Shanna Gustafson

872 total citations
16 papers, 636 citations indexed

About

Shanna Gustafson is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine. According to data from OpenAlex, Shanna Gustafson has authored 16 papers receiving a total of 636 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Shanna Gustafson's work include BRCA gene mutations in cancer (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic factors in colorectal cancer (4 papers). Shanna Gustafson is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Prenatal Screening and Diagnostics (5 papers) and Genetic factors in colorectal cancer (4 papers). Shanna Gustafson collaborates with scholars based in United States, United Kingdom and India. Shanna Gustafson's co-authors include Stephanie A. Cohen, Charis Eng, Monica Marvin, Julie Rousseau, Bronson D. Riley, Victoria M. Raymond, Jessica N. Everett, Kevin Zbuk, Stephen B. Gruber and Elena M. Stoffel and has published in prestigious journals such as Journal of Clinical Oncology, Cochrane Database of Systematic Reviews and Genetics in Medicine.

In The Last Decade

Shanna Gustafson

16 papers receiving 626 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shanna Gustafson United States 12 290 173 122 122 109 16 636
Sarah Scollon United States 17 473 1.6× 158 0.9× 267 2.2× 65 0.5× 130 1.2× 47 991
A Bröcker-Vriends Netherlands 15 177 0.6× 70 0.4× 73 0.6× 84 0.7× 163 1.5× 26 842
Ian Walpole Australia 18 248 0.9× 47 0.3× 187 1.5× 100 0.8× 63 0.6× 49 855
Nicholas Pachter Australia 14 210 0.7× 121 0.7× 45 0.4× 86 0.7× 44 0.4× 30 578
Amanda Gammon United States 18 678 2.3× 251 1.5× 137 1.1× 127 1.0× 282 2.6× 34 1.1k
Carine Courtillot France 13 226 0.8× 43 0.2× 93 0.8× 96 0.8× 93 0.9× 32 774
Holly J. Pederson United States 11 215 0.7× 107 0.6× 35 0.3× 51 0.4× 128 1.2× 34 611
Isabelle Coupier France 14 274 0.9× 275 1.6× 61 0.5× 275 2.3× 73 0.7× 35 834
José Cláudio Casali da Rocha Brazil 13 139 0.5× 162 0.9× 110 0.9× 55 0.5× 126 1.2× 45 704
Tahsin Yakut Türkiye 15 191 0.7× 63 0.4× 174 1.4× 77 0.6× 23 0.2× 78 762

Countries citing papers authored by Shanna Gustafson

Since Specialization
Citations

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

Fields of papers citing papers by Shanna Gustafson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shanna Gustafson

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

All Works

16 of 16 papers shown
1.
Cohen, Stephanie A., et al.. (2016). Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models. Journal of Genetic Counseling. 25(5). 1010–1018. 53 indexed citations
2.
Hercher, Laura, et al.. (2016). Prenatal Testing for Adult‐Onset Conditions: the Position of the National Society of Genetic Counselors. Journal of Genetic Counseling. 25(6). 1139–1145. 21 indexed citations
3.
Benjamin, Caroline, Lois H Thomas, Heather Skirton, et al.. (2015). Interventions to improve patient access to and utilisation of genetic and genomic counselling services.. Cochrane Database of Systematic Reviews. 2015(11). 1 indexed citations
4.
Gustafson, Shanna, Victoria M. Raymond, Monica Marvin, et al.. (2014). Outcomes of genetic evaluation for hereditary cancer syndromes in unaffected individuals. Familial Cancer. 14(1). 167–174. 2 indexed citations
5.
Everett, Jessica N., Shanna Gustafson, & Victoria M. Raymond. (2014). Traditional Roles in a Non‐Traditional Setting: Genetic Counseling in Precision Oncology. Journal of Genetic Counseling. 23(4). 655–660. 19 indexed citations
6.
Everett, Jessica N., Victoria M. Raymond, Monica Dandapani, et al.. (2014). Screening for Germline Mismatch Repair Mutations Following Diagnosis of Sebaceous Neoplasm. JAMA Dermatology. 150(12). 1315–1315. 56 indexed citations
7.
Heald, Brandie, Shanna Gustafson, Jessica L. Mester, et al.. (2013). A Time Study of Cancer Genetic Counselors Using a Genetic Counselor-Only Patient Care Model Versus a Traditional Combined Genetic Counselor Plus Medical Geneticist Care Model. Journal of the National Comprehensive Cancer Network. 11(9). 1076–1081. 12 indexed citations
8.
Raymond, Victoria M., Jessica N. Everett, Larissa V. Furtado, et al.. (2013). Adrenocortical Carcinoma Is a Lynch Syndrome–Associated Cancer. Journal of Clinical Oncology. 31(24). 3012–3018. 134 indexed citations
9.
Cohen, Stephanie A., Monica Marvin, Bronson D. Riley, et al.. (2013). Identification of Genetic Counseling Service Delivery Models in Practice: A Report from the NSGC Service Delivery Model Task Force. Journal of Genetic Counseling. 22(4). 411–421. 90 indexed citations
10.
Cohen, Stephanie A., Shanna Gustafson, Monica Marvin, et al.. (2012). Report from the National Society of Genetic Counselors Service Delivery Model Task Force: A Proposal to Define Models, Components, and Modes of Referral. Journal of Genetic Counseling. 21(5). 645–651. 68 indexed citations
11.
Gustafson, Shanna, et al.. (2012). Psychological Distress with Direct‐to‐Consumer Genetic Testing: A Case Report of an UnexpectedBRCAPositive Test Result. Journal of Genetic Counseling. 21(3). 399–401. 22 indexed citations
12.
Gustafson, Shanna, et al.. (2011). A large health system's approach to utilization of the genetic counselor CPT® 96040 code. Genetics in Medicine. 13(12). 1011–1014. 22 indexed citations
13.
Gulati, Shuchi, Shanna Gustafson, & Hamed Daw. (2011). Lynch Syndrome Associated With PMS2 Mutation: Understanding Current Concepts.. PubMed. 4(5-6). 188–90. 3 indexed citations
14.
Gustafson, Shanna, et al.. (2007). Health beliefs among African American women regarding genetic testing and counseling for sickle cell disease. Genetics in Medicine. 9(5). 303–310. 39 indexed citations
15.
Gustafson, Shanna, et al.. (2007). Cowden Syndrome. Seminars in Oncology. 34(5). 428–434. 91 indexed citations
16.
Gustafson, Shanna. (2006). Knowledge and Health Beliefs of Sickle Cell Disease and Sickle Cell Trait: The Influence on Acceptance of Genetic Screening for Sickle Cell Trait. D-Scholarship@Pitt (University of Pittsburgh). 3 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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