| HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) | Heart Rhythm | 2011 | 737 |
| An absolute requirement for Pax7-positive satellite cells in acute injury-induced skeletal muscle regeneration | Development (Cambridge) | 2011 | 696 |
| HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA) | Europace | 2011 | 557 |
| Cold plasma selectivity and the possibility of a paradigm shift in cancer therapy | British Journal of Cancer | 2011 | 538 |
| Strategies for implementing screening for critical congenital heart disease | Pediatrics | 2011 | 272 |
| The American Clinical Neurophysiology Society's Guideline on Continuous Electroencephalography Monitoring in Neonates | Journal of Clinical Neurophysiology | 2011 | 272 |
| Breastfeeding and reduced risk of sudden infant death syndrome: a meta-analysis | Pediatrics | 2011 | 266 |
| The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation | Nature Genetics | 2011 | 217 |
| A social-ecological model of readiness for transition to adult-oriented care for adolescents and young adults with chronic health conditions | Child: Care, Health and Development | 2011 | 208 |
| Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia | Nature Genetics | 2011 | 201 |
| Adeno-associated virus antibody profiles in newborns, children, and adolescents | Vaccine Journal | 2011 | 197 |
| Symptomatic neonatal arterial ischemic stroke: the International Pediatric Stroke Study | Pediatrics | 2011 | 183 |
| Global and organ-specific chronic graft-versus-host disease severity according to the 2005 NIH Consensus Criteria | Blood | 2011 | 169 |
| The influence of developmental age on the early transcriptomic response of children with septic shock | Molecular Medicine | 2011 | 165 |
| Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy | American Journal of Human Genetics | 2011 | 163 |
| Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases | PLoS Genetics | 2011 | 152 |
| SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy | Neurology | 2011 | 150 |
| GFAP mutations, age at onset, and clinical subtypes in Alexander disease | Neurology | 2011 | 148 |
| School and the concussed youth: recommendations for concussion education and management | Physical Medicine and Rehabilitation Clinics of North America | 2011 | 147 |
| Diagnosis, classification, and genetics of phenylketonuria and tetrahydrobiopterin (BH4) deficiencies | Molecular Genetics and Metabolism | 2011 | 145 |
| Phase I trial of MK-0752 in children with refractory CNS malignancies: a pediatric brain tumor consortium study | Journal of Clinical Oncology | 2011 | 129 |
| Ovarian sex cord-stromal tumors, pleuropulmonary blastoma and DICER1 mutations: a report from the International Pleuropulmonary Blastoma Registry | Gynecologic Oncology | 2011 | 126 |
| Health care transition for youth living with HIV/AIDS | Pediatrics | 2011 | 123 |
| Red blood cell transfusion, feeding and necrotizing enterocolitis in preterm infants | Journal of Perinatology | 2011 | 123 |
| Fragile X syndrome: the GABAergic system and circuit dysfunction | Developmental Neuroscience | 2011 | 119 |
