David W. Stepp

6.0k total citations
106 papers, 4.7k citations indexed

About

David W. Stepp is a scholar working on Physiology, Cardiology and Cardiovascular Medicine and Molecular Biology. According to data from OpenAlex, David W. Stepp has authored 106 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Physiology, 36 papers in Cardiology and Cardiovascular Medicine and 29 papers in Molecular Biology. Recurrent topics in David W. Stepp's work include Nitric Oxide and Endothelin Effects (31 papers), Adipose Tissue and Metabolism (14 papers) and Eicosanoids and Hypertension Pharmacology (11 papers). David W. Stepp is often cited by papers focused on Nitric Oxide and Endothelin Effects (31 papers), Adipose Tissue and Metabolism (14 papers) and Eicosanoids and Hypertension Pharmacology (11 papers). David W. Stepp collaborates with scholars based in United States, China and Canada. David W. Stepp's co-authors include David Fulton, Jefferson C. Frisbee, William M. Chilian, Yasuhiro Nishikawa, James Mintz, Feng Chen, R. Daniel Rudic, Eric J. Belin de Chantemèle, David M. Pollock and Ciprian B. Anea and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Circulation.

In The Last Decade

David W. Stepp

105 papers receiving 4.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David W. Stepp United States	41	2.0k	1.3k	1.3k	667	616	106	4.7k
Lin Chang United States	37	1.6k 0.8×	1.2k 1.0×	1.4k 1.1×	551 0.8×	483 0.8×	98	5.0k
Axel Gödecke Germany	40	2.4k 1.2×	2.4k 1.9×	1.5k 1.2×	357 0.5×	320 0.5×	95	5.9k
Zsolt Bagi United States	38	1.8k 0.9×	1.3k 1.0×	1.2k 1.0×	238 0.4×	391 0.6×	118	4.7k
William G. Mayhan United States	47	2.6k 1.3×	1.3k 1.0×	1.9k 1.5×	640 1.0×	309 0.5×	172	6.6k
Gregory D. Fink United States	43	1.9k 0.9×	1.2k 0.9×	2.7k 2.2×	721 1.1×	250 0.4×	181	5.7k
Pawel M. Kaminski United States	35	2.4k 1.2×	1.5k 1.2×	1.3k 1.0×	206 0.3×	682 1.1×	68	4.9k
Gillian A. Gray United Kingdom	38	2.9k 1.5×	1.4k 1.1×	2.2k 1.7×	252 0.4×	435 0.7×	131	5.5k
Tomio Okamura Japan	33	2.1k 1.1×	781 0.6×	1.2k 0.9×	459 0.7×	182 0.3×	167	4.1k
Hai‐Jian Sun China	39	873 0.4×	2.1k 1.7×	781 0.6×	301 0.5×	579 0.9×	155	5.3k
Jo G. R. De Mey Netherlands	39	2.5k 1.2×	1.8k 1.4×	2.0k 1.6×	289 0.4×	300 0.5×	172	5.9k

Countries citing papers authored by David W. Stepp

Since Specialization

Citations

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

Fields of papers citing papers by David W. Stepp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David W. Stepp

This figure shows the co-authorship network connecting the top 25 collaborators of David W. Stepp. A scholar is included among the top collaborators of David W. Stepp 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 W. Stepp. David W. Stepp 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

Bordán, Zsuzsanna, Yuqing Huo, Feng Chen, et al.. (2025). PFKFB3 Connects Glycolytic Metabolism with Endothelial Dysfunction in Human and Rodent Obesity. Antioxidants. 14(2). 172–172.

Bruder‐Nascimento, Thiago, David W. Stepp, Rodger D. MacArthur, et al.. (2025). CD4 ⁺ T Cells Expressing Viral Proteins Induce HIV-Associated Endothelial Dysfunction and Hypertension Through Interleukin 1α–Mediated Increases in Endothelial NADPH Oxidase 1. Circulation. 151(16). 1187–1203. 5 indexed citations

Larion, Sebastian, James Mintz, Jennifer Thompson, et al.. (2024). NADPH oxidase 1 promotes hepatic steatosis in obese mice and is abrogated by augmented skeletal muscle mass. American Journal of Physiology-Gastrointestinal and Liver Physiology. 326(3). G264–G273. 3 indexed citations

Bordán, Zsuzsanna, Stephen Haigh, Xueyi Li, et al.. (2024). PDZ-Binding Kinase, a Novel Regulator of Vascular Remodeling in Pulmonary Arterial Hypertension. Circulation. 150(5). 393–410. 5 indexed citations

Haigh, Stephen, James Mintz, Ryan A. Harris, et al.. (2023). Galectin-3 Mediates Vascular Dysfunction in Obesity by Regulating NADPH Oxidase 1. Arteriosclerosis Thrombosis and Vascular Biology. 43(10). e381–e395. 10 indexed citations

Mintz, James, Stephen Haigh, Jeremy Sword, et al.. (2023). Early Endothelial Dysfunction in a Novel Model of Sustained Hyperphagia and Obesity in Mice Using a Brain Targeting Adeno-Associated Virus. Arteriosclerosis Thrombosis and Vascular Biology. 43(8). 1592–1594. 3 indexed citations

He, Xiangqin, Jian Shen, Guoqing Hu, et al.. (2023). The Long Noncoding RNA Cardiac Mesoderm Enhancer-Associated Noncoding RNA (Carmn) Is a Critical Regulator of Gastrointestinal Smooth Muscle Contractile Function and Motility. Gastroenterology. 165(1). 71–87. 10 indexed citations

Larion, Sebastian, et al.. (2022). The biological clock enhancer nobiletin ameliorates steatosis in genetically obese mice by restoring aberrant hepatic circadian rhythm. American Journal of Physiology-Gastrointestinal and Liver Physiology. 323(4). G387–G400. 19 indexed citations

Rodriguez‐Miguelez, Paula, Jinhee Jeong, Jeffrey Thomas, et al.. (2022). Endothelin‐1 response to whole‐body vibration in obese and normal weight individuals. Physiological Reports. 10(10). e15335–e15335. 4 indexed citations

10.

Cusworth, Daniel, Andrew K. Thorpe, Alana Ayasse, et al.. (2022). Strong methane point sources contribute a disproportionate fraction of total emissions across multiple basins in the United States. Proceedings of the National Academy of Sciences. 119(38). e2202338119–e2202338119. 67 indexed citations

11.

Guha, Avirup, Xiaoling Wang, Ryan A. Harris, et al.. (2021). Obesity and the Bidirectional Risk of Cancer and Cardiovascular Diseases in African Americans: Disparity vs. Ancestry. Frontiers in Cardiovascular Medicine. 8. 761488–761488. 14 indexed citations

12.

Benson, Tyler W., Neal L. Weintraub, Ha Won Kim, et al.. (2018). A single high-fat meal provokes pathological erythrocyte remodeling and increases myeloperoxidase levels: implications for acute coronary syndrome. Laboratory Investigation. 98(10). 1300–1310. 22 indexed citations

13.

Mohamed, Riyaz, Calpurnia Jayakumar, Feng Chen, et al.. (2015). Low-Dose IL-17 Therapy Prevents and Reverses Diabetic Nephropathy, Metabolic Syndrome, and Associated Organ Fibrosis. Journal of the American Society of Nephrology. 27(3). 745–765. 101 indexed citations

14.

Chantemèle, Eric J. Belin de, M. Irfan Ali, James Mintz, et al.. (2012). Increasing Peripheral Insulin Sensitivity by Protein Tyrosine Phosphatase 1B Deletion Improves Control of Blood Pressure in Obesity. Hypertension. 60(5). 1273–1279. 22 indexed citations

15.

Chantemèle, Eric J. Belin de, James Mintz, William E. Rainey, & David W. Stepp. (2011). Impact of Leptin-Mediated Sympatho-Activation on Cardiovascular Function in Obese Mice. Hypertension. 58(2). 271–279. 82 indexed citations

16.

Romero, Maritza J., Jennifer A. Iddings, Daniel Platt, et al.. (2011). Diabetes-induced vascular dysfunction involves arginase I. American Journal of Physiology-Heart and Circulatory Physiology. 302(1). H159–H166. 74 indexed citations

17.

Ketsawatsomkron, Pimonrat, David W. Stepp, David Fulton, & Mario B. Marrero. (2010). Molecular mechanism of angiotensin II-induced insulin resistance in aortic vascular smooth muscle cells: Roles of Protein Tyrosine Phosphatase-1B. Vascular Pharmacology. 53(3-4). 160–168. 11 indexed citations

18.

Quigley, Jeffrey E., Ahmed A. Elmarakby, Sarah Knight, et al.. (2009). OBESITY INDUCED RENAL OXIDATIVE STRESS CONTRIBUTES TO RENAL INJURY IN SALT‐SENSITIVE HYPERTENSION. Clinical and Experimental Pharmacology and Physiology. 36(7). 724–728. 23 indexed citations

19.

Prakash, Rajan, James Mintz, & David W. Stepp. (2006). Impact of Obesity on Coronary Microvascular Function in the Zucker Rat. Microcirculation. 13(5). 389–396. 24 indexed citations

20.

Stepp, David W., et al.. (2005). Reduced constrictor reactivity balances impaired vasodilation in the mesenteric circulation of the obese Zucker rat. American Journal of Physiology-Heart and Circulatory Physiology. 289(5). H2097–H2102. 36 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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