Joseph Washburn

2.4k total citations
11 papers, 478 citations indexed

About

Joseph Washburn is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Joseph Washburn has authored 11 papers receiving a total of 478 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Pathology and Forensic Medicine and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Joseph Washburn's work include RNA Research and Splicing (3 papers), Genomics and Chromatin Dynamics (3 papers) and Molecular Biology Techniques and Applications (2 papers). Joseph Washburn is often cited by papers focused on RNA Research and Splicing (3 papers), Genomics and Chromatin Dynamics (3 papers) and Molecular Biology Techniques and Applications (2 papers). Joseph Washburn collaborates with scholars based in United States, Puerto Rico and United Kingdom. Joseph Washburn's co-authors include Jill A. Macoska, Marcia Cruz‐Correa, Sang Y. Chun, Long H. Dang, Duyen T. Dang, Craig Johnson, Zeng Quan Yang, Stephen P. Ethier, Donna G. Albertson and Michael E. Ray and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer Research and Oncogene.

In The Last Decade

Joseph Washburn

11 papers receiving 476 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph Washburn United States 8 331 155 72 64 55 11 478
Eric Schordan France 12 294 0.9× 119 0.8× 34 0.5× 107 1.7× 108 2.0× 19 482
Eliot Fletcher-Sananikone United States 4 382 1.2× 165 1.1× 21 0.3× 60 0.9× 28 0.5× 5 573
Dachuan Huang Singapore 12 267 0.8× 93 0.6× 63 0.9× 143 2.2× 56 1.0× 20 488
Alessio Iannetti Italy 6 344 1.0× 266 1.7× 26 0.4× 115 1.8× 64 1.2× 6 595
Zhiyong Deng China 12 413 1.2× 318 2.1× 36 0.5× 59 0.9× 29 0.5× 22 570
Jae Hwi Song South Korea 16 388 1.2× 89 0.6× 82 1.1× 131 2.0× 12 0.2× 27 568
Toshihide Nishishita Japan 12 325 1.0× 50 0.3× 48 0.7× 101 1.6× 17 0.3× 13 476
Liyu Wu United States 6 354 1.1× 81 0.5× 58 0.8× 121 1.9× 11 0.2× 8 451
Shian-ling Ding Taiwan 12 252 0.8× 81 0.5× 102 1.4× 79 1.2× 45 0.8× 13 364
Noga Gadir United States 10 696 2.1× 186 1.2× 29 0.4× 99 1.5× 18 0.3× 18 871

Countries citing papers authored by Joseph Washburn

Since Specialization
Citations

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

Fields of papers citing papers by Joseph Washburn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joseph Washburn

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

All Works

11 of 11 papers shown
1.
Kim, Jin Young, Sean A. Misek, Matthew D. Campbell, et al.. (2016). Differential protein expression and basal lamina remodeling in human heart failure. PROTEOMICS - CLINICAL APPLICATIONS. 10(5). 585–596. 34 indexed citations
2.
Gee, Heon Yung, Shazia Ashraf, Xiaoyang Wan, et al.. (2014). Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome. The American Journal of Human Genetics. 94(6). 884–890. 71 indexed citations
3.
Paulsen, Michelle T., Artur Veloso, Jayendra Prasad, et al.. (2013). Coordinated regulation of synthesis and stability of RNA during the acute TNF-induced proinflammatory response. Proceedings of the National Academy of Sciences. 110(6). 2240–2245. 103 indexed citations
4.
Lehoczky, Jessica A., Peedikayil E. Thomas, Kevin M. Patrie, et al.. (2013). A Novel Intergenic ETnII-β Insertion Mutation Causes Multiple Malformations in Polypodia Mice. PLoS Genetics. 9(12). e1003967–e1003967. 4 indexed citations
5.
Chun, Sang Y., Craig Johnson, Joseph Washburn, et al.. (2010). Oncogenic KRAS modulates mitochondrial metabolism in human colon cancer cells by inducing HIF-1α and HIF-2α target genes. Molecular Cancer. 9(1). 293–293. 94 indexed citations
6.
Tazuke, Yuko, Barbara E. Wildhaber, Hua Yang, Joseph Washburn, & Daniel H. Teitelbaum. (2007). Total Parenteral Nutrition Leads to Alteration of Hepatocyte Cell Cycle Gene Expression and Proliferation in the Mouse. Digestive Diseases and Sciences. 52(4). 920–930. 5 indexed citations
7.
Chun, Sang Y., Joseph Washburn, James W. MacDonald, et al.. (2007). CDX2 promotes anchorage-independent growth by transcriptional repression of IGFBP-3. Oncogene. 26(32). 4725–4729. 19 indexed citations
8.
Ray, Michael E., Zeng Quan Yang, Donna G. Albertson, et al.. (2004). Genomic and Expression Analysis of the 8p11–12 Amplicon in Human Breast Cancer Cell Lines. Cancer Research. 64(1). 40–47. 100 indexed citations
9.
Chaı̈b, Hassan, James W. MacDonald, Robert L. Vessella, et al.. (2003). Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors. Genes Chromosomes and Cancer. 37(3). 306–313. 20 indexed citations
10.
Chaı̈b, Hassan, James W. MacDonald, Robert L. Vessella, et al.. (2003). Haploinsufficiency and reduced expression of genes localized to the 8p chromosomal region in human prostate tumors. European Urology Supplements. 2(6). 61–61. 2 indexed citations
11.
Washburn, Joseph, Kirk J. Wojno, Jyotirmoy Dey, Isaac J. Powell, & Jill A. Macoska. (2000). 8pter-p23 deletion is associated with racial differences in prostate cancer outcome.. PubMed. 6(12). 4647–52. 26 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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