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Plos One|January 11, 2018
Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencingAnn-Marie Patch, Katia Nones, Stephen H Kazakoff, et al.
Neuro-Degenerative Diseases|November 3, 2007
Sorl1 as an Alzheimer's disease predisposition gene?Jennifer A Webster, Amanda J Myers, John V Pearson, et al.
Nucleic Acids Research|May 3, 2018
Telomere sequence content can be used to determine ALT activity in tumoursMichael Lee, Erdahl T Teber, Oliver Holmes, et al.
Genome Medicine|January 11, 2022
Patient-derived xenograft models capture genomic heterogeneity in endometrial cancerVanessa F Bonazzi, Olga Kondrashova, Deborah Smith, et al.
American Journal of Human Genetics|December 13, 2006
Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studiesJohn V Pearson, Matthew J Huentelman, Rebecca F Halperin, et al.
The Journal of Pathology|January 19, 2018
Mixed ductal-lobular carcinomas: evidence for progression from ductal to lobular morphologyAmy E McCart Reed, Jamie R Kutasovic, Katia Nones, et al.
American Journal of Human Genetics|April 14, 2009
Genetic control of human brain transcript expression in Alzheimer diseaseJennifer A Webster, J Raphael Gibbs, Jennifer Clarke, et al.
American Journal of Human Genetics|March 16, 2007
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsStacey Melquist, David W Craig, Matthew J Huentelman, et al.
Genome Medicine|April 30, 2017
Lost in translation: returning germline genetic results in genome-scale cancer researchAmber L Johns, Skye H McKay, Jeremy L Humphris, et al.
Nature Methods|August 1, 2013
Computational approaches to identify functional genetic variants in cancer genomesAbel Gonzalez-Perez, Ville Mustonen, Boris Reva, et al.
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