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

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double‐blind placebo‐controlled crossover trial 2025 ·Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy ·Ian Woodcock, (unknown), Anita Cairns, Zoe E. Davidson, Michael Kean, (unknown), Anneke Grobler, David Metz, Kate Carroll, Nuran Dilek, (unknown), Monique M. Ryan, Martin B. Delatycki, Eppie M. Yiu	1
2	Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents 2025 ·Journal of the Peripheral Nervous System ·(unknown), Monique M. Ryan, Rachel A. Kennedy, Kate Carroll, (unknown), (unknown), Eppie M. Yiu	1
3	Exploring caregivers' attitudes and beliefs about nutrition and weight management for young people with Duchenne muscular dystrophy 2024 ·Muscle & Nerve ·Natassja Billich, Paula Bray, Helen Truby, (unknown), Monique M. Ryan, Kate Carroll, (unknown), (unknown), Andrew J. Kornberg, (unknown), Michelle A. Farrar, Manoj P. Menezes, (unknown), (unknown), Anita Cairns, Zoe E. Davidson	0
4	Correlation between whole body muscle MRI and functional measures in paediatric patients with facioscapulohumeral muscular dystrophy 2022 ·Neuromuscular Disorders ·Ian Woodcock, (unknown), (unknown), Michael Kean, Monique M. Ryan	6
5	The association between dietary factors and body weight and composition in boys with Duchenne muscular dystrophy 2021 ·Journal of Human Nutrition and Dietetics ·Natassja Billich, (unknown), Helen Truby, Monique M. Ryan, Zoe E. Davidson	3
6	Escalating Dose and Randomized, Controlled Study of Nusinersen in Participants With Spinal Muscular Atrophy (SMA); Study Design and Part A Data for the Phase 2/3 DEVOTE (232SM203) Study to Explore High Dose Nusinersen (2343) 2021 ·Neurology ·John Day, Samuel Ignacio Pascual Pascual, Richard S. Finkel, Monique M. Ryan, Eugenio Mercuri, Darryl C. De Vivo, Jacqueline Montes, Juliana Gurgel‐Giannetti, Giulia Gambino, Rebecca Nuzzo, (unknown), Zdenek Berger	1
7	A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy 2020 ·Journal of Medical Genetics ·Macarena Cabrera‐Serrano, David Coote, Dimitar N. Azmanov, Hayley Goullée, Erik Andersen, Catriona McLean, Mark R. Davis, Ryosuke Ishimura, Zornitza Stark, Jean‐Michel Vallat, Masaaki Komatsu, Andrew J. Kornberg, Monique M. Ryan, Nigel G. Laing, Gianina Ravenscroft	19
8	Cerebellar ataxia with normal intellect associated with a homozygous truncating variant in CA8 2019 ·Clinical Genetics ·Christopher M. Richmond, Richard J. Leventer, Monique M. Ryan, Martin B. Delatycki	2
9	Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants 2019 ·Neuromuscular Disorders ·Hannah Jones, Samantha J. Bryen, Leigh B. Waddell, Adam Bournazos, Mark R. Davis, Michelle A. Farrar, Catriona McLean, David Mowat, Hugo Sampaio, Ian Woodcock, Monique M. Ryan, Kristi Jones, Sandra T. Cooper	11
10	Measurement properties and utility of performance-based outcome measures of physical functioning in individuals with facioscapulohumeral dystrophy – A systematic review and evidence synthesis 2019 ·Neuromuscular Disorders ·(unknown), Jennifer L. McGinley, Ian Woodcock, Monique M. Ryan, Fiona Dobson	3
11	Powered standing wheelchairs promote independence, health and community involvement in adolescents with Duchenne muscular dystrophy 2019 ·Neuromuscular Disorders ·(unknown), Kerry Evans, Nada Murphy, Maina Kava, Anita Cairns, Damian Clarke, Monique M. Ryan, Aris Siafarikas, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Peter Jacoby, Donna Cross, Jenny Downs	22
12	Gait and footwear in children and adolescents with Charcot-Marie-Tooth disease: A cross-sectional, case-controlled study 2018 ·Gait & Posture ·Rachel A. Kennedy, Jennifer L. McGinley, Kade L. Paterson, Monique M. Ryan, Kate Carroll	14
13	Neurologic Melioidosis: Case Report of a Rare Cause of Acute Flaccid Paralysis 2016 ·The Journal of Pediatrics ·Erik Andersen, Mark T. Mackay, Monique M. Ryan	2
14	Changing Patterns For The Introduction Of Non-Invasive Ventilation In Children With Neuromuscular Disease 2014 ·Andrew Hughes, (unknown), Monique M. Ryan, Colin Robertson, (unknown), John Massie	2
15	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 2013 ·Human Molecular Genetics ·Marina Kennerson, Eppie M. Yiu, David Chuang, (unknown), Shih-Chia Tso, (unknown), Rama Chaudhry, Alexander P. Drew, Gary Rance, Martin B. Delatycki, Stephan Züchner, Monique M. Ryan, Garth A. Nicholson	56
16	Atypical childhood chronic inflammatory demyelinating polyneuropathy 2010 ·Muscle & Nerve ·Ahmad Rithauddin Mohamed, (unknown), Monique M. Ryan	4
17	Induced dystrophin exon skipping in human muscle explants 2007 ·The Journal of Gene Medicine ·A.M. Adams, Graham McClorey, Hong M. Moulton, Patrick L. Iversen, John E.J. Rasko, Monique M. Ryan, Sue Fletcher, Steve D. Wilton	7
18	Concomitant Transverse Myelitis and Acute Motor Axonal Neuropathy in an Adolescent 2007 ·Pediatric Neurology ·Katherine B. Howell, Jithangi Wanigasinghe, Richard J. Leventer, Monique M. Ryan	14
19	Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene 2001 ·The American Journal of Human Genetics ·Biljana Ilkovski, Sandra T. Cooper, Kristen L. Nowak, Monique M. Ryan, Nan Yang, Christina Schnell, Hayley J. Durling, Laurence G. Roddick, Ian B. Wilkinson, Andrew J. Kornberg, Kevin Collins, Geoff Wallace, Peter W. Gunning, Edna C. Hardeman, Nigel G. Laing, Kathryn N. North	119
20	A Novel Syndrome of Episodic Muscle Weakness Maps to Xp22.3 1999 ·The American Journal of Human Genetics ·Monique M. Ryan, Peter Taylor, Jennifer A. Donald, Robert Ouvrier, Graeme Morgan, G Danta, Michael F. Buckley, Kathryn N. North	8

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.

Explore authors with similar magnitude of impact