Nikolaos Settas

495 total citations
19 papers, 302 citations indexed

About

Nikolaos Settas is a scholar working on Molecular Biology, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Nikolaos Settas has authored 19 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Surgery and 7 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Nikolaos Settas's work include Adrenal and Paraganglionic Tumors (6 papers), Neuroendocrine Tumor Research Advances (3 papers) and Cardiac tumors and thrombi (3 papers). Nikolaos Settas is often cited by papers focused on Adrenal and Paraganglionic Tumors (6 papers), Neuroendocrine Tumor Research Advances (3 papers) and Cardiac tumors and thrombi (3 papers). Nikolaos Settas collaborates with scholars based in United States, Greece and France. Nikolaos Settas's co-authors include Fábio R. Faucz, Constantine A. Stratakis, Antonis Voutetakis, George P. Chrousos, Catherine Dacou‐Voutetakis, Christina Kanaka‐Gantenbein, Maya Lodish, Annabel Berthon, Georgia Pitsava and Christina Tatsi and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Nikolaos Settas

17 papers receiving 295 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nikolaos Settas United States 9 123 111 107 63 51 19 302
Eelco J. Schroor Netherlands 8 89 0.7× 147 1.3× 77 0.7× 50 0.8× 38 0.7× 11 368
Elisabetta Cecconi Italy 8 227 1.8× 130 1.2× 73 0.7× 32 0.5× 9 0.2× 16 324
Amandine Septier France 8 87 0.7× 114 1.0× 63 0.6× 82 1.3× 55 1.1× 12 273
A.M. Guedj France 9 171 1.4× 125 1.1× 94 0.9× 83 1.3× 98 1.9× 13 335
Anne‐Sophie Chong Canada 9 107 0.9× 51 0.5× 113 1.1× 39 0.6× 37 0.7× 16 251
S Khalaf United Kingdom 8 135 1.1× 135 1.2× 48 0.4× 23 0.4× 8 0.2× 13 415
Isabella Finco United States 9 201 1.6× 191 1.7× 153 1.4× 100 1.6× 15 0.3× 15 429
Ninni Mu Sweden 9 117 1.0× 96 0.9× 58 0.5× 44 0.7× 36 0.7× 13 254
Agnes Fresnoza Canada 9 159 1.3× 134 1.2× 48 0.4× 52 0.8× 23 0.5× 11 334
Débora Braslavsky Argentina 12 168 1.4× 239 2.2× 73 0.7× 187 3.0× 86 1.7× 25 454

Countries citing papers authored by Nikolaos Settas

Since Specialization
Citations

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

Fields of papers citing papers by Nikolaos Settas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nikolaos Settas

This figure shows the co-authorship network connecting the top 25 collaborators of Nikolaos Settas. A scholar is included among the top collaborators of Nikolaos Settas 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 Nikolaos Settas. Nikolaos Settas 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.
Settas, Nikolaos, et al.. (2025). Increased METTL3 Expression and m6A Methylation in Myoblasts of Facioscapulohumeral Muscular Dystrophy. International Journal of Molecular Sciences. 26(11). 5170–5170. 1 indexed citations
2.
Xekouki, Paraskevi, Anastasia Konstantinidou, Christina Tatsi, et al.. (2024). HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF. HORMONES. 23(2). 345–350.
3.
Settas, Nikolaos, et al.. (2022). USP13 genetics and expression in a family with thyroid cancer. Endocrine. 77(2). 281–290. 5 indexed citations
4.
Pitsava, Georgia, Nikolaos Settas, Fábio R. Faucz, & Constantine A. Stratakis. (2021). Carney Triad, Carney-Stratakis Syndrome, 3PAS and Other Tumors Due to SDH Deficiency. Frontiers in Endocrinology. 12. 680609–680609. 24 indexed citations
5.
Settas, Nikolaos, Fábio R. Faucz, Ninet Sinaii, et al.. (2021). The PRKAR1B p.R115K Variant is Associated with Lipoprotein Profile in African American Youth with Metabolic Challenges. Journal of the Endocrine Society. 5(8). bvab071–bvab071. 2 indexed citations
6.
Drougat, Ludivine, Nikolaos Settas, Cristina L. Ronchi, et al.. (2020). Genomic and sequence variants of protein kinase A regulatory subunit type 1β (PRKAR1B) in patients with adrenocortical disease and Cushing syndrome. Genetics in Medicine. 23(1). 174–182. 10 indexed citations
7.
Settas, Nikolaos, Eva Kassi, Anna Angelousi, Fábio R. Faucz, & Constantine A. Stratakis. (2020). OR24-06 USP8 Genetic Variants May Contribute to the Development of Bilateral Adrenal Hyperplasia and ACTH-Independent Cushing Syndrome. Journal of the Endocrine Society. 4(Supplement_1).
8.
Tatsi, Christina, Annabel Berthon, Ludivine Drougat, et al.. (2020). ARMC5 variants in PRKAR1A-mutated patients modify cortisol levels and Cushing’s syndrome. Endocrine Related Cancer. 27(9). 509–517. 7 indexed citations
9.
Berthon, Annabel, Nikolaos Settas, Angela Delaney, et al.. (2020). Kisspeptin deficiency leads to abnormal adrenal glands and excess steroid hormone secretion. Human Molecular Genetics. 29(20). 3443–3450. 5 indexed citations
10.
Espiard, Stéphanie, Ludivine Drougat, Nikolaos Settas, et al.. (2020). PRKACB variants in skeletal disease or adrenocortical hyperplasia: effects on protein kinase A. Endocrine Related Cancer. 27(11). 647–656. 9 indexed citations
11.
Settas, Nikolaos, Rebecca Persky, Fábio R. Faucz, et al.. (2018). SGPL1 Deficiency: A Rare Cause of Primary Adrenal Insufficiency. The Journal of Clinical Endocrinology & Metabolism. 104(5). 1484–1490. 27 indexed citations
12.
Scortegagna, Marzia, Annabel Berthon, Nikolaos Settas, et al.. (2017). The E3 ubiquitin ligase Siah1 regulates adrenal gland organization and aldosterone secretion. JCI Insight. 2(23). 10 indexed citations
13.
Settas, Nikolaos, Fábio R. Faucz, & Constantine A. Stratakis. (2017). Succinate dehydrogenase (SDH) deficiency, Carney triad and the epigenome. Molecular and Cellular Endocrinology. 469. 107–111. 36 indexed citations
14.
Faucz, Fábio R., Amit Tirosh, Christina Tatsi, et al.. (2017). Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease. The Journal of Clinical Endocrinology & Metabolism. 102(8). 2836–2843. 75 indexed citations
15.
Angelousi, Anna, Nikolaos Settas, Fábio R. Faucz, et al.. (2017). Medullary thyroid cancer, leukemia, mesothelioma and meningioma associated with germline APC and RASAL1 variants: a new syndrome?. HORMONES. 16(4). 423–428. 4 indexed citations
16.
Faucz, Fábio R., et al.. (2016). Association of a <b><i>PARK2</i></b> Germline Variant and Epithelial Ovarian Cancer in a Southern Brazilian Population. Oncology. 91(2). 101–105. 8 indexed citations
17.
Settas, Nikolaos, Emmanuel Kanavakis, Helen Fryssira, et al.. (2015). A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis–ptosis–epicanthus inversus syndrome. Menopause The Journal of The North American Menopause Society. 22(11). 1264–1268. 6 indexed citations
18.
Settas, Nikolaos, et al.. (2014). Central Precocious Puberty in a Girl and Early Puberty in Her Brother Caused by a Novel Mutation in the MKRN3 Gene. The Journal of Clinical Endocrinology & Metabolism. 99(4). E647–E651. 66 indexed citations
19.
Settas, Nikolaos, Antonia Dastamani, Ilias Katsikis, et al.. (2013). CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS). Hormone and Metabolic Research. 45(5). 383–386. 7 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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