Mary McCullum

522 total citations
15 papers, 362 citations indexed

About

Mary McCullum is a scholar working on Genetics, Sociology and Political Science and Oncology. According to data from OpenAlex, Mary McCullum has authored 15 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 3 papers in Sociology and Political Science and 3 papers in Oncology. Recurrent topics in Mary McCullum's work include BRCA gene mutations in cancer (15 papers), Nutrition, Genetics, and Disease (3 papers) and Global Cancer Incidence and Screening (2 papers). Mary McCullum is often cited by papers focused on BRCA gene mutations in cancer (15 papers), Nutrition, Genetics, and Disease (3 papers) and Global Cancer Incidence and Screening (2 papers). Mary McCullum collaborates with scholars based in Canada. Mary McCullum's co-authors include Lynda G. Balneaves, Joan L. Bottorff, Jessica N. McAlpine, Jane A. Buxton, Thomas F. Hack, Pamela A. Ratner, Janice S. Kwon, Anna V. Tinker, C. Blake Gilks and Chris G. Richardson and has published in prestigious journals such as Journal of Clinical Oncology, Obstetrics and Gynecology and Psycho-Oncology.

In The Last Decade

Mary McCullum

14 papers receiving 352 citations

Peers

Mary McCullum

GENET

ONCOL

PHEOH

PPCH

Steven A. Narod Canada

Lesley Andrews Australia

Tim Rebbeck United States

Christine Lasset France

Amanda Brandt United States

Dorinda Sparacio United States

Raluca Nedelcu United States

Jenna Scott Canada

Evelyn Cantillo United States

Nico Bruyniks Italy

Steven A. Narod Canada

Mary McCullum

365 ×1.4

GENET

181 ×1.4

70 ×0.9

ONCOL

54 ×0.9

PHEOH

55 ×1.0

PPCH

Citations per year, relative to Mary McCullum Mary McCullum (= 1×) peers Steven A. Narod

Countries citing papers authored by Mary McCullum

Since Specialization

Citations

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

Fields of papers citing papers by Mary McCullum

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mary McCullum

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

All Works

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15 of 15 papers shown

Richardson, Matthew, Quan Hong, Mary McCullum, et al.. (2020). Oncology Clinic-Based Hereditary Cancer Genetic Testing in a Population-Based Health Care System. Cancers. 12(2). 338–338. 28 indexed citations

Lee, Michael, Quan Hong, Steve E. Kalloger, et al.. (2019). Unselected germline screening in pancreatic adenocarcinoma yields high rates of pathogenic and likely pathogenic variants (PV) in hereditary cancer susceptibility genes.. Journal of Clinical Oncology. 37(15_suppl). 1582–1582.

Kwon, Janice S., et al.. (2013). Prophylactic Salpingectomy and Delayed Oophorectomy as an Alternative for BRCA Mutation Carriers. Obstetrics and Gynecology. 121(1). 14–24. 110 indexed citations

Kwon, Janice S., et al.. (2013). Prophylactic Salpingectomy and Delayed Oophorectomy as an Alternative for BRCA Mutation Carriers. Obstetrical & Gynecological Survey. 68(6). 442–444. 8 indexed citations

Brotto, Lori A., et al.. (2012). Risk-Reducing Bilateral Salpingo-Oophorectomy and Sexual Health: A Qualitative Study. Journal of Obstetrics and Gynaecology Canada. 34(2). 172–178. 14 indexed citations

McCullum, Mary, et al.. (2009). Evaluation of Group Genetic Counseling for Hereditary Breast and Ovarian Cancer. Journal of Genetic Counseling. 18(1). 87–100. 20 indexed citations

McCullum, Mary, et al.. (2007). Time to decide about risk-reducing mastectomy: A case series of BRCA1/2 gene mutation carriers. BMC Women s Health. 7(1). 3–3. 20 indexed citations

Bottorff, Joan L., et al.. (2005). Canadian Nursing in the Genomic Era: A Call for Leadership. Nursing leadership. 18(2). 56–72. 4 indexed citations

Bottorff, Joan L., et al.. (2005). Establishing roles in genetic nursing: interviews with Canadian nurses.. PubMed. 37(4). 96–115. 18 indexed citations

10.

Bottorff, Joan L., et al.. (2004). Nursing and genetics.. PubMed. 100(8). 24–8. 6 indexed citations

11.

Bottorff, Joan L., Pamela A. Ratner, Chris G. Richardson, et al.. (2003). The influence of question wording on assessments of interest in genetic testing for breast cancer risk. Psycho-Oncology. 12(7). 720–728. 6 indexed citations

12.

Buxton, Jane A., Joan L. Bottorff, Lynda G. Balneaves, et al.. (2003). Women’s Perceptions of Breast Cancer Risk: Are They Accurate?. Canadian Journal of Public Health. 94(6). 422–426. 40 indexed citations

13.

Bottorff, Joan L., Pamela A. Ratner, Lynda G. Balneaves, et al.. (2002). Women's interest in genetic testing for breast cancer risk: the influence of sociodemographics and knowledge.. PubMed. 11(1). 89–95. 69 indexed citations

14.

Bottorff, Joan L., Pamela A. Ratner, Lynda G. Balneaves, et al.. (2002). Women’s Interest in Genetic Testing for Breast Cancer Risk. Cancer Epidemiology and Prevention Biomarkers. 11(1). 89–95. 2 indexed citations

15.

Bottorff, Joan L., Lynda G. Balneaves, Jane A. Buxton, et al.. (2000). Falling through the cracks. Women's experiences of ineligibility for genetic testing for risk of breast cancer.. PubMed. 46. 1449–56. 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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