David Padua

5.1k total citations · 3 hit papers
25 papers, 4.1k citations indexed

About

David Padua is a scholar working on Cancer Research, Molecular Biology and Epidemiology. According to data from OpenAlex, David Padua has authored 25 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cancer Research, 11 papers in Molecular Biology and 7 papers in Epidemiology. Recurrent topics in David Padua's work include Cancer-related molecular mechanisms research (13 papers), MicroRNA in disease regulation (5 papers) and Mycobacterium research and diagnosis (5 papers). David Padua is often cited by papers focused on Cancer-related molecular mechanisms research (13 papers), MicroRNA in disease regulation (5 papers) and Mycobacterium research and diagnosis (5 papers). David Padua collaborates with scholars based in United States, Netherlands and Finland. David Padua's co-authors include Joan Massagué, Qiongqing Wang, William L. Gerald, Paula D. Bos, Sohail F. Tavazoie, Claudio R. Alarcón, Thórdur Óskarsson, Xiang H.-F. Zhang, Cristina Nadal and Roger R. Gomis and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

David Padua

25 papers receiving 4.0k 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.

Endogenous human microRNAs that suppress breast cancer metastasis

2008 1.5k citations Sohail F. Tavazoie, Claudio R. Alarcón et al. Nature profile →
TGFβ Primes Breast Tumors for Lung Metastasis Seeding through Angiopoietin-like 4

2008 747 citations David Padua, Xiang H.-F. Zhang et al. Cell profile →
Roles of TGFβ in metastasis

2008 667 citations David Padua, Joan Massagué Cell Research profile →

Peers

David Padua

ONCOL

PRM

IMMUN

Lingegowda S. Mangala United States

Monica Cantile Italy

Cen Zhang United States

Arthur W. Lambert United States

Miguel F. Segura Spain

Aparna A. Kamat United States

Éric Adriaenssens France

Roger Abounader United States

Johannes H. Schulte Germany

Lin Cheng China

Lingegowda S. Mangala United States

David Padua

2.5k ×0.9

1.3k ×0.7

860 ×0.7

ONCOL

517 ×1.7

PRM

336 ×1.1

IMMUN

Citations per year, relative to David Padua David Padua (= 1×) peers Lingegowda S. Mangala

Countries citing papers authored by David Padua

Since Specialization

Citations

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

Fields of papers citing papers by David Padua

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Padua

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Fang, Kai, Jill M. Hoffman, Ivy Ka Man Law, et al.. (2021). Loss of miR-24-3p promotes epithelial cell apoptosis and impairs the recovery from intestinal inflammation. Cell Death and Disease. 13(1). 8–8. 11 indexed citations

Benhammou, Jihane N., Arthur Ko, Marcus Alvarez, et al.. (2019). Novel Lipid Long Intervening Noncoding RNA, Oligodendrocyte Maturation‐Associated Long Intergenic Noncoding RNA, Regulates the Liver Steatosis Gene Stearoyl‐Coenzyme A Desaturase As an Enhancer RNA. Hepatology Communications. 3(10). 1356–1372. 30 indexed citations

Rankin, Carl R., et al.. (2019). Linear and circular CDKN2B-AS1 expression is associated with Inflammatory Bowel Disease and participates in intestinal barrier formation. Life Sciences. 231. 116571–116571. 34 indexed citations

Rankin, Carl R., et al.. (2019). Overexpressing Long Noncoding RNAs Using Gene-activating CRISPR. Journal of Visualized Experiments. 5 indexed citations

Sauk, Jenny, et al.. (2019). <p>Evaluating tofacitinib citrate in the treatment of moderate-to-severe active ulcerative colitis: design, development and positioning of therapy</p>. Clinical and Experimental Gastroenterology. Volume 12. 179–191. 17 indexed citations

Rankin, Carl R., Christos Polytarchou, Ami Patel, et al.. (2019). miR-24 Is Elevated in Ulcerative Colitis Patients and Regulates Intestinal Epithelial Barrier Function. American Journal Of Pathology. 189(9). 1763–1774. 35 indexed citations

Rankin, Carl R., Ling Shao, Julie Elliott, et al.. (2019). The IBD-associated long noncoding RNA IFNG-AS1 regulates the balance between inflammatory and anti-inflammatory cytokine production after T-cell stimulation. American Journal of Physiology-Gastrointestinal and Liver Physiology. 318(1). G34–G40. 27 indexed citations

Rankin, Carl R., Evangelos A. Theodorou, Ivy Ka Man Law, et al.. (2018). Identification of novel mRNAs and lncRNAs associated with mouse experimental colitis and human inflammatory bowel disease. American Journal of Physiology-Gastrointestinal and Liver Physiology. 315(5). G722–G733. 14 indexed citations

Fang, Kai, Ivy Ka Man Law, David Padua, et al.. (2017). MicroRNA-31-3p Is Involved in Substance P (SP)-Associated Inflammation in Human Colonic Epithelial Cells and Experimental Colitis. American Journal Of Pathology. 188(3). 586–599. 25 indexed citations

10.

Benhammou, Jihane N., et al.. (2017). Gastrointestinal Manifestations of Hereditary Hemorrhagic Telangiectasia (HHT): A Systematic Review of the Literature. Digestive Diseases and Sciences. 62(10). 2623–2630. 39 indexed citations

11.

Law, Ivy Ka Man, David Padua, Dimitrios Iliopoulos, & Charalabos Pothoulakis. (2017). Role of G protein-coupled receptors-microRNA interactions in gastrointestinal pathophysiology. American Journal of Physiology-Gastrointestinal and Liver Physiology. 313(5). G361–G372. 12 indexed citations

12.

Rankin, Carl R., Dimitrios Iliopoulos, Charalabos Pothoulakis, & David Padua. (2017). Gene Expression Profiling Identifies CDKN2B-AS1 as a Long Non-Coding RNA Associated with IBD and Regulated by TGF-Beta. Gastroenterology. 152(5). S144–S144. 4 indexed citations

13.

Law, Ivy Ka Man, David Padua, Dimitrios Iliopoulos, & Charalabos Pothoulakis. (2017). Long Non-Coding RNA (LNCRNA) Profiling Reveals Overexpression of UCA1 and CCAT1 in Human Colonocytes Stimulated by Neurotensin and in Colonic Mucosal Tissues from Ulcerative Colitis (UC) Patients. Gastroenterology. 152(5). S143–S144. 3 indexed citations

14.

Padua, David & Charalabos Pothoulakis. (2015). Novel approaches to treatingClostridium difficile-associated colitis. Expert Review of Gastroenterology & Hepatology. 10(2). 193–204. 7 indexed citations

15.

Padua, David, John P. Vu, Patrizia M. Germano, & Joseph R. Pisegna. (2015). The Role of Neuropeptides in Mouse Models of Colitis. Journal of Molecular Neuroscience. 59(2). 203–210. 24 indexed citations

16.

Pavlović, Svetlana, Yvette Chin, Edi Brogi, et al.. (2013). TGF-β-Id1 Signaling Opposes Twist1 and Promotes Metastatic Colonization via a Mesenchymal-to-Epithelial Transition. Cell Reports. 5(5). 1228–1242. 183 indexed citations

17.

Padua, David & Joan Massagué. (2008). Roles of TGFβ in metastasis. Cell Research. 19(1). 89–102. 667 indexed citations breakdown →

18.

Padua, David, Xiang H.-F. Zhang, Qiongqing Wang, et al.. (2008). TGFβ Primes Breast Tumors for Lung Metastasis Seeding through Angiopoietin-like 4. Cell. 133(1). 66–77. 747 indexed citations breakdown →

19.

Tavazoie, Sohail F., Claudio R. Alarcón, Thórdur Óskarsson, et al.. (2008). Endogenous human microRNAs that suppress breast cancer metastasis. Nature. 451(7175). 147–152. 1527 indexed citations breakdown →

20.

Minn, Andy J., Gaorav P. Gupta, David Padua, et al.. (2007). Lung metastasis genes couple breast tumor size and metastatic spread. Proceedings of the National Academy of Sciences. 104(16). 6740–6745. 299 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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