Rebecca Sutphen

5.8k total citations · 1 hit paper
52 papers, 2.4k citations indexed

About

Rebecca Sutphen is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Rebecca Sutphen has authored 52 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 25 papers in Molecular Biology and 12 papers in Cancer Research. Recurrent topics in Rebecca Sutphen's work include BRCA gene mutations in cancer (20 papers), Cancer Genomics and Diagnostics (8 papers) and Ovarian cancer diagnosis and treatment (7 papers). Rebecca Sutphen is often cited by papers focused on BRCA gene mutations in cancer (20 papers), Cancer Genomics and Diagnostics (8 papers) and Ovarian cancer diagnosis and treatment (7 papers). Rebecca Sutphen collaborates with scholars based in United States, Canada and Australia. Rebecca Sutphen's co-authors include Tuya Pal, Jenny Permuth‐Wey, Alan Cantor, Jeffrey P. Krischer, Martin A Martino, James V. Fiorica, Mitchell Hoffman, James P. LaPolla, Hector Arango and George D. Wilbanks and has published in prestigious journals such as PLoS ONE, Analytical Chemistry and Cancer.

In The Last Decade

Rebecca Sutphen

51 papers receiving 2.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases

2005 524 citations Tuya Pal, Jenny Permuth‐Wey et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rebecca Sutphen United States	25	1.4k	938	466	454	446	52	2.4k
Jean‐Philippe Peyrat France	32	1.8k 1.3×	644 0.7×	167 0.4×	680 1.5×	1.3k 2.9×	86	3.4k
Andy Ryan United Kingdom	29	1.2k 0.8×	512 0.5×	910 2.0×	888 2.0×	712 1.6×	99	3.0k
Karin Sundfeldt Sweden	30	1.3k 0.9×	226 0.2×	927 2.0×	606 1.3×	521 1.2×	91	2.7k
Antoninus Soosaipillai Canada	38	1.3k 1.0×	240 0.3×	391 0.8×	604 1.3×	1.1k 2.4×	91	3.6k
Gerald J. Mizejewski United States	27	1.3k 0.9×	375 0.4×	203 0.4×	334 0.7×	590 1.3×	120	2.6k
Steven McKinney Canada	18	1.2k 0.9×	374 0.4×	503 1.1×	977 2.2×	1.2k 2.7×	30	2.9k
Simone Chevalier Canada	29	1.5k 1.0×	277 0.3×	369 0.8×	445 1.0×	497 1.1×	119	2.9k
Monique A. Spillman United States	23	1.7k 1.2×	735 0.8×	325 0.7×	595 1.3×	581 1.3×	52	2.5k
Stefania Tommasi Italy	28	1.5k 1.1×	688 0.7×	86 0.2×	846 1.9×	828 1.9×	139	2.7k
Anne M. Øyan Norway	37	1.6k 1.2×	282 0.3×	254 0.5×	769 1.7×	809 1.8×	75	2.9k

Countries citing papers authored by Rebecca Sutphen

Since Specialization

Citations

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

Fields of papers citing papers by Rebecca Sutphen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca Sutphen

This figure shows the co-authorship network connecting the top 25 collaborators of Rebecca Sutphen. A scholar is included among the top collaborators of Rebecca Sutphen 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 Rebecca Sutphen. Rebecca Sutphen 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

Armstrong, Joanne, Kristian Lynch, Katherine S. Virgo, et al.. (2021). Utilization, Timing, and Outcomes of BRCA Genetic Testing Among Women With Newly Diagnosed Breast Cancer From a National Commercially Insured Population: The ABOARD Study. JCO Oncology Practice. 17(2). e226–e235. 16 indexed citations

Armstrong, Joanne, Michele Toscano, Sue Friedman, et al.. (2016). Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population. Obstetrical & Gynecological Survey. 71(5). 287–288. 2 indexed citations

Armstrong, Joanne, Michele Toscano, Sue Friedman, et al.. (2014). American BRCA Outcomes and Utilization of Testing (ABOUT) Study: A Pragmatic Research Model that Incorporates Personalized Medicine/Patient‐Centered Outcomes in a Real World Setting. Journal of Genetic Counseling. 24(1). 18–28. 8 indexed citations

Stevens, Kristen N., Linda E. Kelemen, Xianshu Wang, et al.. (2012). Common Variation in Nemo-Like Kinase Is Associated with Risk of Ovarian Cancer. Cancer Epidemiology Biomarkers & Prevention. 21(3). 523–528. 8 indexed citations

Richesson, Rachel, et al.. (2012). The Rare Diseases Clinical Research Network Contact Registry update: Features and functionality. Contemporary Clinical Trials. 33(4). 647–656. 23 indexed citations

Fridley, Brooke L., Prabhakar Chalise, Ya-Yu Tsai, et al.. (2012). Germline Copy Number Variation and Ovarian Cancer Survival. Frontiers in Genetics. 3. 142–142. 9 indexed citations

Sutphen, Rebecca, Heather M. Shappell, Susan T. Vadaparampil, et al.. (2010). Real world experience with cancer genetic counseling via telephone. Familial Cancer. 9(4). 681–689. 34 indexed citations

Sætrom, Pål, Jacob Biesinger, David Smith, et al.. (2009). A Risk Variant in an miR-125b Binding Site in BMPR1B Is Associated with Breast Cancer Pathogenesis. Cancer Research. 69(18). 7459–7465. 118 indexed citations

Carvalho, Marcelo A., Sylvia M. Marsillac, Rachel Karchin, et al.. (2007). Determination of Cancer Risk Associated with Germ Line BRCA1 Missense Variants by Functional Analysis. Cancer Research. 67(4). 1494–1501. 95 indexed citations

10.

Pal, Tuya, et al.. (2007). The presence of germ line mosaicism in cleidocranial dysplasia. Clinical Genetics. 71(6). 589–591. 8 indexed citations

11.

Pal, Tuya, Jenny Permuth‐Wey, Rachna Kapoor, Alan Cantor, & Rebecca Sutphen. (2006). Improved survival in BRCA2 carriers with ovarian cancer. Familial Cancer. 6(1). 113–119. 52 indexed citations

12.

Li, Lihua, Li Chen, Dmitry B. Goldgof, et al.. (2005). Integration of Clinical Information and Gene Expression Profiles for Prediction of Chemo-Response for Ovarian Cancer. PubMed. 2005. 4818–21. 8 indexed citations

13.

Sutphen, Rebecca, et al.. (2004). Comparison of breast magnetic resonance imaging, mammography, and clinical breast exam for surveillance of women at high risk for hereditary breast cancer. Cancer Research. 64. 1094–1094.

14.

Pal, Tuya, et al.. (2004). BRCA1 and BRCA2 mutations in a study of African American breast cancer patients.. PubMed. 13(11 Pt 1). 1794–9. 46 indexed citations

15.

Sutphen, Rebecca, Yan Xu, George D. Wilbanks, et al.. (2004). Lysophospholipids Are Potential Biomarkers of Ovarian Cancer. Cancer Epidemiology Biomarkers & Prevention. 13(7). 1185–1191. 294 indexed citations

16.

Herman, Gail E., Richard I. Kelley, David Glenn Smith, et al.. (2002). Characterization of mutations in 22 females with X-linked dominant chondrodysplasia punctata (Happle syndrome). Genetics in Medicine. 4(6). 434–438. 42 indexed citations

17.

Schurman, Scott J., Rebecca Sutphen, Alfonso Campos, et al.. (2001). Genotype/phenotype observations in African Americans with Bartter syndrome. The Journal of Pediatrics. 139(1). 105–110. 21 indexed citations

18.

Sutphen, Rebecca, et al.. (1999). Severe Lhermitte-Duclos disease with unique germline mutation of PTEN. American Journal of Medical Genetics. 82(4). 290–293. 34 indexed citations

19.

Sutphen, Rebecca, et al.. (1998). Inherited susceptibility to breast and ovarian cancer. Current Opinion in Obstetrics & Gynecology. 10(1). 3–8. 9 indexed citations

20.

Frizell, Edward, et al.. (1998). t(1;18)(q32.1;q22.1) associated with genitourinary malformations. Clinical Genetics. 54(4). 330–333. 4 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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