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Connection

Bennett Leventhal to Genetic Predisposition to Disease

This is a "connection" page, showing publications Bennett Leventhal 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: 0.055
  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: 0.052
  3. Family-based association testing of glutamate transporter genes in autism. Psychiatr Genet. 2011 Aug; 21(4):212-3.
    View in: PubMed
    Score: 0.051
  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: 0.048
  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: 0.048
  6. Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder. Biol Psychiatry. 2007 Oct 15; 62(8):856-62.
    View in: PubMed
    Score: 0.039
  7. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet. 2007 Mar; 39(3):319-28.
    View in: PubMed
    Score: 0.038
  8. Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neurosci Lett. 2007 Apr 24; 417(1):6-9.
    View in: PubMed
    Score: 0.038
  9. Family-based association study of DAT1 and DRD4 polymorphism in Korean children with ADHD. Neurosci Lett. 2005 Dec 30; 390(3):176-81.
    View in: PubMed
    Score: 0.034
  10. Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior. Mol Psychiatry. 2010 Sep; 15(9):928-37.
    View in: PubMed
    Score: 0.011
  11. Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder. Arch Gen Psychiatry. 2006 Jul; 63(7):778-85.
    View in: PubMed
    Score: 0.009
  12. Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder. Am J Med Genet. 1999 Oct 15; 88(5):472-5.
    View in: PubMed
    Score: 0.006
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.