Connection

RUI CHEN to Animals

This is a "connection" page, showing publications RUI CHEN has written about Animals.
Connection Strength

0.789
  1. Integrating short-read and long-read single-cell RNA sequencing for comprehensive transcriptome profiling in mouse retina. Genome Res. 2025 Apr 14; 35(4):740-754.
    View in: PubMed
    Score: 0.052
  2. Genetic diversity of 1,845 rhesus macaques improves genetic variation interpretation and identifies disease models. Nat Commun. 2024 Jul 05; 15(1):5658.
    View in: PubMed
    Score: 0.049
  3. Spatial organization of the mouse retina at single cell resolution by MERFISH. Nat Commun. 2023 08 15; 14(1):4929.
    View in: PubMed
    Score: 0.046
  4. Gene augmentation therapy to rescue degenerative photoreceptors in a Cwc27 mutant mouse model. Exp Eye Res. 2023 09; 234:109596.
    View in: PubMed
    Score: 0.046
  5. Spata7 is required for maintenance of the retinal connecting cilium. Sci Rep. 2022 04 02; 12(1):5575.
    View in: PubMed
    Score: 0.042
  6. SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium. J Cell Biol. 2018 08 06; 217(8):2851-2865.
    View in: PubMed
    Score: 0.032
  7. NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res. 2018 08; 173:32-43.
    View in: PubMed
    Score: 0.032
  8. Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in mice. Exp Eye Res. 2018 01; 166:120-130.
    View in: PubMed
    Score: 0.031
  9. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa. Am J Hum Genet. 2016 Dec 01; 99(6):1305-1315.
    View in: PubMed
    Score: 0.029
  10. Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1. Genet Med. 2016 10; 18(10):1044-51.
    View in: PubMed
    Score: 0.027
  11. Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa. Hum Mol Genet. 2016 Apr 15; 25(8):1479-88.
    View in: PubMed
    Score: 0.027
  12. ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa. Hum Mutat. 2016 Mar; 37(3):246-9.
    View in: PubMed
    Score: 0.027
  13. 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: 0.025
  14. 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: 0.023
  15. Dawn of ocular gene therapy: implications for molecular diagnosis in retinal disease. Sci China Life Sci. 2013 Feb; 56(2):125-33.
    View in: PubMed
    Score: 0.022
  16. Exome capture sequencing identifies a novel mutation in BBS4. Mol Vis. 2011; 17:3529-40.
    View in: PubMed
    Score: 0.021
  17. The Drosophila melanogaster transcriptome by paired-end RNA sequencing. Genome Res. 2011 Feb; 21(2):315-24.
    View in: PubMed
    Score: 0.019
  18. Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing. Genome Res. 2010 Jul; 20(7):981-8.
    View in: PubMed
    Score: 0.018
  19. High-throughput multiplex sequencing to discover copy number variants in Drosophila. Genetics. 2009 Aug; 182(4):935-41.
    View in: PubMed
    Score: 0.017
  20. 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: 0.017
  21. 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: 0.014
  22. Keeping an eye on the fly genome. Dev Biol. 2005 Jun 15; 282(2):285-93.
    View in: PubMed
    Score: 0.013
  23. Dynamic building of a BAC clone tiling path for the Rat Genome Sequencing Project. Genome Res. 2004 Apr; 14(4):679-84.
    View in: PubMed
    Score: 0.012
  24. Comparing vertebrate whole-genome shotgun reads to the human genome. Genome Res. 2001 Nov; 11(11):1807-16.
    View in: PubMed
    Score: 0.010
  25. Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy. Genet Med. 2021 03; 23(3):488-497.
    View in: PubMed
    Score: 0.009
  26. Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies. Am J Hum Genet. 2017 Apr 06; 100(4):592-604.
    View in: PubMed
    Score: 0.007
  27. Identification of novel direct targets of Drosophila Sine oculis and Eyes absent by integration of genome-wide data sets. Dev Biol. 2016 07 01; 415(1):157-167.
    View in: PubMed
    Score: 0.007
  28. Postnatal epigenetic regulation of intestinal stem cells requires DNA methylation and is guided by the microbiome. Genome Biol. 2015 Sep 30; 16:211.
    View in: PubMed
    Score: 0.007
  29. 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: 0.006
  30. Large-scale identification of chemically induced mutations in Drosophila melanogaster. Genome Res. 2014 Oct; 24(10):1707-18.
    View in: PubMed
    Score: 0.006
  31. A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases. Cell. 2014 Sep 25; 159(1):200-214.
    View in: PubMed
    Score: 0.006
  32. TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients. Blood. 2014 Oct 23; 124(17):2705-12.
    View in: PubMed
    Score: 0.006
  33. Notch activation as a driver of osteogenic sarcoma. Cancer Cell. 2014 Sep 08; 26(3):390-401.
    View in: PubMed
    Score: 0.006
  34. Drosophila eyes absent is required for normal cone and pigment cell development. PLoS One. 2014; 9(7):e102143.
    View in: PubMed
    Score: 0.006
  35. Epigenomic profiling of young and aged HSCs reveals concerted changes during aging that reinforce self-renewal. Cell Stem Cell. 2014 May 01; 14(5):673-88.
    View in: PubMed
    Score: 0.006
  36. Regulation of Drosophila eye development by the transcription factor Sine oculis. PLoS One. 2014; 9(2):e89695.
    View in: PubMed
    Score: 0.006
  37. Large conserved domains of low DNA methylation maintained by Dnmt3a. Nat Genet. 2014 Jan; 46(1):17-23.
    View in: PubMed
    Score: 0.006
  38. Onset of atonal expression in Drosophila retinal progenitors involves redundant and synergistic contributions of Ey/Pax6 and So binding sites within two distant enhancers. Dev Biol. 2014 Feb 01; 386(1):152-64.
    View in: PubMed
    Score: 0.006
  39. Drosophila signal peptidase complex member Spase12 is required for development and cell differentiation. PLoS One. 2013; 8(4):e60908.
    View in: PubMed
    Score: 0.006
  40. 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: 0.005
  41. Genome-wide reinforcement of cohesin binding at pre-existing cohesin sites in response to ionizing radiation in human cells. J Biol Chem. 2010 Jul 23; 285(30):22784-92.
    View in: PubMed
    Score: 0.005
  42. Evolutionary and biomedical insights from the rhesus macaque genome. Science. 2007 Apr 13; 316(5822):222-34.
    View in: PubMed
    Score: 0.004
  43. The DNA sequence, annotation and analysis of human chromosome 3. Nature. 2006 Apr 27; 440(7088):1194-8.
    View in: PubMed
    Score: 0.003
  44. The finished DNA sequence of human chromosome 12. Nature. 2006 03 16; 440(7082):346-51.
    View in: PubMed
    Score: 0.003
  45. 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: 0.003
  46. The DNA sequence of the human X chromosome. Nature. 2005 Mar 17; 434(7031):325-37.
    View in: PubMed
    Score: 0.003
  47. Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution. Genome Res. 2005 Jan; 15(1):1-18.
    View in: PubMed
    Score: 0.003
  48. Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature. 2004 04 01; 428(6982):493-521.
    View in: PubMed
    Score: 0.003
  49. The Atlas genome assembly system. Genome Res. 2004 Apr; 14(4):721-32.
    View in: PubMed
    Score: 0.003
  50. Mechanism of hedgehog signaling during Drosophila eye development. Development. 2003 Jul; 130(13):3053-62.
    View in: PubMed
    Score: 0.003
  51. A clone-array pooled shotgun strategy for sequencing large genomes. Genome Res. 2001 Oct; 11(10):1619-23.
    View in: PubMed
    Score: 0.003
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.