Naïma Bellili-Muñoz

426 total citations
12 papers, 321 citations indexed

About

Naïma Bellili-Muñoz is a scholar working on Molecular Biology, Nephrology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Naïma Bellili-Muñoz has authored 12 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Nephrology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Naïma Bellili-Muñoz's work include Birth, Development, and Health (3 papers), Advanced Glycation End Products research (3 papers) and Chronic Kidney Disease and Diabetes (3 papers). Naïma Bellili-Muñoz is often cited by papers focused on Birth, Development, and Health (3 papers), Advanced Glycation End Products research (3 papers) and Chronic Kidney Disease and Diabetes (3 papers). Naïma Bellili-Muñoz collaborates with scholars based in France, Brazil and United States. Naïma Bellili-Muñoz's co-authors include Gilberto Velho, Michel Marre, Ronan Roussel, Frédéric Fumeron, Samy Hadjadj, Kamel Mohammedi, Fathi Driss, Thiago A. Patente, François Alhenc‐Gelas and Nadine Bouby and has published in prestigious journals such as PLoS ONE, Diabetes Care and Diabetes.

In The Last Decade

Naïma Bellili-Muñoz

12 papers receiving 314 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Naïma Bellili-Muñoz France 10 117 68 67 52 49 12 321
Kazuhiko Nishi Japan 11 76 0.6× 52 0.8× 35 0.5× 65 1.3× 23 0.5× 39 368
Ceyda Kabaroğlu Türkiye 12 117 1.0× 35 0.5× 89 1.3× 26 0.5× 48 1.0× 26 439
Liliana Ercole Spain 11 97 0.8× 58 0.9× 82 1.2× 54 1.0× 127 2.6× 14 433
J. Green Israel 10 70 0.6× 41 0.6× 35 0.5× 85 1.6× 56 1.1× 10 339
Bruno Sevá Pessôa Netherlands 7 100 0.9× 104 1.5× 31 0.5× 24 0.5× 143 2.9× 8 322
Carolina Hernández-Carballo Spain 9 97 0.8× 95 1.4× 30 0.4× 185 3.6× 36 0.7× 17 415
Radmila Obrenović Serbia 12 49 0.4× 24 0.4× 29 0.4× 58 1.1× 44 0.9× 39 336
Adela Brahimaj Netherlands 9 116 1.0× 144 2.1× 19 0.3× 79 1.5× 54 1.1× 9 404
Tetsutaro Matayoshi Japan 12 83 0.7× 104 1.5× 68 1.0× 41 0.8× 192 3.9× 25 403
B Łacka Poland 10 99 0.8× 146 2.1× 54 0.8× 63 1.2× 144 2.9× 24 424

Countries citing papers authored by Naïma Bellili-Muñoz

Since Specialization
Citations

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

Fields of papers citing papers by Naïma Bellili-Muñoz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Naïma Bellili-Muñoz. 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 Naïma Bellili-Muñoz. The network helps show where Naïma Bellili-Muñoz may publish in the future.

Co-authorship network of co-authors of Naïma Bellili-Muñoz

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

All Works

12 of 12 papers shown
1.
Mohammedi, Kamel, Jean‐Philippe Bastard, Soraya Fellahi, et al.. (2017). T-cadherin gene variants are associated with nephropathy in subjects with type 1 diabetes. Nephrology Dialysis Transplantation. 32(12). 1987–1993. 3 indexed citations
2.
Mohammedi, Kamel, Jean‐Philippe Bastard, Soraya Fellahi, et al.. (2017). T-cadherin gene variants are associated with nephropathy in subjects with type 1 diabetes. Nephrology Dialysis Transplantation. 32(12). 2144–2144. 5 indexed citations
3.
Gautier, Jean–François, Raphaël Porcher, Charbel Abi Khalil, et al.. (2015). Kidney Dysfunction in Adult Offspring Exposed In Utero to Type 1 Diabetes Is Associated with Alterations in Genome-Wide DNA Methylation. PLoS ONE. 10(8). e0134654–e0134654. 20 indexed citations
4.
Mohammedi, Kamel, Thiago A. Patente, Naïma Bellili-Muñoz, et al.. (2015). Glutathione peroxidase-1 gene (GPX1) variants, oxidative stress and risk of kidney complications in people with type 1 diabetes. Metabolism. 65(2). 12–19. 40 indexed citations
5.
Patente, Thiago A., Kamel Mohammedi, Naïma Bellili-Muñoz, et al.. (2015). Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes. Free Radical Biology and Medicine. 86. 16–24. 20 indexed citations
6.
Velho, Gilberto, Stéphanie Ragot, Kamel Mohammedi, et al.. (2015). Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Kidney Disease in People With Type 2 Diabetes. Diabetes. 64(9). 3262–3272. 13 indexed citations
7.
Lamri, Amel, Naïma Bellili-Muñoz, Jean‐Michel Halimi, et al.. (2015). ABCG8 polymorphisms and renal disease in type 2 diabetic patients. Metabolism. 64(6). 713–719. 11 indexed citations
8.
Mohammedi, Kamel, Naïma Bellili-Muñoz, Fathi Driss, et al.. (2014). Manganese Superoxide Dismutase (SOD2) Polymorphisms, Plasma Advanced Oxidation Protein Products (AOPP) Concentration and Risk of Kidney Complications in Subjects with Type 1 Diabetes. PLoS ONE. 9(5). e96916–e96916. 32 indexed citations
9.
Mohammedi, Kamel, Naïma Bellili-Muñoz, Stefan L. Marklund, et al.. (2014). Plasma extracellular superoxide dismutase concentration, allelic variations in the SOD3 gene and risk of myocardial infarction and all-cause mortality in people with type 1 and type 2 diabetes. Cardiovascular Diabetology. 14(1). 845–845. 42 indexed citations
10.
Velho, Gilberto, Nadine Bouby, Samy Hadjadj, et al.. (2013). Plasma Copeptin and Renal Outcomes in Patients With Type 2 Diabetes and Albuminuria. Diabetes Care. 36(11). 3639–3645. 75 indexed citations
11.
12.
Mohammedi, Kamel, Naïma Bellili-Muñoz, Ronan Roussel, et al.. (2011). Allelic variations in superoxide dismutase-1 (SOD1) gene are associated with increased risk of diabetic nephropathy in type 1 diabetic subjects. Molecular Genetics and Metabolism. 104(4). 654–660. 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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