Salima Assami

407 total citations
8 papers, 268 citations indexed

About

Salima Assami is a scholar working on Cellular and Molecular Neuroscience, Neurology and Cell Biology. According to data from OpenAlex, Salima Assami has authored 8 papers receiving a total of 268 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 3 papers in Neurology and 3 papers in Cell Biology. Recurrent topics in Salima Assami's work include Hereditary Neurological Disorders (5 papers), Skin and Cellular Biology Research (3 papers) and Neurological diseases and metabolism (3 papers). Salima Assami is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Skin and Cellular Biology Research (3 papers) and Neurological diseases and metabolism (3 papers). Salima Assami collaborates with scholars based in Algeria, France and Germany. Salima Assami's co-authors include Mériem Tazir, Djamel Grid, Tarik Hamadouche, Sonia Nouioua, Jean‐Michel Vallat, Traki Benhassine, Michel Kœnig, M. Tazir, Pascale Bomont and Suzanne Lesage and has published in prestigious journals such as Journal of the Neurological Sciences, Human Mutation and Parkinsonism & Related Disorders.

In The Last Decade

Salima Assami

8 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Salima Assami Algeria	8	177	111	106	85	82	8	268
H Drac Poland	10	183 1.0×	75 0.7×	63 0.6×	68 0.8×	133 1.6×	38	293
Sonia Nouioua Algeria	11	298 1.7×	124 1.1×	105 1.0×	136 1.6×	164 2.0×	18	441
H.M.E. Bienfait Netherlands	9	187 1.1×	57 0.5×	77 0.7×	102 1.2×	105 1.3×	10	306
Heike Pawlack Germany	9	165 0.9×	74 0.7×	235 2.2×	26 0.3×	123 1.5×	9	342
Gian Maria Fabrizi Italy	6	301 1.7×	94 0.8×	164 1.5×	35 0.4×	65 0.8×	8	351
Hatice Karasoy Türkiye	10	88 0.5×	52 0.5×	131 1.2×	52 0.6×	147 1.8×	26	332
Sébastien Brot France	10	134 0.8×	29 0.3×	81 0.8×	48 0.6×	92 1.1×	14	268
Xiaohui Duan China	8	108 0.6×	45 0.4×	56 0.5×	21 0.2×	64 0.8×	22	204
S. Chamberlain United Kingdom	10	270 1.5×	55 0.5×	90 0.8×	40 0.5×	245 3.0×	20	377
Antoine Duquette Canada	9	214 1.2×	79 0.7×	95 0.9×	20 0.2×	251 3.1×	21	394

Countries citing papers authored by Salima Assami

Since Specialization

Citations

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

Fields of papers citing papers by Salima Assami

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Salima Assami

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

All Works

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8 of 8 papers shown

1.

Nouioua, Sonia, et al.. (2012). Multicenter Transversal Two-Phase Study to Determine a National Prevalence of Epilepsy in Algeria. Neuroepidemiology. 39(2). 131–134. 9 indexed citations

2.

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

3.

Belarbi, Soreya, Suzanne Lesage, Traki Benhassine, et al.. (2010). LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort. Parkinsonism & Related Disorders. 16(10). 676–679. 64 indexed citations

4.

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

5.

Tazir, Mériem, Lamia Alipacha, Jean‐Pierre Delaunoy, et al.. (2009). Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients. Journal of the Neurological Sciences. 278(1-2). 77–81. 41 indexed citations

6.

Bomont, Pascale, Christine Ioos, Cengiz Yalçınkaya, et al.. (2003). Identification of seven novel mutations in theGAN gene. Human Mutation. 21(4). 446–446. 42 indexed citations

7.

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

8.

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

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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