Scott M. Weissman

2.4k total citations
24 papers, 1.1k citations indexed

About

Scott M. Weissman is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Scott M. Weissman has authored 24 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 10 papers in Pathology and Forensic Medicine and 6 papers in Molecular Biology. Recurrent topics in Scott M. Weissman's work include BRCA gene mutations in cancer (18 papers), Genetic factors in colorectal cancer (10 papers) and Genomics and Rare Diseases (4 papers). Scott M. Weissman is often cited by papers focused on BRCA gene mutations in cancer (18 papers), Genetic factors in colorectal cancer (10 papers) and Genomics and Rare Diseases (4 papers). Scott M. Weissman collaborates with scholars based in United States, Canada and Philippines. Scott M. Weissman's co-authors include Peter J. Hulick, Christina G. Selkirk, Erica Ramos, Andy Anderson, Theodore D. Chung, Wendy Stock, Nadim Mahmud, Terry A. Hewett, Joseph D. Mosca and Robert Deans and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Cancer.

In The Last Decade

Scott M. Weissman

23 papers receiving 1.1k citations

Peers

Scott M. Weissman
T. P. Crotty Ireland
Ana Novokmet Canada
Michael Bremer Germany
Ana Carrió Spain
Tom G.W. Letteboer Netherlands
Jill Hagenkord United States
Yael Goldberg Israel
Rafael Bornstein Spain
Katrin M. Carlson United States
Valérie Bonadona France
T. P. Crotty Ireland
Scott M. Weissman
Citations per year, relative to Scott M. Weissman Scott M. Weissman (= 1×) peers T. P. Crotty

Countries citing papers authored by Scott M. Weissman

Since Specialization
Citations

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

Fields of papers citing papers by Scott M. Weissman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Scott M. Weissman. 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 Scott M. Weissman. The network helps show where Scott M. Weissman may publish in the future.

Co-authorship network of co-authors of Scott M. Weissman

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

All Works

20 of 20 papers shown
1.
Nguyen, Tiffany, Kelly E. Ormond, Scott M. Weissman, Helen J. Kim, & Chloe M. Reuter. (2022). Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services. Translational Behavioral Medicine. 13(2). 104–114.
2.
Weissman, Scott M., et al.. (2021). Utilization of breast cancer risk prediction models by cancer genetic counselors in clinical practice predominantly in the United States. Journal of Genetic Counseling. 30(6). 1737–1747. 3 indexed citations
3.
Thompson, Michael A., Michael P. Mullane, Amanda M. Wilson, et al.. (2019). Coordinating an Oncology Precision Medicine Clinic Within an Integrated Health System: Lessons Learned in Year One. SHILAP Revista de lepidopterología. 6(1). 36–45. 6 indexed citations
4.
Weissman, Scott M., et al.. (2019). At-home genetic testing in pediatrics. Current Opinion in Pediatrics. 31(6). 723–731. 6 indexed citations
5.
Thompson, Michael A., et al.. (2017). Implementing an oncology precision medicine clinic in a large community health system.. PubMed. 23(10 Spec No.). SP425–SP427. 7 indexed citations
6.
Weissman, Scott M., et al.. (2017). Implementing a Virtual Health Telemedicine Program in a Community Setting. Journal of Genetic Counseling. 27(2). 323–325. 22 indexed citations
7.
Postula, Kristen J. Vogel, et al.. (2017). FDA Approval of PARP Inhibitors and the Impact on Genetic Counseling and Genetic Testing Practices. Journal of Genetic Counseling. 27(1). 131–139. 18 indexed citations
8.
Stoll, Jessica, Scott M. Weissman, Christina G. Selkirk, et al.. (2016). Evaluation of laboratory perspectives on hereditary cancer panels. Familial Cancer. 15(4). 689–696. 3 indexed citations
9.
Susswein, Lisa R., Megan L. Marshall, Rachel Nusbaum, et al.. (2015). Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. Genetics in Medicine. 18(8). 823–832. 199 indexed citations
10.
Capuano, Alessandra, Francesco Bucciotti, Kelly D. Farwell, et al.. (2015). Diagnostic Exome Sequencing Identifies a Novel Gene,EMILIN1, Associated with Autosomal‐Dominant Hereditary Connective Tissue Disease. Human Mutation. 37(1). 84–97. 33 indexed citations
11.
Selkirk, Christina G., Kristen J. Vogel, Anna Newlin, et al.. (2014). Cancer genetic testing panels for inherited cancer susceptibility: the clinical experience of a large adult genetics practice. Familial Cancer. 13(4). 527–536. 29 indexed citations
12.
Selkirk, Christina G., Scott M. Weissman, Andy Anderson, & Peter J. Hulick. (2013). Physicians' Preparedness for Integration of Genomic and Pharmacogenetic Testing into Practice Within a Major Healthcare System. Genetic Testing and Molecular Biomarkers. 17(3). 219–225. 104 indexed citations
13.
Weissman, Scott M., et al.. (2012). Genetic Testing by Cancer Site. The Cancer Journal. 18(4). 320–327. 39 indexed citations
14.
Weissman, Scott M., Cecelia Bellcross, Joy Larsen Haidle, et al.. (2010). Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome—A Review. Journal of Genetic Counseling. 20(1). 5–19. 43 indexed citations
15.
Rubinstein, Wendy S. & Scott M. Weissman. (2010). Correction: Managing hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists. Nature Reviews Gastroenterology & Hepatology. 7(9). 477–477. 5 indexed citations
16.
17.
Lynch, Henry T., Pardeep Kaurah, Debrah Wirtzfeld, et al.. (2008). Hereditary diffuse gastric cancer. Cancer. 112(12). 2655–2663. 77 indexed citations
18.
Rubinstein, Wendy S. & Scott M. Weissman. (2008). Managing hereditary gastrointestinal cancer syndromes: the partnership between genetic counselors and gastroenterologists. Nature Clinical Practice Gastroenterology & Hepatology. 5(10). 569–582. 8 indexed citations
19.
Callanan, Nancy P., et al.. (2006). Code of Ethics of the National Society of Genetic Counselors: Explication of Revisions. Journal of Genetic Counseling. 15(5). 313–323. 3 indexed citations
20.
Devine, Steven M., Amelia Bartholomew, Nadim Mahmud, et al.. (2001). Mesenchymal stem cells are capable of homing to the bone marrow of non-human primates following systemic infusion. Experimental Hematology. 29(2). 244–255. 336 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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