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American Journal of Human Genetics|February 8, 2020
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model OrganismsKym M Boycott, Philippe M Campeau, Heather E Howley, et al.
Neurology. Genetics|October 27, 2025
Developing a National Network for Leukodystrophy Research and Care in Canada: The CARELeuko InitiativeAlexandra Chapleau, Adam Le, Justin Simo, et al.
Trials|October 11, 2023
Doxapram versus placebo in preterm newborns: a study protocol for an international double blinded multicentre randomized controlled trial (DOXA-trial)Jarinda A Poppe, Robert B Flint, Anne Smits, et al.
The Lancet. Child & Adolescent Health|June 12, 2026
CONSORT-Children and Adolescents (CONSORT-C) 2026 extension statement: enhancing the reporting and impact of paediatric randomised trialsAmi Baba, Maureen Smith, Beth K Potter, et al.
The Lancet. Child & Adolescent Health|June 12, 2026
SPIRIT-Children and Adolescents (SPIRIT-C) 2026 extension statement: enhancing the reporting and usefulness of paediatric randomised trial protocolsAmi Baba, Maureen Smith, Beth K Potter, et al.
JAMA Pediatrics|February 24, 2026
CONSORT-Children and Adolescents (CONSORT-C) 2026 Extension Statement: Enhancing the Reporting and Impact of Pediatric Randomized TrialsAmi Baba, Maureen Smith, Beth K Potter, et al.
Frontiers in Genetics|May 8, 2023
Combining globally search for a regular expression and print matching lines with bibliographic monitoring of genomic database improves diagnosisFrédéric Tran Mau-Them, Alexis Overs, Ange-Line Bruel, et al.
JAMA Pediatrics|February 24, 2026
SPIRIT-Children and Adolescents (SPIRIT-C) 2026 Extension Statement: Enhancing the Reporting and Usefulness of Pediatric Randomized Trial ProtocolsAmi Baba, Maureen Smith, Beth K Potter, et al.
Nature Communications|January 25, 2020
The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderlyMark Pinese, Paul Lacaze, Emma M Rath, et al.
American Journal of Human Genetics|November 3, 2018
NFIB Haploinsufficiency Is Associated with Intellectual Disability and MacrocephalyIna Schanze, Jens Bunt, Jonathan W C Lim, et al.
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