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HGG Advances|October 4, 2021
Genetic discovery and risk characterization in type 2 diabetes across diverse populationsLinda M Polfus, Burcu F Darst, Heather Highland, et al.Genomics|June 18, 2005
High-density single-nucleotide polymorphism maps of the human genomeRaymond D Miller, Michael S Phillips, Inho Jo, et al.Brain : a Journal of Neurology|August 14, 2025
Connectivity as a universal predictor of tau progression in atypical Alzheimer's diseaseHannah de Bruin, Colin Groot, Henryk Barthel, et al.Nature|January 22, 2025
Scaling and networking a modular photonic quantum computerH Aghaee Rad, T Ainsworth, R N Alexander, et al.Nature Genetics|June 2, 2022
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validationMarijana Vujkovic, Shweta Ramdas, Kim M Lorenz, et al.Physical Review Letters|July 26, 2014
Probing the repulsive core of the nucleon-nucleon interaction via the (4)He(e,e'pN) triple-coincidence reactionI Korover, N Muangma, O Hen, et al.Nature|October 24, 2003
The DNA sequence and analysis of human chromosome 6A J Mungall, S A Palmer, S K Sims, et al.Nature|October 19, 2007
Genome-wide detection and characterization of positive selection in human populationsPardis C Sabeti, Patrick Varilly, Ben Fry, et al.Science (New York, N.Y.)|July 16, 2026
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.Nature|October 19, 2007
A second generation human haplotype map of over 3.1 million SNPs, Kelly A Frazer, Dennis G Ballinger, et al.Pageof 213