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Connection

Latha Soorya to Genetic Predisposition to Disease

This is a "connection" page, showing publications Latha Soorya has written about Genetic Predisposition to Disease.
  1. Individual common variants exert weak effects on the risk for autism spectrum disorders. Hum Mol Genet. 2012 Nov 01; 21(21):4781-92.
    View in: PubMed
    Score: 0.086
  2. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet. 2012 Apr; 131(4):565-79.
    View in: PubMed
    Score: 0.082
  3. Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities. Brain Res. 2011 Mar 22; 1380:98-105.
    View in: PubMed
    Score: 0.077
  4. A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010 Oct 15; 19(20):4072-82.
    View in: PubMed
    Score: 0.075
  5. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 2010 Jul 15; 466(7304):368-72.
    View in: PubMed
    Score: 0.075
  6. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature. 2009 May 28; 459(7246):569-73.
    View in: PubMed
    Score: 0.017
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.