Jessica Profato

586 total citations
10 papers, 135 citations indexed

About

Jessica Profato is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Jessica Profato has authored 10 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Cancer Research and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Jessica Profato's work include BRCA gene mutations in cancer (9 papers), Cancer Genomics and Diagnostics (4 papers) and Nutrition, Genetics, and Disease (3 papers). Jessica Profato is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Cancer Genomics and Diagnostics (4 papers) and Nutrition, Genetics, and Disease (3 papers). Jessica Profato collaborates with scholars based in United States and United Kingdom. Jessica Profato's co-authors include Banu Arun, Jennifer K. Litton, Ashley Woodson, Susan K. Peterson, Denise Nebgen, Yuanqing Ye, Claire N. Singletary, Angelica M. Gutierrez‐Barrera, Haley Streff and Constance T. Albarracin and has published in prestigious journals such as Journal of Clinical Oncology, Cancer and The Oncologist.

In The Last Decade

Jessica Profato

10 papers receiving 127 citations

Peers

Jessica Profato
Marijke R. Wevers Netherlands
Ellen Crepin Netherlands
Yoland Antill Australia
Kelly Kohut United Kingdom
Marion Harris Australia
Thuy M. Vu United States
Marijke R. Wevers Netherlands
Jessica Profato
Citations per year, relative to Jessica Profato Jessica Profato (= 1×) peers Marijke R. Wevers

Countries citing papers authored by Jessica Profato

Since Specialization
Citations

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

Fields of papers citing papers by Jessica Profato

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jessica Profato

This figure shows the co-authorship network connecting the top 25 collaborators of Jessica Profato. A scholar is included among the top collaborators of Jessica Profato 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 Jessica Profato. Jessica Profato 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.
Ademuyiwa, Foluso O., Carolyn Horton, Holly LaDuca, et al.. (2021). Closing the gap: Trends in inconclusive rates on hereditary cancer testing across racial/ethnic groups.. Journal of Clinical Oncology. 39(15_suppl). 10525–10525. 1 indexed citations
2.
Jasperson, Kory, Heather Hampel, Patrick Reineke, et al.. (2018). Concordance of germline multigene panel testing with prior microsatellite instability and immunohistochemistry analyses in endometrial cancer patients. Gynecologic Oncology. 149. 38–39. 1 indexed citations
3.
Streff, Haley, Jessica Profato, Yuanqing Ye, et al.. (2016). Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers. The Oncologist. 21(7). 869–874. 37 indexed citations
4.
Profato, Jessica, Angelica M. Gutierrez‐Barrera, Heather Lin, et al.. (2015). Predictors that Influence Election of Contralateral Prophylactic Mastectomy among Women with Ductal Carcinoma in Situ who are BRCA-Negative. Journal of Cancer. 6(7). 610–615. 6 indexed citations
5.
Sanford, Rachel, Juhee Song, Angelica M. Gutierrez‐Barrera, et al.. (2015). High incidence of germline BRCA mutation in patients with ER low‐positive/PR low‐positive/HER‐2 neu negative tumors. Cancer. 121(19). 3422–3427. 42 indexed citations
6.
Woodson, Ashley, et al.. (2015). Service Delivery Model and Experiences in a Cancer Genetics Clinic for an Underserved Population. Journal of Health Care for the Poor and Underserved. 26(3). 784–791. 11 indexed citations
7.
Profato, Jessica & Banu Arun. (2014). Genetic risk assessment for breast and gynecological malignancies. Current Opinion in Obstetrics & Gynecology. 27(1). 1–5. 3 indexed citations
8.
Woodson, Ashley, Heather Lin, Michelle Jackson, et al.. (2014). Breast Cancer, BRCA Mutations, and Attitudes Regarding Pregnancy and Preimplantation Genetic Diagnosis. The Oncologist. 19(8). 797–804. 18 indexed citations
9.
Profato, Jessica, et al.. (2014). Assessing the Integration of Genomic Medicine in Genetic Counseling Training Programs. Journal of Genetic Counseling. 23(4). 679–688. 8 indexed citations
10.
Woodson, Ashley, et al.. (2013). Breast cancer in the young: role of the geneticist.. PubMed. 5 Suppl 1. S19–26. 8 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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