Monique M. Ryan

12.7k total citations
207 papers, 4.1k citations indexed

About

Monique M. Ryan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Monique M. Ryan has authored 207 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 61 papers in Cellular and Molecular Neuroscience and 53 papers in Genetics. Recurrent topics in Monique M. Ryan's work include Neurogenetic and Muscular Disorders Research (52 papers), Hereditary Neurological Disorders (47 papers) and Muscle Physiology and Disorders (40 papers). Monique M. Ryan is often cited by papers focused on Neurogenetic and Muscular Disorders Research (52 papers), Hereditary Neurological Disorders (47 papers) and Muscle Physiology and Disorders (40 papers). Monique M. Ryan collaborates with scholars based in Australia, United States and Italy. Monique M. Ryan's co-authors include Robert Ouvrier, Joshua Burns, Kathryn N. North, Andrew J. Kornberg, Eppie M. Yiu, Basil T. Darras, Susan T. Iannaccone, H. Royden Jones, Nigel G. Laing and Garth A. Nicholson and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Monique M. Ryan

202 papers receiving 4.0k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Monique M. Ryan 1.7k 1.2k 945 911 597 207 4.1k
Giuseppe Vita 2.5k 1.5× 1.1k 1.0× 590 0.6× 1.1k 1.2× 815 1.4× 245 5.5k
Anne M. Connolly 2.6k 1.5× 747 0.6× 924 1.0× 562 0.6× 658 1.1× 132 4.9k
Elena Pegoraro 3.8k 2.3× 1.6k 1.3× 1.1k 1.1× 1.0k 1.1× 969 1.6× 196 5.6k
Gerald M. Fenichel 2.3k 1.4× 772 0.7× 637 0.7× 786 0.9× 499 0.8× 111 4.7k
Robert Ouvrier 1.0k 0.6× 1.8k 1.6× 527 0.6× 1.2k 1.3× 153 0.3× 131 4.9k
Emma Ciafaloni 2.8k 1.6× 678 0.6× 766 0.8× 896 1.0× 599 1.0× 113 4.3k
Rudolf Korinthenberg 1.2k 0.7× 1.1k 0.9× 577 0.6× 1.2k 1.4× 195 0.3× 184 4.6k
D. Pongratz 2.3k 1.3× 743 0.6× 308 0.3× 825 0.9× 499 0.8× 185 5.0k
Lynne C. Weaver 1.0k 0.6× 2.0k 1.7× 291 0.3× 656 0.7× 953 1.6× 146 6.9k
Atchayaram Nalini 989 0.6× 625 0.5× 642 0.7× 1.3k 1.4× 226 0.4× 239 2.9k

Countries citing papers authored by Monique M. Ryan

Since Specialization
Citations

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

Fields of papers citing papers by Monique M. Ryan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Monique M. Ryan. 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 Monique M. Ryan. The network helps show where Monique M. Ryan may publish in the future.

Co-authorship network of co-authors of Monique M. Ryan

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

All Works

20 of 20 papers shown
1.
Woodcock, Ian, Anita Cairns, Zoe E. Davidson, et al.. (2025). Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double‐blind placebo‐controlled crossover trial. Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy. 45(6). 341–351. 1 indexed citations
2.
Ryan, Monique M., et al.. (2025). Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents. Journal of the Peripheral Nervous System. 30(1). e70002–e70002. 1 indexed citations
3.
Billich, Natassja, Paula Bray, Helen Truby, et al.. (2024). Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy. Muscle & Nerve. 69(4). 448–458.
4.
Woodcock, Ian, et al.. (2022). Correlation between whole body muscle MRI and functional measures in paediatric patients with facioscapulohumeral muscular dystrophy. Neuromuscular Disorders. 33(1). 15–23. 6 indexed citations
5.
Billich, Natassja, et al.. (2021). The association between dietary factors and body weight and composition in boys with Duchenne muscular dystrophy. Journal of Human Nutrition and Dietetics. 35(5). 804–815. 3 indexed citations
6.
Cabrera‐Serrano, Macarena, David Coote, Dimitar N. Azmanov, et al.. (2020). A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy. Journal of Medical Genetics. 57(12). 835–842. 19 indexed citations
7.
Richmond, Christopher M., Richard J. Leventer, Monique M. Ryan, & Martin B. Delatycki. (2019). Cerebellar ataxia with normal intellect associated with a homozygous truncating variant in CA8. Clinical Genetics. 97(3). 516–520. 2 indexed citations
8.
Jones, Hannah, Samantha J. Bryen, Leigh B. Waddell, et al.. (2019). Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants. Neuromuscular Disorders. 29(12). 913–919. 11 indexed citations
9.
10.
Kennedy, Rachel A., Kate Carroll, Kade L. Paterson, et al.. (2019). Physical activity of children and adolescents with Charcot-Marie-Tooth neuropathies: A cross-sectional case-controlled study. PLoS ONE. 14(6). e0209628–e0209628. 9 indexed citations
11.
Kariyawasam, Didu, Arlene D’Silva, Cindy Lin, Monique M. Ryan, & Michelle A. Farrar. (2019). Biomarkers and the Development of a Personalized Medicine Approach in Spinal Muscular Atrophy. Frontiers in Neurology. 10. 898–898. 49 indexed citations
12.
Wen, Sophie, et al.. (2019). Pediatric Neuroschistosomiasis: A Case Report and Review of the Literature. Journal of the Pediatric Infectious Diseases Society. 8(5). 489–491. 7 indexed citations
13.
Kennedy, Rachel A., Kate Carroll, Kade L. Paterson, Monique M. Ryan, & Jennifer L. McGinley. (2017). Deterioration in gait and functional ambulation in children and adolescents with Charcot–Marie–Tooth disease over 12 months. Neuromuscular Disorders. 27(7). 658–666. 19 indexed citations
14.
Yiu, Eppie M., Katherine J. Lee, Kate Carroll, et al.. (2015). Peripheral nerve ultrasound in pediatric Charcot-Marie-Tooth disease type 1A. Neurology. 84(6). 569–574. 35 indexed citations
15.
Hughes, Andrew, et al.. (2014). Changing Patterns For The Introduction Of Non-Invasive Ventilation In Children With Neuromuscular Disease. 16(1). 2 indexed citations
16.
Kennerson, Marina, Eppie M. Yiu, David Chuang, et al.. (2013). A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene. Human Molecular Genetics. 22(7). 1404–1416. 56 indexed citations
17.
Yiu, Eppie M., Geneieve Tai, Roger E. Peverill, et al.. (2013). An Open Label Clinical Pilot Study of Resveratrol as a Treatment for Friedreich Ataxia (S43.006). Neurology. 80(7_supplement). 2 indexed citations
18.
Adams, A.M., Graham McClorey, Hong M. Moulton, et al.. (2007). Induced dystrophin exon skipping in human muscle explants. The Journal of Gene Medicine. 9(6). 534–535. 7 indexed citations
19.
Ilkovski, Biljana, Sandra T. Cooper, Kristen L. Nowak, et al.. (2001). Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene. The American Journal of Human Genetics. 68(6). 1333–1343. 119 indexed citations
20.
Kitchen, W. H., V. Y. H. YU, A. A. ORGILL, et al.. (1982). Infants born before 29 weeks gestation: survival and morbidity at 2 years of age. BJOG An International Journal of Obstetrics & Gynaecology. 89(11). 887–891. 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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