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Top Articles

#TitleJournalYearCitations
1Comprehensive Analysis of Hypermutation in Human CancerCell2017596
2US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosisThorax2016348
3Results of NOPHO ALL2008 treatment for patients aged 1–45 years with acute lymphoblastic leukemiaLeukemia2018297
4US Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus recommendations for the management of non-tuberculous mycobacteria in individuals with cystic fibrosis: executive summaryThorax2016274
5Rett variants: A suggested model for inclusion criteriaPediatric Neurology1994203
6Melatonin Reduces Inflammation and Cell Death in White Matter in the Mid-Gestation Fetal Sheep Following Umbilical Cord OcclusionPediatric Research2007203
7Association Between Year of Birth and 1-Year Survival Among Extremely Preterm Infants in Sweden During 2004-2007 and 2014-2016JAMA - Journal of the American Medical Association2019195
8Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystoniaNature Genetics2017186
9Decrease 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 Immunology1996172
10Cytokine Response in Cerebrospinal Fluid after Birth AsphyxiaPediatric Research1998167
11Intractable Epilepsy in Children. The Efficacy of Lamotrigine Treatment, Including Non-Seizure-Related BenefitsNeuropediatrics1994158
12A two-year prospective study of the effect of ursodeoxycholic acid on urinary bile acid excretion and liver morphology in cystic fibrosis-associated liver diseaseHepatology1998158
13Response-Guided Induction Therapy in Pediatric Acute Myeloid Leukemia With Excellent Remission RateJournal of Clinical Oncology2011156
14Transplantation of an allogeneic vein bioengineered with autologous stem cells: a proof-of-concept studyLancet, The2012151
15Neuropsychiatric disorders in the 22q11 deletion syndromeGenetics in Medicine2001145
16ISPAD Clinical Practice Consensus Guidelines 2018: Exercise in children and adolescents with diabetesPediatric Diabetes2018144
17Epidemiology of chronic renal failure in children: a report from Sweden 1986 - 1994Pediatric Nephrology1997141
18Global prevalence of cerebral palsy: A systematic analysisDevelopmental Medicine and Child Neurology2022139
19Clinical presentation and management of dyskinetic cerebral palsyLancet Neurology, The2017136
20Centralization of Pediatric Heart Surgery in SwedenPediatric Cardiology2000133
21West Sweden Asthma Study: Prevalence trends over the last 18 years argues no recent increase in asthmaRespiratory Research2009133
22Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigationsJournal of Pediatrics1991128
23THE NATURAL HISTORY OF BACTERIURIA IN CHILDHOODInfectious Disease Clinics of North America1997122
24Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent EpilepsyAmerican Journal of Human Genetics2016118
25Speech problems affect more than one in two children with cerebral palsy: Swedish population‐based studyActa Paediatrica, International Journal of Paediatrics2013109
26Increased expression of aquaporin 3 in atopic eczemaAllergy: European Journal of Allergy and Clinical Immunology2006108
27Cardiopulmonary Exercise Testing Provides Additional Prognostic Information in Cystic FibrosisAmerican Journal of Respiratory and Critical Care Medicine2019108
28Epidemiology of nontuberculous mycobacteria among patients with cystic fibrosis in ScandinaviaJournal of Cystic Fibrosis2015107
29Autism spectrum conditons in myotonic dystrophy type 1: A study on 57 individuals with congenital and childhood formsAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics2008105
30Serum Phospholipid Fatty Acids, Adipose Tissue, and Metabolic Markers in Obese AdolescentsObesity2006104
31A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac diseaseTissue Antigens199999
32The 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 disordersTissue Antigens200098
33Medical follow-up study of 5-year-old ICSI childrenReproductive BioMedicine Online200494
34PAN-cancer analysis of S-phase enriched lncRNAs identifies oncogenic drivers and biomarkersNature Communications201893
35Delayed cortical impairment following lipopolysaccharide exposure in preterm fetal sheepAnnals of Neurology201192
36Disappearance of Vesicoureteral Reflux in ChildrenJAMA Pediatrics199891
37Molecular basis of hereditary C1q deficiency—revisited: identification of several novel disease-causing mutationsGenes and Immunity201189
38Differential influence of peripheral and systemic sex steroids on skeletal muscle quality in pre‐ and postmenopausal womenAging Cell201189
39Hematopoietic stem cell transplantation for infantile osteopetrosisBlood201589
40Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromesJournal of Pediatrics199185
41Use of allergen components begins a new era in pediatric allergologyPediatric Allergy and Immunology201183
42Risk factors for cerebral palsy in children born at termActa Obstetricia Et Gynecologica Scandinavica201183
43Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemiaBlood201183
44Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR–Cas9 genome editingNature Biomedical Engineering201783
45The Utility of DXA Assessment at the Forearm, Proximal Femur, and Lateral Distal Femur, and Vertebral Fracture Assessment in the Pediatric Population: 2019 ISCD Official PositionJournal of Clinical Densitometry201983
46Skeletal muscle alterations in patients with chronic heart failureEuropean Heart Journal199782
47D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity?Annals of Neurology199982
48Active epilepsy in mentally retarded children. I. Prevalence and additional neuroimpairmentsActa Paediatrica, International Journal of Paediatrics199581
49Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspectsDevelopmental Medicine and Child Neurology200281
50Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuolesAnnals of Neurology199879