BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

178 related articles for article (PubMed ID: 20680421)

  • 1. Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.
    Shashi V; Keshavan M; Kaczorowski J; Schoch K; Lewandowski KE; McConkie-Rosell A; Hooper SR; Kwapil TR
    J Genet Couns; 2010 Oct; 19(5):535-44. PubMed ID: 20680421
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Social skills and associated psychopathology in children with chromosome 22q11.2 deletion syndrome: implications for interventions.
    Shashi V; Veerapandiyan A; Schoch K; Kwapil T; Keshavan M; Ip E; Hooper S
    J Intellect Disabil Res; 2012 Sep; 56(9):865-78. PubMed ID: 21883601
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: a matched control study.
    Jansen PW; Duijff SN; Beemer FA; Vorstman JA; Klaassen PW; Morcus ME; Heineman-de Boer JA
    Am J Med Genet A; 2007 Mar; 143A(6):574-80. PubMed ID: 17318841
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sex differences in the behavior of children with the 22q11 deletion syndrome.
    Sobin C; Kiley-Brabeck K; Monk SH; Khuri J; Karayiorgou M
    Psychiatry Res; 2009 Mar; 166(1):24-34. PubMed ID: 19217670
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.
    Lewandowski KE; Shashi V; Berry PM; Kwapil TR
    Am J Med Genet B Neuropsychiatr Genet; 2007 Jan; 144B(1):27-36. PubMed ID: 17034021
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications.
    Debbané M; Glaser B; David MK; Feinstein C; Eliez S
    Schizophr Res; 2006 Jun; 84(2-3):187-93. PubMed ID: 16545541
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.
    Allen TM; Hersh J; Schoch K; Curtiss K; Hooper SR; Shashi V
    J Intellect Disabil Res; 2014 Jan; 58(1):31-47. PubMed ID: 23742203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
    Shashi V; Francis A; Hooper SR; Kranz PG; Zapadka M; Schoch K; Ip E; Tandon N; Howard TD; Keshavan MS
    Eur J Hum Genet; 2012 Oct; 20(10):1051-7. PubMed ID: 22763378
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Eye gaze during face processing in children and adolescents with 22q11.2 deletion syndrome.
    Glaser B; Debbané M; Ottet MC; Vuilleumier P; Zesiger P; Antonarakis SE; Eliez S
    J Am Acad Child Adolesc Psychiatry; 2010 Jul; 49(7):665-74. PubMed ID: 20610136
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome.
    Weinberger R; Yi J; Calkins M; Guri Y; McDonald-McGinn DM; Emanuel BS; Zackai EH; Ruparel K; Carmel M; Michaelovsky E; Weizman A; Gur RC; Gur RE; Gothelf D
    Eur Neuropsychopharmacol; 2016 Oct; 26(10):1610-8. PubMed ID: 27524298
    [TBL] [Abstract][Full Text] [Related]  

  • 14. IQ and hemizygosity for the Val
    Franconi CP; McDonald-McGinn D; Zackai EH; McNamara MA; Salmons H; Moss E; Gur RE; Devoto M; Emanuel BS
    Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1112-1115. PubMed ID: 27619075
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [22q11.2 deletion: handicap-related problems and coping strategies of primary caregivers].
    Briegel W; Schneider M; Schwab KO
    Z Kinder Jugendpsychiatr Psychother; 2009 Nov; 37(6):535-40. PubMed ID: 19890816
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Discrepancies in parent and teacher ratings of social-behavioral functioning of children with chromosome 22q11.2 deletion syndrome: implications for assessment.
    Wray E; Shashi V; Schoch K; Curtiss K; Hooper SR
    Am J Intellect Dev Disabil; 2013 Sep; 118(5):339-52. PubMed ID: 24245728
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Assessment of parental disclosure of a 22q11.2 deletion syndrome diagnosis and implications for clinicians.
    Faux D; Schoch K; Eubanks S; Hooper SR; Shashi V
    J Genet Couns; 2012 Dec; 21(6):835-44. PubMed ID: 22936417
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome.
    Shashi V; Muddasani S; Santos CC; Berry MN; Kwapil TR; Lewandowski E; Keshavan MS
    Neuroimage; 2004 Apr; 21(4):1399-406. PubMed ID: 15050565
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Behavior in preschool children with the 22q11.2 deletion syndrome.
    Klaassen P; Duijff S; Swanenburg de Veye H; Vorstman J; Beemer F; Sinnema G
    Am J Med Genet A; 2013 Jan; 161A(1):94-101. PubMed ID: 23239609
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.