Stephanie Gutierrez

1.4k total citations
14 papers, 361 citations indexed

About

Stephanie Gutierrez is a scholar working on Genetics, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Stephanie Gutierrez has authored 14 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 3 papers in Pathology and Forensic Medicine and 3 papers in Oncology. Recurrent topics in Stephanie Gutierrez's work include BRCA gene mutations in cancer (8 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Stephanie Gutierrez is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Stephanie Gutierrez collaborates with scholars based in United States, United Kingdom and Australia. Stephanie Gutierrez's co-authors include Holly LaDuca, Patrick Reineke, Brigette Tippin Davis, Kate Krempely, Phillip Gray, Jill S. Dolinsky, Rachel Pearlman, Heather Hampel, Peter P. Stanich and Kory Jasperson 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

Stephanie Gutierrez

14 papers receiving 353 citations

Author Peers

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

Author						Papers	Cites
Stephanie Gutierrez	212	88	76	73	73	14	361
Patrick Reineke	244 1.2×	61 0.7×	53 0.7×	30 0.4×	132 1.8×	10	355
Rebecca Doherty	182 0.9×	45 0.5×	72 0.9×	71 1.0×	39 0.5×	28	345
Kathryn E. Hatchell	207 1.0×	79 0.9×	82 1.1×	59 0.8×	26 0.4×	40	402
Kristen J. Vogel	231 1.1×	80 0.9×	100 1.3×	125 1.7×	61 0.8×	19	430
Chantal Perret	189 0.9×	76 0.9×	82 1.1×	122 1.7×	32 0.4×	11	329
Karina L. Brierley	305 1.4×	70 0.8×	70 0.9×	49 0.7×	70 1.0×	10	416
Eleni Kakouri	132 0.6×	52 0.6×	70 0.9×	116 1.6×	114 1.6×	17	355
Guochong Jia	88 0.4×	47 0.5×	41 0.5×	65 0.9×	39 0.5×	18	233
Diptasri Mandal	186 0.9×	44 0.5×	67 0.9×	66 0.9×	39 0.5×	24	406
John L. Hopper	180 0.8×	53 0.6×	62 0.8×	129 1.8×	22 0.3×	5	308

Countries citing papers authored by Stephanie Gutierrez

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie Gutierrez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Gutierrez

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

All Works

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14 of 14 papers shown

Taylor, Barbara S., et al.. (2022). Educational Outcomes of a 4-Year MD–MPH Dual-Degree Program: High Completion Rates and Higher Likelihood of Primary Care Residency. Academic Medicine. 97(6). 894–898. 3 indexed citations

Taylor, Barbara S., et al.. (2022). Educational Outcomes of a 4-Year MD-MPH Dual-Degree Program: High Completion Rates and Higher Likelihood of Primary Care Residency.. PubMed. 97(6). 894–898. 3 indexed citations

Black, Mary Helen, Shuwei Li, Holly LaDuca, et al.. (2020). Validation of a prostate cancer polygenic risk score. The Prostate. 80(15). 1314–1321. 19 indexed citations

Tian, Yuan, Patrick Reineke, Aaron J. Stuenkel, et al.. (2020). Diagnosing hereditary cancer predisposition in men with prostate cancer. Genetics in Medicine. 22(9). 1517–1523. 32 indexed citations

Li, Shuwei, et al.. (2020). Prevalence of Germline Pathogenic and Likely Pathogenic Variants in Patients With Second Breast Cancers. JNCI Cancer Spectrum. 4(6). pkaa094–pkaa094. 9 indexed citations

Yadav, Siddhartha, Holly LaDuca, Eric C. Polley, et al.. (2020). Racial and Ethnic Differences in Multigene Hereditary Cancer Panel Test Results for Women With Breast Cancer. JNCI Journal of the National Cancer Institute. 113(10). 1429–1433. 23 indexed citations

Rana, Huma Q., Rosalba Sacca, Stephanie Gutierrez, et al.. (2019). Prevalence of germline variants in inflammatory breast cancer. Cancer. 125(13). 2194–2202. 13 indexed citations

Li, Shuwei, Dajun Qian, Bryony A. Thompson, et al.. (2019). Tumour characteristics provide evidence for germline mismatch repair missense variant pathogenicity. Journal of Medical Genetics. 57(1). 62–69. 2 indexed citations

Yadav, Siddhartha, Holly LaDuca, Eric C. Polley, et al.. (2019). Racial and ethnic differences in the results of multigene panel testing of inherited cancer predisposition genes in breast cancer patients.. Journal of Clinical Oncology. 37(15_suppl). 1514–1514. 3 indexed citations

10.

Stanich, Peter P., Rachel Pearlman, Alice Hinton, et al.. (2018). Prevalence of Germline Mutations in Polyposis and Colorectal Cancer–Associated Genes in Patients With Multiple Colorectal Polyps. Clinical Gastroenterology and Hepatology. 17(10). 2008–2015.e3. 45 indexed citations

11.

Krempely, Kate, Holly LaDuca, Patrick Reineke, et al.. (2018). False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care. Genetics in Medicine. 20(12). 1515–1521. 176 indexed citations

12.

LaDuca, Holly, Rachel McFarland, Stephanie Gutierrez, et al.. (2018). Quality of Clinician-Reported Cancer History When Ordering Genetic Testing. JCO Clinical Cancer Informatics. 2(2). 1–11. 20 indexed citations

13.

Black, Mary Helen, Shuwei Li, Holly LaDuca, et al.. (2018). Polygenic risk score for breast cancer in high-risk women.. Journal of Clinical Oncology. 36(15_suppl). 1508–1508. 9 indexed citations

14.

Scollon, Sarah, Katie Bergstrom, Laurence B. McCullough, et al.. (2015). Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject. The Journal of Law Medicine & Ethics. 43(3). 529–537. 4 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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