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Connection

Bennett Leventhal to Polymorphism, Single Nucleotide

This is a "connection" page, showing publications Bennett Leventhal has written about Polymorphism, Single Nucleotide.
  1. Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. Eur Arch Psychiatry Clin Neurosci. 2018 Apr; 268(3):301-316.
    View in: PubMed
    Score: 0.080
  2. 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: 0.050
  3. Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample. Autism Res. 2008 Apr; 1(2):108-13.
    View in: PubMed
    Score: 0.042
  4. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Neuropsychopharmacology. 2008 Jan; 33(2):353-60.
    View in: PubMed
    Score: 0.040
  5. Deletion polymorphism in the coding region of the human NESP55 alternative transcript of GNAS1. Mol Cell Probes. 2000 Jun; 14(3):191-4.
    View in: PubMed
    Score: 0.025
  6. 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: 0.014
  7. 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: 0.014
  8. Family-based association testing of glutamate transporter genes in autism. Psychiatr Genet. 2011 Aug; 21(4):212-3.
    View in: PubMed
    Score: 0.013
  9. Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder. Biol Psychiatry. 2007 Feb 01; 61(3):322-9.
    View in: PubMed
    Score: 0.010
  10. 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
  11. Transmission disequilibrium studies of the serotonin 5-HT2A receptor gene (HTR2A) in autism. Am J Med Genet. 2002 Apr 08; 114(3):277-83.
    View in: PubMed
    Score: 0.007
  12. Mutation screening and transmission disequilibrium study of ATP10C in autism. Am J Med Genet. 2002 Mar 08; 114(2):137-43.
    View in: PubMed
    Score: 0.007
  13. Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder. Mol Psychiatry. 2001 Mar; 6(2):160-7.
    View in: PubMed
    Score: 0.006
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