Mostafa Kandil

521 total citations
28 papers, 400 citations indexed

About

Mostafa Kandil is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Mostafa Kandil has authored 28 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Sensory Systems. Recurrent topics in Mostafa Kandil's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Forensic and Genetic Research (5 papers) and Forensic Anthropology and Bioarchaeology Studies (4 papers). Mostafa Kandil is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Forensic and Genetic Research (5 papers) and Forensic Anthropology and Bioarchaeology Studies (4 papers). Mostafa Kandil collaborates with scholars based in Morocco, France and Spain. Mostafa Kandil's co-authors include Nourdin Harich, Abdelhamid Barakat, Majida Charif, Redouane Boulouiz, Hassan Rouba, Esther Esteban, Marc Vía, Joana B. Pereira, Marta D. Costa and Omar Abidi and has published in prestigious journals such as Biochemical and Biophysical Research Communications, The American Journal of Human Genetics and Gene.

In The Last Decade

Mostafa Kandil

28 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mostafa Kandil Morocco 11 148 129 95 60 57 28 400
Nicola Bedoni Switzerland 8 70 0.5× 177 1.4× 21 0.2× 5 0.1× 26 0.5× 12 307
Rajini Haraksingh United States 8 217 1.5× 245 1.9× 12 0.1× 7 0.1× 23 0.4× 12 425
Eddie Park United States 10 109 0.7× 502 3.9× 23 0.2× 32 0.5× 22 0.4× 10 675
Sandra Mitrović Switzerland 9 29 0.2× 224 1.7× 35 0.4× 13 0.2× 14 481
Masayasu Yoshino Japan 11 102 0.7× 136 1.1× 17 0.2× 25 0.4× 22 399
Jangsuk Oh United States 8 45 0.3× 198 1.5× 63 0.7× 16 0.3× 11 675
Wenmin Zhang China 11 42 0.3× 144 1.1× 4 0.0× 2 0.0× 74 1.3× 20 313
Francesca Genova Italy 8 165 1.1× 289 2.2× 8 0.1× 2 0.0× 26 0.5× 12 383
Fatimah Rahman United Kingdom 7 209 1.4× 278 2.2× 9 0.1× 19 0.3× 9 439
Christina Yee United States 6 26 0.2× 148 1.1× 21 0.2× 19 0.3× 7 316

Countries citing papers authored by Mostafa Kandil

Since Specialization
Citations

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

Fields of papers citing papers by Mostafa Kandil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mostafa Kandil

This figure shows the co-authorship network connecting the top 25 collaborators of Mostafa Kandil. A scholar is included among the top collaborators of Mostafa Kandil 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 Mostafa Kandil. Mostafa Kandil 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.
Verma, Ramesh Pal Singh, et al.. (2022). CGIAR Barley Breeding Toolbox: A diversity panel to facilitate breeding and genomic research in the developing world. Frontiers in Plant Science. 13. 1034322–1034322. 3 indexed citations
2.
Charoute, Hicham, et al.. (2022). Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies. Orphanet Journal of Rare Diseases. 17(1). 197–197. 8 indexed citations
3.
Bonnet, Crystel, Majida Charif, Mostafa Kandil, et al.. (2020). A homozygous MPZL2 deletion is associated with non syndromic hearing loss in a moroccan family. International Journal of Pediatric Otorhinolaryngology. 140. 110481–110481. 6 indexed citations
4.
Charoute, Hicham, Rym Kéfi, Houda Benrahma, et al.. (2016). Novel variants of mitochondrial DNA associated with Type 2 diabetes mellitus in Moroccan population. Mitochondrial DNA Part A. 29(1). 9–13. 6 indexed citations
5.
Rebbani, Khadija, Agnès Marchio, Sayeh Ezzikouri, et al.. (2015). TP53 R72P polymorphism modulates DNA methylation in hepatocellular carcinoma. Molecular Cancer. 14(1). 74–74. 17 indexed citations
6.
Kandil, Mostafa, et al.. (2015). Activity of Haliscosamine against Fusarium oxysporum f.sp. melonis: in vitro and in vivo analysis. SpringerPlus. 4(1). 16–16. 4 indexed citations
7.
Rebbani, Khadija, Sayeh Ezzikouri, Agnès Marchio, et al.. (2014). Common polymorphic effectors of immunity against hepatitis B and C modulate susceptibility to infection and spontaneous clearance in a Moroccan population. Infection Genetics and Evolution. 26. 1–7. 10 indexed citations
8.
Rebbani, Khadija, Sayeh Ezzikouri, Agnès Marchio, et al.. (2014). MDM2 285G>C and 344T>A gene variants and their association with hepatocellular carcinoma: a Moroccan case–control study. Infectious Agents and Cancer. 9(1). 11–11. 6 indexed citations
9.
Charif, Majida, Omar Abidi, Redouane Boulouiz, et al.. (2013). Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss. Gene. 523(1). 103–105. 8 indexed citations
10.
Barakat, Abdelhamid, Majida Charif, Redouane Boulouiz, et al.. (2013). Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss. Indian journal of human genetics. 19(3). 331–331. 3 indexed citations
11.
Esteban, Esther, et al.. (2012). Usefulness of autosomal STR polymorphisms beyond forensic purposes: data on Arabic- and Berber-speaking populations from central Morocco. Annals of Human Biology. 39(4). 297–304. 12 indexed citations
12.
Charif, Majida, Omar Abidi, Hassan Rouba, et al.. (2012). The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population. Molecular Biology Reports. 39(12). 11011–11016. 22 indexed citations
13.
Charif, Majida, Omar Abidi, Redouane Boulouiz, et al.. (2012). Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss. Biochemical and Biophysical Research Communications. 419(4). 643–647. 16 indexed citations
14.
Jalbout, Majida, Meriem Khyatti, Meriem Abdoun, et al.. (2011). XRCC1 and hOGG1 genes and risk of nasopharyngeal carcinoma in North African countries. Molecular Carcinogenesis. 50(9). 732–737. 33 indexed citations
15.
Attaleb, Mohammed, et al.. (2011). Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma. Infectious Agents and Cancer. 6(1). 3–3. 40 indexed citations
16.
Ezzikouri, Sayeh, Khadija Rebbani, Abdellah Essaid El Feydi, et al.. (2011). Influence of mutation of the HFE gene on the progression of chronic viral hepatitis B and C in Moroccan patients. Journal of Medical Virology. 83(12). 2096–2102. 3 indexed citations
17.
Charif, Majida, Redouane Boulouiz, Houda Benrahma, et al.. (2010). Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss. International Journal of Pediatric Otorhinolaryngology. 74(9). 1071–1074. 18 indexed citations
18.
Harich, Nourdin, Marta D. Costa, Verónica Fernandes, et al.. (2010). The trans-Saharan slave trade - clues from interpolation analyses and high-resolution characterization of mitochondrial DNA lineages. BMC Evolutionary Biology. 10(1). 138–138. 49 indexed citations
19.
Esteban, Esther, et al.. (2010). Genetic differences among North African Berber and Arab-speaking populations revealed by Y-STR diversity. Annals of Human Biology. 38(2). 228–236. 7 indexed citations
20.
Esteban, Esther, Marc Vía, Magdalena Gayà‐Vidal, et al.. (2009). Population relationships in the Mediterranean revealed by autosomal genetic data (Alu and Alu/STR compound systems). American Journal of Physical Anthropology. 141(3). 430–439. 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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