Beth N. Peshkin

8.7k total citations
129 papers, 4.8k citations indexed

About

Beth N. Peshkin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Sociology and Political Science. According to data from OpenAlex, Beth N. Peshkin has authored 129 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 116 papers in Genetics, 51 papers in Pediatrics, Perinatology and Child Health and 46 papers in Sociology and Political Science. Recurrent topics in Beth N. Peshkin's work include BRCA gene mutations in cancer (116 papers), Family Support in Illness (44 papers) and Childhood Cancer Survivors' Quality of Life (26 papers). Beth N. Peshkin is often cited by papers focused on BRCA gene mutations in cancer (116 papers), Family Support in Illness (44 papers) and Childhood Cancer Survivors' Quality of Life (26 papers). Beth N. Peshkin collaborates with scholars based in United States, Iceland and Spain. Beth N. Peshkin's co-authors include Marc D. Schwartz, Claudine Isaacs, Tiffani A. DeMarco, Kenneth P. Tercyak, Caryn Lerman, Caryn Lerman, Chanita Hughes, Kristi D. Graves, Heiðdís Valdimarsdóttir and David Main and has published in prestigious journals such as The Lancet, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Beth N. Peshkin

125 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Beth N. Peshkin United States	39	3.9k	1.2k	1.1k	934	740	129	4.8k
Kathy Tucker Australia	35	2.4k 0.6×	818 0.7×	745 0.7×	744 0.8×	549 0.7×	142	3.4k
Kelly Metcalfe Canada	41	3.7k 0.9×	588 0.5×	506 0.4×	1.4k 1.5×	843 1.1×	176	5.9k
Caryn Lerman United States	53	4.7k 1.2×	1.3k 1.1×	1.7k 1.5×	2.4k 2.6×	1.1k 1.5×	94	8.2k
Margreet G.E.M. Ausems Netherlands	35	2.0k 0.5×	596 0.5×	346 0.3×	1.0k 1.1×	415 0.6×	157	3.6k
Clara Gaff Australia	35	2.5k 0.6×	682 0.6×	440 0.4×	428 0.5×	723 1.0×	152	3.9k
Kelly‐Anne Phillips Australia	38	1.8k 0.5×	451 0.4×	289 0.3×	2.3k 2.4×	810 1.1×	158	5.2k
Shari Gelber United States	35	1.2k 0.3×	883 0.7×	540 0.5×	3.1k 3.4×	1.7k 2.4×	108	5.9k
Jill E. Stopfer United States	31	2.1k 0.5×	392 0.3×	232 0.2×	598 0.6×	382 0.5×	69	2.6k
Angela R. Bradbury United States	28	1.4k 0.4×	450 0.4×	204 0.2×	638 0.7×	431 0.6×	121	2.8k
Andrew Balshem United States	25	1.5k 0.4×	453 0.4×	630 0.6×	1.7k 1.9×	550 0.7×	44	3.6k

Countries citing papers authored by Beth N. Peshkin

Since Specialization

Citations

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

Fields of papers citing papers by Beth N. Peshkin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beth N. Peshkin. 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 Beth N. Peshkin. The network helps show where Beth N. Peshkin may publish in the future.

Co-authorship network of co-authors of Beth N. Peshkin

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

All Works

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20 of 20 papers shown

1.

Peshkin, Beth N., Jada G. Hamilton, Mingqian Liu, et al.. (2025). Parental Communication With their Children about Cancer Risk and DTC Cascade Genetic Testing: Implications for Genetic Education and Counseling. American Journal of Medical Genetics Part A. 197(9). e64115–e64115.

2.

Peshkin, Beth N., Jada G. Hamilton, Jamie Brower, et al.. (2023). Measuring high‐risk parents' opinions about direct‐to‐consumer genetic testing for adult‐onset inherited cancer syndromes in their adolescent and young adult children. Journal of Genetic Counseling. 32(4). 768–777. 2 indexed citations

3.

Marshall, John L., Beth N. Peshkin, Takayuki Yoshino, et al.. (2022). The Essentials of Multiomics. The Oncologist. 27(4). 272–284. 12 indexed citations

4.

Peshkin, Beth N., Claudine Isaacs, Shawna C. Willey, et al.. (2020). Predictors of contralateral prophylactic mastectomy in genetically high risk newly diagnosed breast cancer patients. Breast Cancer Research and Treatment. 180(1). 177–185. 9 indexed citations

5.

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

6.

Graves, Kristi D., Rachel Nusbaum, Gillian W. Hooker, et al.. (2013). Behavioral and psychosocial responses to genomic testing for colorectal cancer risk. Genomics. 102(2). 123–130. 31 indexed citations

7.

DeMarco, Tiffani A., Darren Mays, Beth N. Peshkin, et al.. (2011). Parenting Through Genetic Uncertainty: Themes in the Disclosure of Breast Cancer Risk Information to Children. Genetic Testing and Molecular Biomarkers. 16(5). 376–382. 31 indexed citations

8.

Graves, Kristi D., et al.. (2011). BRCA1/2 genetic testing uptake and psychosocial outcomes in men. Familial Cancer. 10(2). 213–223. 29 indexed citations

9.

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

10.

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

11.

O’Neill, S C, et al.. (2008). Adolescent Medical Providers' Willingness to Recommend Genetic Susceptibility Testing for Nicotine Addiction and Lung Cancer Risk to Adolescents. Journal of Pediatric Psychology. 34(6). 617–626. 9 indexed citations

12.

Tercyak, Kenneth P., Beth N. Peshkin, Tiffani A. DeMarco, et al.. (2007). Information Needs of Mothers Regarding Communicating BRCA1/2 Cancer Genetic Test Results to Their Children. Genetic Testing. 11(3). 249–255. 40 indexed citations

13.

DeMarco, Tiffani A., Karen L. Smith, Rachel Nusbaum, et al.. (2007). Practical Aspects of Delivering Hereditary Cancer Risk Counseling. Seminars in Oncology. 34(5). 369–378. 23 indexed citations

14.

Peshkin, Beth N., et al.. (2007). Genetic Discrimination in Health Insurance: Current Legal Protections and Industry Practices. INQUIRY The Journal of Health Care Organization Provision and Financing. 44(3). 350–368. 10 indexed citations

15.

O’Neill, Suzanne C., Tiffani A. DeMarco, Beth N. Peshkin, et al.. (2006). Tolerance for uncertainty and perceived risk among women receiving uninformativeBRCA1/2test results. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 142C(4). 251–259. 58 indexed citations

16.

Tercyak, Kenneth P., et al.. (2005). Interest of adolescents in genetic testing for nicotine addiction susceptibility. Preventive Medicine. 42(1). 60–65. 17 indexed citations

17.

Tercyak, Kenneth P., et al.. (2004). Women's satisfaction with genetic counseling for hereditary breast‐ovarian cancer: Psychological aspects. American Journal of Medical Genetics Part A. 131A(1). 36–41. 28 indexed citations

18.

Tercyak, Kenneth P., Beth N. Peshkin, Randi Streisand, & Caryn Lerman. (2001). Psychological issues among children of hereditary breast cancer gene (BRCA1/2) testing participants. Psycho-Oncology. 10(4). 336–346. 62 indexed citations

19.

Peshkin, Beth N. & Caryn Lerman. (1999). Genetic counselling for hereditary breast cancer. The Lancet. 353(9171). 2176–2177. 11 indexed citations

20.

Lerman, Caryn, Beth N. Peshkin, Chanita Hughes, & Claudine Isaacs. (1998). Family Disclosure in Genetic Testing for Cancer Susceptibility: Determinants and Consequences. 1(2). 353. 42 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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