Roula Ghaoui

2.3k total citations
22 papers, 486 citations indexed

About

Roula Ghaoui is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Roula Ghaoui has authored 22 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Roula Ghaoui's work include Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiomyopathy and Myosin Studies (5 papers). Roula Ghaoui is often cited by papers focused on Muscle Physiology and Disorders (12 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiomyopathy and Myosin Studies (5 papers). Roula Ghaoui collaborates with scholars based in Australia, United States and United Kingdom. Roula Ghaoui's co-authors include Carolyn M. Sue, Daniel G. MacArthur, Sandra T. Cooper, Nigel F. Clarke, Roser Pons, Monkol Lek, Toni S. Pearson, Kathryn N. North, Leigh B. Waddell and Mark R. Davis and has published in prestigious journals such as Brain, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Roula Ghaoui

21 papers receiving 477 citations

Peers

Roula Ghaoui

CMN

GENET

CCM

Karlla W. Brigatti United States

Gina O’Grady New Zealand

Carmen Paradas Spain

Meyke Schouten Netherlands

David S. Lynch United Kingdom

Soledad Monges Argentina

Edgard Verdura Spain

Carlos Cervera Spain

Dong-Hui Chen United States

Simona Brajkovic Italy

Karlla W. Brigatti United States

Roula Ghaoui

364 ×1.2

180 ×1.4

CMN

75 ×0.6

GENET

73 ×0.6

GENET

34 ×0.4

CCM

Citations per year, relative to Roula Ghaoui Roula Ghaoui (= 1×) peers Karlla W. Brigatti

Countries citing papers authored by Roula Ghaoui

Since Specialization

Citations

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

Fields of papers citing papers by Roula Ghaoui

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roula Ghaoui

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

Davis, Ryan L., Karl Ng, Roula Ghaoui, et al.. (2025). Long-read sequencing for diagnosis of genetic myopathies. BMJ Neurology Open. 7(1). e000990–e000990. 1 indexed citations

Burton, E. F., et al.. (2024). Tetrodotoxin toxicity: an increasing threat. Practical Neurology. 25(4). 377–379. 1 indexed citations

Ghaoui, Roula, Thuong Ha, Jennifer Kerkhof, et al.. (2023). Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis. Neuromuscular Disorders. 33(6). 484–489. 3 indexed citations

Scriba, Carolin K., Igor Stevanovski, Sanjog R. Chintalaphani, et al.. (2023). RFC1 in an Australasian neurological disease cohort: extending the genetic heterogeneity and implications for diagnostics. Brain Communications. 5(4). fcad208–fcad208. 9 indexed citations

Ghaoui, Roula, et al.. (2023). Segmental Uniparental Isodisomy Causing an “Inside-to-Outside” Limb-Girdle Muscular Dystrophy Due to a Homozygous Mutation in POGLUT1. JAMA Neurology. 80(8). 868–868. 1 indexed citations

Mroczek, Magdalena, Hacer Durmuş, Sunita Bijarnia‐Mahay, et al.. (2020). Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patients. Neuromuscular Disorders. 30(4). 310–314. 16 indexed citations

Khoo, Anthony, et al.. (2019). Progressive cranial neuropathy and uterine involvement in myeloid sarcoma. BMJ Neurology Open. 1(1). e000006–e000006.

Bryen, Samantha J., Himanshu Joshi, Frances J. Evesson, et al.. (2019). Pathogenic Abnormal Splicing Due to Intronic Deletions that Induce Biophysical Space Constraint for Spliceosome Assembly. The American Journal of Human Genetics. 105(3). 573–587. 20 indexed citations

Riley, Lisa G., Leigh B. Waddell, Roula Ghaoui, et al.. (2019). Recessive DES cardio/myopathy without myofibrillar aggregates: intronic splice variant silences one allele leaving only missense L190P-desmin. European Journal of Human Genetics. 27(8). 1267–1273. 14 indexed citations

10.

Pearson, Toni S., Roser Pons, Roula Ghaoui, & Carolyn M. Sue. (2019). Genetic mimics of cerebral palsy. Movement Disorders. 34(5). 625–636. 66 indexed citations

11.

Ghaoui, Roula & Carolyn M. Sue. (2018). Movement disorders in mitochondrial disease. Journal of Neurology. 265(5). 1230–1240. 34 indexed citations

12.

Mathey, Emily K., Nidhi Garg, Tuan Nghia Nguyen, et al.. (2017). Autoantibody responses to nodal and paranodal antigens in chronic inflammatory neuropathies. Journal of Neuroimmunology. 309. 41–46. 41 indexed citations

13.

Ghaoui, Roula, Tatiana Benavides Damm, Monkol Lek, et al.. (2016). TOR1AIP1 as a cause of cardiac failure and recessive limb-girdle muscular dystrophy. Neuromuscular Disorders. 26(8). 500–503. 29 indexed citations

14.

O’Grady, Gina, Alan Ma, Deborah A. Sival, et al.. (2016). Prominent scapulae mimicking an inherited myopathy expands the phenotype of CHD7-related disease. European Journal of Human Genetics. 24(8). 1216–1219. 2 indexed citations

15.

O’Grady, Gina, Monkol Lek, Shireen R. Lamandé, et al.. (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there. Annals of Neurology. 80(1). 101–111. 49 indexed citations

16.

Cabrera‐Serrano, Macarena, Roula Ghaoui, Gianina Ravenscroft, et al.. (2015). Expanding the phenotype of GMPPB mutations. Brain. 138(4). 836–844. 43 indexed citations

17.

Ghaoui, Roula, Sandra T. Cooper, Monkol Lek, et al.. (2015). Use of whole-exome sequencing for diagnosis of Limb-Girdle muscular dystrophy. Murdoch Research Repository (Murdoch University). 2 indexed citations

18.

Cabrera‐Serrano, Macarena, et al.. (2014). T.P.33. Neuromuscular Disorders. 24(9-10). 874–874. 2 indexed citations

19.

Ghaoui, Roula, et al.. (2014). Axonal excitability in primary amyloidotic neuropathy. Muscle & Nerve. 51(3). 443–445. 4 indexed citations

20.

Ghaoui, Roula, Nigel F. Clarke, P. Hollingworth, & Merrilee Needham. (2013). Muscle disorders: the latest investigations. Internal Medicine Journal. 43(9). 970–978. 4 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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