| # | Title | Journal | Year | Citations |
|---|
| 1 | Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 | Autophagy | 2021 | 1,430 |
| 2 | Autism spectrum disorder | Lancet, The | 2018 | 1,220 |
| 3 | Cerebral palsy | Nature Reviews Disease Primers | 2016 | 603 |
| 4 | Bispectral index values during elective rigid bronchoscopy: a prospective observational pilot study | Anaesthesia | 2007 | 531 |
| 5 | British Association for Psychopharmacology consensus statement on evidence-based treatment of insomnia, parasomnias and circadian rhythm disorders | Journal of Psychopharmacology | 2010 | 484 |
| 6 | The Standardization of Terminology of Lower Urinary Tract Function in Children and Adolescents: Update Report from the Standardization Committee of the International Children's Continence Society | Journal of Urology | 2014 | 466 |
| 7 | Cerebral palsy | Lancet, The | 2014 | 423 |
| 8 | GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction | Nature Genetics | 2013 | 380 |
| 9 | Intensive care admissions of children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the UK: a multicentre observational study | The Lancet Child and Adolescent Health | 2020 | 352 |
| 10 | Childhood arterial ischaemic stroke incidence, presenting features, and risk factors: a prospective population-based study | Lancet Neurology, The | 2014 | 291 |
| 11 | Targeted Neonatal Echocardiography in the Neonatal Intensive Care Unit: Practice Guidelines and Recommendations for Training | Journal of the American Society of Echocardiography | 2011 | 285 |
| 12 | Centronuclear (myotubular) myopathy | Orphanet Journal of Rare Diseases | 2008 | 267 |
| 13 | The wide spectrum of tubulinopathies: what are the key features for the diagnosis? | Brain | 2014 | 252 |
| 14 | BSACI guidelines for the management of chronic urticaria and angio‐oedema | Clinical and Experimental Allergy | 2007 | 235 |
| 15 | New-Onset Heart Failure Due to Heart Muscle Disease in Childhood | Circulation | 2008 | 188 |
| 16 | The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation | Journal of Inherited Metabolic Disease | 2015 | 186 |
| 17 | Associated risk factors for silent cerebral infarcts in sickle cell anemia: low baseline hemoglobin, sex, and relative high systolic blood pressure | Blood | 2012 | 180 |
| 18 | Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study | Lancet Neurology, The | 2011 | 179 |
| 19 | The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype | Journal of Inherited Metabolic Disease | 2015 | 175 |
| 20 | Swine-origin influenza virus H1N1, seasonal influenza virus, and critical illness in children | Lancet, The | 2009 | 162 |
| 21 | Coronary arterial fistulas | Orphanet Journal of Rare Diseases | 2006 | 156 |
| 22 | Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids) | JAMA Cardiology | 2019 | 147 |
| 23 | The use of Z-scores in paediatric cardiology | Annals of Pediatric Cardiology | 2012 | 145 |
| 24 | Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene-associated myopathies | Human Mutation | 2012 | 145 |
| 25 | Neurological Manifestations of Influenza Infection in Children and Adults: Results of a National British Surveillance Study | Clinical Infectious Diseases | 2014 | 143 |
| 26 | Proportion of life lived with dystonia inversely correlates with response to pallidal deep brain stimulation in both primary and secondary childhood dystonia | Developmental Medicine and Child Neurology | 2013 | 142 |
| 27 | Central core disease | Orphanet Journal of Rare Diseases | 2007 | 140 |
| 28 | Specificity Characteristics of 7 Commercial Creatinine Measurement Procedures by Enzymatic and Jaffe Method Principles | Clinical Chemistry | 2012 | 135 |
| 29 | Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation | American Journal of Medical Genetics, Part A | 2006 | 125 |
| 30 | GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex | Brain | 2010 | 125 |
| 31 | Development of a Functional Assessment Scale for Ambulatory Boys with Duchenne Muscular Dystrophy | Physiotherapy Research International | 2012 | 121 |
| 32 | Obstructive Sleep Apnea and Sickle Cell Anemia | Pediatrics | 2014 | 116 |
| 33 | Neurological manifestations of SARS-CoV-2 infection in hospitalised children and adolescents in the UK: a prospective national cohort study | The Lancet Child and Adolescent Health | 2021 | 114 |
| 34 | The use of rituximab in myasthenia gravis and Lambert-Eaton myasthenic syndrome | Journal of Neurology, Neurosurgery and Psychiatry | 2011 | 107 |
| 35 | Hepatocyte Transplantation Followed by Auxiliary Liver Transplantation—a Novel Treatment for Ornithine Transcarbamylase Deficiency | American Journal of Transplantation | 2008 | 101 |
| 36 | Beyond the Burke–Fahn–Marsden Dystonia Rating Scale: Deep brain stimulation in childhood secondary dystonia | European Journal of Paediatric Neurology | 2012 | 101 |
| 37 | An organization‐ and category‐level comparison of diagnostic requirements for mental disorders in ICD‐11 and DSM‐5 | World Psychiatry | 2021 | 100 |
| 38 | Treatment mechanism in the MRC preschool autism communication trial: implications for study design and parent‐focussed therapy for children | Journal of Child Psychology and Psychiatry and Allied Disciplines | 2015 | 95 |
| 39 | Treatment of short stature in renal disease with recombinant human growth hormone. | Archives of Disease in Childhood | 1990 | 93 |
| 40 | Initial Steroid Sensitivity in Children with Steroid-Resistant Nephrotic Syndrome Predicts Post-Transplant Recurrence | Journal of the American Society of Nephrology: JASN | 2014 | 93 |
| 41 | Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number | American Journal of Human Genetics | 2016 | 93 |
| 42 | Diagnostic delays in paediatric stroke | Journal of Neurology, Neurosurgery and Psychiatry | 2015 | 92 |
| 43 | Once-daily, subcutaneous vosoritide therapy in children with achondroplasia: a randomised, double-blind, phase 3, placebo-controlled, multicentre trial | Lancet, The | 2020 | 92 |
| 44 | European consensus on the concepts and measurement of the pathophysiological neuromuscular responses to passive muscle stretch | European Journal of Neurology | 2017 | 90 |
| 45 | Growth and endocrine function in steroid sensitive nephrotic syndrome. | Archives of Disease in Childhood | 1988 | 89 |
| 46 | Prevalence of Abnormal Lipid Profiles and the Relationship With the Development of Microalbuminuria in Adolescents With Type 1 Diabetes | Diabetes Care | 2009 | 89 |
| 47 | Impregnated central venous catheters for prevention of bloodstream infection in children (the CATCH trial): a randomised controlled trial | Lancet, The | 2016 | 89 |
| 48 | The Relationship Among Thromboelastography, Hemostatic Variables, and Bleeding After Cardiopulmonary Bypass Surgery in Children | Anesthesia and Analgesia | 2010 | 88 |
| 49 | Growth and endocrine function after renal transplantation. | Archives of Disease in Childhood | 1988 | 86 |
| 50 | A clinical and safety review of paracetamol and ibuprofen in children | Inflammopharmacology | 2017 | 85 |
