8× 11 199
Marion Harris Australia 6 194 1.5× 69 1.1× 59 1.2× 48 1.0× 44 1.3× 9 218
Ellen Crepin Netherlands 3 114 0.9× 68 1.0× 36 0.7× 28 0.6× 32 0.9× 4 150
Theodore Turnquest Canada 5 143 1.1× 54 0.8× 48 1.0× 28 0.6× 56 1.6× 7 177
Thuy M. Vu United States 5 82 0.6× 35 0.5× 22 0.4× 72 1.5× 46 1.4× 8 138
Valérie Bonadona France 4 63 0.5× 35 0.5× 28 0.6× 27 0.6× 38 1.1× 8 104
Mariana Niell‐Swiller United States 4 131 1.0× 45 0.7× 38 0.8× 60 1.3× 23 0.7× 6 159

Countries citing papers authored by Tracy Graham

Since Specialization
Citations

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

Fields of papers citing papers by Tracy Graham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracy Graham

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

All Works

8 of 8 papers shown
1.
Shickh, Salma, Chloe Mighton, Marc Clausen, et al.. (2023). P409: Clinical utility of genomic sequencing for hereditary cancer syndromes: An observational chart review. SHILAP Revista de lepidopterología. 1(1). 100445–100445.
2.
Metcalfe, Kelly, Steven A. Narod, Andrea Eisen, et al.. (2022). Genetic testing women with newly diagnosed breast cancer: What criteria are the most predictive of a positive test?. Cancer Medicine. 12(6). 7580–7587. 3 indexed citations
3.
Zyla, Roman, Tracy Graham, Melyssa Aronson, et al.. (2021). MLH1 epimutation is a rare mechanism for Lynch syndrome: A case report and review of the literature. Genes Chromosomes and Cancer. 60(9). 635–639. 4 indexed citations
4.
Metcalfe, Kelly, Andrea Eisen, Aletta Poll, et al.. (2020). Rapid Genetic Testing for BRCA1 and BRCA2 Mutations at the Time of Breast Cancer Diagnosis: An Observational Study. Annals of Surgical Oncology. 28(4). 2219–2226. 11 indexed citations
5.
Raphael, Jacques, et al.. (2016). Abstract P6-10-17: Rates of prophylactic surgeries among BRCA 1 or 2 mutation carriers: A single institution experience. Cancer Research. 76(4_Supplement). P6–10. 1 indexed citations
6.
Graham, Tracy, et al.. (2013). Variants of unknown significance in BRCA testing: impact on risk perception, worry, prevention and counseling. Annals of Oncology. 24. viii69–viii74. 83 indexed citations
7.
Graham, Tracy, Aletta Poll, Ping Sun, et al.. (2011). Reasons for risk-reducing mastectomy versus MRI-screening in a cohort of women at high hereditary risk of breast cancer. The Breast. 20(3). 254–258. 31 indexed citations
8.
Thiffault, Isabelle, Nancy Hamel, Tuya Pal, et al.. (2004). Germline truncating mutations in both MSH2 and BRCA2 in a single kindred. British Journal of Cancer. 90(2). 483–491. 31 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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