# | Title | Journal | Year | Citations |
---|
1 | Comprehensive Analysis of Hypermutation in Human Cancer | Cell | 2017 | 596 |
2 | US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis | Thorax | 2016 | 348 |
3 | Results of NOPHO ALL2008 treatment for patients aged 1–45 years with acute lymphoblastic leukemia | Leukemia | 2018 | 297 |
4 | US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summary | Thorax | 2016 | 274 |
5 | Rett variants: A suggested model for inclusion criteria | Pediatric Neurology | 1994 | 203 |
6 | Melatonin Reduces Inflammation and Cell Death in White Matter in the Mid-Gestation Fetal Sheep Following Umbilical Cord Occlusion | Pediatric Research | 2007 | 203 |
7 | Association Between Year of Birth and 1-Year Survival Among Extremely Preterm Infants in Sweden During 2004-2007 and 2014-2016 | JAMA - Journal of the American Medical Association | 2019 | 195 |
8 | Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia | Nature Genetics | 2017 | 186 |
9 | Decrease in hospitalization for treatment of childhood asthma with increased use of antiinflammatory treatment, despite an increase in the prevalence of asthma† | Journal of Allergy and Clinical Immunology | 1996 | 172 |
10 | Cytokine Response in Cerebrospinal Fluid after Birth Asphyxia | Pediatric Research | 1998 | 167 |
11 | Intractable Epilepsy in Children. The Efficacy of Lamotrigine Treatment, Including Non-Seizure-Related Benefits | Neuropediatrics | 1994 | 158 |
12 | A two-year prospective study of the effect of ursodeoxycholic acid on urinary bile acid excretion and liver morphology in cystic fibrosis-associated liver disease | Hepatology | 1998 | 158 |
13 | Response-Guided Induction Therapy in Pediatric Acute Myeloid Leukemia With Excellent Remission Rate | Journal of Clinical Oncology | 2011 | 156 |
14 | Transplantation of an allogeneic vein bioengineered with autologous stem cells: a proof-of-concept study | Lancet, The | 2012 | 151 |
15 | Neuropsychiatric disorders in the 22q11 deletion syndrome | Genetics in Medicine | 2001 | 145 |
16 | ISPAD Clinical Practice Consensus Guidelines 2018: Exercise in children and adolescents with diabetes | Pediatric Diabetes | 2018 | 144 |
17 | Epidemiology of chronic renal failure in children: a report from Sweden 1986 - 1994 | Pediatric Nephrology | 1997 | 141 |
18 | Global prevalence of cerebral palsy: A systematic analysis | Developmental Medicine and Child Neurology | 2022 | 139 |
19 | Clinical presentation and management of dyskinetic cerebral palsy | Lancet Neurology, The | 2017 | 136 |
20 | Centralization of Pediatric Heart Surgery in Sweden | Pediatric Cardiology | 2000 | 133 |
21 | West Sweden Asthma Study: Prevalence trends over the last 18 years argues no recent increase in asthma | Respiratory Research | 2009 | 133 |
22 | Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations | Journal of Pediatrics | 1991 | 128 |
23 | THE NATURAL HISTORY OF BACTERIURIA IN CHILDHOOD | Infectious Disease Clinics of North America | 1997 | 122 |
24 | Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy | American Journal of Human Genetics | 2016 | 118 |
25 | Speech problems affect more than one in two children with cerebral palsy: Swedish population‐based study | Acta Paediatrica, International Journal of Paediatrics | 2013 | 109 |
26 | Increased expression of aquaporin 3 in atopic eczema | Allergy: European Journal of Allergy and Clinical Immunology | 2006 | 108 |
27 | Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic Fibrosis | American Journal of Respiratory and Critical Care Medicine | 2019 | 108 |
28 | Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in Scandinavia | Journal of Cystic Fibrosis | 2015 | 107 |
29 | Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood forms | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2008 | 105 |
30 | Serum Phospholipid Fatty Acids, Adipose Tissue, and Metabolic Markers in Obese Adolescents | Obesity | 2006 | 104 |
31 | A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease | Tissue Antigens | 1999 | 99 |
32 | The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders | Tissue Antigens | 2000 | 98 |
33 | Medical follow-up study of 5-year-old ICSI children | Reproductive BioMedicine Online | 2004 | 94 |
34 | PAN-cancer analysis of S-phase enriched lncRNAs identifies oncogenic drivers and biomarkers | Nature Communications | 2018 | 93 |
35 | Delayed cortical impairment following lipopolysaccharide exposure in preterm fetal sheep | Annals of Neurology | 2011 | 92 |
36 | Disappearance of Vesicoureteral Reflux in Children | JAMA Pediatrics | 1998 | 91 |
37 | Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutations | Genes and Immunity | 2011 | 89 |
38 | Differential influence of peripheral and systemic sex steroids on skeletal muscle quality in pre‐ and postmenopausal women | Aging Cell | 2011 | 89 |
39 | Hematopoietic stem cell transplantation for infantile osteopetrosis | Blood | 2015 | 89 |
40 | Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes | Journal of Pediatrics | 1991 | 85 |
41 | Use of allergen components begins a new era in pediatric allergology | Pediatric Allergy and Immunology | 2011 | 83 |
42 | Risk factors for cerebral palsy in children born at term | Acta Obstetricia Et Gynecologica Scandinavica | 2011 | 83 |
43 | Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemia | Blood | 2011 | 83 |
44 | Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR–Cas9 genome editing | Nature Biomedical Engineering | 2017 | 83 |
45 | The Utility of DXA Assessment at the Forearm, Proximal Femur, and Lateral Distal Femur, and Vertebral Fracture Assessment in the Pediatric Population: 2019 ISCD Official Position | Journal of Clinical Densitometry | 2019 | 83 |
46 | Skeletal muscle alterations in patients with chronic heart failure | European Heart Journal | 1997 | 82 |
47 | D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity? | Annals of Neurology | 1999 | 82 |
48 | Active epilepsy in mentally retarded children. I. Prevalence and additional neuroimpairments | Acta Paediatrica, International Journal of Paediatrics | 1995 | 81 |
49 | Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects | Developmental Medicine and Child Neurology | 2002 | 81 |
50 | Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles | Annals of Neurology | 1998 | 79 |