Connection

NOAH SHROYER to Mutation

This is a "connection" page, showing publications NOAH SHROYER has written about Mutation.
Connection Strength

0.149
  1. Complex inheritance of ABCR mutations in Stargardt disease: linkage disequilibrium, complex alleles, and pseudodominance. Hum Genet. 2000 Feb; 106(2):244-8.
    View in: PubMed
    Score: 0.065
  2. BMP signaling in the intestine: cross-talk is key. Gastroenterology. 2007 Sep; 133(3):1035-8.
    View in: PubMed
    Score: 0.027
  3. Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration. Hum Mol Genet. 2001 Nov 01; 10(23):2671-8.
    View in: PubMed
    Score: 0.018
  4. Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration. Science. 1997 Sep 19; 277(5333):1805-7.
    View in: PubMed
    Score: 0.014
  5. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet. 1997 Mar; 15(3):236-46.
    View in: PubMed
    Score: 0.013
  6. Atonal homolog 1 is a tumor suppressor gene. PLoS Biol. 2009 Feb 24; 7(2):e39.
    View in: PubMed
    Score: 0.008
  7. Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease. Am J Hum Genet. 1999 Feb; 64(2):422-34.
    View in: PubMed
    Score: 0.004
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.