Nesrine Abboud

468 total citations
19 papers, 351 citations indexed

About

Nesrine Abboud is a scholar working on Immunology, Immunology and Allergy and Hematology. According to data from OpenAlex, Nesrine Abboud has authored 19 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Immunology, 6 papers in Immunology and Allergy and 5 papers in Hematology. Recurrent topics in Nesrine Abboud's work include Atherosclerosis and Cardiovascular Diseases (7 papers), Cell Adhesion Molecules Research (6 papers) and Adipokines, Inflammation, and Metabolic Diseases (4 papers). Nesrine Abboud is often cited by papers focused on Atherosclerosis and Cardiovascular Diseases (7 papers), Cell Adhesion Molecules Research (6 papers) and Adipokines, Inflammation, and Metabolic Diseases (4 papers). Nesrine Abboud collaborates with scholars based in Tunisia, Bahrain and France. Nesrine Abboud's co-authors include Touhami Mahjoub, Wassim Y. Almawi, Lakhdar Ghazouani, Sonia Stefanovic, Michel Pucéat, David Nury, Chad A. Cowan, Sarra Saidi, Nabil Mtiraoui and Walid Zammiti and has published in prestigious journals such as Nature Communications, The Journal of Experimental Medicine and The Journal of Cell Biology.

In The Last Decade

Nesrine Abboud

19 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nesrine Abboud Tunisia 12 129 88 81 73 70 19 351
Thalia Romani de Wit Netherlands 7 83 0.6× 173 2.0× 210 2.6× 58 0.8× 47 0.7× 8 446
Patrick Brien United Kingdom 6 245 1.9× 158 1.8× 98 1.2× 20 0.3× 51 0.7× 8 460
Masatoshi Kanda Japan 11 94 0.7× 161 1.8× 28 0.3× 33 0.5× 11 0.2× 37 363
Mohamed Sabry Egypt 12 196 1.5× 26 0.3× 30 0.4× 30 0.4× 52 0.7× 38 425
Negah Ahmadvand Germany 11 143 1.1× 45 0.5× 25 0.3× 13 0.2× 25 0.4× 16 298
Blanca Soler Palacios Spain 8 116 0.9× 152 1.7× 33 0.4× 20 0.3× 24 0.3× 12 319
Kiave-Yune HoWangYin France 6 210 1.6× 233 2.6× 16 0.2× 28 0.4× 128 1.8× 6 464
Marta Mazzucato Italy 7 95 0.7× 189 2.1× 10 0.1× 47 0.6× 51 0.7× 9 371
Chiara Baggio Italy 10 85 0.7× 46 0.5× 24 0.3× 29 0.4× 86 1.2× 28 275
Xiaocai Yan United States 15 88 0.7× 158 1.8× 23 0.3× 46 0.6× 5 0.1× 26 530

Countries citing papers authored by Nesrine Abboud

Since Specialization
Citations

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

Fields of papers citing papers by Nesrine Abboud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nesrine Abboud

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

All Works

19 of 19 papers shown
1.
Abboud, Nesrine, et al.. (2016). Culture conditions have an impact on the maturation of traceable, transplantable mouse embryonic stem cell-derived otic progenitor cells. Journal of Tissue Engineering and Regenerative Medicine. 11(9). 2629–2642. 14 indexed citations
2.
Abboud, Nesrine, Thomas Moore‐Morris, Henry Yang, et al.. (2015). A cohesin–OCT4 complex mediates Sox enhancers to prime an early embryonic lineage. Nature Communications. 6(1). 6749–6749. 21 indexed citations
3.
Ghazouani, Lakhdar, et al.. (2011). -174G>C interleukin-6 gene polymorphism in Tunisian patients with coronary artery disease. Annals of Saudi Medicine. 31(1). 40–44. 26 indexed citations
4.
Ghazouani, Lakhdar, et al.. (2011). -174G>C Interleukin-6 Gene Polymorphism in Tunisian Patients with Coronary Artery Disease. Annals of Saudi Medicine. 31(1). 40–44. 1 indexed citations
5.
Ghazouani, Lakhdar, et al.. (2010). TNF-α −308G > A and IL-6 −174G > C polymorphisms in Tunisian patients with coronary artery disease. Clinical Biochemistry. 43(13-14). 1085–1089. 25 indexed citations
6.
Abboud, Nesrine, et al.. (2010). Evaluation of the Contribution of Renin Angiotensin System Polymorphisms to the Risk of Coronary Artery Disease Among Tunisians. Genetic Testing and Molecular Biomarkers. 14(5). 661–666. 11 indexed citations
7.
Ghazouani, Lakhdar, Nesrine Abboud, Claire Perret, et al.. (2010). Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians. Molecular Biology Reports. 38(1). 495–501. 7 indexed citations
8.
Ghazouani, Lakhdar, et al.. (2010). Functional interleukin-10 promoter variants in coronary artery disease patients in Tunisia.. PubMed. 21(2). 136–41. 10 indexed citations
9.
Abboud, Nesrine, et al.. (2009). Association of PAI-1 4G/5G and -844G/A Gene Polymorphisms and Changes in PAI-1/Tissue Plasminogen Activator Levels in Myocardial Infarction: A Case–Control Study. Genetic Testing and Molecular Biomarkers. 14(1). 23–27. 30 indexed citations
10.
Abboud, Nesrine, et al.. (2009). Polymorphisms of human platelet alloantigens HPA-1 and HPA-2 associated with severe coronary artery disease. Cardiovascular Pathology. 19(5). 302–307. 9 indexed citations
11.
Ghazouani, Lakhdar, et al.. (2009). –308G>A and –1031T>C tumor necrosis factor gene polymorphisms in Tunisian patients with coronary artery disease. Clinical Chemistry and Laboratory Medicine (CCLM). 47(10). 1247–51. 18 indexed citations
12.
Abboud, Nesrine, et al.. (2009). Human platelet alloantigens HPA-1, HPA-2, and HPA-3 polymorphisms associated with extent of severe coronary artery disease. Journal of Thrombosis and Thrombolysis. 29(4). 409–415. 11 indexed citations
13.
Ghazouani, Lakhdar, Nesrine Abboud, Claire Perret, et al.. (2009). Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population. Journal of Thrombosis and Thrombolysis. 29(1). 114–118. 4 indexed citations
14.
Stefanovic, Sonia, et al.. (2009). Interplay of Oct4 with Sox2 and Sox17: a molecular switch from stem cell pluripotency to specifying a cardiac fate. The Journal of Experimental Medicine. 206(10). i20–i20. 3 indexed citations
15.
Stefanovic, Sonia, et al.. (2009). Interplay of Oct4 with Sox2 and Sox17: a molecular switch from stem cell pluripotency to specifying a cardiac fate. The Journal of Cell Biology. 186(5). 665–673. 84 indexed citations
16.
Ghazouani, Lakhdar, Nesrine Abboud, Claire Perret, et al.. (2008). P-selectin gene polymorphisms and risk of coronary heart disease among Tunisians. Journal of Thrombosis and Thrombolysis. 28(3). 314–319. 4 indexed citations
17.
Ghazouani, Lakhdar, Nesrine Abboud, Nabil Mtiraoui, et al.. (2008). Homocysteine and methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Tunisian patients with severe coronary artery disease. Journal of Thrombosis and Thrombolysis. 27(2). 191–197. 25 indexed citations
18.
Zammiti, Walid, Nabil Mtiraoui, Éric Mercier, et al.. (2006). Association of factor V gene polymorphisms (Leiden; Cambridge; Hong Kong and HR2 haplotype) with recurrent idiopathic pregnancy loss in Tunisia. Thrombosis and Haemostasis. 95(4). 612–617. 25 indexed citations
19.
Zammiti, Walid, Nabil Mtiraoui, Éric Mercier, et al.. (2006). Association of factor V gene polymorphisms (Leiden; Cambridge; Hong Kong and HR2 haplotype) with recurrent idiopathic pregnancy loss in Tunisia. A case-control study.. PubMed. 95(4). 612–7. 23 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

Rankless by CCL
2026