N. Gouider‐Khouja

1.6k total citations
47 papers, 879 citations indexed

About

N. Gouider‐Khouja is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, N. Gouider‐Khouja has authored 47 papers receiving a total of 879 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Neurology, 13 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in N. Gouider‐Khouja's work include Parkinson's Disease Mechanisms and Treatments (11 papers), Neurological disorders and treatments (11 papers) and Neurological diseases and metabolism (9 papers). N. Gouider‐Khouja is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (11 papers), Neurological disorders and treatments (11 papers) and Neurological diseases and metabolism (9 papers). N. Gouider‐Khouja collaborates with scholars based in Tunisia, France and Belgium. N. Gouider‐Khouja's co-authors include Yves Agid, Marie Vidailhet, B. Pillon, Muriel Bonnet, S. Rivaud, Bertrand Gaymard, Charles Pierrot‐Deseilligny, Samir Belal, M. Ben Hamida and Fayçal Hentati and has published in prestigious journals such as Neurology, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

N. Gouider‐Khouja

42 papers receiving 856 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. Gouider‐Khouja Tunisia 16 496 271 236 167 98 47 879
Nataša Dragašević Serbia 19 690 1.4× 478 1.8× 229 1.0× 165 1.0× 99 1.0× 47 1.2k
Pierre Castelnau France 16 268 0.5× 160 0.6× 283 1.2× 135 0.8× 79 0.8× 50 826
Vera Tadić Germany 18 556 1.1× 327 1.2× 190 0.8× 153 0.9× 76 0.8× 43 833
Yasushi Takehisa Japan 19 500 1.0× 260 1.0× 359 1.5× 183 1.1× 198 2.0× 35 1.0k
Farzad Sina Iran 11 445 0.9× 242 0.9× 231 1.0× 300 1.8× 86 0.9× 24 706
Amanda Singleton United States 14 666 1.3× 490 1.8× 290 1.2× 170 1.0× 202 2.1× 17 985
Yaping Yan China 18 363 0.7× 286 1.1× 257 1.1× 127 0.8× 145 1.5× 59 814
Daniel Kremens United States 11 734 1.5× 241 0.9× 230 1.0× 85 0.5× 64 0.7× 26 993
Elena Lorenzo Spain 13 403 0.8× 179 0.7× 234 1.0× 237 1.4× 185 1.9× 20 741
Cathérine C.S. Delnooz Netherlands 15 523 1.1× 242 0.9× 96 0.4× 133 0.8× 83 0.8× 21 923

Countries citing papers authored by N. Gouider‐Khouja

Since Specialization
Citations

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

Fields of papers citing papers by N. Gouider‐Khouja

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. Gouider‐Khouja. 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 N. Gouider‐Khouja. The network helps show where N. Gouider‐Khouja may publish in the future.

Co-authorship network of co-authors of N. Gouider‐Khouja

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

All Works

20 of 20 papers shown
2.
Kraoua, Ichraf, et al.. (2015). Status dystonicus in childhood.. PubMed. 93(12). 756–9. 19 indexed citations
3.
Benrhouma, Hanène, et al.. (2015). Secondary parkinsonism with bilateral involvement of substantia nigra in cerebral malaria. Journal of Pediatric Neurology. 10(3). 225–227. 1 indexed citations
4.
Kraoua, Ichraf, et al.. (2014). Lesch Nyhan syndrome: A novel complex mutation in a Tunisian child. Brain and Development. 36(10). 921–923. 2 indexed citations
5.
Achour, N. Ben, et al.. (2013). Cognitive and psychological profile in Tunisian children with Duchenne muscular dystrophy. Journal of the Neurological Sciences. 333. e445–e445.
6.
Achour, N. Ben, et al.. (2013). Une sténose congénitale des foramens interventriculaires révélée par une hypertension intracrânienne à rechute. Neurochirurgie. 59(2). 93–96. 2 indexed citations
7.
Benrhouma, Hanène, et al.. (2011). Epilepsy Aspects and EEG Patterns in Neuro-Metabolic Diseases. Journal of Behavioral and Brain Science. 1(2). 69–74. 3 indexed citations
8.
Messaoud, Olfa, Mariem Ben Rekaya, Héla Azaiez, et al.. (2011). Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity. Archives of Dermatological Research. 304(2). 171–176. 18 indexed citations
9.
Benrhouma, Hanène, et al.. (2011). Methylmalonic acidemia and hyperglycemia: An unusual association. Brain and Development. 34(2). 113–114. 11 indexed citations
10.
Ahmed, Mohamed Ben, et al.. (2010). Enrichissement d'ontologie par une base générique minimale de règles associatives - application aux maladies neurologies : les dystonies.. 289–300. 2 indexed citations
11.
Messaoud, Olfa, Mariem Ben Rekaya, Rym Kéfi, et al.. (2010). Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family. British Journal of Dermatology. 162(4). 883–886. 15 indexed citations
12.
Kraoua, Ichraf, et al.. (2008). [Slow channel syndrome: clinical and neurophysiological aspects].. PubMed. 86(2). 202–4. 1 indexed citations
13.
Gouider‐Khouja, N., et al.. (2006). Étude comparative des aspects cliniques et paracliniques de la sclérose en plaques en Tunisie. Revue Neurologique. 162(6-7). 729–733. 16 indexed citations
14.
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
15.
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
16.
Gouider‐Khouja, N., et al.. (2000). Intrafamilial phenotypic variability of Hallervorden–Spätz syndrome in a Tunisian family. Parkinsonism & Related Disorders. 6(3). 175–179. 7 indexed citations
17.
Gouider‐Khouja, N., et al.. (2000). Hemiparkinsonian syndrome due to a cerebral tumor infiltrating the substantia nigra. Parkinsonism & Related Disorders. 6(2). 115–117. 1 indexed citations
18.
Gouider‐Khouja, N., et al.. (1999). [Hemifacial spasm and its treatment with botulinum toxin].. PubMed. 77(1). 41–4. 1 indexed citations
19.
Bonnet, A. M., J. Pichon, Marie Vidailhet, et al.. (1999). Urinary Disturbances in Striatonigral Degeneration and Parkinson's Disease: Clinical and Urodynamic Aspects. The Journal of Urology. 161(6). 2033–2033. 2 indexed citations
20.
Gouider‐Khouja, N., Marie Vidailhet, Muriel Bonnet, J. Pichon, & Yves Agid. (1995). “Pure” striatonigral degeneration and Parkinson's disease: A comparative clinical study. Movement Disorders. 10(3). 288–294. 39 indexed citations

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