Fayçal Hentati

12.1k citations

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

Neurology top 0.5%
- Neurological diseases and metabolism 22
- Parkinson's Disease Mechanisms and Treatments 20
- Amyotrophic Lateral Sclerosis Research 10
Neurology top 0.5%
- Neurological diseases and metabolism 22
- Parkinson's Disease Mechanisms and Treatments 20
- Amyotrophic Lateral Sclerosis Research 10
Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases 28
- Hereditary Neurological Disorders 19
Genetics top 1%
- Neurogenetic and Muscular Disorders Research 12
Cell Biology top 1%
Molecular Biology
- Muscle Physiology and Disorders 22
- Mitochondrial Function and Pathology 21

Co-authors: Mongi Ben Hamida Rim Amouri Christiane Ben Hamida Samir Belal Karim Ouahchi M. Ben Hamida M. Kœnig Teepu Siddique
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Science (1 paper)Nature Genetics (7 papers)Brain (1 paper)
Partner nations: Tunisia United States France

In The Last Decade

Fayçal Hentati

122 papers receiving 5.8k citations

Hit Papers

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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

The 25 scholars most cited alongside Fayçal Hentati, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fayçal Hentati Line = papers co-authored together Fayçal Hentati links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Heterodimerization of Lrrk1–Lrrk2: Implications for LRRK2-associated Parkinson disease 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	2010	19
2	A novel mitochondrial tRNAIle point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia Journal of the Neurological Sciences ·Sihem Souilem,S. Chebel,Michelangelo Mancuso,Lucia Petrozzi,Gabriele Siciliano,Mahbouba Frih-Ayed,Fayçal Hentati,Rim Amouri	2010	10
3	Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration The American Journal of Human Genetics ·Maria K. Tsaousidou,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,P. Lamont,Teepu Siddique,Andrew H. Crosby	2008	117
4	ATP13A2variability in Parkinson disease 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	2008	33
5	A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease 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	2007	31
6	Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes Neuromuscular Disorders ·Khaled Fendri,M. Kéfi,Fayçal Hentati,Rim Amouri	2006	12
7	Spectrum ofHSPG2(Perlecan) mutations in patients with Schwartz-Jampel syndrome 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,EL-Hadi Hammouda,Phuc Canh Quan,Bertrand Fontaine,Sophie Nicole	2006	71
8	Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia Archives of Neurology ·Ghada El Euch-Fayache,Irfan Lalani,Rim Amouri,Ilhem Turki,Karim Ouahchi,Wu-Yen Hung,Samir Belal,Teepu Siddique,Fayçal Hentati	2003	75
9	Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation Neuromuscular Disorders ·M. Kéfi,Rim Amouri,Adel Driss,C. Ben Hamida,M. Ben Hamida,Louis M. Kunkel,Fayçal Hentati	2003	35
10	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease Neuromuscular Disorders ·Nadia Ammar,Eva Nelis,Luciano Merlini,Nina Barišić,Rim Amouri,C. Ceuterick,Jean‐Jacques Martin,Vincent Timmerman,Fayçal Hentati,Peter De Jonghe	2003	37
11	Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 European Journal of Human Genetics ·Maria-Ceù Moreira,Sandra Klur,Clara Barbot,Nobutada Tachi,Pascale Bomont,Masao Watanabe,Mikio Shoji,J Warter,Pauline Aubourg,Alexandra Dürr,Andrea H. Németh,Rim Amouri,Fayçal Hentati,A Alurkar,D Divekar,P Mendoca,Jorge Sequeiros,Paula Coutinho,Michel Kœnig	2002	3
12	Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children Neuromuscular Disorders ·Stéphanie Decary,C. Ben Hamida,Vincent Mouly,Jacques Barbet,Fayçal Hentati,Gillian Butler‐Browne	2000	151
13	Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia) Nature Genetics ·Sophie Nicole,Claire-Sophie Davoine,Haluk Topaloğlu,Laurence Cattolico,Duarte C. Barral,Peter Beighton,Christiane Ben Hamida,Hadi Hammouda,Corinne Cruaud,Peter S. White,Delphine Samson,J. Andoni Urtizberea,F. Lehmann‐Horn,Jean Weissenbach,Fayçal Hentati,Bertrand Fontaine	2000	198
14	Progress in Neuropathology of the Neuronal Ceroid Lipofuscinoses Molecular Genetics and Metabolism ·Hans H. Goebel,Sydney S. Schochet,Margaret Jaynes,Wolfgang Brück,Alfried Kohlschütter,Fayçal Hentati	1999	27
15	Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study Journal of Inherited Metabolic Disease ·A. Larnaout,M. A. Mongalgi,Naziha Kaabachi,D. Khiari,A Debbabi,Alexandre Mebazza,M. Ben Hamida,Fayçal Hentati	1998	23
16	LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3 Neuromuscular Disorders ·Carsten G. Bönnemann,Jenny Wong,Ch. Ben Hamida,M. Ben Hamida,Fayçal Hentati,Louis M. Kunkel	1998	28
17	Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers Human Molecular Genetics ·Afif Hentati,Margaret A. Pericak‐Vance,Felicia Lennon,Brad Wasserman,Fayçal Hentati,T.R. Juneja,Misha Angrist,W.‐Y. Hung,Rose-Mary Boustany,Saeed Bohlega,Zafar Iqbal,Carl H. Huether,Mongi Ben Hamida,Teepu Siddique	1994	71
18	Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy Journal of the Neurological Sciences ·Christiane Ben Hamida,Nadia Soussi‐Yanicostas,Khemissa Bejaoui,Gillian Butler‐Browne,Fayçal Hentati,M. Ben Hamida	1994	4
19	Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. PubMed ·Samir Belal,Kyproula Panayides,Giorgio Sirugo,C Ben Hamida,P.A. Ioannou,Fayçal Hentati,J. Beckmann,M. Koenig,Jean‐Louis Mandel,M. Ben Hamida	1992	11
20	Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome Journal of the Neurological Sciences ·Nadia Soussi‐Yanicostas,Christiane Ben Hamida,Gillian Butler‐Browne,Fayçal Hentati,Khemissa Bejaoui,M. Ben Hamida	1991	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), Muscle Physiology and Disorders (22 papers), Mitochondrial Function and Pathology (21 papers), Parkinson's Disease Mechanisms and Treatments (20 papers), Hereditary Neurological Disorders (19 papers), Neurogenetic and Muscular Disorders Research (12 papers) and Amyotrophic Lateral Sclerosis Research (10 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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