Suzanne M. O’Neill

883 total citations
23 papers, 650 citations indexed

About

Suzanne M. O’Neill is a scholar working on Genetics, Oncology and Sociology and Political Science. According to data from OpenAlex, Suzanne M. O’Neill has authored 23 papers receiving a total of 650 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Oncology and 5 papers in Sociology and Political Science. Recurrent topics in Suzanne M. O’Neill's work include BRCA gene mutations in cancer (12 papers), Global Cancer Incidence and Screening (6 papers) and Family Support in Illness (4 papers). Suzanne M. O’Neill is often cited by papers focused on BRCA gene mutations in cancer (12 papers), Global Cancer Incidence and Screening (6 papers) and Family Support in Illness (4 papers). Suzanne M. O’Neill collaborates with scholars based in United States, Philippines and Germany. Suzanne M. O’Neill's co-authors include Wendy S. Rubinstein, Mack T. Ruffin, Catharine Wang, Louise S. Acheson, Nan Rothrock, Robert Gramling, Donald E. Nease, Jennifer L. Beaumont, Ananda Sen and June A. Peters and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Preventive Medicine and Preventive Medicine.

In The Last Decade

Suzanne M. O’Neill

21 papers receiving 629 citations

Peers

Suzanne M. O’Neill
Beatty G. Watts United States
Mariëlle S. van Roosmalen Netherlands
Suzanne A. Miller United States
Janet Seay United States
Aliya Collier United States
Margaret Gleeson Australia
Reneé Royak-Schaler United States
Jennifer Hilgart United Kingdom
Debra Duquette United States
Heather Howley Canada
Beatty G. Watts United States
Suzanne M. O’Neill
Citations per year, relative to Suzanne M. O’Neill Suzanne M. O’Neill (= 1×) peers Beatty G. Watts

Countries citing papers authored by Suzanne M. O’Neill

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne M. O’Neill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suzanne M. O’Neill. 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 Suzanne M. O’Neill. The network helps show where Suzanne M. O’Neill may publish in the future.

Co-authorship network of co-authors of Suzanne M. O’Neill

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne M. O’Neill. A scholar is included among the top collaborators of Suzanne M. O’Neill 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 Suzanne M. O’Neill. Suzanne M. O’Neill 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.
O’Neill, Suzanne M., et al.. (2019). The impact of insurance coverage on the prenatal genetic counseling process: An exploration of genetic counselors' experiences with TRICARE. Prenatal Diagnosis. 39(6). 448–455. 4 indexed citations
2.
MacLeod, Heather, et al.. (2018). Genetic Counselors’ Approach To Postmortem Genetic Testing After Sudden Death. Academic Forensic Pathology. 8(3). 738–751. 8 indexed citations
3.
4.
Peshkin, Beth N., Susan T. Vadaparampil, Lindsey Hoskins, Suzanne M. O’Neill, & James Barter. (2015). Genetic counseling and testing for hereditary cancer risk in young adult women: Facilitating autonomy and informed decision making is key. SHILAP Revista de lepidopterología. 14. 44–45. 6 indexed citations
5.
Tercyak, Kenneth P., Andrea C. Johnson, Sarah E. Murphy, et al.. (2015). Survey on Addressing the Information and Support Needs of Jewish Women at Increased Risk for or Diagnosed with Breast Cancer: The Sharsheret Experience. Healthcare. 3(2). 324–337. 7 indexed citations
6.
O’Neill, Suzanne M., et al.. (2013). Evaluation of a One-Call Center for Utah's Wasatch Front Region. Transportation Research Board 92nd Annual MeetingTransportation Research Board.
7.
O’Neill, Suzanne M., et al.. (2013). Standardizing Data for Mobility Management. Transportation Research Board eBooks. 2 indexed citations
8.
Dorman, Janice S., Rodolfo Valdéz, Tiebin Liu, et al.. (2012). Health beliefs among individuals at increased familial risk for type 2 diabetes: Implications for prevention. Diabetes Research and Clinical Practice. 96(2). 156–162. 25 indexed citations
9.
Wang, Catharine, Ananda Sen, Mack T. Ruffin, et al.. (2012). Family History Assessment. American Journal of Preventive Medicine. 43(4). 392–398. 37 indexed citations
10.
Rubinstein, Wendy S., Louise S. Acheson, Suzanne M. O’Neill, et al.. (2011). Clinical utility of family history for cancer screening and referral in primary care: A report from the Family Healthware Impact Trial. Genetics in Medicine. 13(11). 956–965. 70 indexed citations
11.
O’Neill, Suzanne M., et al.. (2011). Family Physicians’ Awareness and Knowledge of the Genetic Information Non‐Discrimination Act (GINA). Journal of Genetic Counseling. 21(2). 345–352. 45 indexed citations
12.
Fitzpatrick, Patricia, et al.. (2011). False-positive Mammographic Screening: Factors Influencing Re-attendance over a Decade of Screening. Journal of Medical Screening. 18(1). 30–33. 19 indexed citations
13.
Rubinstein, Wendy S., Suzanne M. O’Neill, Nan Rothrock, et al.. (2010). Components of family history associated with women's disease perceptions for cancer: A report from the Family Healthware™ Impact Trial. Genetics in Medicine. 13(1). 52–62. 15 indexed citations
14.
Acheson, Louise S., Catharine Wang, Stephen J. Zyzanski, et al.. (2010). Family history and perceptions about risk and prevention for chronic diseases in primary care: A report from the Family Healthware™ Impact Trial. Genetics in Medicine. 12(4). 212–218. 68 indexed citations
15.
O’Neill, Suzanne M., Wendy S. Rubinstein, Catharine Wang, et al.. (2009). Familial Risk for Common Diseases in Primary Care. American Journal of Preventive Medicine. 36(6). 506–514. 92 indexed citations
16.
Wang, Catharine, Suzanne M. O’Neill, Nan Rothrock, et al.. (2008). Comparison of risk perceptions and beliefs across common chronic diseases. Preventive Medicine. 48(2). 197–202. 108 indexed citations
17.
O’Neill, Suzanne M., June A. Peters, Victor G. Vogel, Eleanor Feingold, & Wendy S. Rubinstein. (2006). Referral to cancer genetic counseling: Are there stages of readiness?. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 142C(4). 221–231. 41 indexed citations
18.
Kaufman, Elizabeth, Beth N. Peshkin, William Lawrence, et al.. (2003). Development of an Interactive Decision Aid for Female BRCA1/BRCA2 Carriers. Journal of Genetic Counseling. 12(2). 109–129. 28 indexed citations
19.
Rubinstein, Wendy S., et al.. (2002). Mathematical Modeling for Breast Cancer Risk Assessment. 6 indexed citations
20.
Rubinstein, Wendy S., et al.. (2002). Mathematical modeling for breast cancer risk assessment. State of the art and role in medicine.. PubMed. 16(8). 1082–94; discussion 1094, 1097. 17 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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