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C. Campbell · SciRah

Researcher profile · Semantic Scholar

C. Campbell

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C. Campbell — researcher profile on SciRah

h-index: 31
Works: 126
Citations: 4,781

Most-cited papers

Nusinersen versus Sham Control in Later‐Onset Spinal Muscular Atrophy
E. Mercuri, B. Darras, C. Chiriboga, J. Day +19 more
2018New England Journal of Medicine1,189 citations Open access
Semantic Scholar
Ataluren treatment of patients with nonsense mutation dystrophinopathy
K. Bushby, R. Finkel, B. Wong, R. Barohn +30 more
2014Muscle and Nerve416 citations Open access
Semantic Scholar
Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial.
Craig M. McDonald, C. Campbell, R. Torricelli, R. Finkel +69 more
2017The Lancet376 citations Open access
Semantic Scholar
Myostatin inhibitor ACE‐031 treatment of ambulatory boys with Duchenne muscular dystrophy: Results of a randomized, placebo‐controlled clinical trial
C. Campbell, Hugh J. McMillan, Jean K. Mah, M. Tarnopolsky +6 more
2017Muscle and Nerve223 citations
Semantic Scholar
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database
Z. Koeks, C. Bladen, David Salgado, E. V. van Zwet +60 more
2017Journal of Neuromuscular Diseases157 citations Open access
Semantic Scholar
Effect of Different Corticosteroid Dosing Regimens on Clinical Outcomes in Boys With Duchenne Muscular Dystrophy: A Randomized Clinical Trial.
M. Guglieri, K. Bushby, M. McDermott, K. Hart +59 more
2022Journal of the American Medical Association (JAMA)132 citations Open access
Semantic Scholar
Myotonic dystrophy type 1
C. Nguyen, C. Campbell
2016Canadian Medical Association Journal127 citations Open access
Semantic Scholar
Treating pediatric neuromuscular disorders: The future is now
J. Dowling, H. Gonorazky, R. Cohn, C. Campbell
2017American Journal of Medical Genetics. Part A113 citations Open access
Semantic Scholar
A randomized placebo-controlled phase 3 trial of an antisense oligonucleotide, drisapersen, in Duchenne muscular dystrophy.
N. Goemans, E. Mercuri, E. Belousova, H. Komaki +8 more
2018Neuromuscular Disorders107 citations Open access
Semantic Scholar
The TREAT‐NMD Duchenne Muscular Dystrophy Registries: Conception, Design, and Utilization by Industry and Academia
C. Bladen, K. Rafferty, V. Straub, S. Monges +61 more
2013Human Mutation105 citations Open access
Semantic Scholar
Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe
C. Bladen, R. Thompson, J. M. Jackson, C. Garland +58 more
2013Journal of Neurology100 citations Open access
Semantic Scholar
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
M. Zarrei, D. Fehlings, K. Mawjee, L. Switzer +22 more
2017Genetics in Medicine88 citations Open access
Semantic Scholar
Developing Standardized Corticosteroid Treatment for Duchenne Muscular Dystrophy
M. Guglieri, K. Bushby, M. McDermott, K. Hart +43 more
2017Contemporary Clinical Trials70 citations Open access
Semantic Scholar
Congenital myotonic dystrophy: Canadian population-based surveillance study.
C. Campbell, S. Levin, V. Siu, S. Venance +1 more
2013Jornal de Pediatria69 citations
Semantic Scholar
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy
Nicholas Johnson, Anne-Berit Ekstrom, C. Campbell, Man Hung +6 more
2015Developmental Medicine & Child Neurology56 citations Open access
Semantic Scholar
Meta-analyses of ataluren randomized controlled trials in nonsense mutation Duchenne muscular dystrophy.
C. Campbell, R. Barohn, E. Bertini, B. Chabrol +31 more
2020Journal of Comparative Effectiveness Research55 citations Open access
Semantic Scholar
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1
N. Johnson, E. Z. Aldana, N. Angeard, T. Ashizawa +8 more
2019Neurology Clinical Practice47 citations Open access
Semantic Scholar
A checklist for clinical trials in rare disease: obstacles and anticipatory actions—lessons learned from the FOR-DMD trial
Rebecca A. Crow, K. Hart, M. McDermott, R. Tawil +44 more
2018Trials47 citations Open access
Semantic Scholar
Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up Recommendations
H. McMillan, Kristin D. Kernohan, E. Yeh, K. Amburgey +9 more
2020Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques44 citations Open access
Semantic Scholar
Factors Associated With Health-Related Quality of Life in Children With Duchenne Muscular Dystrophy
Yi-yun Wei, K. Speechley, G. Zou, C. Campbell
2016Journal of Child Neurology40 citations
Semantic Scholar
Neuroplastic Sensorimotor Resting State Network Reorganization in Children With Hemiplegic Cerebral Palsy Treated With Constraint-Induced Movement Therapy
Kathryn Y. Manning, Ravi S. Menon, J. Gorter, R. Mesterman +3 more
2016Journal of Child Neurology34 citations
Semantic Scholar
Reldesemtiv in Patients with Spinal Muscular Atrophy: a Phase 2 Hypothesis-Generating Study
S. Rudnicki, Jinsy A. Andrews, T. Duong, Bettina M. Cockroft +19 more
2021Neurotherapeutics32 citations Open access
Semantic Scholar
Resting State and Diffusion Neuroimaging Predictors of Clinical Improvements Following Constraint-Induced Movement Therapy in Children With Hemiplegic Cerebral Palsy
Kathryn Y. Manning, D. Fehlings, R. Mesterman, J. Gorter +3 more
2015Journal of Child Neurology32 citations
Semantic Scholar
Orofacial strength, dysarthria, and dysphagia in Congenital Myotonic Dystrophy
Kiera N. Berggren, Man Hung, Melissa M. Dixon, Jerry Bounsanga +6 more
2018Muscle and Nerve31 citations Open access
Semantic Scholar
Fatigue in young people with Duchenne muscular dystrophy
B. El-Aloul, K. Speechley, Yi-yun Wei, P. Wilk +1 more
2020Developmental Medicine & Child Neurology30 citations Open access
Semantic Scholar
Brain biomarkers and pre-injury cognition are associated with long-term cognitive outcome in children with traumatic brain injury
Amy A Wilkinson, M. Dennis, N. Simić, Margot J. Taylor +9 more
2017BMC Pediatrics29 citations Open access
Semantic Scholar
Disease burden and functional outcomes in congenital myotonic dystrophy
N. Johnson, R. Butterfield, Kiera N. Berggren, Man Hung +8 more
2016Neurology28 citations Open access
Semantic Scholar
Pharmacological therapy for the prevention and management of cardiomyopathy in Duchenne muscular dystrophy: A systematic review.
B. El-Aloul, L. Altamirano-Diaz, E. Zapata-Aldana, Rébecca Rodrigues +3 more
2017Neuromuscular Disorders27 citations
Semantic Scholar
Prenatal, Neonatal, and Early Childhood Features in Congenital Myotonic Dystrophy
E. Zapata-Aldana, D. Ceballos-Sáenz, R. Hicks, C. Campbell
2018Journal of Neuromuscular Diseases25 citations
Semantic Scholar
Randomized phase 2 study of ACE‐083, a muscle‐promoting agent, in facioscapulohumeral muscular dystrophy
J. Statland, C. Campbell, U. Desai, C. Karam +25 more
2022Muscle and Nerve24 citations Open access
Semantic Scholar
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
L. Wood, G. Bassez, C. Bleyenheuft, C. Campbell +35 more
2018Orphanet Journal of Rare Diseases24 citations Open access
Semantic Scholar
A National Spinal Muscular Atrophy Registry for Real-World Evidence
V. Hodgkinson, M. Oskoui, J. Lounsberry, S. M'Dahoma +46 more
2020Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques23 citations Open access
Semantic Scholar
The Canadian Neuromuscular Disease Registry 2010–2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry
V. Hodgkinson, J. Lounsberry, S. M'Dahoma, A. Russell +59 more
2020Journal of Neuromuscular Diseases22 citations Open access
Semantic Scholar
Seizures Related to Hypomagnesemia
Becky Biqi Chen, C. Prasad, M. Kobrzynski, C. Campbell +1 more
2016Child Neurology Open22 citations Open access
Semantic Scholar
Neurodevelopmental profiles of children with unilateral cerebral palsy associated with middle cerebral artery and periventricular venous infarctions
D. Fehlings, P. Krishnan, Renee-Marie Ragguett, G. deVeber +10 more
2021Developmental Medicine & Child Neurology18 citations Open access
Semantic Scholar
Ontario Newborn Screening for Spinal Muscular Atrophy: The First Year
Kristin D. Kernohan, H. McMillan, Ed Yeh, Melanie Lacaria +9 more
2021Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques17 citations Open access
Semantic Scholar
Twinkle-Associated Mitochondrial DNA Depletion.
S. Remtulla, Cam-Tu Emilie Nguyen, C. Prasad, C. Campbell
2019Pediatric Neurology17 citations Open access
Semantic Scholar
Further delineation of TBCK - Infantile hypotonia with psychomotor retardation and characteristic facies type 3.
E. Zapata-Aldana, D. D. Kim, S. Remtulla, C. Prasad +2 more
2019European Journal of Medical Genetics17 citations
Semantic Scholar
Physical Function and Mobility in Children with Congenital Myotonic Dystrophy
E. Pucillo, D. Dibella, Man Hung, Jerry Bounsanga +5 more
2017Muscle and Nerve17 citations Open access
Semantic Scholar
The Canadian Neuromuscular Disease Registry: Connecting patients to national and international research opportunities.
Yi-yun Wei, A. Mccormick, A. MacKenzie, E. O'Ferrall +13 more
2018Paediatrics & child health16 citations Open access
Semantic Scholar
Health-Related Quality of Life in Children with DuchenneMuscular Dystrophy: A Review
Yi-yun Wei, K. Speechley, C. Campbell
2015Journal of Neuromuscular Diseases16 citations Open access
Semantic Scholar
Serum Biomarkers Help Predict Attention Problems in Critically Ill Children With Traumatic Brain Injury
Amy A Wilkinson, N. Simić, H. Frndova, Margot J. Taylor +12 more
2016Pediatric Critical Care Medicine15 citations
Semantic Scholar
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy.
P. Shieh, G. Elfring, P. Trifillis, Claudio L Santos +6 more
2021Journal of Comparative Effectiveness Research13 citations Open access
Semantic Scholar
The relationship between quality of life and health‐related quality of life in young males with Duchenne muscular dystrophy
Yi-yun Wei, K. Speechley, G. Zou, C. Campbell
2017Developmental Medicine & Child Neurology13 citations Open access
Semantic Scholar
Corrigendum to "Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy" [Neuromuscular Disorders, Vol. 30 (6) 2020, 492-502].
K. Wagner, H. Abdel-Hamid, J. Mah, C. Campbell +20 more
2021Neuromuscular Disorders12 citations Open access
Semantic Scholar
Patient-reported study of the impact of pediatric-onset myotonic dystrophy
M. Hunter, Anne-Berit Ekstrom, C. Campbell, Man Hung +7 more
2019Muscle and Nerve12 citations Open access
Semantic Scholar
Case of Multiple Sulfatase Deficiency and Ocular Albinism: A Diagnostic Odyssey
C. Prasad, C. Rupar, C. Campbell, M. Napier +4 more
2014Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques12 citations Open access
Semantic Scholar
12-Month Progression of Motor and Functional Outcomes in Congenital Myotonic Dystrophy
Kellen H. Quigg, Kiera N. Berggren, Melissa McIntyre, K. Bates +11 more
2020Muscle and Nerve11 citations Open access
Semantic Scholar
Distal arthrogryposis type 5 and PIEZO2 novel variant in a Canadian family
E. Zapata-Aldana, S. Al-Mobarak, N. Karp, C. Campbell
2019American Journal of Medical Genetics. Part A10 citations
Semantic Scholar
Agitated behavior scale in pediatric traumatic brain injury
M. Nowicki, Lisa S Pearlman, C. Campbell, R. Hicks +2 more
2019Brain Injury8 citations
Semantic Scholar

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