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Nature Genetics|April 12, 2011
A framework for variation discovery and genotyping using next-generation DNA sequencing dataMark A DePristo, Eric Banks, Ryan Poplin, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 2, 2018
Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from EstoniaMaris Alver, Marili Palover, Aet Saar, et al.Nature Genetics|March 31, 2004
Assessing the impact of population stratification on genetic association studiesMatthew L Freedman, David Reich, Kathryn L Penney, et al.Nature|October 25, 2002
Detecting recent positive selection in the human genome from haplotype structurePardis C Sabeti, David E Reich, John M Higgins, et al.Nature Genetics|September 7, 2010
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiencySarah E Calvo, Elena J Tucker, Alison G Compton, et al.Circulation Research|January 1, 2014
Increased burden of cardiovascular disease in carriers of APOL1 genetic variantsKaoru Ito, Alexander G Bick, Jason Flannick, et al.Cancer Cell|March 12, 2015
A functional landscape of resistance to ALK inhibition in lung cancerFrederick H Wilson, Cory M Johannessen, Federica Piccioni, et al.Journal of the International Neuropsychological Society : JINS|February 3, 2016
Decreased Fronto-Limbic Activation and Disrupted Semantic-Cued List Learning in Major Depressive DisorderMichelle T Kassel, Julia A Rao, Sara J Walker, et al.Plos One|June 1, 2022
COVID-19 vaccines uptake: Public knowledge, awareness, perception and acceptance among adult AfricansJohn K Ahiakpa, Nanma T Cosmas, Felix E Anyiam, et al.Cell|March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO MutationAh Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.Pageof 28