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Connection

Alan Sanders to Schizophrenia

This is a "connection" page, showing publications Alan Sanders has written about Schizophrenia.
Connection Strength

4.805
  1. Transcriptome sequencing study implicates immune-related genes differentially expressed in schizophrenia: new data and a meta-analysis. Transl Psychiatry. 2017 04 18; 7(4):e1093.
    View in: PubMed
    Score: 0.394
  2. Transcriptome study of differential expression in schizophrenia. Hum Mol Genet. 2013 Dec 15; 22(24):5001-14.
    View in: PubMed
    Score: 0.304
  3. [The etiology of schizophrenia]. Medicina (B Aires). 2012; 72(3):227-34.
    View in: PubMed
    Score: 0.273
  4. No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. Am J Psychiatry. 2008 Apr; 165(4):497-506.
    View in: PubMed
    Score: 0.207
  5. Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. Mol Psychiatry. 2005 Apr; 10(4):353-65.
    View in: PubMed
    Score: 0.171
  6. Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell-Derived Neurons. Biol Psychiatry. 2023 07 15; 94(2):153-163.
    View in: PubMed
    Score: 0.145
  7. Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. Am J Hum Genet. 2022 08 04; 109(8):1500-1519.
    View in: PubMed
    Score: 0.142
  8. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 2022 04; 604(7906):502-508.
    View in: PubMed
    Score: 0.139
  9. Influential ideas and experimental progress in schizophrenia genetics research. JAMA. 2001 Jun 13; 285(22):2831-3.
    View in: PubMed
    Score: 0.131
  10. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biol Psychiatry. 2022 01 01; 91(1):102-117.
    View in: PubMed
    Score: 0.129
  11. Major corrections are indicated for 'Comparative proteome analysis of the hippocampus implicates chromosome 6q in schizophrenia'. Mol Psychiatry. 2001 Jan; 6(1):10-2.
    View in: PubMed
    Score: 0.127
  12. Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants. Science. 2020 07 31; 369(6503):561-565.
    View in: PubMed
    Score: 0.124
  13. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Am J Psychiatry. 2019 08 01; 176(8):651-660.
    View in: PubMed
    Score: 0.114
  14. Dopamine perturbation of gene co-expression networks reveals differential response in schizophrenia for translational machinery. Transl Psychiatry. 2018 12 13; 8(1):278.
    View in: PubMed
    Score: 0.110
  15. Transcriptomic signatures of schizophrenia revealed by dopamine perturbation in an ex vivo model. Transl Psychiatry. 2018 08 16; 8(1):158.
    View in: PubMed
    Score: 0.108
  16. Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci. Cell Stem Cell. 2017 09 07; 21(3):305-318.e8.
    View in: PubMed
    Score: 0.101
  17. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects. Nat Genet. 2017 01; 49(1):27-35.
    View in: PubMed
    Score: 0.096
  18. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. PLoS Genet. 2016 05; 12(5):e1005993.
    View in: PubMed
    Score: 0.092
  19. New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. Int J Epidemiol. 2015 Oct; 44(5):1706-21.
    View in: PubMed
    Score: 0.088
  20. Transcriptome outlier analysis implicates schizophrenia susceptibility genes and enriches putatively functional rare genetic variants. Hum Mol Genet. 2015 Aug 15; 24(16):4674-85.
    View in: PubMed
    Score: 0.086
  21. A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorder. Am J Hum Genet. 2014 Dec 04; 95(6):744-53.
    View in: PubMed
    Score: 0.083
  22. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet. 2013 Oct; 45(10):1150-9.
    View in: PubMed
    Score: 0.076
  23. Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia. Biol Psychiatry. 2014 Mar 01; 75(5):371-7.
    View in: PubMed
    Score: 0.076
  24. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry. 2013 Mar; 70(3):253-60.
    View in: PubMed
    Score: 0.074
  25. Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia. Schizophr Res. 1993 Jan; 8(3):211-21.
    View in: PubMed
    Score: 0.073
  26. Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. Am J Psychiatry. 2012 Dec; 169(12):1309-17.
    View in: PubMed
    Score: 0.073
  27. Genome-wide association study of multiplex schizophrenia pedigrees. Am J Psychiatry. 2012 Sep; 169(9):963-73.
    View in: PubMed
    Score: 0.071
  28. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Mol Psychiatry. 2012 Feb; 17(2):193-201.
    View in: PubMed
    Score: 0.064
  29. Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. Alcohol Clin Exp Res. 2011 May; 35(5):963-75.
    View in: PubMed
    Score: 0.064
  30. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry. 2011 Mar; 168(3):302-16.
    View in: PubMed
    Score: 0.064
  31. Genetics of schizophrenia: new findings and challenges. Annu Rev Genomics Hum Genet. 2011; 12:121-44.
    View in: PubMed
    Score: 0.064
  32. Genome-wide approaches to schizophrenia. Brain Res Bull. 2010 Sep 30; 83(3-4):93-102.
    View in: PubMed
    Score: 0.061
  33. The role of genetics in the etiology of schizophrenia. Psychiatr Clin North Am. 2010 Mar; 33(1):35-66.
    View in: PubMed
    Score: 0.060
  34. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature. 2009 Aug 06; 460(7256):753-7.
    View in: PubMed
    Score: 0.057
  35. Genomewide linkage scan of schizophrenia in a large multicenter pedigree sample using single nucleotide polymorphisms. Mol Psychiatry. 2009 Aug; 14(8):786-95.
    View in: PubMed
    Score: 0.056
  36. Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry. 2009 Aug; 14(8):774-85.
    View in: PubMed
    Score: 0.055
  37. Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2. Mol Psychiatry. 2009 Jan; 14(1):30-6.
    View in: PubMed
    Score: 0.054
  38. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat Genet. 2008 Sep; 40(9):1053-5.
    View in: PubMed
    Score: 0.054
  39. DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the gene. Hum Hered. 2007; 64(2):97-106.
    View in: PubMed
    Score: 0.049
  40. Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample. Am J Hum Genet. 2006 Feb; 78(2):315-33.
    View in: PubMed
    Score: 0.045
  41. Neuregulin 1 (NRG1 ) and schizophrenia: analysis of a US family sample and the evidence in the balance. Psychol Med. 2005 Nov; 35(11):1599-610.
    View in: PubMed
    Score: 0.044
  42. Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia. Am J Hum Genet. 2004 Oct; 75(4):624-38.
    View in: PubMed
    Score: 0.041
  43. Multicenter linkage study of schizophrenia loci on chromosome 22q. Mol Psychiatry. 2004 Aug; 9(8):784-95.
    View in: PubMed
    Score: 0.041
  44. Polymorphisms in the 5'-untranslated region of the human serotonin receptor 1B (HTR1B) gene affect gene expression. Mol Psychiatry. 2003 Nov; 8(11):901-10.
    View in: PubMed
    Score: 0.039
  45. No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science. 2002 Apr 26; 296(5568):739-41.
    View in: PubMed
    Score: 0.035
  46. Linkage analysis of schizophrenia to chromosome 15. Am J Med Genet. 2001 Dec 08; 105(8):789-93.
    View in: PubMed
    Score: 0.034
  47. Genetic diversity of the human serotonin receptor 1B (HTR1B) gene. Genomics. 2001 Feb 15; 72(1):1-14.
    View in: PubMed
    Score: 0.032
  48. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet. 2000 Sep; 67(3):652-63.
    View in: PubMed
    Score: 0.031
  49. Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q. Am J Med Genet. 1999 Aug 20; 88(4):337-43.
    View in: PubMed
    Score: 0.029
  50. Closing in on genes for manic-depressive illness and schizophrenia. Neuropsychopharmacology. 1998 Apr; 18(4):233-42.
    View in: PubMed
    Score: 0.026
  51. Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees. Genomics. 1997 Jul 01; 43(1):1-8.
    View in: PubMed
    Score: 0.025
  52. Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples. Am J Med Genet. 1996 Nov 22; 67(6):505-14.
    View in: PubMed
    Score: 0.024
  53. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 2016 05 26; 533(7604):539-42.
    View in: PubMed
    Score: 0.023
  54. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. 2013 Sep; 45(9):984-94.
    View in: PubMed
    Score: 0.019
  55. A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. Proc Natl Acad Sci U S A. 1999 May 11; 96(10):5604-9.
    View in: PubMed
    Score: 0.007
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.