The University of Chicago Header Logo

Connection

Bennett Leventhal to Genotype

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

0.338
  1. A pharmacogenetic study of escitalopram in autism spectrum disorders. Autism Res. 2010 Feb; 3(1):1-7.
    View in: PubMed
    Score: 0.064
  2. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Transl Psychiatry. 2021 01 18; 11(1):56.
    View in: PubMed
    Score: 0.034
  3. 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: 0.027
  4. 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: 0.019
  5. 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: 0.018
  6. 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: 0.017
  7. Dopamine transporter genotype and stimulant side effect factors in youth diagnosed with attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2009 Jun; 19(3):233-9.
    View in: PubMed
    Score: 0.015
  8. 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: 0.015
  9. 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: 0.014
  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: 0.013
  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: 0.013
  12. 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. Am J Psychiatry. 2006 Dec; 163(12):2148-56.
    View in: PubMed
    Score: 0.013
  13. 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: 0.012
  14. 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: 0.012
  15. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. Am J Med Genet. 2002 Jul 08; 114(5):541-52.
    View in: PubMed
    Score: 0.009
  16. 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: 0.009
  17. 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: 0.009
  18. 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: 0.009
  19. 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: 0.008
  20. High throughput fluorescent CE-SSCP SNP genotyping. Mol Psychiatry. 1999 Jul; 4(4):339-43.
    View in: PubMed
    Score: 0.008
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.