Daniel M. Evans
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 11 publications
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
RAPIDOMICS: rapid genome-wide sequencing in a neonatal intensive care unit-successes and challenges.
Journal: European journal of pediatrics
Published: January 04, 2019
Diagnostic Yield and Treatment Impact of Targeted Exome Sequencing in Early-Onset Epilepsy.
Journal: Frontiers in neurology
Published: November 17, 2018
Whole-Exome Sequencing of an Exceptional Longevity Cohort.
Journal: The journals of gerontology. Series A, Biological sciences and medical sciences
Published: January 31, 2018
De Novo Mutations in YWHAG Cause Early-Onset Epilepsy.
Journal: American journal of human genetics
Published: April 11, 2017
Neurobehavioral characterization of adult-onset Alexander disease: A family study.
Journal: Neurology. Clinical practice
Published: January 14, 2017
An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2.
Journal: Pediatric neurology
Published: September 24, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy.
Journal: Neurology. Genetics
Published: June 16, 2016
α-synuclein genetic variability: A biomarker for dementia in Parkinson disease.
Journal: Annals of neurology
Published: December 09, 2015
Defining neurodegeneration on Guam by targeted genomic sequencing.
Journal: Annals of neurology
Published: August 14, 2014
The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber population.
Journal: European journal of neurology
Published: April 04, 2014
DNAJC13 mutations in Parkinson disease.
Journal: Human molecular genetics
Published: November 13, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026