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Nature Communications|May 9, 2022
Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritabilityMarcin Kierczak, Nima Rafati, Julia Höglund, et al.
European Journal of Human Genetics : EJHG|October 15, 2009
Comparison of participant information and informed consent forms of five European studies in genetic isolated populationsDeborah Mascalzoni, A Cecile J W Janssens, Alison Stewart, et al.
Cancer Research|October 3, 2014
TGFβ receptor 1: an immune susceptibility gene in HPV-associated cancerChaya Levovitz, Dan Chen, Emma Ivansson, et al.
Neuro-Oncology|June 23, 2022
Novel cancer gene discovery using a forward genetic screen in RCAS-PDGFB-driven gliomasHolger Weishaupt, Matko Čančer, Gabriela Rosén, et al.
Genome Biology|December 2, 2020
Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activityIda Höijer, Josefin Johansson, Sanna Gudmundsson, et al.
BMC Genomics|February 27, 2010
Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic dataOzren Polasek, Caroline Hayward, Celine Bellenguez, et al.
Journal of Molecular Neuroscience : MN|October 12, 2012
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genesIrene Pichler, Christine Schwienbacher, Alessandra Zanon, et al.
Cancer Research|December 4, 2020
Patterns of Human Leukocyte Antigen Class I and Class II Associations and CancerZhiwei Liu, Andriy Derkach, Kelly J Yu, et al.
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