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Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.Nature Communications|December 14, 2017
Identification and characterization of two functional variants in the human longevity gene FOXO3Friederike Flachsbart, Janina Dose, Liljana Gentschew, et al.Nature Communications|January 18, 2018
Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3Friederike Flachsbart, Janina Dose, Liljana Gentschew, et al.Journal of Community Genetics|March 31, 2019
Linking pre-existing biorepositories for medical research: the PopGen 2.0 NetworkWolfgang Lieb, Gunnar Jacobs, Andreas Wolf, et al.HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.Gut|July 26, 2022
GWAS meta-analysis of 16 790 patients with Barrett's oesophagus and oesophageal adenocarcinoma identifies 16 novel genetic risk loci and provides insights into disease aetiology beyond the single marker levelJulia Schröder, Laura Chegwidden, Carlo Maj, et al.Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.The New England Journal of Medicine|June 20, 2020
Genomewide Association Study of Severe Covid-19 with Respiratory Failure, David Ellinghaus, Frauke Degenhardt, et al.Human Molecular Genetics|July 18, 2022
Detailed stratified GWAS analysis for severe COVID-19 in four European populationsFrauke Degenhardt, David Ellinghaus, Simonas Juzenas, et al.Pageof 2