Rod M. Gardner
Dunedin, OTA, New Zealand
Last Updated: 09/26/2026
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Found 35 publications
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Half-Siblings.
Journal: Annals of clinical and translational neurology
Published: August 16, 2025
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndrome.
Journal: Frontiers in genetics
Published: January 02, 2023
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25.
Journal: Annals of neurology
Published: November 07, 2021
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy.
Journal: Molecular genetics & genomic medicine
Published: May 21, 2018
The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: November 23, 2017
Mutations in the netrin-1 gene cause congenital mirror movements.
Journal: The Journal of clinical investigation
Published: June 05, 2017
A novel role for the DNA repair gene Rad51 in Netrin-1 signalling.
Journal: Scientific reports
Published: May 13, 2016
SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia.
Journal: Microarrays (Basel, Switzerland)
Published: January 01, 2015
Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.
Journal: Journal of the neurological sciences
Published: December 01, 2014
Expanded transition spaces: the case of Garrwa.
Journal: Frontiers in psychology
Published: October 30, 2014
Diagnostic genetics at a distance: von hippel-lindau disease and a novel mutation.
Journal: Genetics research international
Published: March 31, 2013
Framing the consultation: the role of the referral in surgeon-patient consultations.
Journal: Health communication
Published: February 14, 2013
Last Updated: 09/26/2026