David M. Winder

1.3k total citations
17 papers, 980 citations indexed

About

David M. Winder is a scholar working on Molecular Biology, Epidemiology and Surgery. According to data from OpenAlex, David M. Winder has authored 17 papers receiving a total of 980 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Epidemiology and 6 papers in Surgery. Recurrent topics in David M. Winder's work include Cervical Cancer and HPV Research (8 papers), Head and Neck Cancer Studies (5 papers) and Genital Health and Disease (3 papers). David M. Winder is often cited by papers focused on Cervical Cancer and HPV Research (8 papers), Head and Neck Cancer Studies (5 papers) and Genital Health and Disease (3 papers). David M. Winder collaborates with scholars based in United Kingdom, Germany and Austria. David M. Winder's co-authors include Margaret Stanley, Peter Goon, Brian Salmons, Jane Sterling, Volker Erfle, Mark R. Pett, Ian Roberts, Nicholas Coleman, Balaji Muralidhar and Walter H. Günzburg and has published in prestigious journals such as Cancer Research, Biochemical and Biophysical Research Communications and The Journal of Pathology.

In The Last Decade

David M. Winder

17 papers receiving 945 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David M. Winder United Kingdom 16 415 384 232 210 189 17 980
Caroline A.J. Horvath Belgium 11 379 0.9× 271 0.7× 119 0.5× 71 0.3× 80 0.4× 13 722
Peter C. Angeletti United States 17 437 1.1× 427 1.1× 125 0.5× 97 0.5× 228 1.2× 38 975
Davin C. Dillon United States 18 591 1.4× 547 1.4× 171 0.7× 25 0.1× 157 0.8× 23 1.4k
Deílson Elgui de Oliveira Brazil 16 208 0.5× 201 0.5× 72 0.3× 15 0.1× 493 2.6× 38 862
Valerie Zacny United States 9 497 1.2× 319 0.8× 64 0.3× 17 0.1× 364 1.9× 10 925
Joongho Joh United States 13 339 0.8× 185 0.5× 69 0.3× 27 0.1× 160 0.8× 31 654
Harald zur Hausen Germany 5 750 1.8× 333 0.9× 186 0.8× 49 0.2× 267 1.4× 5 1.0k
Joanna L. Parish United Kingdom 21 590 1.4× 561 1.5× 103 0.4× 24 0.1× 310 1.6× 41 1.2k
Günter Krämmer Germany 7 720 1.7× 449 1.2× 139 0.6× 54 0.3× 173 0.9× 7 1.1k
Min Tan United States 14 418 1.0× 367 1.0× 55 0.2× 5 0.0× 292 1.5× 39 965

Countries citing papers authored by David M. Winder

Since Specialization
Citations

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

Fields of papers citing papers by David M. Winder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David M. Winder

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

All Works

17 of 17 papers shown
1.
Masterson, Liam, David M. Winder, Martin Lehmann, et al.. (2016). Molecular analyses of unselected head and neck cancer cases demonstrates that human papillomavirus transcriptional activity is positively associated with survival and prognosis. BMC Cancer. 16(1). 367–367. 4 indexed citations
2.
Masterson, Liam, Frédéric Sorgeloos, David M. Winder, et al.. (2015). Deregulation of SYCP2 predicts early stage human papillomavirus‐positive oropharyngeal carcinoma: A prospective whole transcriptome analysis. Cancer Science. 106(11). 1568–1575. 42 indexed citations
3.
Winder, David M., et al.. (2013). Detection of specific HPV subtypes responsible for the pathogenesis of condylomata acuminata. Virology Journal. 10(1). 137–137. 44 indexed citations
4.
Stanley, Margaret, David M. Winder, Jane Sterling, & Peter Goon. (2012). HPV infection, anal intra-epithelial neoplasia (AIN) and anal cancer: current issues. BMC Cancer. 12(1). 398–398. 68 indexed citations
5.
Muralidhar, Balaji, David M. Winder, Matthew J. Murray, et al.. (2011). Functional evidence that Drosha overexpression in cervical squamous cell carcinoma affects cell phenotype and microRNA profiles. The Journal of Pathology. 224(4). 496–507. 62 indexed citations
6.
Crawford, Robin, Sarah Kitson, David M. Winder, et al.. (2011). High prevalence of HPV in non-cervical sites of women with abnormal cervical cytology. BMC Cancer. 11(1). 473–473. 35 indexed citations
7.
Winder, David M., Anasuya Chattopadhyay, Balaji Muralidhar, et al.. (2011). Overexpression of the oncostatin M receptor in cervical squamous cell carcinoma cells is associated with a pro‐angiogenic phenotype and increased cell motility and invasiveness. The Journal of Pathology. 225(3). 448–462. 35 indexed citations
8.
Sudhoff, Holger, Hartmut Schwarze, David M. Winder, et al.. (2011). Evidence for a causal association for HPV in head and neck cancers. European Archives of Oto-Rhino-Laryngology. 268(11). 1541–1547. 42 indexed citations
9.
Winder, David M., et al.. (2011). Analyses of human papillomavirus genotypes and viral loads in anogenital warts. Journal of Medical Virology. 83(8). 1345–1350. 66 indexed citations
10.
Gray, Elizabeth H., Mark R. Pett, David M. Winder, et al.. (2010). In vitro Progression of Human Papillomavirus 16 Episome-Associated Cervical Neoplasia Displays Fundamental Similarities to Integrant-Associated Carcinogenesis. Cancer Research. 70(10). 4081–4091. 71 indexed citations
11.
Winder, David M., Yin Ling Woo, Jane Sterling, et al.. (2009). Sensitive HPV detection in oropharyngeal cancers. BMC Cancer. 9(1). 440–440. 31 indexed citations
12.
Scarpini, Cinzia G., Ian Roberts, David M. Winder, et al.. (2008). Characterization of Naturally Occurring HPV16 Integration Sites Isolated from Cervical Keratinocytes under Noncompetitive Conditions. Cancer Research. 68(20). 8249–8259. 77 indexed citations
13.
Ng, Grace, David M. Winder, Balaji Muralidhar, et al.. (2007). Gain and overexpression of the oncostatin M receptor occur frequently in cervical squamous cell carcinoma and are associated with adverse clinical outcome. The Journal of Pathology. 212(3). 325–334. 39 indexed citations
14.
Sparmann, Gisela, Christine Hohenadl, Jens Tornøe, et al.. (2004). Generation and characterization of immortalized rat pancreatic stellate cells. American Journal of Physiology-Gastrointestinal and Liver Physiology. 287(1). G211–G219. 52 indexed citations
15.
Nikol, Sigrid, Tanya Y. Huehns, Eberhard Krausz, et al.. (1999). Needle injection catheter delivery of the gene for an antibacterial agent inhibits neointimal formation. Gene Therapy. 6(5). 737–748. 34 indexed citations
16.
Erfle, Volker, Markus Neumann, David M. Winder, et al.. (1998). Antimicrobial peptides melittin and cecropin inhibit replication of human immunodeficiency virus 1 by suppressing viral gene expression.. Journal of General Virology. 79(4). 731–740. 196 indexed citations
17.
Winder, David M., Walter H. Günzburg, Volker Erfle, & Brian Salmons. (1998). Expression of Antimicrobial Peptides Has an Antitumour Effect in Human Cells. Biochemical and Biophysical Research Communications. 242(3). 608–612. 82 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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