Marios Kambouris

2.7k total citations
50 papers, 1.3k citations indexed

About

Marios Kambouris is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Marios Kambouris has authored 50 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Marios Kambouris's work include Genomics and Rare Diseases (5 papers), Cystic Fibrosis Research Advances (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Marios Kambouris is often cited by papers focused on Genomics and Rare Diseases (5 papers), Cystic Fibrosis Research Advances (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Marios Kambouris collaborates with scholars based in United States, Saudi Arabia and Qatar. Marios Kambouris's co-authors include Brian F. Meyer, Saeed Bohlega, Juliette Harris, Robert J. Desnick, Wassim Eid, Oonagh Dowling, Mohamed H. Al‐Hamed, Marc Glucksman, Sultan Bahabri and K. Sheth and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Marios Kambouris

47 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marios Kambouris United States 18 436 430 286 169 128 50 1.3k
Kazuhiro Kobuke Japan 18 503 1.2× 426 1.0× 210 0.7× 185 1.1× 272 2.1× 52 1.3k
Takashi Miyazawa Japan 16 647 1.5× 327 0.8× 193 0.7× 86 0.5× 139 1.1× 50 1.5k
Lorin E. Olson United States 19 833 1.9× 222 0.5× 160 0.6× 156 0.9× 202 1.6× 31 1.6k
Marie Paule Jacob France 17 272 0.6× 423 1.0× 255 0.9× 364 2.2× 185 1.4× 35 1.2k
Clarissa S. Craft United States 21 413 0.9× 209 0.5× 116 0.4× 193 1.1× 72 0.6× 29 1.1k
Fernando Gianfrancesco Italy 23 613 1.4× 268 0.6× 199 0.7× 150 0.9× 57 0.4× 73 1.4k
Nicoletta Resta Italy 27 887 2.0× 408 0.9× 253 0.9× 288 1.7× 373 2.9× 115 2.0k
Nicoletta Zoppi Italy 23 517 1.2× 847 2.0× 182 0.6× 116 0.7× 131 1.0× 54 1.4k
Christel van Erp United States 7 681 1.6× 667 1.6× 529 1.8× 114 0.7× 253 2.0× 8 1.6k
Mats Sjöquist Sweden 14 397 0.9× 189 0.4× 151 0.5× 129 0.8× 179 1.4× 27 976

Countries citing papers authored by Marios Kambouris

Since Specialization
Citations

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

Fields of papers citing papers by Marios Kambouris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marios Kambouris

This figure shows the co-authorship network connecting the top 25 collaborators of Marios Kambouris. A scholar is included among the top collaborators of Marios Kambouris 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 Marios Kambouris. Marios Kambouris 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.
Ahram, Dina, et al.. (2017). A chromosomal microdeletion of 15q in a female patient with epilepsy, ID , and autism spectrum disorder: a case report. Clinical Case Reports. 5(6). 1013–1017. 4 indexed citations
2.
Lepelletier, C., Yasser Al‐Sarraj, Christine Bodemer, et al.. (2017). Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis. Acta Dermato Venereologica. 97(7). 858–859. 10 indexed citations
3.
Hadj‐Rabia, S., Gaëlle Brideau, Yasser Al‐Sarraj, et al.. (2017). Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome. Genetics in Medicine. 20(2). 190–201. 68 indexed citations
4.
Fadda, Abeer, Sara Tomei, Sara Deola, et al.. (2016). Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype. BMC Medical Genetics. 17(1). 84–84. 15 indexed citations
5.
Hamilos, Michalis, Emmanuel I. Skalidis, Marios Kambouris, et al.. (2015). Comparison of the antiplatelet effect of clopidogrel hydrogenosulfate and clopidogrel besylate in patients with stable coronary artery disease. Journal of Thrombosis and Thrombolysis. 40(3). 288–293. 4 indexed citations
6.
Kambouris, Marios, Rachid C. Maroun, Tawfeg Ben‐Omran, et al.. (2014). Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome. Orphanet Journal of Rare Diseases. 9(1). 80–80. 16 indexed citations
7.
Kambouris, Marios, et al.. (2014). Genomics DNA profiling in elite professional soccer players: a pilot study.. PubMed. 9. 18–22. 9 indexed citations
8.
Coucke, Paul, Andy Willaert, Marja W. Wessels, et al.. (2006). Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome. Nature Genetics. 38(4). 452–457. 246 indexed citations
9.
Wahab, Abdul, et al.. (2004). Rare CFTR Mutation 1525-1G〉A in a Pakistani Patient. Journal of Tropical Pediatrics. 50(2). 120–122. 11 indexed citations
10.
Khan, Arif O., Farrukh A. Shamsi, Amr Al‐Saif, & Marios Kambouris. (2004). A Novel Missense Norrie Disease Mutation Associated With a Severe Ocular Phenotype. Journal of Pediatric Ophthalmology & Strabismus. 41(6). 361–363. 4 indexed citations
11.
Abu‐Amero, Khaled K., et al.. (2003). Lack of association of lipoprotein lipase gene polymorphisms with coronary artery disease in the Saudi Arab population.. Archives of Pathology & Laboratory Medicine. 127(5). 597–600. 28 indexed citations
12.
Díaz, George A., Bruce D. Gelb, Marios Kambouris, et al.. (2002). Mutation of a tubulin folding gene, TCFE, causes the autosomal recessive Kenny-Caffey syndrome. Journal of Investigative Medicine. 50(2). 161. 1 indexed citations
13.
Bohlega, Saeed, et al.. (2000). Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC). Neurology. 54(1). 261–261. 47 indexed citations
14.
Kambouris, Marios, et al.. (1999). A novel autosomal recessive "Huntington's disease-like" neurodegenerative disorder in a Saudi family.. PubMed. 20(1). 85–9. 7 indexed citations
15.
Qari, Mohammed, et al.. (1998). Mutation of p16, p21 or cyclin dependent kinase 4 is rare in acute lymphoblastic leukaemia. British Journal of Haematology. 103(2). 467–472. 4 indexed citations
16.
17.
Feldman, Gerald L., et al.. (1995). Relationship of Familial Prominent Corneal Nerves and Lesions of the Tongue Resembling Neuromas to Multiple Endocrine Neoplasia Type 2B. American Journal of Ophthalmology. 120(4). 456–461. 16 indexed citations
18.
Goldstein, D., Marios Kambouris, & Richard E. Ward. (1994). Familial crossed polysyndactyly. American Journal of Medical Genetics. 50(3). 215–223. 12 indexed citations
19.
Feldman, Gerald L., Marios Kambouris, Gary B. Talpos, et al.. (1994). Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A.. PubMed. 116(6). 1042–7. 11 indexed citations
20.
Kambouris, Marios, Stephen R. Dlouhy, James A. Trofatter, et al.. (1988). Localization of the gene for X‐linked nephrogenic diabetes insipidus to Xq28. American Journal of Medical Genetics. 29(1). 239–246. 35 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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