Rosaline C. M. Quinlivan

Author

Also Known As

Anna Ambrosini, Claire Rylance, Genomics England, Gisèle Bonne, Phadke, R, Quinlivan, R, Quinlivan, R., Quinlivan, Ros, R C. M. Quinlivan, R M Quinlivan

904

Publications

9.8K

Citations

H-Index

151

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery Great Ormond Street Hospital Robert Jones and Agnes Hunt Orthopaedic Hospital Newcastle University

About

Rosaline C. M. Quinlivan is an author at University College London specializing in medicine, pathology, and neuromuscular pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	46	2.5K
2	Health Sciences	14	15	732
3	Nursing	2	2	51
4	Education	1	1	14
5	Natural Sciences	1	1	132

Rosaline C. M. Quinlivan

Publications

6.9K

Citations

H-Index

Page 1

	Year	Citations
Consensus on Exercise Reporting Template (CERT): Modified Delphi Study Susan C. Slade, Clermont E. Dionne, Martin Underwood, Physical Therapy	2016	447
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan C. Godfrey, Emma Clement, R. Mein, Brain	2007	433
Ataluren treatment of patients with nonsense mutation dystrophinopathy K. Bushby, Richard S. Finkel, Brenda Wong, Muscle & Nerve	2014	416
Changes in Spirometry Over Time as a Prognostic Marker in Patients with Duchenne Muscular Dystrophy Margaret Phillips, Rosaline C. M. Quinlivan, R. H. T. Edwards, American Journal of Respiratory and Critical Care Medicine	2001	280
<i>RYR1</i> mutations are a common cause of congenital myopathies with central nuclei Jo M. Wilmshurst, Suzanne Lillis, Haiyan Zhou, Annals of Neurology	2010	261
Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy Valeria Ricotti, Deborah Ridout, E. Scott, Journal of Neurology Neurosurgery & Psychiatry	2012	255
Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan Keren Carss, Elizabeth Stevens, A. Reghan Foley, The American Journal of Human Genetics	2013	236
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis Nomazulu Dlamini, Nicol C. Voermans, S. Lillis, Neuromuscular Disorders Neuromusculoskeletal DisorderMendelian DisorderGeneticsMolecular BiologyPathology	2013	195
Brain involvement in muscular dystrophies with defective dystroglycan glycosylation Emma Clement, Eugenio Mercuri, Caroline Godfrey, Annals of Neurology	2008	177
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies Haiyan Zhou, Heinz Jungbluth, C. Sewry, Brain Mendelian DisorderRyr1-related Congenital MyopathiesSkeletal MuscleMalignant Hyperthermia SusceptibilityGenetics	2007	173

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