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Neurology. Genetics|April 29, 2016
Analysis of rare copy number variation in absence epilepsiesLaura Addis, Richard E Rosch, Antonio Valentin, et al.
Forensic Science International. Genetics|February 16, 2022
Coral-ID: A forensically validated genetic test to identify precious coral material and its application to objects seized from illegal trafficBertalan Lendvay, Laurent E Cartier, Federica Costantini, et al.
Plos One|November 1, 2016
Large-Scale Genotyping-by-Sequencing Indicates High Levels of Gene Flow in the Deep-Sea Octocoral Swiftia simplex (Nutting 1909) on the West Coast of the United StatesMeredith V Everett, Linda K Park, Ewann A Berntson, et al.
European Journal of Human Genetics : EJHG|May 15, 2008
Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24Kate V Everett, Francesca Capon, Christina Georgoula, et al.
Journal of Medical Case Reports|April 6, 2023
Presacral malakoplakia presenting as foot drop: a case reportTom A Yates, Katie Devlin, Abed Arnaout, et al.
Plos One|December 1, 2025
eDNA reveals spatial differences in species composition of protected rockfishesStephanie A Matthews, Olivia M Scott, Meredith V Everett, et al.
Molecular Ecology Resources|October 23, 2015
An integrated linkage map reveals candidate genes underlying adaptive variation in Chinook salmon (Oncorhynchus tshawytscha)G J McKinney, L W Seeb, W A Larson, et al.
American Journal of Human Genetics|March 1, 2008
Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23Kate V Everett, Barry A Chioza, Christina Georgoula, et al.
Rheumatology (Oxford, England)|August 25, 2014
Inadequate pain relief and large functional loss among patients with knee osteoarthritis: evidence from a prospective multinational longitudinal study of osteoarthritis real-world therapiesPhilip G Conaghan, Paul M Peloso, Sharlette V Everett, et al.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
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