Most cited papers from SickKids Foundation

SickKids Foundation

What are the most cited papers from SickKids Foundation?

The most cited paper from SickKids Foundation is "The 2021 WHO Classification of Tumors of the Central Nervous System: a summary" (David N. Louis, Arie Perry, Pieter Wesseling et al., 2021), with 12,579 citations. Next come "Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines" (11,535) and "Identification of human brain tumour initiating cells" (7,487).

Published TypeFieldAccessAuthorsCitations

Showing 50 of 60 papers. Every paper with more than 1,430 citations is listed.

Most cited papers, sortable by citations and release date
#	Paper
1	The 2021 WHO Classification of Tumors of the Central Nervous System: a summary David N. Louis, Arie Perry, Pieter Wesseling et al. · Neuro-Oncology Open access	3 May 2021	12,579
2	Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines Clotilde Théry et al. · Journal of Extracellular Vesicles Open access382 authors	23 Nov 2018	11,535
3	Identification of human brain tumour initiating cells Sheila Kumari Singh, Cynthia E Hawkins, Ian D. Clarke et al. · Nature	Nov 2004	7,487
4	Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell Dominique A. Bonnet, John Edgar Dick · Nature Medicine	Jul 1997	7,031
5	The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement Eric I. Benchimol, Liam L Smeeth, Astrid Guttmann et al. · PLoS Medicine Open access	6 Oct 2015	5,721
6	Histological grading and staging of chronic hepatitis Kamal G. Ishak, Amélia Baptista, Leonardo Bianchi et al. · Journal of Hepatology	Jun 1995	5,081
7	Identification of a cancer stem cell in human brain tumors. Sheila Kumari Singh, Ian D. Clarke, Mizuhiko Terasaki et al. · PubMed	15 Sep 2003	4,896
8	Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease Robin P. Sherrington et al. · Nature	Jun 1995	4,080
9	The repertoire of mutational signatures in human cancer Ludmil B. Alexandrov et al. · Nature Open access1,384 authors	5 Feb 2020	3,854
10	Defining consensus: A systematic review recommends methodologic criteria for reporting of Delphi studies Ivan R. Diamond, Robert C. Grant, Brian Michael Feldman et al. · Journal of Clinical Epidemiology Review	26 Feb 2014	3,802
11	TRIPOD+AI statement: updated guidance for reporting clinical prediction models that use regression or machine learning methods Professor Gary S. Collins et al. · BMJ Open access	16 Apr 2024	3,581
12	Hematological Problems in Pediatric Intensive Care Shoshana Revel‐Vilk, Peter N. Cox, Nancy Robitaille et al. · Pediatric and adolescent medicine Book chapter	28 Nov 2013	3,516
13	The Treatment-Naive Microbiome in New-Onset Crohn’s Disease Dirk Gevers et al. · Cell Host & Microbe Open access	Mar 2014	3,362
14	Pan-cancer analysis of whole genomes Lauri A. Aaltonen et al. · Nature Open access1,324 authors	5 Feb 2020	3,360
15	DNA methylation-based classification of central nervous system tumours David Capper et al. · Nature Open access143 authors	13 Mar 2018	3,228
16	Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies David T. Miller et al. · The American Journal of Human Genetics Open access	May 2010	2,934
17	STRIDE-II: An Update on the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE) Initiative of the International Organization for the Study of IBD (IOIBD): Determining Therapeutic Goals for Treat-to-Target strategies in IBD Dan Turner, Amanda Ricciuto, Ayanna E. Lewis et al. · Gastroenterology Open access	20 Feb 2021	2,882
18	Nanoparticle-mediated cellular response is size-dependent Wen Jiang, Betty Y.S. Kim, James T. Rutka et al. · Nature Nanotechnology	Mar 2008	2,772
19	Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1 Daniel J. Klionsky et al. · Autophagy Open access2,930 authors	2 Jan 2021	2,743
20	Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Jeremy Schwartzentruber et al. · Nature	27 Jan 2012	2,736
21	Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group Francesco Rodeghiero, Roberto Stasi, Terry Gernsheimer et al. · Blood Open access	12 Nov 2008	2,707
22	Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease Jeffrey C. Barrett et al. · Nature Genetics Open access	29 Jun 2008	2,644
23	New insights into the genetic etiology of Alzheimer’s disease and related dementias Céline Bellenguez et al. · Nature Genetics Open access1,266 authors	Apr 2022	2,608
24	Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci André Franke et al. · Nature Genetics Open access	21 Nov 2010	2,592
25	Combination therapy in combating cancer Reza Bayat Mokhtari, Tina S. Homayouni, Narges Baluch et al. · Oncotarget Open access	30 Mar 2017	2,568
26	Angiotensin-converting enzyme 2 protects from severe acute lung failure Yumiko Imai, Keiji Kuba, Shuan Rao et al. · Nature Open access	6 Jul 2005	2,566
27	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs S Hong Lee et al. · Nature Genetics Open access370 authors	11 Aug 2013	2,374
28	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder Ditte Demontis et al. · Nature Genetics Open access	23 Nov 2018	2,356
29	International standards for newborn weight, length, and head circumference by gestational age and sex: the Newborn Cross-Sectional Study of the INTERGROWTH-21st Project José Villar, Leila Cheikh Ismail, Cesar Gomes Victora et al. · The Lancet	Sep 2014	2,352
30	Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap Jüri Reimand, Ruth Isserlin, Véronique Voisin et al. · Nature Protocols Open access	21 Jan 2019	2,219
31	Similarity network fusion for aggregating data types on a genomic scale Bo Wang, Aziz M. Mezlini, Feyyaz Demir et al. · Nature Methods	26 Jan 2014	2,167
32	Structural variation in the human genome Lars Feuk, Andrew R. Carson, Stephen W. Scherer · Nature Reviews Genetics Review	18 Jan 2006	2,093
33	Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto et al. · Nature Open access177 authors	8 Jun 2010	2,073
34	Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene Evgeny Ivanovich Rogaev et al. · Nature	Aug 1995	2,073
35	Canadian 24-Hour Movement Guidelines for Children and Youth: An Integration of Physical Activity, Sedentary Behaviour, and Sleep Mark Stephen Tremblay et al. · Applied Physiology Nutrition and Metabolism Open access	Jun 2016	2,061
36	Analysis of shared heritability in common disorders of the brain Verneri Anttila et al. · Science Open access577 authors	21 Jun 2018	2,056
37	Intercellular transfer of the oncogenic receptor EGFRvIII by microvesicles derived from tumour cells Khalid N I Al-Nedawi, Brian Meehan, Johann Micallef et al. · Nature Cell Biology	20 Apr 2008	2,045
38	The Burden of Primary Liver Cancer and Underlying Etiologies From 1990 to 2015 at the Global, Regional, and National Level Tomi Akinyemiju et al. · JAMA Oncology Open access	5 Oct 2017	2,044
39	WFH Guidelines for the Management of Hemophilia, 3rd edition Alok Srivastava, Elena Santagostino, Alison Dougall et al. · Haemophilia Open access	Aug 2020	2,029
40	Molecular subgroups of medulloblastoma: the current consensus Michael D. Taylor, Paul A. Northcott, Andrey Korshunov et al. · Acta Neuropathologica Open access	2 Dec 2011	1,993
41	Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles Timothy J. Nott, Evangelia Petsalaki, Patrick J. Farber et al. · Molecular Cell Open access	Mar 2015	1,978
42	CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia Haydar Frangoul et al. · New England Journal of Medicine Open access	5 Dec 2020	1,969
43	The 2017 international classification of the Ehlers–Danlos syndromes Fransiska Malfait et al. · American Journal of Medical Genetics Part C Seminars in Medical Genetics Open access	Mar 2017	1,940
44	Hotspot Mutations in H3F3A and IDH1 Define Distinct Epigenetic and Biological Subgroups of Glioblastoma Dominik Sturm et al. · Cancer Cell Open access	Oct 2012	1,881
45	Structural Variation of Chromosomes in Autism Spectrum Disorder Christian R. Marshall et al. · The American Journal of Human Genetics Open access	22 Jan 2008	1,867
46	Microglia emerge as central players in brain disease Michael W. Salter, Beth A. Stevens · Nature Medicine	Sep 2017	1,842
47	The Diploid Genome Sequence of an Individual Human Samuel Lévy et al. · PLoS Biology Open access	31 Aug 2007	1,838
48	Clinical recommendations for cardiovascular magnetic resonance mapping of T1, T2, T2* and extracellular volume: A consensus statement by the Society for Cardiovascular Magnetic Resonance (SCMR) endorsed by the European Association for Cardiovascular Imaging (EACVI) Daniel Messroghli, James Moon, Vanessa M. Ferreira et al. · Journal of Cardiovascular Magnetic Resonance Open access	Dec 2016	1,753
49	Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray Y. Ann Chen, Mathieu Lemire, Sanaa Choufani et al. · Epigenetics Open access	11 Jan 2013	1,738
50	Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency Angela R Brooks-Wilson et al. · Nature Genetics	Aug 1999	1,720

Citations are OpenAlex's own counts, from its 2026-09-23 snapshot, so the ranking can differ from Google Scholar or Web of Science. A paper is listed for an institution when any of its authors gave it as an affiliation; retracted papers and papers whose citation count cannot be traced to citing works are left out, and a preprint and the article it became are shown once. Release dates are OpenAlex's: where a source gave only a month or a year, that is what is shown. How the lists are chosen.