Smaragda Kamakari

751 total citations
27 papers, 315 citations indexed

About

Smaragda Kamakari is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Smaragda Kamakari has authored 27 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Oncology. Recurrent topics in Smaragda Kamakari's work include Neuroendocrine Tumor Research Advances (4 papers), DNA Repair Mechanisms (3 papers) and RNA modifications and cancer (3 papers). Smaragda Kamakari is often cited by papers focused on Neuroendocrine Tumor Research Advances (4 papers), DNA Repair Mechanisms (3 papers) and RNA modifications and cancer (3 papers). Smaragda Kamakari collaborates with scholars based in Greece, United Kingdom and United States. Smaragda Kamakari's co-authors include Susan Lindsay, Siladitya Bhattacharya, A Curtis, Dawn L. Thiselton, Maroulio Pertesi, George Fountzilas, Drakoulis Yannoukakos, Irene Konstantopoulou, S. Raptis and Μelpomeni Peppa and has published in prestigious journals such as Human Molecular Genetics, British Journal of Cancer and Genomics.

In The Last Decade

Smaragda Kamakari

27 papers receiving 304 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Smaragda Kamakari Greece	11	150	132	60	41	40	27	315
Asma I. Tahir Saudi Arabia	11	129 0.9×	90 0.7×	34 0.6×	15 0.4×	21 0.5×	19	294
R Lahl Germany	10	164 1.1×	76 0.6×	67 1.1×	19 0.5×	19 0.5×	37	424
Daniela Radl Argentina	11	144 1.0×	56 0.4×	30 0.5×	21 0.5×	18 0.5×	15	333
Ariane Sadr‐Nabavi Iran	10	119 0.8×	68 0.5×	15 0.3×	27 0.7×	21 0.5×	38	323
Valeria Cinquina Italy	11	112 0.7×	193 1.5×	10 0.2×	34 0.8×	44 1.1×	22	388
Jens Schallner Germany	11	182 1.2×	120 0.9×	32 0.5×	6 0.1×	43 1.1×	15	324
Göran Brandberg Sweden	8	244 1.6×	116 0.9×	10 0.2×	12 0.3×	80 2.0×	10	442
Ling‐Jia Hu France	12	203 1.4×	63 0.5×	109 1.8×	44 1.1×	32 0.8×	16	486
Emmanuelle Ranza Switzerland	12	137 0.9×	103 0.8×	18 0.3×	18 0.4×	15 0.4×	22	295
Sonya A. Gunter United States	4	237 1.6×	166 1.3×	23 0.4×	16 0.4×	22 0.6×	4	400

Countries citing papers authored by Smaragda Kamakari

Since Specialization

Citations

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

Fields of papers citing papers by Smaragda Kamakari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Smaragda Kamakari

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

All Works

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20 of 20 papers shown

Rotsos, Tryfon, et al.. (2022). Wolfram Syndrome: A case report of two sisters Wolfram Syndrome: Case report of two sisters. American Journal of Ophthalmology Case Reports. 26. 101452–101452. 2 indexed citations

Chauhan, Bharesh K., Matthew P. Baumgartner, Smaragda Kamakari, et al.. (2018). Case series: Pyramidal cataracts, intact irides and nystagmus from three novel PAX6 mutations. American Journal of Ophthalmology Case Reports. 10. 172–179. 3 indexed citations

Bozi, Maria, Dimitra Papadimitriou, Marina Moraitou, et al.. (2013). Genetic assessment of familial and early‐onset Parkinson's disease in a Greek population. European Journal of Neurology. 21(7). 963–968. 53 indexed citations

Kostakis, George, et al.. (2010). Absence of hotspot mutations in exons 9 and 20 of the PIK3CA gene in human oral squamous cell carcinoma in the Greek population. Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology. 109(5). e53–e58. 14 indexed citations

Peppa, Μelpomeni, Smaragda Kamakari, Eleni Boutati, et al.. (2009). A novel germline mutation of theVHLgene in a Greek family with Von Hippel–Lindau disease. BMJ Case Reports. 2009. bcr0220091574–bcr0220091574. 1 indexed citations

Pertesi, Maroulio, Florentia Fostira, Panagiotis S. Athanasopoulos, et al.. (2009). Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases. British Journal of Cancer. 101(1). 32–37. 25 indexed citations

Golfinopoulos, Vassilis, et al.. (2008). Donor-derived breast cancer in a bone marrow transplantation recipient. Breast Cancer Research and Treatment. 113(2). 215–215. 1 indexed citations

Peppa, Μelpomeni, Eleni Boutati, Smaragda Kamakari, et al.. (2008). Novel germline mutations of the MEN1 gene in Greek families with multiple endocrine neoplasia type 1. Clinical Endocrinology. 70(1). 75–81. 5 indexed citations

Pertesi, Maroulio, Irene Konstantopoulou, Smaragda Kamakari, et al.. (2007). G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history. Breast Cancer Research and Treatment. 110(2). 377–385. 29 indexed citations

10.

Kamakari, Smaragda, et al.. (2004). Structural analysis and expression profile of a novel gene on chromosome 5q23 encoding a Golgi-associated protein with six splice variants, and involved within the 5q deletion of a Ph(−) CML patient. Leukemia Research. 29(1). 17–31. 3 indexed citations

11.

Kontaraki, Joanna, et al.. (1999). Assignment of a human cold shock domain protein A intronless pseudogene (CSDAP1) to human chromosome 16 band p11.2 by in situ hybridization. Cytogenetic and Genome Research. 84(1-2). 53–54. 4 indexed citations

12.

Kamakari, Smaragda, et al.. (1997). Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17. Human Genetics. 99(2). 233–236. 10 indexed citations

13.

Marzella, R., Maria Kokkinaki, M. Kapsetaki, et al.. (1997). Map integration at human chromosome 10: molecular and cytogenetic analysis of a chromosome-specific somatic cell hybrid panel and genomic clones, based on a well-supported genetic map. Cytogenetic and Genome Research. 79(3-4). 257–265. 3 indexed citations

14.

Thiselton, Dawn L., et al.. (1995). Genetic and physical mapping of five novel microsatellite markers on human Xp21.1–p11.22. Genomics. 25(1). 279–281. 2 indexed citations

15.

Thiselton, Dawn L., Smaragda Kamakari, Michel P. Coleman, et al.. (1993). Dinucleotide repeat polymorphism at the DXS556 locus. Human Molecular Genetics. 2(5). 613–613. 3 indexed citations

16.

Lindsay, Susan, et al.. (1993). Isolation and Characterization of Three Microsatellite Markers in the Proximal Long Arm of the Human X Chromosome. Genomics. 17(1). 208–210. 4 indexed citations

17.

Kamakari, Smaragda, et al.. (1993). Dinucleotide repeat polymorphism at the DXS573 locus. Human Molecular Genetics. 2(1). 92–92. 5 indexed citations

18.

Kamakari, Smaragda, et al.. (1992). Dinucleotide repeat polymorphism at the DXS559 locus. Human Molecular Genetics. 1(9). 778–778. 18 indexed citations

19.

Porteous, Mary, A Curtis, Susan Lindsay, et al.. (1992). The gene for aarskog syndrome is located between DXS255 and DXS566 (Xp11.2–Xq13). Genomics. 14(2). 298–301. 19 indexed citations

20.

Kamakari, Smaragda, et al.. (1992). Two dinucleotide repeat polymorphisms at the DXS571 locus. Human Molecular Genetics. 1(9). 776–776. 2 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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