Charles Lee

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2018-12 FusorSV: an algorithm for optimally combining data from multiple structural variation detection methods in GENOME BIOLOGY
  • 2018-12 High-resolution deconstruction of evolution induced by chemotherapy treatments in breast cancer xenografts in SCIENTIFIC REPORTS
  • 2018-08 Studying cancer immunotherapy using patient-derived xenografts (PDXs) in humanized mice in EXPERIMENTAL & MOLECULAR MEDICINE
  • 2017-04 High prevalence of TP53 mutations is associated with poor survival and an EMT signature in gliosarcoma patients in EXPERIMENTAL & MOLECULAR MEDICINE
  • 2016-06 Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences in NATURE GENETICS
  • 2016-03 Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR in NATURE NEUROSCIENCE
  • 2015-12 Erratum: Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms in NATURE COMMUNICATIONS
  • 2015-12 Analysis of deletion breakpoints from 1,092 humans reveals details of mutation mechanisms in NATURE COMMUNICATIONS
  • 2015-10 An integrated map of structural variation in 2,504 human genomes in NATURE
  • 2014-03 Does germ-line deletion of the PIP gene constitute a widespread risk for cancer? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-12 Copy number variation genotyping using family information in BMC BIOINFORMATICS
  • 2013-11 ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013 in GENETICS IN MEDICINE
  • 2012-07 Evolutionary genetics of the human Rh blood group system in HUMAN GENETICS
  • 2012-04 Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration in NATURE GENETICS
  • 2011-10 Shared acquired genomic changes in zebrafish and human T-ALL in ONCOGENE
  • 2011-08 Extensive genomic and transcriptional diversity identified through massively parallel DNA and RNA sequencing of eighteen Korean individuals in NATURE GENETICS
  • 2011-06 Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants in NATURE BIOTECHNOLOGY
  • 2011-05 Refinement of primate copy number variationhotspots identifies candidate genomic regions evolving under positive selection in GENOME BIOLOGY
  • 2011-02-03 Mapping copy number variation by population-scale genome sequencing in NATURE
  • 2011-02 Activation of a novel palmitoyltransferase ZDHHC14 in acute biphenotypic leukemia and subsets of acute myeloid leukemia in LEUKEMIA
  • 2010-05 Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing in NATURE GENETICS
  • 2010-05 Mutation spectrum revealed by breakpoint sequencing of human germline CNVs in NATURE GENETICS
  • 2010-05 Towards a comprehensive structural variation map of an individual human genome in GENOME BIOLOGY
  • 2010-04 Amplification of EGFR T790M causes resistance to an irreversible EGFR inhibitor in ONCOGENE
  • 2010-04 Origins and functional impact of copy number variation in the human genome in NATURE
  • 2009-08 A highly annotated whole-genome sequence of a Korean individual in NATURE
  • 2008-10 Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs in NATURE GENETICS
  • 2007-12 Definition of the zebrafish genome using flow cytometry and cytogenetic mapping in BMC GENOMICS
  • 2007-10 Diet and the evolution of human amylase gene copy number variation in NATURE GENETICS
  • 2007-09 Structural variation in the human genome: the impact of copy number variants on clinical diagnosis in GENETICS IN MEDICINE
  • 2007-07 Challenges and standards in integrating surveys of structural variation in NATURE GENETICS
  • 2007-07 TMPRSS2:ERG gene fusion associated with lethal prostate cancer in a watchful waiting cohort in ONCOGENE
  • 2007-07 Copy number variations and clinical cytogenetic diagnosis of constitutional disorders in NATURE GENETICS
  • 2007-05 Completing the map of human genetic variation in NATURE
  • 2006-12 Genome assembly comparison identifies structural variants in the human genome in NATURE GENETICS
  • 2006-11 Global variation in copy number in the human genome in NATURE
  • 2006-07 A new recurrent 9q34 duplication in pediatric T-cell acute lymphoblastic leukemia in LEUKEMIA
  • 2006-01 Common deletion polymorphisms in the human genome in NATURE GENETICS
  • 2005-07 Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma in NATURE
  • 2004-09 Detection of large-scale variation in the human genome in NATURE GENETICS
  • 2003-05 Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency in NATURE GENETICS
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