Robert D. Burk

922 total citations
13 papers, 696 citations indexed

About

Robert D. Burk is a scholar working on Epidemiology, Surgery and Molecular Biology. According to data from OpenAlex, Robert D. Burk has authored 13 papers receiving a total of 696 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Epidemiology, 2 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Robert D. Burk's work include Cervical Cancer and HPV Research (12 papers), Genital Health and Disease (2 papers) and Reproductive tract infections research (2 papers). Robert D. Burk is often cited by papers focused on Cervical Cancer and HPV Research (12 papers), Genital Health and Disease (2 papers) and Reproductive tract infections research (2 papers). Robert D. Burk collaborates with scholars based in United States, Canada and Costa Rica. Robert D. Burk's co-authors include Seymour L. Romney, Anna S. Kadish, L. Stewart Massad, Joel M. Palefsky, Gloria Y. F. Ho, Jayasri Basu, Prabhudas R. Palan, Magdy S. Mikhail, Rachel G. Fruchter and Laila I. Muderspach and has published in prestigious journals such as Nucleic Acids Research, JNCI Journal of the National Cancer Institute and American Journal of Obstetrics and Gynecology.

In The Last Decade

Robert D. Burk

13 papers receiving 653 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert D. Burk United States 9 620 278 160 156 85 13 696
A. J. C. van den Brule Netherlands 12 876 1.4× 497 1.8× 237 1.5× 151 1.0× 109 1.3× 15 982
Mariana García Panama 9 605 1.0× 210 0.8× 92 0.6× 181 1.2× 53 0.6× 13 757
Xiao-Wei Sun China 7 515 0.8× 279 1.0× 125 0.8× 142 0.9× 37 0.4× 12 627
Rolando Herrero United States 6 692 1.1× 297 1.1× 102 0.6× 140 0.9× 74 0.9× 7 765
Eileen Dareng United States 16 498 0.8× 161 0.6× 154 1.0× 178 1.1× 132 1.6× 30 685
Brahim Qadadri United States 13 628 1.0× 333 1.2× 154 1.0× 85 0.5× 63 0.7× 22 697
Cornelis J.A. Hogewoning Netherlands 12 774 1.2× 607 2.2× 127 0.8× 78 0.5× 64 0.8× 16 910
M. Santamaria Spain 9 962 1.6× 432 1.6× 128 0.8× 244 1.6× 114 1.3× 11 1.1k
Joel Palefsky United States 5 471 0.8× 252 0.9× 84 0.5× 99 0.6× 29 0.3× 8 524
Michelle Garcia Discacciati Brazil 14 320 0.5× 102 0.4× 206 1.3× 81 0.5× 52 0.6× 35 502

Countries citing papers authored by Robert D. Burk

Since Specialization
Citations

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

Fields of papers citing papers by Robert D. Burk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert D. Burk. 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 Robert D. Burk. The network helps show where Robert D. Burk may publish in the future.

Co-authorship network of co-authors of Robert D. Burk

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

All Works

13 of 13 papers shown
1.
Castle, Philip E., Ana Cecilia Rodríguez, Robert D. Burk, et al.. (2009). Short term persistence of human papillomavirus and risk of cervical precancer and cancer: population based cohort study. BMJ. 339(jul28 2). b2569–b2569. 149 indexed citations
2.
Rojas, Mary, et al.. (2007). 7: Cervical, anal, and oral HPV among sexually active urban adolescent females. Journal of Adolescent Health. 40(2). S9–S9. 1 indexed citations
3.
Li, Rui, A Levine, L. Stewart Massad, et al.. (2004). Highly Active Antiretroviral Therapy and Cervical Squamous Intraepithelial Lesions in Human Immunodeficiency Virus-Positive Women. JNCI Journal of the National Cancer Institute. 96(14). 1070–1076. 81 indexed citations
4.
Einstein, Mark H. & Robert D. Burk. (2001). Persistent human papillomavirus infection: Definitions and clinical implications. 12(5). 119–123. 9 indexed citations
5.
Terai, Masanori & Robert D. Burk. (2001). Complete Nucleotide Sequence and Analysis of a Novel Human Papillomavirus (HPV 84) Genome Cloned by an Overlapping PCR Method. Virology. 279(1). 109–115. 29 indexed citations
6.
Massad, L. Stewart, Katherine Riester, Kathryn Anastos, et al.. (1999). Prevalence and Predictors of Squamous Cell Abnormalities in Papanicolaou Smears From Women Infected With HIV-1. JAIDS Journal of Acquired Immune Deficiency Syndromes. 21(1). 33–41. 163 indexed citations
7.
Ho, Gloria Y. F., Anna S. Kadish, Robert D. Burk, et al.. (1998). HPV 16 and cigarette smoking as risk factors for high-grade cervical intra-epithelial neoplasia. International Journal of Cancer. 78(3). 281–285. 123 indexed citations
8.
Bierman, Robert, et al.. (1998). Natural History of Cervicovaginal Papillomavirus Infection in Young Women GYF Ho. Journal of Lower Genital Tract Disease. 2(4). 235–235. 27 indexed citations
9.
Maiman, Mitchell, et al.. (1998). Prevalence, Risk Factors, and Accuracy of Cytologic Screening for Cervical Intraepithelial Neoplasia in Women with the Human Immunodeficiency Virus. Journal of Lower Genital Tract Disease. 2(4). 233–233. 8 indexed citations
10.
Ranst, Marc Van, et al.. (1992). Primary structure of the E6 protein ofMicromys minutuspapillomavirus andMastomys natalensispapillomavirus. Nucleic Acids Research. 20(11). 2889–2889. 7 indexed citations
11.
Brandsma, Janet L., Robert D. Burk, Wayne D. Lancaster, Herbert Pfister, & Mark H. Schiffman. (1989). Inter‐laboratory variation as an explanation for varying prevalence estimates of human papillomavirus infection. International Journal of Cancer. 43(2). 260–262. 48 indexed citations
12.
Kadish, Anna S., et al.. (1988). Detection of human papillomavirus deoxyribonucleic acid in exfoliated cervicovaginal cells as a predictor of cervical neoplasia in a high-risk population. American Journal of Obstetrics and Gynecology. 159(6). 1517–1525. 50 indexed citations
13.
Sundberg, J P, et al.. (1987). Host immune responses to genital and laryngeal papillomavirus infections.. The Mouseion at the JAXlibrary (Jackson Laboratory). 387. 1 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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