Amina Chaouch

1.0k total citations
14 papers, 314 citations indexed

About

Amina Chaouch is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Amina Chaouch has authored 14 papers receiving a total of 314 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 4 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Amina Chaouch's work include Amyotrophic Lateral Sclerosis Research (6 papers), Myasthenia Gravis and Thymoma (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Amina Chaouch is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (6 papers), Myasthenia Gravis and Thymoma (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Amina Chaouch collaborates with scholars based in United Kingdom, France and Bulgaria. Amina Chaouch's co-authors include Hanns Lochmüller, Juliane S. Müller, Ulrike Schara, Velina Guergueltcheva, Marina Dusl, Angela Abicht, Rosana Hermínia Scola, Violeta Mihaylova, David Beeson and Maja von der Hagen and has published in prestigious journals such as Journal of the Neurological Sciences, Human Mutation and Journal of Neurology.

In The Last Decade

Amina Chaouch

12 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amina Chaouch United Kingdom	7	190	146	115	37	33	14	314
Stéphanie Bauché France	10	113 0.6×	150 1.0×	71 0.6×	40 1.1×	58 1.8×	20	271
Marina Dusl Germany	8	218 1.1×	139 1.0×	127 1.1×	39 1.1×	28 0.8×	10	313
Annabel K. Wang United States	6	105 0.6×	127 0.9×	50 0.4×	28 0.8×	29 0.9×	10	280
Cécile Cauquil France	9	69 0.4×	150 1.0×	46 0.4×	13 0.4×	46 1.4×	20	268
Stayko Sarafov Bulgaria	9	68 0.4×	215 1.5×	37 0.3×	40 1.1×	29 0.9×	20	297
Daniel Natera‐de Benito Spain	13	73 0.4×	214 1.5×	60 0.5×	59 1.6×	55 1.7×	59	399
Paloma González-Pérez United States	8	85 0.4×	92 0.6×	70 0.6×	52 1.4×	61 1.8×	13	247
Ulf Drugge Sweden	11	118 0.6×	328 2.2×	101 0.9×	29 0.8×	89 2.7×	26	501
Josiah Chai Singapore	7	142 0.7×	72 0.5×	24 0.2×	27 0.7×	51 1.5×	18	308
Sheng Yao China	12	118 0.6×	253 1.7×	31 0.3×	51 1.4×	184 5.6×	33	434

Countries citing papers authored by Amina Chaouch

Since Specialization

Citations

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

Fields of papers citing papers by Amina Chaouch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amina Chaouch

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

All Works

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14 of 14 papers shown

Young, Carolyn, Amina Chaouch, Christopher McDermott, et al.. (2025). Fatigue in amyotrophic lateral sclerosis/motor neuron disease: prevalence, influences and trajectories. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 27(1-2). 78–89.

Young, Carolyn, Amina Chaouch, Christopher McDermott, et al.. (2025). Determinants and progression of stigma in amyotrophic lateral sclerosis/motor neuron disease. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 26(3-4). 192–202. 1 indexed citations

Alder, J.F., Chrysanthus Chukwuma, Tracey Farragher, et al.. (2025). Impact of relative deprivation and ethnicity on the incidence rate of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 26(5-6). 558–565.

Young, Carolyn, Amina Chaouch, Christopher McDermott, et al.. (2024). Improving the measurement properties of the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R): deriving a valid measurement total for the calculation of change. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(3-4). 400–409. 5 indexed citations

Chaouch, Amina, et al.. (2024). Delayed onset post-traumatic wound botulism. Practical Neurology. 24(4). 320–325. 1 indexed citations

Young, Carolyn, Amina Chaouch, Christopher McDermott, et al.. (2024). Dyspnea (breathlessness) in amyotrophic lateral sclerosis/motor neuron disease: prevalence, progression, severity, and correlates. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(5-6). 475–485. 3 indexed citations

Chaouch, Amina, et al.. (2022). Perry Syndrome with Intrafamilial Heterogeneity in Presentation and Survival Including Acute Respiratory Failure: Case Series. Movement Disorders Clinical Practice. 9(6). 816–820. 1 indexed citations

Hiller, Monika, Pietro Spitali, Stijn Oonk, et al.. (2014). Fibronectin is a serum biomarker for Duchenne muscular dystrophy. PROTEOMICS - CLINICAL APPLICATIONS. 8(3-4). 269–278. 70 indexed citations

Lorenzoni, Paulo José, Rosana Hermínia Scola, Cláudia Suemi Kamoi Kay, et al.. (2013). Salbutamol therapy in congenital myasthenic syndrome due to DOK7 mutation. Journal of the Neurological Sciences. 331(1-2). 155–157. 39 indexed citations

10.

Wagner, Matias, Amina Chaouch, Juliane Müller, et al.. (2012). Presymptomatic late-onset Pompe disease identified by the dried blood spot test. Neuromuscular Disorders. 23(1). 89–92. 8 indexed citations

11.

Chaouch, Amina, David Beeson, Daniel Hantaı̈, & Hanns Lochmüller. (2012). 186th ENMC International Workshop: Congenital myasthenic syndromes 24–26 June 2011, Naarden, The Netherlands. Neuromuscular Disorders. 22(6). 566–576. 29 indexed citations

12.

Abicht, Angela, Marina Dusl, Constanze Gallenmüller, et al.. (2012). Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients. Human Mutation. 33(10). 1474–1484. 91 indexed citations

13.

Chaouch, Amina, Juliane S. Müller, Velina Guergueltcheva, et al.. (2011). A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome. Journal of Neurology. 259(3). 474–481. 50 indexed citations

14.

Barišić, Nina, Amina Chaouch, Juliane S. Müller, & Hanns Lochmüller. (2011). Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes. European Journal of Paediatric Neurology. 15(3). 189–196. 16 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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