F. Hentati

643 total citations
14 papers, 450 citations indexed

About

F. Hentati is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, F. Hentati has authored 14 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 8 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in F. Hentati's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (8 papers) and Neurological diseases and metabolism (3 papers). F. Hentati is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (8 papers) and Neurological diseases and metabolism (3 papers). F. Hentati collaborates with scholars based in Tunisia, United States and France. F. Hentati's co-authors include Samir Belal, M. Ben Hamida, Christiane Ben Hamida, Jean‐Louis Mandel, Ilhem Turki, Nathalie Doerflinger, Colette Dib, Vahe Mokini, Gàbor Gyapay and Giuseppe Novelli and has published in prestigious journals such as Nature Genetics, Neurology and Acta Neuropathologica.

In The Last Decade

F. Hentati

14 papers receiving 426 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
F. Hentati Tunisia	7	288	224	126	92	80	14	450
S. Di Donato Italy	12	331 1.1×	283 1.3×	36 0.3×	19 0.2×	149 1.9×	17	487
Surabhi Bhatia Australia	13	217 0.8×	63 0.3×	23 0.2×	32 0.3×	67 0.8×	16	447
Koji Matsushita Japan	5	192 0.7×	80 0.4×	15 0.1×	21 0.2×	42 0.5×	10	386
Motoko Kawaguchi Japan	9	158 0.5×	34 0.2×	19 0.2×	24 0.3×	176 2.2×	9	383
Ruth Darrow United States	8	283 1.0×	64 0.3×	50 0.4×	34 0.4×	6 0.1×	9	382
Marie‐Elise Martin France	9	129 0.4×	63 0.3×	11 0.1×	217 2.4×	155 1.9×	9	591
En Huang Canada	10	337 1.2×	73 0.3×	6 0.0×	33 0.4×	87 1.1×	14	504
Mingshu Mo China	12	218 0.8×	100 0.4×	14 0.1×	9 0.1×	70 0.9×	14	376
Chye Yun Yu Singapore	10	361 1.3×	92 0.4×	6 0.0×	26 0.3×	30 0.4×	10	497
Mariana Rodova United States	6	506 1.8×	36 0.2×	9 0.1×	11 0.1×	61 0.8×	8	649

Countries citing papers authored by F. Hentati

Since Specialization

Citations

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

Fields of papers citing papers by F. Hentati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of F. Hentati

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

All Works

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14 of 14 papers shown

Sassi, Samia Ben, et al.. (2009). Man-in-the-Barrel Syndrome with Combination of Infarctions in the Anterior Spinal Artery and Posterior Inferior Cerebellar Artery Territories. Cerebrovascular Diseases. 27(2). 201–202. 8 indexed citations

Ammar, Naglaa M., et al.. (2006). [Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report].. PubMed. 84(6). 361–4. 2 indexed citations

Hentati, F., et al.. (2006). [Study of dyslexia within school kids that suffer from epilepsia].. PubMed. 84(12). 803–4. 1 indexed citations

Romdhane, Habiba Ben, et al.. (2005). [Secondary prevention of cardiovascular diseases: knowledge and practices of patients].. PubMed. 83 Suppl 5. 30–5. 1 indexed citations

Gouider‐Khouja, N., Samir Belal, Moncef Feki, et al.. (2001). Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency. European Journal of Neurology. 8(5). 477–481. 96 indexed citations

Belal, Samir, C. Ben Hamida, Rim Amouri, et al.. (2000). Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54(7). 1408–1414. 52 indexed citations

Belal, Samir, C. Ben Hamida, Rim Amouri, et al.. (2000). LINKAGE TO CHROMOSOME 13Q11‐12 OF AN AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA IN A TUNISIAN FAMILY. Journal of the Peripheral Nervous System. 5(4). 241–242. 1 indexed citations

Hentati, F., et al.. (1995). Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.. PubMed. 3(1). 39–42. 11 indexed citations

Hamida, Christiane Ben, Nathalie Doerflinger, Samir Belal, et al.. (1993). Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping. Nature Genetics. 5(2). 195–200. 163 indexed citations

10.

Hamida, M. Ben, Samir Belal, Giorgio Sirugo, et al.. (1993). Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology. 43(11). 2179–2179. 96 indexed citations

11.

Hentati, F., et al.. (1991). [Fatal acute pancreatitis in systemic lupus erythematosus].. PubMed. 142(3). 230–2. 5 indexed citations

12.

Hentati, F., et al.. (1991). [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].. PubMed. 147(12). 798–808. 8 indexed citations

13.

Hamida, M. Ben, et al.. (1987). Hypertrophic neuropathy in spinocerebellar degeneration. Acta Neuropathologica. 75(1). 51–61. 2 indexed citations

14.

Hamida, M. Ben, et al.. (1986). [Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].. PubMed. 34(3-4). 267–74. 4 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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