BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 26853120)

  • 1. A Common Polymorphism in a Williams Syndrome Gene Predicts Amygdala Reactivity and Extraversion in Healthy Adults.
    Swartz JR; Waller R; Bogdan R; Knodt AR; Sabhlok A; Hyde LW; Hariri AR
    Biol Psychiatry; 2017 Feb; 81(3):203-210. PubMed ID: 26853120
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variation in the Williams syndrome GTF2I gene and anxiety proneness interactively affect prefrontal cortical response to aversive stimuli.
    Jabbi M; Chen Q; Turner N; Kohn P; White M; Kippenhan JS; Dickinson D; Kolachana B; Mattay V; Weinberger DR; Berman KF
    Transl Psychiatry; 2015 Aug; 5(8):e622. PubMed ID: 26285132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cognitive-behavioral phenotypes of Williams syndrome are associated with genetic variation in the GTF2I gene, in a healthy population.
    Crespi BJ; Hurd PL
    BMC Neurosci; 2014 Nov; 15():127. PubMed ID: 25429715
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The contribution of GTF2I haploinsufficiency to Williams syndrome.
    Chailangkarn T; Noree C; Muotri AR
    Mol Cell Probes; 2018 Aug; 40():45-51. PubMed ID: 29305905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Williams syndrome prosociality gene
    Procyshyn TL; Spence J; Read S; Watson NV; Crespi BJ
    Biol Lett; 2017 Apr; 13(4):. PubMed ID: 28424317
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic influences on sociability: heightened amygdala reactivity and event-related responses to positive social stimuli in Williams syndrome.
    Haas BW; Mills D; Yam A; Hoeft F; Bellugi U; Reiss A
    J Neurosci; 2009 Jan; 29(4):1132-9. PubMed ID: 19176822
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.
    Morris CA; Mervis CB; Hobart HH; Gregg RG; Bertrand J; Ensing GJ; Sommer A; Moore CA; Hopkin RJ; Spallone PA; Keating MT; Osborne L; Kimberley KW; Stock AD
    Am J Med Genet A; 2003 Nov; 123A(1):45-59. PubMed ID: 14556246
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Consistent hypersocial behavior in mice carrying a deletion of
    Martin LA; Iceberg E; Allaf G
    Brain Behav; 2018 Jan; 8(1):e00895. PubMed ID: 29568691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common and distinct neural correlates of facial emotion processing in social anxiety disorder and Williams syndrome: A systematic review and voxel-based meta-analysis of functional resonance imaging studies.
    Binelli C; Subirà S; Batalla A; Muñiz A; Sugranyés G; Crippa JA; Farré M; Pérez-Jurado L; Martín-Santos R
    Neuropsychologia; 2014 Nov; 64():205-17. PubMed ID: 25194208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An oxytocin receptor polymorphism predicts amygdala reactivity and antisocial behavior in men.
    Waller R; Corral-Frías NS; Vannucci B; Bogdan R; Knodt AR; Hariri AR; Hyde LW
    Soc Cogn Affect Neurosci; 2016 Aug; 11(8):1218-26. PubMed ID: 27036876
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug.
    Barak B; Zhang Z; Liu Y; Nir A; Trangle SS; Ennis M; Levandowski KM; Wang D; Quast K; Boulting GL; Li Y; Bayarsaihan D; He Z; Feng G
    Nat Neurosci; 2019 May; 22(5):700-708. PubMed ID: 31011227
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of GTF2I promotes neuronal apoptosis and synaptic reduction in human cellular models of neurodevelopment.
    Adams JW; Vinokur A; de Souza JS; Austria C; Guerra BS; Herai RH; Wahlin KJ; Muotri AR
    Cell Rep; 2024 Mar; 43(3):113867. PubMed ID: 38416640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models.
    Kopp N; McCullough K; Maloney SE; Dougherty JD
    Hum Mol Genet; 2019 Oct; 28(20):3443-3465. PubMed ID: 31418010
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuronal deletion of Gtf2i results in developmental microglial alterations in a mouse model related to Williams syndrome.
    Bar E; Fischer I; Rokach M; Elad-Sfadia G; Shirenova S; Ophir O; Trangle SS; Okun E; Barak B
    Glia; 2024 Jun; 72(6):1117-1135. PubMed ID: 38450767
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A susceptibility gene for affective disorders and the response of the human amygdala.
    Hariri AR; Drabant EM; Munoz KE; Kolachana BS; Mattay VS; Egan MF; Weinberger DR
    Arch Gen Psychiatry; 2005 Feb; 62(2):146-52. PubMed ID: 15699291
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.
    Borralleras C; Sahun I; Pérez-Jurado LA; Campuzano V
    Mol Ther; 2015 Nov; 23(11):1691-1699. PubMed ID: 26216516
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.
    Malenfant P; Liu X; Hudson ML; Qiao Y; Hrynchak M; Riendeau N; Hildebrand MJ; Cohen IL; Chudley AE; Forster-Gibson C; Mickelson EC; Rajcan-Separovic E; Lewis ME; Holden JJ
    J Autism Dev Disord; 2012 Jul; 42(7):1459-69. PubMed ID: 22048961
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Williams syndrome deletions and duplications: Genetic windows to understanding anxiety, sociality, autism, and schizophrenia.
    Crespi BJ; Procyshyn TL
    Neurosci Biobehav Rev; 2017 Aug; 79():14-26. PubMed ID: 28499504
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.
    Sakurai T; Dorr NP; Takahashi N; McInnes LA; Elder GA; Buxbaum JD
    Autism Res; 2011 Feb; 4(1):28-39. PubMed ID: 21328569
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Functional Interleukin-18 Haplotype Predicts Depression and Anxiety through Increased Threat-Related Amygdala Reactivity in Women but Not Men.
    Swartz JR; Prather AA; Di Iorio CR; Bogdan R; Hariri AR
    Neuropsychopharmacology; 2017 Jan; 42(2):419-426. PubMed ID: 27430614
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.