These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 17653112)

  • 1. Disrupted dopaminergic neurotransmission in 22q11 deletion syndrome.
    Boot E; Booij J; Zinkstok J; Abeling N; de Haan L; Baas F; Linszen D; van Amelsvoort T
    Neuropsychopharmacology; 2008 May; 33(6):1252-8. PubMed ID: 17653112
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatology.
    Boot E; Booij J; Abeling N; Meijer J; da Silva Alves F; Zinkstok J; Baas F; Linszen D; van Amelsvoort T
    J Psychopharmacol; 2011 Jul; 25(7):888-95. PubMed ID: 21447540
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Startle reactivity and prepulse inhibition of the acoustic startle response are modulated by catechol-O-methyl-transferase Val(158) Met polymorphism in adults with 22q11 deletion syndrome.
    de Koning MB; Boot E; Bloemen OJ; van Duin ED; Abel KM; de Haan L; Linszen DH; van Amelsvoort TA
    J Psychopharmacol; 2012 Dec; 26(12):1548-60. PubMed ID: 22952320
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lower [
    van Duin EDA; Ceccarini J; Booij J; Kasanova Z; Vingerhoets C; van Huijstee J; Heinzel A; Mohammadkhani-Shali S; Winz O; Mottaghy F; Myin-Germeys I; van Amelsvoort T
    Psychol Med; 2020 Apr; 50(5):799-807. PubMed ID: 30935427
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Executive functions and memory abilities in children with 22q11.2 deletion syndrome.
    Campbell LE; Azuma R; Ambery F; Stevens A; Smith A; Morris RG; Murphy DG; Murphy KC
    Aust N Z J Psychiatry; 2010 Apr; 44(4):364-71. PubMed ID: 20307169
    [TBL] [Abstract][Full Text] [Related]  

  • 6. COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.
    Baker K; Baldeweg T; Sivagnanasundaram S; Scambler P; Skuse D
    Biol Psychiatry; 2005 Jul; 58(1):23-31. PubMed ID: 15935994
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Striatal dopamine release and impaired reinforcement learning in adults with 22q11.2 deletion syndrome.
    van Duin EDA; Kasanova Z; Hernaus D; Ceccarini J; Heinzel A; Mottaghy F; Mohammadkhani-Shali S; Winz O; Frank M; Beck MCH; Booij J; Myin-Germeys I; van Amelsvoort T
    Eur Neuropsychopharmacol; 2018 Jun; 28(6):732-742. PubMed ID: 29703646
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
    Schaer M; Debbané M; Bach Cuadra M; Ottet MC; Glaser B; Thiran JP; Eliez S
    Schizophr Res; 2009 Dec; 115(2-3):182-90. PubMed ID: 19836927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dopamine in high-risk populations: A comparison of subjects with 22q11.2 deletion syndrome and subjects at ultra high-risk for psychosis.
    Vingerhoets C; Bloemen OJN; Boot E; Bakker G; de Koning MB; da Silva Alves F; Booij J; van Amelsvoort TAMJ
    Psychiatry Res Neuroimaging; 2018 Feb; 272():65-70. PubMed ID: 29174435
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Serotonergic, noradrenergic and dopaminergic markers are related to cognitive function in adults with 22q11 deletion syndrome.
    Evers LJ; Curfs LM; Bakker JA; Boot E; da Silva Alves F; Abeling N; Bierau J; Drukker M; van Amelsvoort TA
    Int J Neuropsychopharmacol; 2014 Aug; 17(8):1159-65. PubMed ID: 24713114
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Striatal D₂ receptor binding in 22q11 deletion syndrome: an [¹²³I]IBZM SPECT study.
    Boot E; Booij J; Zinkstok JR; de Haan L; Linszen DH; Baas F; van Amelsvoort TA
    J Psychopharmacol; 2010 Oct; 24(10):1525-31. PubMed ID: 19406852
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dopamine dysfunction in 22q11 deletion syndrome: possible cause of motor symptoms.
    Casarelli L; Minnei M; Pitzianti M; Armando M; Pontillo M; Vicari S; Pasini A
    Psychiatr Genet; 2016 Oct; 26(5):187-92. PubMed ID: 27548835
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.
    Shashi V; Keshavan MS; Howard TD; Berry MN; Basehore MJ; Lewandowski E; Kwapil TR
    Clin Genet; 2006 Mar; 69(3):234-8. PubMed ID: 16542388
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.
    Sinderberry B; Brown S; Hammond P; Stevens AF; Schall U; Murphy DG; Murphy KC; Campbell LE
    Res Dev Disabil; 2013 Jan; 34(1):116-25. PubMed ID: 22940165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.
    Campbell LE; Stevens A; Daly E; Toal F; Azuma R; Karmiloff-Smith A; Murphy DG; Murphy KC
    Neuropsychologia; 2009 Mar; 47(4):1034-44. PubMed ID: 19061904
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Childhood neglect and parental care perception in cocaine addicts: relation with psychiatric symptoms and biological correlates.
    Gerra G; Leonardi C; Cortese E; Zaimovic A; Dell'agnello G; Manfredini M; Somaini L; Petracca F; Caretti V; Raggi MA; Donnini C
    Neurosci Biobehav Rev; 2009 Apr; 33(4):601-10. PubMed ID: 17904221
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.
    Magnée MJ; Lamme VA; de Sain-van der Velden MG; Vorstman JA; Kemner C
    PLoS One; 2011; 6(10):e25882. PubMed ID: 21998713
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome.
    Rockers K; Ousley O; Sutton T; Schoenberg E; Coleman K; Walker E; Cubells JF
    J Intellect Disabil Res; 2009 Jul; 53(7):665-76. PubMed ID: 19460069
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Plasma homovanillic acid: a significant association with alcoholism is independent of a functional polymorphism of the human catechol-O-methyltransferase gene.
    Köhnke MD; Wiatr G; Kolb W; Köhnke AM; Schick S; Lutz U; Vonthein R; Gaertner I
    Neuropsychopharmacology; 2003 May; 28(5):1004-10. PubMed ID: 12741370
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
    Gothelf D; Schaer M; Eliez S
    Dev Disabil Res Rev; 2008; 14(1):59-68. PubMed ID: 18636637
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.