Connection

Co-Authors

This is a "connection" page, showing publications co-authored by RUI CHEN and GRAEME MARDON.
Connection Strength

1.717
  1. Keeping an eye on the fly genome. Dev Biol. 2005 Jun 15; 282(2):285-93.
    View in: PubMed
    Score: 0.261
  2. CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes. Sci Rep. 2015 Feb 10; 5:8366.
    View in: PubMed
    Score: 0.127
  3. Genome-wide DNA binding pattern of the homeodomain transcription factor Sine oculis (So) in the developing eye of Drosophila melanogaster. Genom Data. 2014 Dec 01; 2:153-155.
    View in: PubMed
    Score: 0.126
  4. Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina. Hum Mol Genet. 2015 Mar 15; 24(6):1584-601.
    View in: PubMed
    Score: 0.125
  5. Drosophila eyes absent is required for normal cone and pigment cell development. PLoS One. 2014; 9(7):e102143.
    View in: PubMed
    Score: 0.122
  6. Regulation of Drosophila eye development by the transcription factor Sine oculis. PLoS One. 2014; 9(2):e89695.
    View in: PubMed
    Score: 0.119
  7. optix functions as a link between the retinal determination network and the dpp pathway to control morphogenetic furrow progression in Drosophila. Dev Biol. 2013 Sep 01; 381(1):50-61.
    View in: PubMed
    Score: 0.114
  8. Drosophila signal peptidase complex member Spase12 is required for development and cell differentiation. PLoS One. 2013; 8(4):e60908.
    View in: PubMed
    Score: 0.112
  9. MAPK target sites of eyes absent are not required for eye development or survival in Drosophila. PLoS One. 2012; 7(12):e50776.
    View in: PubMed
    Score: 0.110
  10. Exome capture sequencing identifies a novel mutation in BBS4. Mol Vis. 2011; 17:3529-40.
    View in: PubMed
    Score: 0.103
  11. Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis. Hum Mutat. 2011 Dec; 32(12):1450-9.
    View in: PubMed
    Score: 0.101
  12. Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa. Am J Hum Genet. 2009 Mar; 84(3):380-7.
    View in: PubMed
    Score: 0.084
  13. Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless. Genome Res. 2006 Apr; 16(4):466-76.
    View in: PubMed
    Score: 0.069
  14. Dual regulation and redundant function of two eye-specific enhancers of the Drosophila retinal determination gene dachshund. Development. 2005 Jun; 132(12):2895-905.
    View in: PubMed
    Score: 0.065
  15. Mechanism of hedgehog signaling during Drosophila eye development. Development. 2003 Jul; 130(13):3053-62.
    View in: PubMed
    Score: 0.057
  16. Potential involvement of more than one locus in trait manifestation for individuals with Leber congenital amaurosis. Hum Genet. 2011 Mar; 129(3):319-27.
    View in: PubMed
    Score: 0.024
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.