Robyn Labrum

2.9k total citations
21 papers, 772 citations indexed

About

Robyn Labrum is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Robyn Labrum has authored 21 papers receiving a total of 772 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Robyn Labrum's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (6 papers) and Ion channel regulation and function (5 papers). Robyn Labrum is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (6 papers) and Ion channel regulation and function (5 papers). Robyn Labrum collaborates with scholars based in United Kingdom, United States and Australia. Robyn Labrum's co-authors include Michael G. Hanna, Dimitri M. Kullmann, Stéphanie Schorge, Mary B. Davis, Mary G. Sweeney, Richa Sud, Emma Matthews, Patrick F. Chinnery, Paola Giunti and Sanjeev Rajakulendran and has published in prestigious journals such as Brain, Neurology and The Journal of Physiology.

In The Last Decade

Robyn Labrum

21 papers receiving 754 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robyn Labrum United Kingdom 14 488 400 175 145 93 21 772
Giovanni Vazza Italy 17 360 0.7× 227 0.6× 98 0.6× 87 0.6× 79 0.8× 33 752
Barbara Leube Germany 16 269 0.6× 504 1.3× 492 2.8× 44 0.3× 31 0.3× 27 989
Enrico Bugiardini Italy 20 567 1.2× 439 1.1× 252 1.4× 139 1.0× 21 0.2× 44 932
Giuseppe Piscosquito Italy 20 371 0.8× 641 1.6× 558 3.2× 47 0.3× 51 0.5× 55 1.2k
Ana María Cobo Spain 14 703 1.4× 393 1.0× 138 0.8× 193 1.3× 93 1.0× 28 979
Nobuyoshi Fukuhara Japan 17 693 1.4× 205 0.5× 139 0.8× 126 0.9× 25 0.3× 35 1.1k
Hiroto Fujigasaki Japan 21 988 2.0× 888 2.2× 380 2.2× 28 0.2× 28 0.3× 39 1.3k
Rosangela Ferese Italy 16 577 1.2× 108 0.3× 117 0.7× 38 0.3× 12 0.1× 43 879
J. Colomer Spain 17 479 1.0× 214 0.5× 213 1.2× 143 1.0× 12 0.1× 42 934
M.L. Mostacciuolo Italy 12 289 0.6× 113 0.3× 45 0.3× 119 0.8× 65 0.7× 18 466

Countries citing papers authored by Robyn Labrum

Since Specialization
Citations

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

Fields of papers citing papers by Robyn Labrum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robyn Labrum

This figure shows the co-authorship network connecting the top 25 collaborators of Robyn Labrum. A scholar is included among the top collaborators of Robyn Labrum 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 Robyn Labrum. Robyn Labrum 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.
Macken, William L., Micol Falabella, Cathy E. Woodward, et al.. (2023). Enhanced mitochondrial genome analysis: bioinformatic and long-read sequencing advances and their diagnostic implications. Expert Review of Molecular Diagnostics. 23(9). 797–814. 10 indexed citations
2.
Labrum, Robyn, Charlotte L. Alston, Cathy E. Woodward, et al.. (2022). Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European Journal of Human Genetics. 31(2). 148–163. 33 indexed citations
3.
Parkinson, Michael, Héctor García‐Moreno, Ese Mudanohwo, et al.. (2021). Friedreich's Ataxia Frequency in a Large Cohort of Genetically Undetermined Ataxia Patients. Frontiers in Neurology. 12. 736253–736253. 3 indexed citations
4.
Nethisinghe, Suran, Robyn Labrum, James M. Polke, et al.. (2021). Interruptions of the FXN GAA Repeat Tract Delay the Age at Onset of Friedreich’s Ataxia in a Location Dependent Manner. International Journal of Molecular Sciences. 22(14). 7507–7507. 12 indexed citations
5.
Nethisinghe, Suran, Sally Pemble, Mary G. Sweeney, et al.. (2018). PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption. Frontiers in Cellular Neuroscience. 12. 200–200. 16 indexed citations
6.
Tomlinson, Susan E, S. Veronica Tan, David Burke, et al.. (2016). In vivoimpact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2. Brain. 139(2). 380–391. 10 indexed citations
7.
Gardiner, A., Fatima Jaffer, Russell C. Dale, et al.. (2015). The clinical and genetic heterogeneity of paroxysmal dyskinesias. Brain. 138(12). 3567–3580. 101 indexed citations
8.
Galea, Charles A., Aamira Huq, Paul J. Lockhart, et al.. (2015). Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia. Annals of Neurology. 79(3). 485–495. 106 indexed citations
9.
Tomlinson, Susan E, Sanjeev Rajakulendran, S. Veronica Tan, et al.. (2013). Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1. Journal of Neurology Neurosurgery & Psychiatry. 84(10). 1107–1112. 38 indexed citations
10.
Spatola, Marianna, Pierre‐Yves Jeannet, Claudio Pollo, et al.. (2012). Effect of Vagus Nerve Stimulation in an Adult Patient with Dravet Syndrome: Contribution to Sudden Unexpected Death in Epilepsy Risk Reduction?. European Neurology. 69(2). 119–121. 13 indexed citations
11.
Proukakis, Christos, David Moore, Robyn Labrum, Nicholas Wood, & Henry Houlden. (2011). Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males. Journal of the Neurological Sciences. 306(1-2). 62–65. 23 indexed citations
12.
Rajakulendran, Sanjeev, Tracey D. Graves, Robyn Labrum, et al.. (2010). Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. The Journal of Physiology. 588(11). 1905–1913. 71 indexed citations
13.
Matthews, Emma, Reeteka Sud, Robyn Labrum, et al.. (2010). P91 Using MRI as a diagnostic tool in the skeletal muscle channelopathies. Neuromuscular Disorders. 20. S29–S30. 1 indexed citations
14.
Ramsay, Michèle, Zané Lombard, Robyn Labrum, et al.. (2009). Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals. Journal of Dermatological Science. 54(3). 198–204. 8 indexed citations
15.
Labrum, Robyn, Sanjeev Rajakulendran, Tracey D. Graves, et al.. (2009). Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing. Journal of Medical Genetics. 46(11). 786–791. 47 indexed citations
16.
Rajakulendran, Sanjeev, S. Veronica Tan, Emma Matthews, et al.. (2009). A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A. Neurology. 73(12). 993–995. 7 indexed citations
17.
Matthews, Emma, Robyn Labrum, Mary G. Sweeney, et al.. (2008). Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis. Neurology. 72(18). 1544–1547. 144 indexed citations
18.
Labrum, Robyn, et al.. (2007). The molecular basis of Spinal Muscular Atrophy (SMA) in South African black patients. Neuromuscular Disorders. 17(9-10). 684–692. 20 indexed citations
19.
Markus, Hugh S., Robyn Labrum, Steve Bevan, et al.. (2006). Genetic and Acquired Inflammatory Conditions Are Synergistically Associated With Early Carotid Atherosclerosis. Stroke. 37(9). 2253–2259. 36 indexed citations
20.
Goldman, A, Robyn Labrum, Mireille Claustres, et al.. (2001). The molecular basis of cystic fibrosis in South Africa. Clinical Genetics. 59(1). 37–41. 31 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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