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Items: 1 to 20 of 199

1.

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. doi: 10.1016/j.schres.2009.09.016.

PMID:
19836927
2.

Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome.

Gothelf D, Hoeft F, Hinard C, Hallmayer JF, Stoecker JV, Antonarakis SE, Morris MA, Reiss AL.

Hum Brain Mapp. 2007 Jun;28(6):533-42.

PMID:
17427209
3.

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.

PMID:
16542388
4.

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. doi: 10.1002/ddrr.9. Review.

PMID:
18636637
5.

Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.

Vorstman JA, Breetvelt EJ, Duijff SN, Eliez S, Schneider M, Jalbrzikowski M, Armando M, Vicari S, Shashi V, Hooper SR, Chow EW, Fung WL, Butcher NJ, Young DA, McDonald-McGinn DM, Vogels A, van Amelsvoort T, Gothelf D, Weinberger R, Weizman A, Klaassen PW, Koops S, Kates WR, Antshel KM, Simon TJ, Ousley OY, Swillen A, Gur RE, Bearden CE, Kahn RS, Bassett AS; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome..

JAMA Psychiatry. 2015 Apr;72(4):377-85. doi: 10.1001/jamapsychiatry.2014.2671.

6.

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.

PMID:
16234808
7.

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.

Carmel M, Zarchi O, Michaelovsky E, Frisch A, Patya M, Green T, Gothelf D, Weizman A.

J Psychiatr Res. 2014 Sep;56:28-35. doi: 10.1016/j.jpsychires.2014.04.019.

PMID:
24853458
8.

A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.

Hooper SR, Curtiss K, Schoch K, Keshavan MS, Allen A, Shashi V.

Res Dev Disabil. 2013 May;34(5):1758-69. doi: 10.1016/j.ridd.2012.12.003.

9.

Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.

Schreiner MJ, Karlsgodt KH, Uddin LQ, Chow C, Congdon E, Jalbrzikowski M, Bearden CE.

Soc Cogn Affect Neurosci. 2014 Sep;9(9):1261-7. doi: 10.1093/scan/nst114.

10.

COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Shashi V, Howard TD, Keshavan MS, Kaczorowski J, Berry MN, Schoch K, Spence EJ, Kwapil TR.

Psychiatry Res. 2010 Jul 30;178(2):433-6. doi: 10.1016/j.psychres.2010.04.048.

11.

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 1;58(1):23-31.

PMID:
15935994
12.

Aberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.

Schmitt JE, Vandekar S, Yi J, Calkins ME, Ruparel K, Roalf DR, Whinna D, Souders MC, Satterwaite TD, Prabhakaran K, McDonald-McGinn DM, Zackai EH, Gur RC, Emanuel BS, Gur RE.

Biol Psychiatry. 2015 Jul 15;78(2):135-43. doi: 10.1016/j.biopsych.2014.10.025.

13.

Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndrome.

Takarae Y, Schmidt L, Tassone F, Simon TJ.

Cogn Affect Behav Neurosci. 2009 Mar;9(1):83-90. doi: 10.3758/CABN.9.1.83.

14.

Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.

Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR.

Biol Psychiatry. 2014 Mar 1;75(5):406-13. doi: 10.1016/j.biopsych.2013.07.021.

15.

Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study.

Gothelf D, Penniman L, Gu E, Eliez S, Reiss AL.

Schizophr Res. 2007 Nov;96(1-3):72-81.

16.

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.

van Amelsvoort T, Zinkstok J, Figee M, Daly E, Morris R, Owen MJ, Murphy KC, De Haan L, Linszen DH, Glaser B, Murphy DG.

Psychol Med. 2008 Jan;38(1):89-100.

PMID:
17493297
17.

Resting-state networks in adolescents with 22q11.2 deletion syndrome: associations with prodromal symptoms and executive functions.

Debbané M, Lazouret M, Lagioia A, Schneider M, Van De Ville D, Eliez S.

Schizophr Res. 2012 Aug;139(1-3):33-9. doi: 10.1016/j.schres.2012.05.021.

PMID:
22704643
18.

Hippocampal volume reduction in chromosome 22q11.2 deletion syndrome (22q11.2DS): a longitudinal study of morphometry and symptomatology.

Flahault A, Schaer M, Ottet MC, Debbané M, Eliez S.

Psychiatry Res. 2012 Jul 30;203(1):1-5. doi: 10.1016/j.pscychresns.2011.09.003.

PMID:
22920836
19.

Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls.

Raznahan A, Greenstein D, Lee Y, Long R, Clasen L, Gochman P, Addington A, Giedd JN, Rapoport JL, Gogtay N.

Neuroimage. 2011 Aug 15;57(4):1517-23. doi: 10.1016/j.neuroimage.2011.05.032.

20.

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. doi: 10.1371/journal.pone.0025882.

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