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Items: 1 to 20 of 58

1.

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

Antshel KM, Fremont W, Roizen NJ, Shprintzen R, Higgins AM, Dhamoon A, Kates WR.

J Am Acad Child Adolesc Psychiatry. 2006 May;45(5):596-603.

PMID:
16670654
2.

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome).

Kates WR, Miller AM, Abdulsabur N, Antshel KM, Conchelos J, Fremont W, Roizen N.

J Am Acad Child Adolesc Psychiatry. 2006 May;45(5):587-95.

PMID:
16670653
3.

Sex differences in cognitive functioning in velocardiofacial syndrome (VCFS).

Antshel KM, AbdulSabur N, Roizen N, Fremont W, Kates WR.

Dev Neuropsychol. 2005;28(3):849-69.

PMID:
16266252
4.

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.

Gothelf D, Eliez S, Thompson T, Hinard C, Penniman L, Feinstein C, Kwon H, Jin S, Jo B, Antonarakis SE, Morris MA, Reiss AL.

Nat Neurosci. 2005 Nov;8(11):1500-2. Epub 2005 Oct 23.

PMID:
16234808
5.

COMT genetic variation confers risk for psychotic and affective disorders: a case control study.

Funke B, Malhotra AK, Finn CT, Plocik AM, Lake SL, Lencz T, DeRosse P, Kane JM, Kucherlapati R.

Behav Brain Funct. 2005 Oct 18;1:19.

6.

Effect of COMT Val158Met polymorphism on the Continuous Performance Test, Identical Pairs Version: tuning rather than improving performance.

Stefanis NC, van Os J, Avramopoulos D, Smyrnis N, Evdokimidis I, Stefanis CN.

Am J Psychiatry. 2005 Sep;162(9):1752-4.

PMID:
16135641
7.

Behavior and corpus callosum morphology relationships in velocardiofacial syndrome (22q11.2 deletion syndrome).

Antshel KM, Conchelos J, Lanzetta G, Fremont W, Kates WR.

Psychiatry Res. 2005 Apr 30;138(3):235-45.

PMID:
15854791
8.

Executive dysfunction and its relation to language ability in verbal school-age children with autism.

Joseph RM, McGrath LM, Tager-Flusberg H.

Dev Neuropsychol. 2005;27(3):361-78.

9.

Gender-moderated dorsolateral prefrontal reductions in 22q11.2 Deletion Syndrome: implications for risk for schizophrenia.

Kates WR, Antshel K, Willhite R, Bessette BA, AbdulSabur N, Higgins AM.

Child Neuropsychol. 2005 Feb;11(1):73-85.

PMID:
15823984
10.

Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype.

Meyer-Lindenberg A, Kohn PD, Kolachana B, Kippenhan S, McInerney-Leo A, Nussbaum R, Weinberger DR, Berman KF.

Nat Neurosci. 2005 May;8(5):594-6. Epub 2005 Apr 10.

PMID:
15821730
11.

Differential effects of DRD4 and DAT1 genotype on fronto-striatal gray matter volumes in a sample of subjects with attention deficit hyperactivity disorder, their unaffected siblings, and controls.

Durston S, Fossella JA, Casey BJ, Hulshoff Pol HE, Galvan A, Schnack HG, Steenhuis MP, Minderaa RB, Buitelaar JK, Kahn RS, van Engeland H.

Mol Psychiatry. 2005 Jul;10(7):678-85.

PMID:
15724142
12.

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.

Simon TJ, Bearden CE, Mc-Ginn DM, Zackai E.

Cortex. 2005 Apr;41(2):145-55.

13.

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow.

Ho BC, Wassink TH, O'Leary DS, Sheffield VC, Andreasen NC.

Mol Psychiatry. 2005 Mar;10(3):229, 287-98.

PMID:
15668720
14.

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis.

Fan JB, Zhang CS, Gu NF, Li XW, Sun WW, Wang HY, Feng GY, St Clair D, He L.

Biol Psychiatry. 2005 Jan 15;57(2):139-44. Review.

PMID:
15652872
15.

Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome.

Bish JP, Ferrante SM, McDonald-McGinn D, Zackai E, Simon TJ.

Dev Sci. 2005 Jan;8(1):36-43.

PMID:
15647065
16.

The molecular genetics of the 22q11-associated schizophrenia.

Karayiorgou M, Gogos JA.

Brain Res Mol Brain Res. 2004 Dec 20;132(2):95-104. Review.

PMID:
15582150
17.

Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain.

Chen J, Lipska BK, Halim N, Ma QD, Matsumoto M, Melhem S, Kolachana BS, Hyde TM, Herman MM, Apud J, Egan MF, Kleinman JE, Weinberger DR.

Am J Hum Genet. 2004 Nov;75(5):807-21. Epub 2004 Sep 27. Erratum in: Am J Hum Genet. 2005 Jun;76(6):1089.

18.

Networks of attention in children with the 22q11 deletion syndrome.

Sobin C, Kiley-Brabeck K, Daniels S, Blundell M, Anyane-Yeboa K, Karayiorgou M.

Dev Neuropsychol. 2004;26(2):611-26.

19.

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

Bearden CE, Jawad AF, Lynch DR, Sokol S, Kanes SJ, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ.

Am J Psychiatry. 2004 Sep;161(9):1700-2.

PMID:
15337663
20.

Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome.

van Amelsvoort T, Henry J, Morris R, Owen M, Linszen D, Murphy K, Murphy D.

Schizophr Res. 2004 Oct 1;70(2-3):223-32.

PMID:
15329299

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