Andrea Forman

1.4k total citations
28 papers, 732 citations indexed

About

Andrea Forman is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Sociology and Political Science. According to data from OpenAlex, Andrea Forman has authored 28 papers receiving a total of 732 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 11 papers in Pediatrics, Perinatology and Child Health and 8 papers in Sociology and Political Science. Recurrent topics in Andrea Forman's work include BRCA gene mutations in cancer (27 papers), Family Support in Illness (8 papers) and Genomics and Rare Diseases (7 papers). Andrea Forman is often cited by papers focused on BRCA gene mutations in cancer (27 papers), Family Support in Illness (8 papers) and Genomics and Rare Diseases (7 papers). Andrea Forman collaborates with scholars based in United States, Iceland and United Kingdom. Andrea Forman's co-authors include Michael J. Hall, Mary B. Daly, Veda N. Giri, Heiðdís Valdimarsdóttir, Marc D. Schwartz, Georgia L. Wiesner, Robert Pilarski, Karen Brown, Lina Jandorf and Dana H. Bovbjerg and has published in prestigious journals such as Journal of Clinical Oncology, Scientific Reports and Journal of Medical Internet Research.

In The Last Decade

Andrea Forman

28 papers receiving 719 citations

Peers

Andrea Forman
Rachel Nusbaum United States
Vickie L. Venne United States
Sue Friedman United States
Carolyn Durham United States
Clinton Finch United States
Kara J. Milliron United States
Cecelia Bellcross United States
Brita Arver Sweden
Christine Lasset France
Monica Marvin United States
Rachel Nusbaum United States
Andrea Forman
Citations per year, relative to Andrea Forman Andrea Forman (= 1×) peers Rachel Nusbaum

Countries citing papers authored by Andrea Forman

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Forman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Forman

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Forman. A scholar is included among the top collaborators of Andrea Forman 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 Andrea Forman. Andrea Forman 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.
Usher‐Smith, Juliet A., Abdul Badran, Andrea Forman, et al.. (2024). Patterns of referrals to regional clinical genetics services for women potentially at above-population level risk of breast cancer. PubMed. 2(1). 2–2. 1 indexed citations
2.
Badran, Abdul, et al.. (2023). Proactive familial cancer risk assessment: a service development study in UK primary care. BJGP Open. 7(4). BJGPO.2023.0076–BJGPO.2023.0076. 1 indexed citations
3.
Hartman, Tiffiney R., Lily Hoang, Marcy E. Richardson, et al.. (2020). Prevalence of pathogenic variants in DNA damage response and repair genes in patients undergoing cancer risk assessment and reporting a personal history of early-onset renal cancer. Scientific Reports. 10(1). 13518–13518. 15 indexed citations
4.
Forman, Andrea, et al.. (2019). Tumor-Based Genetic Testing and Familial Cancer Risk. Cold Spring Harbor Perspectives in Medicine. 10(8). a036590–a036590. 22 indexed citations
5.
Forman, Andrea, et al.. (2019). Guidelines-Based Cancer Risk Assessment. Seminars in Oncology Nursing. 35(1). 34–46. 3 indexed citations
6.
Bradbury, Angela R., Linda Patrick‐Miller, Diana Harris, et al.. (2016). Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study. Journal of Medical Internet Research. 18(2). e23–e23. 75 indexed citations
7.
Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations
8.
Jain, Rishi, et al.. (2016). The Relevance of Hereditary Cancer Risks to Precision Oncology: What Should Providers Consider When Conducting Tumor Genomic Profiling?. Journal of the National Comprehensive Cancer Network. 14(6). 795–806. 14 indexed citations
9.
Hall, Michael J., et al.. (2016). Genetic testing for hereditary cancer predisposition: BRCA1/2, Lynch syndrome, and beyond. Gynecologic Oncology. 140(3). 565–574. 34 indexed citations
10.
Peshkin, Beth N., Scott P. Kelly, Rachel Nusbaum, et al.. (2015). Patient Perceptions of Telephone vs. In‐Person BRCA1/BRCA2 Genetic Counseling. Journal of Genetic Counseling. 25(3). 472–482. 46 indexed citations
11.
Patrick‐Miller, Linda, Brian L. Egleston, Dominique Fetzer, et al.. (2014). Development of a Communication Protocol for Telephone Disclosure of Genetic Test Results for Cancer Predisposition. JMIR Research Protocols. 3(4). e49–e49. 16 indexed citations
12.
Hall, Michael J., Andrea Forman, Robert Pilarski, Georgia L. Wiesner, & Veda N. Giri. (2014). Gene Panel Testing for Inherited Cancer Risk. Journal of the National Comprehensive Cancer Network. 12(9). 1339–1346. 87 indexed citations
13.
Patrick‐Miller, Linda, Brian L. Egleston, Mary B. Daly, et al.. (2013). Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results. Patient Education and Counseling. 93(3). 413–419. 17 indexed citations
14.
Thompson, Hayley S., Katarina M. Sussner, Marc D. Schwartz, et al.. (2012). Receipt of Genetic Counseling Recommendations Among Black Women at High Risk for BRCA Mutations. Genetic Testing and Molecular Biomarkers. 16(11). 1257–1262. 20 indexed citations
15.
Sussner, Katarina M., Hayley S. Thompson, Lina Jandorf, et al.. (2011). Ethnic, Racial and Cultural Identity and Perceived Benefits and Barriers Related to Genetic Testing for Breast Cancer among At-Risk Women of African Descent in New York City. Public Health Genomics. 14(6). 356–370. 34 indexed citations
16.
Patrick‐Miller, Linda, et al.. (2010). Genetic counselor opinions of, and experiences with telephone communication of BRCA1/2 test results. Clinical Genetics. 79(2). 125–131. 37 indexed citations
17.
Forman, Andrea & Michael J. Hall. (2009). Influence of Race/Ethnicity on Genetic Counseling and Testing for Hereditary Breast and Ovarian Cancer. The Breast Journal. 15. S56–S62. 85 indexed citations
18.
Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 0(0). 2685938514–2685938514. 1 indexed citations
19.
Peshkin, Beth N., Tiffani A. DeMarco, Kristi D. Graves, et al.. (2008). Telephone Genetic Counseling for High-Risk Women Undergoing BRCA1 and BRCA2 Testing: Rationale and Development of a Randomized Controlled Trial. Genetic Testing. 12(1). 37–52. 41 indexed citations
20.
Thompson, Hayley S., Naa Oyo A. Kwate, Karen Brown, et al.. (2008). Association between temporal orientation and attitudes about BRCA1/2 testing among women of African descent with family histories of breast cancer. Patient Education and Counseling. 72(2). 276–282. 23 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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