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Nature Communications|February 7, 2017
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemiaPhilip J Law, Sonja I Berndt, Helen E Speedy, et al.Circulation|September 26, 2022
Cross-Ancestry Investigation of Venous Thromboembolism Genomic PredictorsFlorian Thibord, Derek Klarin, Jennifer A Brody, et al.Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.Nature Communications|March 15, 2023
Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular diseaseWilliam J Young, Jeffrey Haessler, Jan-Walter Benjamins, et al.Nature Communications|July 8, 2015
Genome-wide association study of colorectal cancer identifies six new susceptibility lociFredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, et al.Nature Communications|January 9, 2015
A genome-wide association study of marginal zone lymphoma shows association to the HLA regionJoseph Vijai, Zhaoming Wang, Sonja I Berndt, et al.Lupus Science & Medicine|December 8, 2017
Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphomaSasha Bernatsky, Héctor A Velásquez García, John J Spinelli, et al.American Journal of Human Genetics|February 11, 2014
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacksGina M Peloso, Paul L Auer, Joshua C Bis, et al.American Journal of Human Genetics|February 11, 2014
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterolLeslie A Lange, Youna Hu, He Zhang, et al.Contemporary Nurse|August 18, 2020
A unified call to action from Australian nursing and midwifery leaders: ensuring that Black lives matterL Geia, K Baird, K Bail, et al.Pageof 223