Raja Fayad

3.0k total citations
47 papers, 2.2k citations indexed

About

Raja Fayad is a scholar working on Epidemiology, Immunology and Molecular Biology. According to data from OpenAlex, Raja Fayad has authored 47 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Epidemiology, 16 papers in Immunology and 10 papers in Molecular Biology. Recurrent topics in Raja Fayad's work include Adipokines, Inflammation, and Metabolic Diseases (16 papers), IL-33, ST2, and ILC Pathways (6 papers) and Regulation of Appetite and Obesity (5 papers). Raja Fayad is often cited by papers focused on Adipokines, Inflammation, and Metabolic Diseases (16 papers), IL-33, ST2, and ILC Pathways (6 papers) and Regulation of Appetite and Obesity (5 papers). Raja Fayad collaborates with scholars based in United States, India and Hong Kong. Raja Fayad's co-authors include Arpit Saxena, Giamila Fantuzzi, Manjeshwar Shrinath Baliga, Joseph A. Sennello, Maria Pini, E. Angela Murphy, Mitzi Nagarkatti, Prakash Nagarkatti, Robert L. Price and Udai P. Singh and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Immunology and Gastroenterology.

In The Last Decade

Raja Fayad

46 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raja Fayad United States 29 581 547 419 373 370 47 2.2k
Fausto Sánchez‐Muñoz Mexico 26 779 1.3× 470 0.9× 435 1.0× 347 0.9× 337 0.9× 117 2.3k
Marina Korotkova Sweden 30 709 1.2× 382 0.7× 324 0.8× 316 0.8× 271 0.7× 77 2.5k
Isaías Dichi Brazil 29 649 1.1× 366 0.7× 369 0.9× 515 1.4× 199 0.5× 96 2.5k
Junpeng Wang China 28 819 1.4× 319 0.6× 648 1.5× 190 0.5× 143 0.4× 102 2.7k
Fabrício Rios-Santos Brazil 19 531 0.9× 214 0.4× 276 0.7× 229 0.6× 251 0.7× 42 1.8k
Joilson O. Martins Brazil 26 360 0.6× 466 0.9× 373 0.9× 237 0.6× 173 0.5× 67 1.8k
Elizabeth A. Mann United States 29 812 1.4× 432 0.8× 274 0.7× 246 0.7× 275 0.7× 63 2.4k
Caroline B. Appleyard Puerto Rico 24 577 1.0× 246 0.4× 482 1.2× 210 0.6× 421 1.1× 65 2.0k
Belén Beltrán Spain 29 887 1.5× 786 1.4× 424 1.0× 444 1.2× 960 2.6× 117 3.1k

Countries citing papers authored by Raja Fayad

Since Specialization
Citations

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

Fields of papers citing papers by Raja Fayad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raja Fayad

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

All Works

20 of 20 papers shown
1.
Narsale, Aditi, Reilly T. Enos, Melissa Puppa, et al.. (2015). Liver Inflammation and Metabolic Signaling in ApcMin/+ Mice: The Role of Cachexia Progression. PLoS ONE. 10(3). e0119888–e0119888. 46 indexed citations
2.
Rothenberg, Sarah E., Susan Korrick, & Raja Fayad. (2015). The influence of obesity on blood mercury levels for U.S. non-pregnant adults and children: NHANES 2007–2010. Environmental Research. 138. 173–180. 55 indexed citations
3.
Kaur, Kamaljeet, Arpit Saxena, Emma Fletcher, et al.. (2015). Mucus mediated protection against acute colitis in adiponectin deficient mice. Journal of Inflammation. 12(1). 35–35. 17 indexed citations
4.
Singh, Udai P., Narendra P. Singh, E. Angela Murphy, et al.. (2015). Chemokine and cytokine levels in inflammatory bowel disease patients. Cytokine. 77. 44–49. 240 indexed citations
5.
Khori, Vahid, Sadegh Amani-Shalamzari, Ali Mohammad Alizadeh, et al.. (2015). Effects of exercise training together with tamoxifen in reducing mammary tumor burden in mice: Possible underlying pathway of miR-21. European Journal of Pharmacology. 765. 179–187. 66 indexed citations
6.
Turner‐McGrievy, Gabrielle, Michael D. Wirth, Nitin Shivappa, et al.. (2014). Randomization to plant-based dietary approaches leads to larger short-term improvements in Dietary Inflammatory Index scores and macronutrient intake compared with diets that contain meat. Nutrition Research. 35(2). 97–106. 84 indexed citations
7.
Steiner, Jennifer L., John M. Davis, James A. Carson, et al.. (2014). Dose-dependent benefits of quercetin on tumorigenesis in the C3(1)/SV40Tag transgenic mouse model of breast cancer. Cancer Biology & Therapy. 15(11). 1456–1467. 36 indexed citations
8.
Saxena, Arpit, Manjeshwar Shrinath Baliga, Venkatesh Ponemone, et al.. (2013). Mucus and adiponectin deficiency: role in chronic inflammation-induced colon cancer. International Journal of Colorectal Disease. 28(9). 1267–1279. 40 indexed citations
9.
Jung, Seung Ho, Arpit Saxena, Kamaljeet Kaur, et al.. (2012). The role of adipose tissue-associated macrophages and T lymphocytes in the pathogenesis of inflammatory bowel disease. Cytokine. 61(2). 459–468. 14 indexed citations
10.
Saxena, Arpit, et al.. (2012). Effect of exercise on chemically-induced colitis in adiponectin deficient mice. Journal of Inflammation. 9(1). 30–30. 47 indexed citations
11.
Saxena, Arpit, Alexander A. Chumanevich, Emma Fletcher, et al.. (2011). Adiponectin and Selenium: Role in chronic inflammation induced colon cancer. Inflammatory Bowel Diseases. 17. S77–S77. 1 indexed citations
12.
Saxena, Arpit, Alexander A. Chumanevich, Emma Fletcher, et al.. (2011). Adiponectin deficiency: Role in chronic inflammation induced colon cancer. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(4). 527–536. 69 indexed citations
13.
Ponemone, Venkatesh, Ali Keshavarzian, Marc I. Brand, et al.. (2010). Apoptosis and Inflammation: Role of Adipokines in Inflammatory Bowel Disease. Clinical and Translational Gastroenterology. 1(10). e1–e1. 25 indexed citations
14.
15.
16.
Pini, Maria, et al.. (2008). Adiponectin deficiency does not affect development and progression of spontaneous colitis in IL-10 knockout mice. American Journal of Physiology-Gastrointestinal and Liver Physiology. 296(2). G382–G387. 23 indexed citations
17.
Fayad, Raja, et al.. (2006). Apoptosis resistance in ulcerative colitis: High expression of decoy receptors by lamina propria T cells. European Journal of Immunology. 36(8). 2215–2222. 36 indexed citations
18.
Huang, Yujun, et al.. (2005). Induction of Mucosal and Systemic Immune Responses against Human Carcinoembryonic Antigen by an Oral Vaccine. Cancer Research. 65(15). 6990–6999. 18 indexed citations
19.
Sennello, Joseph A., Raja Fayad, Alison Morris, et al.. (2005). Regulation of T Cell-Mediated Hepatic Inflammation by Adiponectin and Leptin. Endocrinology. 146(5). 2157–2164. 80 indexed citations
20.
Fayad, Raja, Hongtao Zhang, Daniel G. Quinn, Yujun Huang, & Liang Qiao. (2004). Oral Administration with Papillomavirus Pseudovirus Encoding IL-2 Fully Restores Mucosal and Systemic Immune Responses to Vaccinations in Aged Mice. The Journal of Immunology. 173(4). 2692–2698. 15 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Fausto Sánchez‐Muñoz Breakdown of academic impact, for papers by Marina Korotkova Breakdown of academic impact, for papers by Isaías Dichi Breakdown of academic impact, for papers by Junpeng Wang Breakdown of academic impact, for papers by Fabrício Rios-Santos Breakdown of academic impact, for papers by Joilson O. Martins Breakdown of academic impact, for papers by Elizabeth A. Mann Breakdown of academic impact, for papers by Caroline B. Appleyard Breakdown of academic impact, for papers by Belén Beltrán
Rankless by CCL
2026