2.7K
Articles
100.9K
Citations
3
avg. Impact Factor
132
h-index

Most Cited Articles of Department of Pediatrics

TitleJournalYearCitations
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductaseNature Genetics19954.7K
A genome-wide association study identifies novel risk loci for type 2 diabetesNature20072.3K
Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastomaCancer Cell20121.2K
A new and improved population-based Canadian reference for birth weight for gestational agePediatrics20011.1K
Clinical biostatistics. LIV. The biostatistics of concordanceClinical Pharmacology and Therapeutics1981917
Canadian 24-Hour Movement Guidelines for Children and Youth: An Integration of Physical Activity, Sedentary Behaviour, and SleepApplied Physiology, Nutrition and Metabolism2016687
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locusNature Genetics1997671
An update on the prevalence of cerebral palsy: a systematic review and meta-analysisDevelopmental Medicine and Child Neurology2013658
Breastfeeding and child cognitive development: new evidence from a large randomized trialArchives of General Psychiatry2008637
Differential in situ cytokine gene expression in acute versus chronic atopic dermatitisJournal of Clinical Investigation1994580
Eosinophil-associated TGF-beta1 mRNA expression and airways fibrosis in bronchial asthmaAmerican Journal of Respiratory Cell and Molecular Biology1997567
Socio-economic disparities in pregnancy outcome: why do the poor fare so poorly?Paediatric and Perinatal Epidemiology2000554
Intertumoral Heterogeneity within Medulloblastoma SubgroupsCancer Cell2017511
Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalitiesProceedings of the National Academy of Sciences of the United States of America1998507
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomasCancer Cell2013478
The whole-genome landscape of medulloblastoma subtypesNature2017472
Optimal duration of exclusive breastfeedingThe Cochrane Library2012465
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid depositionHuman Molecular Genetics2001458
Epigenomic alterations define lethal CIMP-positive ependymomas of infancyNature2014434
Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damageScience2013424
A genome-wide association study identifies KIAA0350 as a type 1 diabetes geneNature2007424
Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine GliomaCancer Cell2017423
Brain volume and metabolism in fetuses with congenital heart disease: evaluation with quantitative magnetic resonance imaging and spectroscopyCirculation2010421
Handwriting development, competency, and interventionDevelopmental Medicine and Child Neurology2007412
The melanocortin-1 receptor gene mediates female-specific mechanisms of analgesia in mice and humansProceedings of the National Academy of Sciences of the United States of America2003412