Imelda Hughes

4.9k total citations
29 papers, 978 citations indexed

About

Imelda Hughes is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Imelda Hughes has authored 29 papers receiving a total of 978 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 7 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Imelda Hughes's work include Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Metabolism and Genetic Disorders (6 papers). Imelda Hughes is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Neurogenetic and Muscular Disorders Research (7 papers) and Metabolism and Genetic Disorders (6 papers). Imelda Hughes collaborates with scholars based in United Kingdom, United States and Australia. Imelda Hughes's co-authors include Richard Newton, J. Gallagher, Anita K. Simonds, Julian Forton, Robert Ross Russell, Renée McCulloch, Elaine Chan, Neil Gibson, Michelle Chatwin and Jeremy Hull and has published in prestigious journals such as PLoS ONE, Neurology and PEDIATRICS.

In The Last Decade

Imelda Hughes

28 papers receiving 957 citations

Peers

Countries citing papers authored by Imelda Hughes

Since Specialization

Citations

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

Fields of papers citing papers by Imelda Hughes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imelda Hughes

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

#	Work	Indexed citations
1	Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain 2024 ·Journal of Neuromuscular Diseases ·(unknown), Anne‐Marie Childs, Elizabeth Wraige, Pinki Munot, Gautam Ambegaonkar, Gabriel Chow, Imelda Hughes, Marjorie Illingworth, Anirban Majumdar, Chiara Marini‐Bettolo, (unknown), Stefan Spinty, Tracey Willis, Mariacristina Scoto, Giovanni Baranello, (unknown)	5
2	Prediagnosis pathway benchmarking audit in patients with Duchenne muscular dystrophy 2021 ·Archives of Disease in Childhood ·Vasantha Gowda, Miguel Ángel Luque-Fernández, (unknown), Anne‐Marie Childs, Imelda Hughes, Sandya Tirupathi, Christian de Goede, Declan O’Rourke, (unknown), Tracey Willis, (unknown), I. A. Davidson	0
3	Presynaptic congenital myasthenic syndrome due to three novel mutations in SLC5A7 encoding the sodium-dependant high-affinity choline transporter 2020 ·Neuromuscular Disorders ·Pedro M. Rodríguez Cruz, Imelda Hughes, Adnan Manzur, Pinki Munot, Sithara Ramdas, Ronnie Wright, Catherine Breen, (unknown), Alistair T. Pagnamenta, Jenny C. Taylor, Jacqueline Palace, David Beeson	14
4	242nd ENMC International Workshop: Diagnosis and management of juvenile myasthenia gravis Hoofddorp, the Netherlands, 1–3 March 2019 2020 ·Neuromuscular Disorders ·Pinki Munot, S. Robb, E. Niks, Jacqueline Palace, Amelia Evoli, Andrea Klein, (unknown), B. Eymard, Heinz Jungbluth, Corrie E. Erasmus, Adela Della Marina, Fulvio Baggi, Nancy L. Kuntz, (unknown), Imelda Hughes, Sithara Ramdas, Monique M. Ryan, Matthew Pitt	14
5	Mortality and respiratory support in X-linked myotubular myopathy: a RECENSUS retrospective analysis 2019 ·Archives of Disease in Childhood ·Robert J. Graham, Francesco Muntoni, Imelda Hughes, Sabrina W. Yum, Nancy L. Kuntz, Michele Yang, Barry J. Byrne, Suyash Prasad, (unknown), Casie A. Genetti, Tmirah Haselkorn, Emma S. James, (unknown), Mojtaba Noursalehi, Salvador Rico, Alan H. Beggs	25
6	Growth, bone health & ambulatory status of boys with DMD treated with daily vs. intermittent oral glucocorticoid regimen 2018 ·Bone ·Nicola Crabtree, J.E. Adams, Raja Padidela, Nick J. Shaw, Wolfgang Högler, Helen Roper, Imelda Hughes, (unknown), Zahir Mughal	33
7	Overcoming pharmacokinetic challenges to drug administration in Duchenne muscular dystrophy: Lessons from Phase 1 development of ezutromid 2017 ·European Journal of Paediatric Neurology ·(unknown), Stefan Spinty, Helen Roper, Imelda Hughes, Adhip P.N. Majumdar, Shawn Harriman, Kelvin P. Davies, Francesco Muntoni	1
8	A multicenter, retrospective medical record review of patients with X-Linked Myotubular myopathy (XLMTM): the RECENSUS study 2017 ·Neuromuscular Disorders ·Alan H. Beggs, B. Byrne, (unknown), Tmirah Haselkorn, Imelda Hughes, Emma S. James, (unknown), (unknown), Lindsay C. Swanson, Michele Yang, (unknown), Sabrina W. Yum, (unknown)	1
9	Safety, Tolerability, and Pharmacokinetics of SMT C1100, a 2-Arylbenzoxazole Utrophin Modulator, following Single- and Multiple-Dose Administration to Pediatric Patients with Duchenne Muscular Dystrophy 2016 ·PLoS ONE ·Valeria Ricotti, Stefan Spinty, Helen Roper, Imelda Hughes, (unknown), (unknown), Gary Layton, Kay E. Davies, Francesco Muntoni, Jonathon M. Tinsley	46
10	British Thoracic Society guideline for respiratory management of children with neuromuscular weakness 2012 ·Thorax ·Jeremy Hull, (unknown), Elaine Chan, Michelle Chatwin, Julian Forton, J. Gallagher, Neil Gibson, Jill Gordon, Imelda Hughes, Renée McCulloch, Robert Ross Russell, Anita K. Simonds	249
11	The clinical utility of an SCN1A genetic diagnosis in infantile‐onset epilepsy 2012 ·Developmental Medicine & Child Neurology ·Andreas Brunklaus, Liam Dorris, Rachael Ellis, Eleanor Reavey, Elizabeth Lee, (unknown), Richard Appleton, J. Helen Cross, Colin D. Ferrie, Imelda Hughes, Alice Jollands, Mary D. King, (unknown), Bryan Lynch, Sunny Philip, Ingrid E. Scheffer, Ruth Williams, Sameer M. Zuberi	54
12	Maternally inherited mitochondrial DNA disease in consanguineous families 2011 ·European Journal of Human Genetics ·Charlotte L. Alston, Langping He, Andrew A. M. Morris, Imelda Hughes, Christian de Goede, Douglass M. Turnbull, Robert McFarland, Robert W. Taylor	13
13	Thymectomy for inducing remission in juvenile myasthenia gravis 2011 ·Pediatric Surgery International ·(unknown), (unknown), Imelda Hughes, Gillian Humphrey	17
14	Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease 2011 ·Journal of Medical Genetics ·Johanna Uusimaa, Heinz Jungbluth, Carl Fratter, Guido Crisponi, Longhua Feng, Massimo Zeviani, Imelda Hughes, Eileen P. Treacy, Jacqueline Birks, Grace Brown, Caroline A. Sewry, Michael McDermott, F. Muntoni, Joanna Poulton	44
15	Sustained response to intrathecal rituximab in EBV associated Post‐transplant lymphoproliferative disease confined to the central nervous system following haematopoietic stem cell transplant 2011 ·Pediatric Blood & Cancer ·Denise Bonney, (unknown), Andrew Turner, Anna Kelsey, (unknown), Stephen Hughes, Imelda Hughes, Robert Wynn	29
16	Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis 2010 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Lesley MacPherson, Katharine Foster, Peter Lunt, Imelda Hughes, Angela F. Brady, Michael Pike, (unknown), Neil V. Morgan, Carol Hardy, (unknown), Fiona MacDonald, Eamonn R. Maher, Manju A. Kurian	27
17	Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita 2008 ·Journal of Medical Genetics ·M Guftar Shaikh, (unknown), (unknown), Rose C. Collins, G. T. N. Besley, (unknown), (unknown), Imelda Hughes, C. M. Hall, (unknown), John C. Achermann, Peter Clayton	30
18	Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy 2008 ·Neuromuscular Disorders ·Emma L. Blakely, Langping He, (unknown), Gavin Hudson, John H. Walter, Imelda Hughes, Douglass M. Turnbull, Robert W. Taylor	34
19	Minicore myopathy in children: a clinical and histopathological study of 19 cases 2000 ·Neuromuscular Disorders ·Heinz Jungbluth, Caroline A. Sewry, S. Brown, Adnan Y. Manzur, Eugenio Mercuri, Kate Bushby, (unknown), Margaret Johnson, Imelda Hughes, Anna Kelsey, Victor Dubowitz, Francesco Muntoni	40
20	Mitochondrial myopathy with skeletal muscle cytochrome oxidase deficiency 1982 ·Journal of Inherited Metabolic Disease ·D. Stansbie, Robert L. Dormer, Imelda Hughes, (unknown), G. A. F. Hendry, O. T. G. Jones, Andrew R. Cross, H. S. A. Sherratt, Douglass M. Turnbull, Mark A. Johnson	27

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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