Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Eunjung Alice Lee, Ph.D.

Co-Author

This page shows the publications co-authored by Eunjung Alice Lee and Peter Park.
Connection Strength

1.917
  1. Identification and Genotyping of Transposable Element Insertions From Genome Sequencing Data. Curr Protoc Hum Genet. 2020 09; 107(1):e102.
    View in: PubMed
    Score: 0.231
  2. An enhanced genetic model of colorectal cancer progression history. Genome Biol. 2019 08 15; 20(1):168.
    View in: PubMed
    Score: 0.215
  3. NGSCheckMate: software for validating sample identity in next-generation sequencing studies within and across data types. Nucleic Acids Res. 2017 Jun 20; 45(11):e103.
    View in: PubMed
    Score: 0.185
  4. Intron retention is a widespread mechanism of tumor-suppressor inactivation. Nat Genet. 2015 Nov; 47(11):1242-8.
    View in: PubMed
    Score: 0.165
  5. The Cancer Genome Atlas Pan-Cancer analysis project. Nat Genet. 2013 Oct; 45(10):1113-20.
    View in: PubMed
    Score: 0.143
  6. Landscape of somatic retrotransposition in human cancers. Science. 2012 Aug 24; 337(6097):967-71.
    View in: PubMed
    Score: 0.131
  7. Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. Proc Natl Acad Sci U S A. 2011 Nov 15; 108(46):E1128-36.
    View in: PubMed
    Score: 0.125
  8. Parallel RNA and DNA analysis after deep sequencing (PRDD-seq) reveals cell type-specific lineage patterns in human brain. Proc Natl Acad Sci U S A. 2020 06 23; 117(25):13886-13895.
    View in: PubMed
    Score: 0.057
  9. Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition. Nat Genet. 2020 03; 52(3):306-319.
    View in: PubMed
    Score: 0.056
  10. Global impact of somatic structural variation on the DNA methylome of human cancers. Genome Biol. 2019 10 15; 20(1):209.
    View in: PubMed
    Score: 0.054
  11. Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease. N Engl J Med. 2019 10 24; 381(17):1644-1652.
    View in: PubMed
    Score: 0.054
  12. A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases. Cell Rep. 2018 07 10; 24(2):515-527.
    View in: PubMed
    Score: 0.050
  13. A Pan-Cancer Proteogenomic Atlas of PI3K/AKT/mTOR Pathway Alterations. Cancer Cell. 2017 06 12; 31(6):820-832.e3.
    View in: PubMed
    Score: 0.046
  14. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science. 2017 04 28; 356(6336).
    View in: PubMed
    Score: 0.046
  15. The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts. PLoS Genet. 2016 10; 12(10):e1006385.
    View in: PubMed
    Score: 0.044
  16. Next-generation sequencing-based detection of germline L1-mediated transductions. BMC Genomics. 2016 05 10; 17:342.
    View in: PubMed
    Score: 0.043
  17. Resolving rates of mutation in the brain using single-neuron genomics. Elife. 2016 Feb 22; 5.
    View in: PubMed
    Score: 0.042
  18. Pericentromeric satellite repeat expansions through RNA-derived DNA intermediates in cancer. Proc Natl Acad Sci U S A. 2015 Dec 08; 112(49):15148-53.
    View in: PubMed
    Score: 0.041
  19. Somatic mutation in single human neurons tracks developmental and transcriptional history. Science. 2015 Oct 02; 350(6256):94-98.
    View in: PubMed
    Score: 0.041
  20. Cell lineage analysis in human brain using endogenous retroelements. Neuron. 2015 Jan 07; 85(1):49-59.
    View in: PubMed
    Score: 0.039
  21. The somatic genomic landscape of chromophobe renal cell carcinoma. Cancer Cell. 2014 Sep 08; 26(3):319-330.
    View in: PubMed
    Score: 0.038
  22. Primate genome architecture influences structural variation mechanisms and functional consequences. Proc Natl Acad Sci U S A. 2013 Sep 24; 110(39):15764-9.
    View in: PubMed
    Score: 0.036
  23. Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain. Cell. 2012 Oct 26; 151(3):483-96.
    View in: PubMed
    Score: 0.034
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.