Djamel Grid

2.3k total citations
28 papers, 1.3k citations indexed

About

Djamel Grid is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Djamel Grid has authored 28 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 12 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Djamel Grid's work include Hereditary Neurological Disorders (21 papers), Neurological diseases and metabolism (8 papers) and RNA Research and Splicing (5 papers). Djamel Grid is often cited by papers focused on Hereditary Neurological Disorders (21 papers), Neurological diseases and metabolism (8 papers) and RNA Research and Splicing (5 papers). Djamel Grid collaborates with scholars based in France, Algeria and Switzerland. Djamel Grid's co-authors include Mériem Tazir, Nicolas Lévy, Jean-Michel Vallat, Malika Chaouch, Annachiara De Sandre‐Giovannoli, T. Hammadouche, Serguei Kozlov, Pierre Szepetowski, Antoon Vandenberghe and Colin L. Stewart and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Djamel Grid

28 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Djamel Grid France	17	710	692	309	272	251	28	1.3k
A. Löfgren Belgium	18	878 1.2×	1.1k 1.6×	308 1.0×	164 0.6×	304 1.2×	37	1.8k
Nazha Birouk France	17	1.0k 1.4×	344 0.5×	362 1.2×	263 1.0×	463 1.8×	47	1.3k
P. F. Chance United States	21	608 0.9×	373 0.5×	258 0.8×	113 0.4×	315 1.3×	28	1.1k
Е. Л. Дадали Russia	10	454 0.6×	260 0.4×	208 0.7×	152 0.6×	207 0.8×	115	760
Tine Deconinck Belgium	17	376 0.5×	376 0.5×	149 0.5×	89 0.3×	107 0.4×	28	733
John Wolff United States	18	411 0.6×	481 0.7×	81 0.3×	54 0.2×	154 0.6×	23	844
Gaoying Ren United States	12	312 0.4×	449 0.6×	76 0.2×	59 0.2×	176 0.7×	19	928
Alice B. Schindler United States	15	396 0.6×	607 0.9×	128 0.4×	132 0.5×	202 0.8×	37	1.0k
Hideji Hashida Japan	19	520 0.7×	672 1.0×	111 0.4×	46 0.2×	434 1.7×	49	1.2k
H.-M. Meinck Germany	13	553 0.8×	362 0.5×	113 0.4×	146 0.5×	952 3.8×	18	1.4k

Countries citing papers authored by Djamel Grid

Since Specialization

Citations

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

Fields of papers citing papers by Djamel Grid

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Djamel Grid

This figure shows the co-authorship network connecting the top 25 collaborators of Djamel Grid. A scholar is included among the top collaborators of Djamel Grid 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 Djamel Grid. Djamel Grid 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

Nouioua, Sonia, Tarik Hamadouche, Benoît Funalot, et al.. (2011). Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes. Neuromuscular Disorders. 21(8). 543–550. 18 indexed citations

Tazir, Mériem, Sonia Nouioua, Laurent Magy, et al.. (2009). Phenotypic variability in giant axonal neuropathy. Neuromuscular Disorders. 19(4). 270–274. 40 indexed citations

Klebe, Stephan, Alexandra Dürr, Naïma Bouslam, et al.. (2007). Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(7). 854–861. 14 indexed citations

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). G.O.3 Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H. Neuromuscular Disorders. 17(9-10). 767–767. 3 indexed citations

Delague, Valérie, Arnaud Jacquier, Tarik Hamadouche, et al.. (2007). Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H. The American Journal of Human Genetics. 81(1). 1–16. 117 indexed citations

Elleuch, Nizar, Naïma Bouslam, Sylvain Hanein, et al.. (2007). Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families. Neurogenetics. 8(4). 307–315. 15 indexed citations

Vallat, Jean‐Michel, Laurent Magy, É. Lagrange, et al.. (2007). Diagnostic value of ultrastructural nerve examination in Charcot-Marie-Tooth disease: two CMT 1B cases with pseudo-recessive inheritance. Acta Neuropathologica. 113(4). 443–449. 16 indexed citations

Vallat, Jean‐Michel, Djamel Grid, Corinne Magdelaine, et al.. (2005). Formes autosomales récessives de la maladie de Charcot-Marie-Tooth. Bulletin de l Académie Nationale de Médecine. 189(1). 55–69. 2 indexed citations

Vallat, Jean-Michel, Mériem Tazir, Corinne Magdelaine, Franck Sturtz, & Djamel Grid. (2005). Autosomal-Recessive Charcot-Marie-Tooth Diseases. Journal of Neuropathology & Experimental Neurology. 64(5). 363–370. 30 indexed citations

10.

Tazir, Mériem, Jean-Michel Vallat, Pascale Bomont, et al.. (2002). Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1. Neuromuscular Disorders. 12(9). 849–852. 21 indexed citations

11.

Chaouch, M., Annachiara De Sandre‐Giovannoli, J.M. Vallat, et al.. (2002). The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene. Neuromuscular Disorders. 13(1). 60–67. 65 indexed citations

12.

Sandre‐Giovannoli, Annachiara De, Malika Chaouch, Serguei Kozlov, et al.. (2002). Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse. The American Journal of Human Genetics. 70(3). 726–736. 417 indexed citations

13.

Moore, Tom, Dorothée Ville, Djamel Grid, et al.. (2001). Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME. Epilepsy Research. 46(2). 157–167. 30 indexed citations

14.

Azzedine, Hamid, Salima Assami, Jean‐Michel Vallat, et al.. (2000). Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy. Neuromuscular Disorders. 10(8). 592–598. 33 indexed citations

15.

Salih, Mustafa A., Thierry Maisonobe, Mohammad M. Kabiraj, et al.. (2000). Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity. Neuromuscular Disorders. 10(1). 10–15. 12 indexed citations

16.

Sáenz, Amets, Juan Carlos Galán, Christophe Caloustian, et al.. (1999). Autosomal Dominant Nocturnal Frontal Lobe Epilepsy in a Spanish Family With a Ser252Phe Mutation in the CHRNA4 Gene. Archives of Neurology. 56(8). 1004–1004. 71 indexed citations

17.

Coutinho, Paula, José Barros, Cristina Alves, et al.. (1999). Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias. Archives of Neurology. 56(8). 943–943. 56 indexed citations

18.

Poza, Juan José, Ana María Cobo, Miguel Urtasun, et al.. (1999). Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large basque pedigree linked to chromosome 10q. Annals of Neurology. 45(2). 182–188. 103 indexed citations

19.

Lalioti, Maria D., Hamish S. Scott, Pierre Genton, et al.. (1998). A PCR Amplification Method Reveals Instability of the Dodecamer Repeat in Progressive Myoclonus Epilepsy (EPM1) and No Correlation between the Size of the Repeat and Age at Onset. The American Journal of Human Genetics. 62(4). 842–847. 52 indexed citations

20.

Labauge, Pierre, Réda Ouazzani, A. Mrabet, et al.. (1997). Allelic heterogeneity of mediterranean myoclonus and the cystatin B gene. Annals of Neurology. 41(5). 686–689. 3 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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