Connection

RINKI RATNA PRIYA to DNA Mutational Analysis

This is a "connection" page, showing publications RINKI RATNA PRIYA has written about DNA Mutational Analysis.
Connection Strength

0.116
  1. Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing. Invest Ophthalmol Vis Sci. 2016 11 01; 57(14):6374-6381.
    View in: PubMed
    Score: 0.058
  2. A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3. Hum Genet. 2009 Jun; 125(5-6):541-9.
    View in: PubMed
    Score: 0.034
  3. Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration. Hum Mol Genet. 2014 Nov 01; 23(21):5827-37.
    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.