Connection

Co-Authors

This is a "connection" page, showing publications co-authored by JASON HEANEY and MARY DICKINSON.
Connection Strength

1.116
  1. Comparative analysis of single-stranded DNA donors to generate conditional null mouse alleles. BMC Biol. 2018 Jun 21; 16(1):69.
    View in: PubMed
    Score: 0.159
  2. Alzheimer's disease risk gene CD2AP is a dose-sensitive determinant of synaptic structure and plasticity. Hum Mol Genet. 2024 10 07; 33(20):1815-1832.
    View in: PubMed
    Score: 0.061
  3. Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines. Sci Rep. 2024 09 30; 14(1):22626.
    View in: PubMed
    Score: 0.061
  4. A Comprehensive Atlas of AAV Tropism in the Mouse. bioRxiv. 2024 Sep 10.
    View in: PubMed
    Score: 0.061
  5. Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity. Commun Biol. 2023 06 10; 6(1):626.
    View in: PubMed
    Score: 0.056
  6. Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice. Mamm Genome. 2023 06; 34(2):180-199.
    View in: PubMed
    Score: 0.056
  7. Genome-wide screening reveals the genetic basis of mammalian embryonic eye development. BMC Biol. 2023 02 03; 21(1):22.
    View in: PubMed
    Score: 0.055
  8. Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes. Sci Rep. 2022 12 01; 12(1):20791.
    View in: PubMed
    Score: 0.054
  9. Mendelian gene identification through mouse embryo viability screening. Genome Med. 2022 10 13; 14(1):119.
    View in: PubMed
    Score: 0.053
  10. AAV5 delivery of CRISPR-Cas9 supports effective genome editing in mouse lung airway. Mol Ther. 2022 Jan 05; 30(1):238-243.
    View in: PubMed
    Score: 0.050
  11. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
    View in: PubMed
    Score: 0.049
  12. The NIH Somatic Cell Genome Editing program. Nature. 2021 04; 592(7853):195-204.
    View in: PubMed
    Score: 0.048
  13. A resource of targeted mutant mouse lines for 5,061 genes. Nat Genet. 2021 04; 53(4):416-419.
    View in: PubMed
    Score: 0.048
  14. Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density. PLoS Genet. 2020 12; 16(12):e1009190.
    View in: PubMed
    Score: 0.047
  15. A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance. Hum Mol Genet. 2020 08 03; 29(13):2171-2184.
    View in: PubMed
    Score: 0.046
  16. Soft windowing application to improve analysis of high-throughput phenotyping data. Bioinformatics. 2020 03 01; 36(5):1492-1500.
    View in: PubMed
    Score: 0.045
  17. The Deep Genome Project. Genome Biol. 2020 02 03; 21(1):18.
    View in: PubMed
    Score: 0.044
  18. Human and mouse essentiality screens as a resource for disease gene discovery. Nat Commun. 2020 01 31; 11(1):655.
    View in: PubMed
    Score: 0.044
  19. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438.
    View in: PubMed
    Score: 0.041
  20. Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features. Am J Hum Genet. 2017 Apr 06; 100(4):676-688.
    View in: PubMed
    Score: 0.036
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.