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This is a "connection" page, showing publications co-authored by Jubao Duan and Alan Sanders.
Jubao Duan
Connection Strength
5.314
Alan Sanders
  1. Scaled and efficient derivation of loss-of-function alleles in risk genes for neurodevelopmental and psychiatric disorders in human iPSCs. Stem Cell Reports. 2024 Oct 08; 19(10):1489-1504.
    View in: PubMed
    Score: 0.247
  2. Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication. medRxiv. 2024 Aug 15.
    View in: PubMed
    Score: 0.246
  3. Alzheimer's disease risk allele of PICALM causes detrimental lipid droplets in microglia. Res Sq. 2024 May 24.
    View in: PubMed
    Score: 0.242
  4. Scaled and Efficient Derivation of Loss of Function Alleles in Risk Genes for Neurodevelopmental and Psychiatric Disorders in Human iPSC. bioRxiv. 2024 Mar 19.
    View in: PubMed
    Score: 0.239
  5. Brain Lipids and Lipid Droplet Dysregulation in Alzheimer's Disease and Neuropsychiatric Disorders. Complex Psychiatry. 2023 Jan-Dec; 9(1-4):154-171.
    View in: PubMed
    Score: 0.233
  6. Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons. Cell Genom. 2023 Sep 13; 3(9):100399.
    View in: PubMed
    Score: 0.230
  7. Modeling PTSD neuronal stress responses in a dish. Nat Neurosci. 2022 11; 25(11):1402-1404.
    View in: PubMed
    Score: 0.217
  8. 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: 0.214
  9. Cell type-specific and cross-population polygenic risk score analyses of MIR137 gene pathway in schizophrenia. iScience. 2021 Jul 23; 24(7):102785.
    View in: PubMed
    Score: 0.198
  10. Sex-specific nicotine sensitization and imprinting of self-administration in rats inform GWAS findings on human addiction phenotypes. Neuropsychopharmacology. 2021 09; 46(10):1746-1756.
    View in: PubMed
    Score: 0.196
  11. Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants. Science. 2020 07 31; 369(6503):561-565.
    View in: PubMed
    Score: 0.186
  12. From Schizophrenia Genetics to Disease Biology: Harnessing New Concepts and Technologies. J Psychiatr Brain Sci. 2019; 4.
    View in: PubMed
    Score: 0.175
  13. The Genetic Relevance of Human Induced Pluripotent Stem Cell-Derived Microglia to Alzheimer's Disease and Major Neuropsychiatric Disorders. Mol Neuropsychiatry. 2020 Apr; 5(Suppl 1):85-96.
    View in: PubMed
    Score: 0.173
  14. 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: 0.162
  15. Open chromatin dynamics reveals stage-specific transcriptional networks in hiPSC-based neurodevelopmental model. Stem Cell Res. 2018 05; 29:88-98.
    View in: PubMed
    Score: 0.158
  16. Genome-Wide Association Study of Male Sexual Orientation. Sci Rep. 2017 12 07; 7(1):16950.
    View in: PubMed
    Score: 0.155
  17. 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: 0.151
  18. 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: 0.130
  19. 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: 0.125
  20. Transcriptome study of differential expression in schizophrenia. Hum Mol Genet. 2013 Dec 15; 22(24):5001-14.
    View in: PubMed
    Score: 0.114
  21. Genome-wide survey of interindividual differences of RNA stability in human lymphoblastoid cell lines. Sci Rep. 2013; 3:1318.
    View in: PubMed
    Score: 0.110
  22. The Internet-based MGS2 control sample: self report of mental illness. Am J Psychiatry. 2010 Jul; 167(7):854-65.
    View in: PubMed
    Score: 0.092
  23. Genome-wide approaches to schizophrenia. Brain Res Bull. 2010 Sep 30; 83(3-4):93-102.
    View in: PubMed
    Score: 0.091
  24. The role of genetics in the etiology of schizophrenia. Psychiatr Clin North Am. 2010 Mar; 33(1):35-66.
    View in: PubMed
    Score: 0.090
  25. 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: 0.078
  26. 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: 0.074
  27. 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: 0.067
  28. Lipid Trajectories Improve Risk Models for Alzheimer's Disease and Mild Cognitive Impairment. medRxiv. 2024 Sep 28.
    View in: PubMed
    Score: 0.062
  29. 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: 0.062
  30. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum Mol Genet. 2003 Feb 01; 12(3):205-16.
    View in: PubMed
    Score: 0.055
  31. 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: 0.054
  32. DNA variation and psychopharmacology of the human serotonin receptor 1B (HTR1B) gene. Pharmacogenomics. 2002 Nov; 3(6):745-62.
    View in: PubMed
    Score: 0.054
  33. Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature. 2022 04; 604(7906):502-508.
    View in: PubMed
    Score: 0.052
  34. 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: 0.042
  35. Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395).
    View in: PubMed
    Score: 0.040
  36. Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data. PLoS Genet. 2016 Dec; 12(12):e1006493.
    View in: PubMed
    Score: 0.036
  37. 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: 0.036
  38. 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: 0.035
  39. 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: 0.033
  40. The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. PLoS Genet. 2015 Oct; 11(10):e1005378.
    View in: PubMed
    Score: 0.033
  41. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet. 2013 Oct; 45(10):1150-9.
    View in: PubMed
    Score: 0.029
  42. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet. 2013 Sep; 45(9):984-94.
    View in: PubMed
    Score: 0.029
  43. 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: 0.029
  44. 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: 0.027
  45. Genome-wide association study of multiplex schizophrenia pedigrees. Am J Psychiatry. 2012 Sep; 169(9):963-73.
    View in: PubMed
    Score: 0.027
  46. Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. Arch Gen Psychiatry. 2012 Aug; 69(8):854-60.
    View in: PubMed
    Score: 0.027
  47. Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25. Genet Epidemiol. 2012 May; 36(4):340-51.
    View in: PubMed
    Score: 0.026
  48. 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: 0.024
  49. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010 Nov; 42(11):937-48.
    View in: PubMed
    Score: 0.024
  50. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 2010 Oct 14; 467(7317):832-8.
    View in: PubMed
    Score: 0.024
  51. Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature. 2009 Aug 06; 460(7256):753-7.
    View in: PubMed
    Score: 0.022
  52. 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: 0.020
  53. 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: 0.017
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.