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Connection

Bennett Leventhal to Linkage Disequilibrium

This is a "connection" page, showing publications Bennett Leventhal has written about Linkage Disequilibrium.
Connection Strength

0.409
  1. 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: 0.045
  2. 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: 0.045
  3. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry. 2002; 7(3):278-88.
    View in: PubMed
    Score: 0.045
  4. Transmission disequilibrium testing of arginine vasopressin receptor 1A (AVPR1A) polymorphisms in autism. Mol Psychiatry. 2002; 7(5):503-7.
    View in: PubMed
    Score: 0.045
  5. 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: 0.038
  6. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Hum Genet. 1998 May; 62(5):1077-83.
    View in: PubMed
    Score: 0.035
  7. 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: 0.032
  8. 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: 0.022
  9. 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: 0.016
  10. 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: 0.016
  11. 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: 0.016
  12. 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: 0.015
  13. Family-based association study of the serotonin transporter gene polymorphisms in Korean ADHD trios. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 05; 139B(1):14-8.
    View in: PubMed
    Score: 0.015
  14. 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: 0.014
  15. 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: 0.011
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.