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Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
by Chu, Van Trung
Nature biotechnology, 2015-05, Vol.33 (5), p.543-548
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Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks
by Peloso, Gina M
American journal of human genetics, 2014-02-06, Vol.94 (2), p.223-232
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Multiscale Analysis of Independent Alzheimer’s Cohorts Finds Disruption of Molecular, Genetic, and Clinical Networks by Human Herpesvirus
by Readhead, Ben
Neuron (Cambridge, Mass.), 2018-07-11, Vol.99 (1), p.64-82.e7
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Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
by Miraoui, Hichem
American journal of human genetics, 2013-05-02, Vol.92 (5), p.725-743
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Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining
by Maruyama, Takeshi
Nature biotechnology, 2015-05, Vol.33 (5), p.538-542
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Efficient generation of targeted large insertions by microinjection into two-cell-stage mouse embryos
by Gu, Bin
Nature biotechnology, 2018-08, Vol.36 (7), p.632-637
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Regulation of Transcription by Long Noncoding RNAs
by Bonasio, Roberto
Annual review of genetics, 2014-11-23, Vol.48 (1), p.433-455
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Fibrinogen as a key regulator of inflammation in disease
by Davalos, Dimitrios
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The diploid genome sequence of an Asian individual
by Wang, Jun
Nature, 2008-11-06, Vol.456 (7218), p.60-65
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Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells
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Nature biotechnology, 2015-02, Vol.33 (2), p.155-160
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Functional genetic screens for enhancer elements in the human genome using CRISPR-Cas9
by Korkmaz, Gozde
Nature biotechnology, 2016-02, Vol.34 (2), p.192-198
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Inducible in vivo genome editing with CRISPR-Cas9
by Dow, Lukas E
Nature biotechnology, 2015-04, Vol.33 (4), p.390-394
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Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype
by Yin, Hao
Nature biotechnology, 2014-06, Vol.32 (6), p.551-553
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Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis
by Ling, Shuo-Chien
Neuron (Cambridge, Mass.), 2013-08-07, Vol.79 (3), p.416-438
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Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia
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A “Copernican” Reassessment of the Human Mitochondrial DNA Tree from its Root
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Annual review of neuroscience, 2014, Vol.37 (1), p.17-38
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Genetic Removal of p70 S6 Kinase 1 Corrects Molecular, Synaptic, and Behavioral Phenotypes in Fragile X Syndrome Mice
by Bhattacharya, Aditi
Neuron (Cambridge, Mass.), 2012-10-18, Vol.76 (2), p.325-337
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Advancing the understanding of autism disease mechanisms through genetics
by de la Torre-Ubieta, Luis
Nature medicine, 2016-04, Vol.22 (4), p.345-361
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