Emma Matthews - Concepedia

Author

Emma Matthews

Also Known As

A Maclean, Andrew Marshall, Axel Jensen, Christian Babbs, D Broughton, David G. Kiely, Dirksen, Robert T., E L Matthews, E MATTHEWS, E Matthews

214

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery Great Ormond Street Hospital King's College London St George’s University Hospitals NHS Foundation Trust

About

Emma Matthews is an author at University College London specializing in medicine, physiology, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	14	547
2	Health Sciences	9	9	524
3	Applied Physiology	3	3	176
4	Engineering	2	2	29
5	Public Health	1	1	26

Emma Matthews

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
To tell or not to tell: barriers and facilitators in family communication about genetic risk Karen Forrest, SA Simpson, Wilson Bj, Clinical Genetics	2003	370
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis Emma Matthews, Robyn Labrum, Mary G. Sweeney, Neurology	2008	195
Prevalence study of genetically defined skeletal muscle channelopathies in England Alejandro Horga, D.L. Raja Rayan, Emma Matthews, Neurology	2013	135
Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy Vanessa Schartner, Norma B. Romero, Sandra Donkervoort, Acta Neuropathologica Congenital MyopathyMendelian DisorderDegenerative DiseaseGenetic Disorder	2016	132
Effect of Mexiletine on Muscle Stiffness in Patients With Nondystrophic Myotonia Evaluated Using Aggregated N-of-1 Trials Bas C. Stunnenberg, Joost Raaphorst, Hans Groenewoud, JAMA	2018	129
Loss-of-function mutations in<i>SCN4A</i>cause severe foetal hypokinesia or ‘classical’ congenital myopathy Irina Zaharieva, Michael G. Thor, Emily C. Oates, Brain Congenital MyopathyMuscle FunctionGeneticsPathologyClinical Genetics	2015	120
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype Emma Matthews, Simona Portaro, Richa Sud, Neurology	2011	106
Refined exercise testing can aid dna‐based diagnosis in muscle channelopathies S. Veronica Tan, Emma Matthews, Melissa Barber, Annals of Neurology	2011	102
Non-dystrophic myotonia: prospective study of objective and patient reported outcomes Jaya Trivedi, Brian N. Bundy, Jeffrey Statland, Brain Skeletal Muscle ChlorideMuscle FunctionNon-dystrophic MyotoniaKinesiologyMuscle Injury	2013	96
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene Haiyan Zhou, Suzanne Lillis, Ryan E. Loy, Neuromuscular Disorders Muscle FunctionSkeletal MusclePhysiologyMulti-minicore DiseaseNovel Mutations	2010	88

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