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Nature Genetics|April 13, 2021
Chromothripsis as an on-target consequence of CRISPR-Cas9 genome editingMitchell L Leibowitz, Stamatis Papathanasiou, Phillip A Doerfler, et al.Nature|January 20, 2012
DNA breaks and chromosome pulverization from errors in mitosisKaren Crasta, Neil J Ganem, Regina Dagher, et al.Nature|April 18, 2014
Oncogene-like induction of cellular invasion from centrosome amplificationSusana A Godinho, Remigio Picone, Mithila Burute, et al.RNA (New York, N.Y.)|December 13, 2018
Human nuclear RNAi-defective 2 (NRDE2) is an essential RNA splicing factorAlan L Jiao, Roberto Perales, Neil T Umbreit, et al.Oncogene|March 30, 2004
High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell linesPasi A Jänne, Cheng Li, Xiaojun Zhao, et al.Molecular and Cellular Biology|January 6, 2005
The parafibromin tumor suppressor protein is part of a human Paf1 complexOrit Rozenblatt-Rosen, Christina M Hughes, Suraj J Nannepaga, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2008
The T790M mutation in EGFR kinase causes drug resistance by increasing the affinity for ATPCai-Hong Yun, Kristen E Mengwasser, Angela V Toms, et al.Plos Pathogens|April 1, 2022
Long-read sequencing reveals complex patterns of wraparound transcription in polyomavirusesJason Nomburg, Wei Zou, Thomas C Frost, et al.Nature Communications|April 17, 2015
Calibrating genomic and allelic coverage bias in single-cell sequencingCheng-Zhong Zhang, Viktor A Adalsteinsson, Joshua Francis, et al.Genome Research|November 6, 2012
Somatic rearrangements across cancer reveal classes of samples with distinct patterns of DNA breakage and rearrangement-induced hypermutabilityYotam Drier, Michael S Lawrence, Scott L Carter, et al.Pageof 44