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Christopher A. Walsh, M.D., Ph.D.

Co-Author

This page shows the publications co-authored by Christopher Walsh and Peter Park.
Connection Strength

2.526
  1. Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 Apr; 24(4):611.
    View in: PubMed
    Score: 0.238
  2. Landmarks of human embryonic development inscribed in somatic mutations. Science. 2021 03 19; 371(6535):1249-1253.
    View in: PubMed
    Score: 0.238
  3. The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 02; 24(2):176-185.
    View in: PubMed
    Score: 0.235
  4. 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: 0.225
  5. Accurate detection of mosaic variants in sequencing data without matched controls. Nat Biotechnol. 2020 03; 38(3):314-319.
    View in: PubMed
    Score: 0.219
  6. Linked-read analysis identifies mutations in single-cell DNA-sequencing data. Nat Genet. 2019 04; 51(4):749-754.
    View in: PubMed
    Score: 0.207
  7. PaSD-qc: quality control for single cell whole-genome sequencing data using power spectral density estimation. Nucleic Acids Res. 2018 02 28; 46(4):e20.
    View in: PubMed
    Score: 0.193
  8. Aging and neurodegeneration are associated with increased mutations in single human neurons. Science. 2018 02 02; 359(6375):555-559.
    View in: PubMed
    Score: 0.190
  9. Resolving rates of mutation in the brain using single-neuron genomics. Elife. 2016 Feb 22; 5.
    View in: PubMed
    Score: 0.167
  10. Somatic mutation in single human neurons tracks developmental and transcriptional history. Science. 2015 Oct 02; 350(6256):94-98.
    View in: PubMed
    Score: 0.163
  11. Cell lineage analysis in human brain using endogenous retroelements. Neuron. 2015 Jan 07; 85(1):49-59.
    View in: PubMed
    Score: 0.155
  12. 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: 0.133
  13. Comprehensive identification of somatic nucleotide variants in human brain tissue. Genome Biol. 2021 03 29; 22(1):92.
    View in: PubMed
    Score: 0.060
  14. Large mosaic copy number variations confer autism risk. Nat Neurosci. 2021 02; 24(2):197-203.
    View in: PubMed
    Score: 0.059
  15. Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network. Science. 2017 04 28; 356(6336).
    View in: PubMed
    Score: 0.045
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.