A. Larnaout

789 total citations
26 papers, 528 citations indexed

About

A. Larnaout is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Larnaout has authored 26 papers receiving a total of 528 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Larnaout's work include Metabolism and Genetic Disorders (8 papers), Biochemical and Molecular Research (4 papers) and Genetic Neurodegenerative Diseases (4 papers). A. Larnaout is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Biochemical and Molecular Research (4 papers) and Genetic Neurodegenerative Diseases (4 papers). A. Larnaout collaborates with scholars based in Tunisia, Belgium and France. A. Larnaout's co-authors include Fayçal Hentati, M. Ben Hamida, Samir Belal, Mongi Ben Hamida, Christiane Ben Hamida, Richard P. Copp, Thomas Wısnıewskı, Herbert J. Kayden, Rim Amouri and Naziha Kaabachi and has published in prestigious journals such as Brain Research, Acta Neuropathologica and Journal of Neurology.

In The Last Decade

A. Larnaout

26 papers receiving 508 citations

Peers

A. Larnaout

CMN

NEURO

BIOCH

Marco Piccardi Italy

M. Doly France

P. Homayoun France

Sophie Belin United States

Annalisa Lo Gerfo Italy

Surabhi Bhatia Australia

Gianfrancesco Goracci Italy

Sarah Almond United Kingdom

Eddie O’Gorman Switzerland

Sachit Shah United Kingdom

Marco Piccardi Italy

A. Larnaout

442 ×1.8

138 ×1.0

CMN

69 ×0.5

NEURO

20 ×0.2

78 ×0.9

BIOCH

Citations per year, relative to A. Larnaout A. Larnaout (= 1×) peers Marco Piccardi

Countries citing papers authored by A. Larnaout

Since Specialization

Citations

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

Fields of papers citing papers by A. Larnaout

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Larnaout

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Amouri, Rim, et al.. (2009). Allelic ROBO3 Heterogeneity in Tunisian Patients with Horizontal Gaze Palsy with Progressive Scoliosis. Journal of Molecular Neuroscience. 39(3). 337–341. 25 indexed citations

Larnaout, A., et al.. (2008). Wilson's Disease: Appreciable Improvement of Sub-cortical White Matter Abnormalities after Copper Chelating Treatment: Five Years Follow-up. Neuropediatrics. 39(3). 176–178. 4 indexed citations

Larnaout, A., Rim Amouri, M. Kéfi, & Fayçal Hentati. (2008). l‐2‐Hydroxyglutaric aciduria: Clinical and molecular study in three Tunisian families. Identification of a new mutation and inter‐familial phenotype variability. Journal of Inherited Metabolic Disease. 31(S2). 375–379. 11 indexed citations

Gouider‐Khouja, N., et al.. (2004). Paralysie du regard latéral et scoliose progressive : à propos de 4 familles tunisiennes. Revue Neurologique. 160(3). 307–310. 2 indexed citations

Gouider‐Khouja, N., A. Larnaout, Rim Amouri, et al.. (2003). Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism & Related Disorders. 9(5). 247–251. 69 indexed citations

Chaabane, Mohamed, et al.. (2000). Nasu-Hakola disease in two Tunisian siblings: new radiological findings. Neuroradiology. 42(5). 375–378. 6 indexed citations

Copp, Richard P., Thomas Wısnıewskı, Fayçal Hentati, et al.. (1999). Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders. Brain Research. 822(1-2). 80–87. 97 indexed citations

Larnaout, A., et al.. (1998). Methylmalonic acidaemia with bilateral globus pallidus involvement: A neuropathological study. Journal of Inherited Metabolic Disease. 21(6). 639–644. 23 indexed citations

Larnaout, A., M. Ben Hamida, & Fayçal Hentati. (1998). A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities. Acta Neurologica Scandinavica. 98(6). 452–457. 4 indexed citations

10.

Larnaout, A., et al.. (1998). Juvenile Form of Dihydropteridine Reductase Deficiency in 2 Tunisian Patients. Neuropediatrics. 29(6). 322–323. 2 indexed citations

11.

Larnaout, A., Samir Belal, Christiane Ben Hamida, M. Ben Hamida, & Fayçal Hentati. (1998). Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings. Journal of Neurology. 245(4). 231–235. 13 indexed citations

12.

Zouari, M., Moncef Feki, Christiane Ben Hamida, et al.. (1998). Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. Neuromuscular Disorders. 8(6). 416–425. 44 indexed citations

13.

Larnaout, A., et al.. (1998). Dihydropteridine Reductase Deficiency in a Large Consanguineous Tunisian Family: Clinical, Biochemical, and Neuropathologic Findings. Journal of Child Neurology. 13(10). 475–480. 5 indexed citations

14.

Larnaout, A., Samir Belal, M. Zouari, et al.. (1997). Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. Acta Neuropathologica. 93(6). 633–637. 42 indexed citations

15.

Larnaout, A., et al.. (1994). Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria. Acta Neuropathologica. 88(4). 367–370. 32 indexed citations

16.

Hamida, M. Ben, et al.. (1993). Prevalence Study of Neurologic Disorders in Kelibia (Tunisia). Neuroepidemiology. 12(5). 285–299. 67 indexed citations

17.

Kaabachi, Naziha, A. Larnaout, Daniel Rabier, et al.. (1993). Familial encephalopathy andl‐2‐hydroxyglutaric aciduria. Journal of Inherited Metabolic Disease. 16(5). 893–893. 9 indexed citations

18.

Larnaout, A., et al.. (1992). [Candida albicans meningitis and neurosarcoidosis].. PubMed. 148(12). 762–6. 4 indexed citations

19.

Rocco, Maja Di, et al.. (1990). Arthrogryposis, cholestatic pigmentary liver disease and renal dysfunction: Report of a second family. American Journal of Medical Genetics. 37(2). 237–240. 18 indexed citations

20.

Mbonda, Elie, et al.. (1990). Multiple sclerosis in a black Cameroonian woman.. PubMed. 90(4). 218–22. 6 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.

Explore authors with similar magnitude of impact