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Plos One|October 3, 2012
Three-dimensional genome architecture influences partner selection for chromosomal translocations in human diseaseJesse M Engreitz, Vineeta Agarwala, Leonid A MirnyNature Genetics|October 22, 2013
Evaluating empirical bounds on complex disease genetic architectureVineeta Agarwala, Jason Flannick, Shamil Sunyaev, et al.Nature Protocols|October 26, 2013
Genome engineering using the CRISPR-Cas9 systemF Ann Ran, Patrick D Hsu, Jason Wright, et al.American Journal of Human Genetics|April 29, 2014
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in FinlandSophie R Wang, Vineeta Agarwala, Jason Flannick, et al.Health Affairs (Project Hope)|May 8, 2018
Real-World Evidence In Support Of Precision Medicine: Clinico-Genomic Cancer Data As A Case StudyVineeta Agarwala, Sean Khozin, Gaurav Singal, et al.Plos Genetics|April 24, 2015
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseLoukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, et al.American Journal of Human Genetics|February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathyDaniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.Nature Genetics|July 22, 2011
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarctionJessica Shea, Vineeta Agarwala, Anthony A Philippakis, et al.Nature Biotechnology|July 23, 2013
DNA targeting specificity of RNA-guided Cas9 nucleasesPatrick D Hsu, David A Scott, Joshua A Weinstein, et al.JAMA|August 9, 2018
Association of Broad-Based Genomic Sequencing With Survival Among Patients With Advanced Non-Small Cell Lung Cancer in the Community Oncology SettingCarolyn J Presley, Daiwei Tang, Pamela R Soulos, et al.Pageof 2