Fayçal Hentati

12.1k citations

122 papers · 6.0k indexed · 1 hit paper · h-index 37

Molecular Biology top 2%
Cellular and Molecular Neuroscience top 0.5%
Neurology top 0.5%
Neurology top 0.5%
Cell Biology top 1%

Co-authors: Mongi Ben Hamida Rim Amouri Christiane Ben Hamida Samir Belal Karim Ouahchi M. Ben Hamida M. Kœnig Teepu Siddique
Topics: Genetic Neurodegenerative Diseases (28 papers)Neurological diseases and metabolism (22 papers)Muscle Physiology and Disorders (22 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Science Nature Genetics Brain
Partner nations: Tunisia United States France

In The Last Decade

Fayçal Hentati

122 papers receiving 5.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

2001 548 citations Yi Yang, Afif Hentati et al. Nature Genetics profile →

Peers

Countries citing papers authored by Fayçal Hentati

Since Specialization

Citations

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

Fields of papers citing papers by Fayçal Hentati

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fayçal Hentati

This figure shows the co-authorship network connecting the top 25 collaborators of Fayçal Hentati. A scholar is included among the top collaborators of Fayçal 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 Fayçal Hentati. Fayçal 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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20 of 20 papers shown

#	Work	Indexed citations
1	Heterodimerization of Lrrk1–Lrrk2: Implications for LRRK2-associated Parkinson disease 2010 ·Mechanisms of Ageing and Development ·Justus C. Dächsel,Kenya Nishioka,Carles Vilariño‐Güell,Sarah Lincoln,Alexandra I. Soto‐Ortolaza,Jennifer M. Kachergus,Kelly M. Hinkle,Michael G. Heckman,Barbara Jasińska‐Myga,Julie P. Taylor,Dennis W. Dickson,Rachel A. Gibson,Fayçal Hentati,Owen A. Ross,Matthew J. Farrer	19
2	A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia 2010 ·Journal of the Neurological Sciences ·(unknown),(unknown),Michelangelo Mancuso,Lucia Petrozzi,Gabriele Siciliano,(unknown),Fayçal Hentati,Rim Amouri	10
3	Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration 2008 ·The American Journal of Human Genetics ·(unknown),Karim Ouahchi,Thomas T. Warner,Yi Yang,Michael A. Simpson,Nigel G. Laing,Philip A. Wilkinson,R. E. Madrid,Heema Patel,Fayçal Hentati,Michael A. Patton,Afif Hentati,(unknown),Teepu Siddique,Andrew H. Crosby	117
4	ATP13A2variability in Parkinson disease 2008 ·Human Mutation ·Carles Vilariño‐Güell,Alexandra I. Soto,Sarah Lincoln,Samia Ben Yahmed,Mounir Kefi,Michael G. Heckman,Mary Hulihan,Hua Chai,Nancy N. Diehl,Rim Amouri,Alex Rajput,Deborah C. Mash,Dennis W. Dickson,Lefkos Middleton,Rachel A. Gibson,Fayçal Hentati,Matthew J. Farrer	33
5	A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease 2007 ·Parkinsonism & Related Disorders ·Liling Warren,Rachel A. Gibson,Lianna Ishihara,Ramu Elango,Zhengyu Xue,P. Anthony Akkari,Leigh Ragone,Rajesh Pahwa,Joseph Jankovic,Martha Nance,Alan Freeman,Ray L. Watts,Fayçal Hentati	31
6	Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes 2006 ·Neuromuscular Disorders ·(unknown),M. Kéfi,Fayçal Hentati,Rim Amouri	12
7	Spectrum ofHSPG2(Perlecan) mutations in patients with Schwartz-Jampel syndrome 2006 ·Human Mutation ·Morgane Stum,Claire-Sophie Davoine,Savine Vicart,Léna Guillot‐Noël,Haluk Topaloğlu,Francisco Javier Carod-Artal,Hülya Kayserili,Fayçal Hentati,Luciano Merlini,Jon Andoni Urtizberea,(unknown),Phuc Canh Quan,Bertrand Fontaine,Sophie Nicole	71
8	Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia 2003 ·Archives of Neurology ·(unknown),(unknown),Rim Amouri,Ilhem Turki,Karim Ouahchi,Wu-Yen Hung,Samir Belal,Teepu Siddique,Fayçal Hentati	75
9	Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation 2003 ·Neuromuscular Disorders ·M. Kéfi,Rim Amouri,Adel Driss,C. Ben Hamida,M. Ben Hamida,Louis M. Kunkel,Fayçal Hentati	35
10	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease 2003 ·Neuromuscular Disorders ·(unknown),Eva Nelis,Luciano Merlini,Nina Barišić,Rim Amouri,C. Ceuterick,Jean‐Jacques Martin,Vincent Timmerman,Fayçal Hentati,Peter De Jonghe	37
11	Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 2002 ·European Journal of Human Genetics ·(unknown),(unknown),Clara Barbot,Nobutada Tachi,Pascale Bomont,Masao Watanabe,Mikio Shoji,J Warter,(unknown),Alexandra Dürr,Andrea H. Németh,Rim Amouri,Fayçal Hentati,(unknown),(unknown),(unknown),Jorge Sequeiros,Paula Coutinho,Michel Kœnig	3
12	Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children 2000 ·Neuromuscular Disorders ·Stéphanie Decary,C. Ben Hamida,Vincent Mouly,Jacques Barbet,Fayçal Hentati,Gillian Butler‐Browne	151
13	Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) 2000 ·Nature Genetics ·Sophie Nicole,Claire-Sophie Davoine,Haluk Topaloğlu,Laurence Cattolico,Duarte C. Barral,Peter Beighton,Christiane Ben Hamida,(unknown),Corinne Cruaud,Peter S. White,Delphine Samson,J. Andoni Urtizberea,F. Lehmann‐Horn,Jean Weissenbach,Fayçal Hentati,Bertrand Fontaine	198
14	Progress in Neuropathology of the Neuronal Ceroid Lipofuscinoses 1999 ·Molecular Genetics and Metabolism ·(unknown),Sydney S. Schochet,(unknown),(unknown),Alfried Kohlschütter,Fayçal Hentati	27
15	Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study 1998 ·Journal of Inherited Metabolic Disease ·A. Larnaout,(unknown),Naziha Kaabachi,(unknown),(unknown),(unknown),M. Ben Hamida,Fayçal Hentati	23
16	LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3 1998 ·Neuromuscular Disorders ·Carsten G. Bönnemann,Jenny Wong,(unknown),M. Ben Hamida,Fayçal Hentati,Louis M. Kunkel	28
17	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers 1994 ·Human Molecular Genetics ·Afif Hentati,Margaret A. Pericak‐Vance,Felicia Lennon,(unknown),Fayçal Hentati,T.R. Juneja,Misha Angrist,W.‐Y. Hung,Rose-Mary Boustany,Saeed Bohlega,Zafar Iqbal,(unknown),Mongi Ben Hamida,Teepu Siddique	71
18	Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy 1994 ·Journal of the Neurological Sciences ·Christiane Ben Hamida,Nadia Soussi‐Yanicostas,Khemissa Bejaoui,Gillian Butler‐Browne,Fayçal Hentati,M. Ben Hamida	4
19	Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. 1992 ·PubMed ·Samir Belal,(unknown),Giorgio Sirugo,(unknown),P.A. Ioannou,Fayçal Hentati,J. Beckmann,M. Koenig,Jean‐Louis Mandel,M. Ben Hamida	11
20	Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome 1991 ·Journal of the Neurological Sciences ·Nadia Soussi‐Yanicostas,Christiane Ben Hamida,Gillian Butler‐Browne,Fayçal Hentati,Khemissa Bejaoui,M. Ben Hamida	10

About Fayçal Hentati

Fayçal Hentati is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience, having authored 122 papers that have together received 6.0k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (28 papers), Neurological diseases and metabolism (22 papers) and Muscle Physiology and Disorders (22 papers). The work is most often cited by research in Neurology (1.1k citations), Neurology (1.9k citations) and Cellular and Molecular Neuroscience (2.2k citations). Fayçal Hentati has collaborated with scholars based in Tunisia, United States and France. Frequent co-authors include Mongi Ben Hamida, Rim Amouri, Christiane Ben Hamida, Samir Belal, Karim Ouahchi, M. Ben Hamida, M. Kœnig, Teepu Siddique, Jeffery M. Vance and Kamel Ben Othmane. Their work appears in journals such as Science, Nature Genetics and Brain.

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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