Erica M. Bednar

566 total citations
17 papers, 360 citations indexed

About

Erica M. Bednar is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine. According to data from OpenAlex, Erica M. Bednar has authored 17 papers receiving a total of 360 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Erica M. Bednar's work include BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (6 papers) and Genetic factors in colorectal cancer (4 papers). Erica M. Bednar is often cited by papers focused on BRCA gene mutations in cancer (14 papers), Genomics and Rare Diseases (6 papers) and Genetic factors in colorectal cancer (4 papers). Erica M. Bednar collaborates with scholars based in United States. Erica M. Bednar's co-authors include Karen H. Lu, Charlotte C. Sun, Emily Hinchcliff, J. Alejandro Rauh‐Hain, Banu Arun, Kent Hoskins, Stephanie A. Cohen, Angela R. Bradbury, Vida Henderson and Sheryl McCurdy and has published in prestigious journals such as Cancer Research, Health Affairs and Gynecologic Oncology.

In The Last Decade

Erica M. Bednar

17 papers receiving 355 citations

Peers

Erica M. Bednar

GENET

PFM

PPCH

PHEOH

Kimberly Childers United States

Anne Weidner United States

Sara Pirzadeh‐Miller United States

Sherry Grumet United States

Elizabeth Hoodfar United States

Devon Bonner United States

Amanda Brandt United States

Karina L. Brierley United States

Ingrid Slade United Kingdom

Ryan Noss United States

Kimberly Childers United States

Erica M. Bednar

276 ×1.0

GENET

68 ×0.8

56 ×0.8

PFM

64 ×0.9

PPCH

41 ×0.8

PHEOH

Citations per year, relative to Erica M. Bednar Erica M. Bednar (= 1×) peers Kimberly Childers

Countries citing papers authored by Erica M. Bednar

Since Specialization

Citations

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

Fields of papers citing papers by Erica M. Bednar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erica M. Bednar

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

All Works

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17 of 17 papers shown

Bednar, Erica M., Sara Pirzadeh‐Miller, Isabel C. Scarinci, et al.. (2024). Cascade genetic testing: an underutilized pathway to equitable cancer care?. Familial Cancer. 23(2). 141–145. 1 indexed citations

Hashmi, S. Shahrukh, et al.. (2024). Status of abortion curriculum in genetic counseling: Survey of graduate programs and recent graduates in the United States. Journal of Genetic Counseling. 34(1). e1875–e1875. 2 indexed citations

Bednar, Erica M., Jose Alejandro Rauh‐Hain, Roni Nitecki, et al.. (2023). Experiences of Family Communication and Cascade Genetic Testing for Hereditary Cancer in Medically Underserved Populations—A Qualitative Study. Cancer Prevention Research. 17(1). 19–28. 2 indexed citations

Walsh, Michael T., Katherine Oestman, Stephanie Nutt, et al.. (2023). Creating and Activating an Implementation Community to Drive HPV Vaccine Uptake in Texas: The Role of an NCI-Designated Cancer Center. Vaccines. 11(6). 1128–1128. 2 indexed citations

Bednar, Erica M., Roni Nitecki, Kate J. Krause, & Jose Alejandro Rauh‐Hain. (2022). Interventions to improve delivery of cancer genetics services in the United States: A scoping review. Genetics in Medicine. 24(6). 1176–1186. 8 indexed citations

Roth, Michael, et al.. (2022). Factors impacting adolescent and young adult cancer patients’ decision to pursue genetic counseling and testing. Supportive Care in Cancer. 30(6). 5481–5489. 6 indexed citations

Bednar, Erica M., Michael T. Walsh, Ruth Rechis, et al.. (2022). Implementation and outcome evaluations of a multi‐site improvement program in cancer genetics. Journal of Genetic Counseling. 32(1). 182–196. 1 indexed citations

Bednar, Erica M., et al.. (2021). Clinical management among individuals with variant of uncertain significance in hereditary cancer: A systematic review and meta‐analysis. Clinical Genetics. 100(2). 119–131. 19 indexed citations

Smith, Hadley Stevens, et al.. (2021). Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication. Journal of Community Genetics. 12(3). 439–447. 4 indexed citations

10.

Hinchcliff, Emily, Erica M. Bednar, Karen H. Lu, & J. Alejandro Rauh‐Hain. (2019). Disparities in gynecologic cancer genetics evaluation. Gynecologic Oncology. 153(1). 184–191. 56 indexed citations

11.

Bednar, Erica M., Charlotte C. Sun, Sheryl McCurdy, & Sally W. Vernon. (2019). Assessing relatives’ readiness for hereditary cancer cascade genetic testing. Genetics in Medicine. 22(4). 719–726. 32 indexed citations

12.

Bannon, Sarah A., et al.. (2019). Clinical applicability of proposed algorithm for identifying individuals at risk for hereditary hematologic malignancies. Leukemia & lymphoma. 60(12). 3020–3027. 3 indexed citations

13.

Cohen, Stephanie A., Angela R. Bradbury, Vida Henderson, et al.. (2019). Genetic Counseling and Testing in a Community Setting: Quality, Access, and Efficiency. American Society of Clinical Oncology Educational Book. e34–e44. 55 indexed citations

14.

Bednar, Erica M., Charlotte C. Sun, Alyssa G. Rieber, et al.. (2018). Disseminating universal genetic testing to a diverse, indigent patient population at a county hospital gynecologic oncology clinic. Gynecologic Oncology. 152(2). 328–333. 9 indexed citations

15.

Roberts, Megan C., W. David Dotson, Erica M. Bednar, et al.. (2018). Delivery Of Cascade Screening For Hereditary Conditions: A Scoping Review Of The Literature. Health Affairs. 37(5). 801–808. 113 indexed citations

16.

Bednar, Erica M., Holly D. Oakley, Charlotte C. Sun, et al.. (2017). A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment. Gynecologic Oncology. 146(2). 399–404. 44 indexed citations

17.

Bednar, Erica M., et al.. (2016). Abstract P2-09-08: Universal BRCA testing and family outreach for women with triple negative breast cancer. Cancer Research. 76(4_Supplement). P2–9. 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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