Alan J. Mears
Ottawa, ON, Canada
Last Updated: 09/26/2026
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Found 20 publications
FGF14 GAA Intronic Expansion in Unsolved Adult-Onset Ataxia in the Care4Rare Canada Consortium.
Journal: Annals of clinical and translational neurology
Published: October 23, 2024
Next generation sequencing reveals novel compound heterozygous deletions in NDUFAF2 in a child with mitochondrial complex I deficiency, nuclear type 10.
Journal: American journal of medical genetics. Part A
Published: January 03, 2024
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia.
Journal: European journal of medical genetics
Published: April 09, 2020
Validation and in-field testing of a new on-site qPCR system for quantification of Legionella pneumophila according to ISO/TS 12869:2012 in HVAC cooling towers.
Journal: Journal of water and health
Published: April 04, 2019
Identification of therapeutics that target eEF1A2 and upregulate utrophin A translation in dystrophic muscles.
Journal: Nature communications
Published: April 02, 2019
Transcriptomic RNAseq drug screen in cerebrocortical cultures: toward novel neurogenetic disease therapies.
Journal: Human molecular genetics
Published: March 17, 2018
Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screen.
Journal: NPJ genomic medicine
Published: January 16, 2017
Norrin/Frizzled4 signalling in the preneoplastic niche blocks medulloblastoma initiation.
Journal: eLife
Published: April 08, 2016
A Notch-Gli2 axis sustains Hedgehog responsiveness of neural progenitors and Müller glia.
Journal: Developmental biology
Published: July 02, 2015
A novel mutation in two Hmong families broadens the range of STRA6-related malformations to include contractures and camptodactyly.
Journal: American journal of medical genetics. Part A
Published: February 03, 2015
Last Updated: 09/26/2026