S. Samet

406 total citations
9 papers, 320 citations indexed

About

S. Samet is a scholar working on Surgery, Neurology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, S. Samet has authored 9 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Surgery, 2 papers in Neurology and 2 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in S. Samet's work include Schizophrenia research and treatment (2 papers), Galectins and Cancer Biology (1 paper) and Genetic Syndromes and Imprinting (1 paper). S. Samet is often cited by papers focused on Schizophrenia research and treatment (2 papers), Galectins and Cancer Biology (1 paper) and Genetic Syndromes and Imprinting (1 paper). S. Samet collaborates with scholars based in Tunisia and United States. S. Samet's co-authors include Deborah S. Hasin, Kristin Dietz Trautman, Gloria M. Miele, J Endicott, Shubuladè Smith, S. Younes, S. Hammami, Imen Ghzaiel, Mohamed Hammami and Amira Zarrouk and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Psychiatry and Prostaglandins Leukotrienes and Essential Fatty Acids.

In The Last Decade

S. Samet

8 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Samet Tunisia	3	132	112	69	49	45	9	320
Carla Back‐Madruga United States	11	238 1.8×	198 1.8×	51 0.7×	34 0.7×	44 1.0×	13	579
Robert B. Whitney United States	13	172 1.3×	67 0.6×	61 0.9×	19 0.4×	18 0.4×	22	398
Massimo Di Giannantonio Italy	10	74 0.6×	112 1.0×	160 2.3×	45 0.9×	39 0.9×	18	372
Cornelis A. J. De Jong Netherlands	9	91 0.7×	67 0.6×	104 1.5×	36 0.7×	33 0.7×	24	335
Taryn Williams South Africa	8	39 0.3×	48 0.4×	113 1.6×	47 1.0×	28 0.6×	15	279
Y. Riemer Austria	10	199 1.5×	39 0.3×	25 0.4×	31 0.6×	88 2.0×	20	418
Krista J. Siefried Australia	12	161 1.2×	67 0.6×	58 0.8×	17 0.3×	107 2.4×	45	537
Yiyang Liu United States	8	126 1.0×	29 0.3×	64 0.9×	19 0.4×	58 1.3×	39	365
Linda Abadjian United States	13	71 0.5×	111 1.0×	75 1.1×	20 0.4×	13 0.3×	20	538
Alfio Lucchini Italy	10	109 0.8×	47 0.4×	28 0.4×	24 0.5×	78 1.7×	20	370

Countries citing papers authored by S. Samet

Since Specialization

Citations

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

Fields of papers citing papers by S. Samet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Samet

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

All Works

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9 of 9 papers shown

1.

Samet, S., et al.. (2022). Fahr syndrome discovered in adulthood revealing a rare GNAS mutation in pseudohypoparathyroidism type 1a in a Tunisian family. SHILAP Revista de lepidopterología. 10(5). e05849–e05849. 1 indexed citations

2.

Samet, S., et al.. (2021). Neurofibromatose découverte en post opératoire suite à une rupture spontanée d’un phéochromocytome méconnu. Annales d Endocrinologie. 82(5). 439–440.

3.

Ghzaiel, Imen, S. Hammami, S. Younes, et al.. (2020). Genetic variants in FADS1 and ELOVL2 increase level of arachidonic acid and the risk of Alzheimer's disease in the Tunisian population. Prostaglandins Leukotrienes and Essential Fatty Acids. 160. 102159–102159. 36 indexed citations

4.

Salah, Afif Ben, et al.. (2018). Une insuffisance rénale aiguë révélant une hypothyroïdie primaire. Annales d Endocrinologie. 79(4). 355–355. 1 indexed citations

5.

Samet, S., et al.. (2017). Encéphalopathie corticosensible associée à une thyroïdite auto-immune. Annales d Endocrinologie. 78(4). 346–346. 2 indexed citations

6.

Samet, S., et al.. (2001). [Carcinomatous meningitis revealing a cancer: study of two cases].. PubMed. 79(4). 257–60. 2 indexed citations

7.

Gouider, Riadh, S. Samet, Amina Gargouri, et al.. (1999). [Neurological manifestations indicative of brucellosis].. PubMed. 155(3). 215–8. 9 indexed citations

8.

Hasin, Deborah S., Kristin Dietz Trautman, Gloria M. Miele, et al.. (1996). Psychiatric Research Interview for Substance and Mental Disorders (PRISM): reliability for substance abusers. American Journal of Psychiatry. 153(9). 1195–1201. 267 indexed citations

9.

Girard, Thierry, et al.. (1994). [Haloperidol, a new cause of rhabdomyolysis, in the absence of neuroleptic malignant syndrome].. PubMed. 23(32). 1493–1493. 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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