Karima Ghorab

1.3k total citations
19 papers, 476 citations indexed

About

Karima Ghorab is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Karima Ghorab has authored 19 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 9 papers in Cellular and Molecular Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Karima Ghorab's work include Peripheral Neuropathies and Disorders (9 papers), Hereditary Neurological Disorders (7 papers) and Genetic Neurodegenerative Diseases (4 papers). Karima Ghorab is often cited by papers focused on Peripheral Neuropathies and Disorders (9 papers), Hereditary Neurological Disorders (7 papers) and Genetic Neurodegenerative Diseases (4 papers). Karima Ghorab collaborates with scholars based in France, United States and Switzerland. Karima Ghorab's co-authors include Laurent Magy, Jean‐Michel Vallat, Stéphane Mathis, Laurence Richard, Christiane Caudie, Pascal Laforêt, Johann Böhm, Shahram Attarian, Marc Bartoli and Michel Fardeau and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and The American Journal of Human Genetics.

In The Last Decade

Karima Ghorab

18 papers receiving 469 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karima Ghorab France 11 205 194 190 93 54 19 476
M G Sweeney United Kingdom 18 314 1.5× 128 0.7× 1.0k 5.5× 10 0.1× 41 0.8× 21 1.2k
Meriel McEntagart United Kingdom 14 157 0.8× 49 0.3× 273 1.4× 81 0.9× 41 0.8× 24 576
Jonathan D. Louie United States 8 40 0.2× 110 0.6× 82 0.4× 34 0.4× 15 0.3× 12 294
Joshua Menke United States 7 87 0.4× 320 1.6× 63 0.3× 17 0.2× 14 0.3× 20 504
Li Wu China 14 86 0.4× 132 0.7× 435 2.3× 10 0.1× 15 0.3× 36 738
Francesco Laschena Italy 12 172 0.8× 41 0.2× 419 2.2× 43 0.5× 20 0.4× 18 534
Andreas Woppmann United States 8 184 0.9× 354 1.8× 385 2.0× 7 0.1× 44 0.8× 8 724
Anthony P. Turel United States 8 101 0.5× 115 0.6× 124 0.7× 32 0.3× 5 0.1× 10 444
Katie Mayne United Kingdom 8 91 0.4× 56 0.3× 164 0.9× 6 0.1× 16 0.3× 10 397
H. Goebel Germany 13 53 0.3× 53 0.3× 263 1.4× 13 0.1× 58 1.1× 37 475

Countries citing papers authored by Karima Ghorab

Since Specialization
Citations

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

Fields of papers citing papers by Karima Ghorab

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karima Ghorab

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

All Works

19 of 19 papers shown
1.
Vicart, Savine, Yann Péréon, Karima Ghorab, et al.. (2024). Self-reported outcomes and quality of life of patients with non-dystrophic myotonia: The French IMPACT 2022 survey. Revue Neurologique. 180(8). 791–797.
2.
Richard, Laurence, Jean‐Michel Vallat, Karima Ghorab, et al.. (2023). The First Large Deletion of ATL3 Identified in a Patient Presenting with a Sensory Polyneuropathy. Biomedicines. 11(6). 1565–1565. 2 indexed citations
3.
Richard, Laurence, Foudil Lamari, Karima Ghorab, et al.. (2022). GM2 gangliosidosis AB variant: first case of late onset and review of the literature. Neurological Sciences. 43(11). 6517–6527. 5 indexed citations
4.
Deschamps, Nathalie, Stéphane Mathis, Mathilde Duchesne, et al.. (2021). CIDP and hemopathies, an underestimated association. Journal of the Neurological Sciences. 429. 118055–118055. 1 indexed citations
5.
Viollet, Louis, Kathryn J. Swoboda, Rong Mao, et al.. (2020). A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies. European Journal of Medical Genetics. 63(12). 104063–104063. 5 indexed citations
6.
Vallat, Jean‐Michel, Mathilde Duchesne, Philippe Corcia, et al.. (2020). The Wide Spectrum of Pathophysiologic Mechanisms of Paraproteinemic Neuropathy. Neurology. 96(5). 214–225. 12 indexed citations
7.
Lerat, Justine, Corinne Magdelaine, Caroline Espil, et al.. (2019). A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next‐generation sequencing and review of the literature. Journal of the Peripheral Nervous System. 24(1). 139–144. 14 indexed citations
8.
Mathis, Stéphane, Laurent Magy, Gwendal Le Masson, et al.. (2018). Value of nerve biopsy in the management of peripheral neuropathies. Expert Review of Neurotherapeutics. 18(7). 589–602. 8 indexed citations
9.
Mathis, Stéphane, Mériem Tazir, Laurent Magy, et al.. (2017). History and current difficulties in classifying inherited myopathies and muscular dystrophies. Journal of the Neurological Sciences. 384. 50–54. 16 indexed citations
10.
Marziniak, Martin, Karima Ghorab, Wojciech Kozubski, et al.. (2016). Variations in multiple sclerosis practice within Europe – Is it time for a new treatment guideline?. Multiple Sclerosis and Related Disorders. 8. 35–44. 20 indexed citations
11.
Mathis, Stéphane, Laurent Magy, Philippe Corcia, et al.. (2016). Simultaneous Combined Myositis, Inflammatory Polyneuropathy, and Overlap Myasthenic Syndrome. SHILAP Revista de lepidopterología. 2016. 1–11. 2 indexed citations
12.
Duchesne, Mathilde, Stéphane Mathis, Philippe Corcia, et al.. (2015). Value of Nerve Biopsy in Patients With Latent Malignant Hemopathy and Peripheral Neuropathy. Medicine. 94(3). e394–e394. 18 indexed citations
13.
Vallat, Jean‐Michel, et al.. (2015). Natalizumab as a Disease-Modifying Therapy in Chronic Inflammatory Demyelinating Polyneuropathy - A Report of Three Cases. European Neurology. 73(5-6). 294–302. 20 indexed citations
14.
Magy, Laurent, et al.. (2015). Heterogeneity of Polyneuropathy Associated with Anti-MAG Antibodies. Journal of Immunology Research. 2015. 1–9. 56 indexed citations
15.
Böhm, Johann, Frédéric Chevessier, Catherine Koch, et al.. (2013). Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy. The American Journal of Human Genetics. 92(2). 271–278. 149 indexed citations
16.
Fauchais, A.L., Laurence Richard, G. Gondran, et al.. (2010). Neuropathie des petites fibres au cours du syndrome de Sjögren primitif. La Revue de Médecine Interne. 32(3). 142–148. 22 indexed citations
17.
Funalot, Benoît, Robert Ouvrier, Leïla Lazaro, et al.. (2009). Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Type 2 Caused by Mitofusin 2 Mutations. Archives of Neurology. 66(12). 1511–6. 92 indexed citations
18.
Magy, Laurent, et al.. (2008). Intranervous immunoglobulin deposits: An underestimated mechanism of neuropathy. Muscle & Nerve. 38(1). 904–911. 26 indexed citations
19.
Ghorab, Karima, et al.. (2007). Carotid Angioplasty Stenting Revisited: Clinical and Radiological (MRI) Outcome. Cerebrovascular Diseases. 25(1-2). 21–25. 8 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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