Robyn Labrum

2.9k citations

21 papers · 772 indexed · h-index 14

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Neurology top 10%
- Neurological disorders and treatments

Papers in ⓘ

Cellular and Molecular Neuroscience 12
- Genetic Neurodegenerative Diseases 11
- Hereditary Neurological Disorders 2
Neurology 5
- Neurological disorders and treatments 3

Co-authors: Michael G. Hanna (9 shared papers)Dimitri M. Kullmann (7 shared papers)Stéphanie Schorge (5 shared papers)Mary B. Davis (4 shared papers)Mary G. Sweeney (5 shared papers)Emma Matthews (3 shared papers)Richa Sud (2 shared papers)G. Meola (1 shared paper)
Journals: Brain (2 papers)Neurology (2 papers)Neuromuscular Disorders (2 papers)Stroke (2 papers)European Journal of Human Genetics (1 paper)
Partner nations: United Kingdom United States Australia

In The Last Decade

Robyn Labrum

21 papers receiving 754 citations

Peers

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-authors

The 25 scholars most cited alongside Robyn Labrum, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Robyn Labrum Line = papers co-authored together Robyn Labrum links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 21 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis Neurology ·Emma Matthews, Robyn Labrum, Mary G. Sweeney, Richa Sud, A. Haworth, Patrick F. Chinnery, G. Meola, Stéphanie Schorge, Dimitri M. Kullmann, Mary B. Davis, Michael G. Hanna	2008	144
2	Compound heterozygous FXN mutations and clinical outcome in friedreich ataxia Annals of Neurology ·Charles A. Galea, Aamira Huq, Paul J. Lockhart, Geneieve Tai, Louise A. Corben, Eppie M. Yiu, Lyle C. Gurrin, David R. Lynch, Sarah Gelbard, Alexandra Dürr, Françoise Pousset, Michael Parkinson, Robyn Labrum, Paola Giunti, Susan Perlman, Martin B. Delatycki, Marguerite V. Evans‐Galea	2015	106
3	The clinical and genetic heterogeneity of paroxysmal dyskinesias Brain ·A. Gardiner, Fatima Jaffer, Russell C. Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, María Stamelou, Matthew C. Walker, Dimitri M. Kullmann, Thomas T. Warner, Paul Jarman, Michael G. Hanna, Manju A. Kurian, Kailash P. Bhatia, Henry Houlden	2015	101
4	Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy The Journal of Physiology ·Sanjeev Rajakulendran, Tracey D. Graves, Robyn Labrum, Dimitrios Kotzadimitriou, L. H. Eunson, Mary B. Davis, Rosalyn Davies, Nicholas Wood, Dimitri M. Kullmann, Michael G. Hanna, Stéphanie Schorge	2010	71
5	Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing Journal of Medical Genetics ·Robyn Labrum, Sanjeev Rajakulendran, Tracey D. Graves, L. H. Eunson, R. T. Bevan, Mary G. Sweeney, Simon Hammans, Niall Tubridy, TC Britton, Lucinda Carr, John R. Østergaard, C Kennedy, A. Al‐Memar, Dimitri M. Kullmann, Stéphanie Schorge, I. Karen Temple, Mary B. Davis, Michael G. Hanna	2009	47
6	Toll Receptor Polymorphisms and Carotid Artery Intima-Media Thickness Stroke ·Robyn Labrum, Steve Bevan, Matthias Sitzer, Matthias Lorenz, Hugh S. Markus	2007	42
7	Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1 Journal of Neurology Neurosurgery & Psychiatry ·Susan E Tomlinson, Sanjeev Rajakulendran, S. Veronica Tan, Tracey D. Graves, Doris‐Eva Bamiou, Robyn Labrum, David Burke, Carolyn M. Sue, Paola Giunti, Stéphanie Schorge, Dimitri M. Kullmann, Michael G. Hanna	2013	38
8	Genetic and Acquired Inflammatory Conditions Are Synergistically Associated With Early Carotid Atherosclerosis Stroke ·Hugh S. Markus, Robyn Labrum, Steve Bevan, Markus Reindl, Georg Egger, Christian J. Wiedermann, Qingbo Xu, Stefan Kiechl, Johann Willeit	2006	36
9	Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines European Journal of Human Genetics ·Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L. Alston, Cathy E. Woodward, Conrad Smith, Charlotte V. Y. Knowles, Yogen Patel, Philip Hodsdon, Jack P. Baines, Emma L. Blakely, James M. Polke, Robert W. Taylor, Carl Fratter	2022	33
10	The molecular basis of cystic fibrosis in South Africa Clinical Genetics ·A Goldman, Robyn Labrum, Mireille Claustres, Marie Desgeorges, Caroline Guittard, Andrew J. Wallace, Michèle Ramsay	2001	31
11	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 ·Christos Proukakis, David Moore, Robyn Labrum, Nicholas Wood, Henry Houlden	2011	23
12	The molecular basis of Spinal Muscular Atrophy (SMA) in South African black patients Neuromuscular Disorders ·Robyn Labrum, J. Rodda, Amanda Krause	2007	20
13	PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption Frontiers in Cellular Neuroscience ·Suran Nethisinghe, Maria Lucia Pigazzini, Sally Pemble, Mary G. Sweeney, Robyn Labrum, Katarina Manso, David Moore, Jon Warner, Mary B. Davis, Paola Giunti	2018	16
14	Effect of Vagus Nerve Stimulation in an Adult Patient with Dravet Syndrome: Contribution to Sudden Unexpected Death in Epilepsy Risk Reduction? European Neurology ·Marianna Spatola, Pierre‐Yves Jeannet, Claudio Pollo, Christian Wider, Robyn Labrum, Andrea O. Rossetti	2012	13
15	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 ·Suran Nethisinghe, Maheswaran Kesavan, Heather Ging, Robyn Labrum, James M. Polke, Saiful Islam, Héctor García‐Moreno, Martina F. Callaghan, Francesca Cavalcanti, Mark A. Pook, Paola Giunti	2021	12
16	In vivoimpact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2 Brain ·Susan E Tomlinson, S. Veronica Tan, David Burke, Robyn Labrum, Andrea Haworth, Vaneesha Gibbons, Mary G. Sweeney, Robert C. Griggs, Dimitri M. Kullmann, Hugh Bostock, Michael G. Hanna	2016	10
17	Enhanced mitochondrial genome analysis: bioinformatic and long-read sequencing advances and their diagnostic implications Expert Review of Molecular Diagnostics ·William L. Macken, Micol Falabella, Chiara Pizzamiglio, Cathy E. Woodward, Elizabeth Scotchman, Lyn S. Chitty, James M. Polke, Enrico Bugiardini, Michael G. Hanna, Jana Vandrovcová, Natalie Chandler, Robyn Labrum, Robert D. S. Pitceathly	2023	10
18	Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals Journal of Dermatological Science ·Michèle Ramsay, Tarryn S. Greenberg, Zané Lombard, Robyn Labrum, Steven Lubbe, Shaun Aron, Anna-Susan Marais, Sharon F. Terry, Lionel Bercovitch, Denis Viljoen	2009	8
19	A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A Neurology ·Sanjeev Rajakulendran, S. Veronica Tan, Emma Matthews, Susan E Tomlinson, Robyn Labrum, Richa Sud, Dimitri M. Kullmann, Stéphanie Schorge, Michael G. Hanna	2009	7
20	Friedreich's Ataxia Frequency in a Large Cohort of Genetically Undetermined Ataxia Patients Frontiers in Neurology ·Alexander Brown, Michael Parkinson, Héctor García‐Moreno, Ese Mudanohwo, Robyn Labrum, Mary G. Sweeney, Paola Giunti	2021	3

About Robyn Labrum

Robyn Labrum is a scholar working on Cellular and Molecular Neuroscience, Neurology, Clinical Biochemistry, Neurology and Psychiatry and Mental health, having authored 21 papers that have together received 772 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (6 papers), Ion channel regulation and function (5 papers), Neurological disorders and treatments (3 papers), Cardiac electrophysiology and arrhythmias (3 papers), Metabolism and Genetic Disorders (2 papers), Hereditary Neurological Disorders (2 papers) and Epilepsy research and treatment (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (400 citations), Neurology (175 citations), Clinical Biochemistry (54 citations), Neurology (62 citations) and Molecular Biology (488 citations). Robyn Labrum has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Michael G. Hanna, Dimitri M. Kullmann, Stéphanie Schorge, Mary B. Davis, Mary G. Sweeney, Emma Matthews, Richa Sud, G. Meola, A. Haworth and Paola Giunti. Their work appears in journals such as Brain, Neurology, Neuromuscular Disorders, Stroke and European Journal of Human Genetics.

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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