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Results: 1 to 20 of 23

Cited In for PubMed (Select 16511839)

1.

White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosis.

Kates WR, Olszewski AK, Gnirke MH, Kikinis Z, Nelson J, Antshel KM, Fremont W, Radoeva PD, Middleton FA, Shenton ME, Coman IL.

Schizophr Res. 2015 Jan;161(1):76-84. doi: 10.1016/j.schres.2014.07.010. Epub 2014 Jul 25.

PMID:
25066496
2.

The development of cognitive control in children with chromosome 22q11.2 deletion syndrome.

Shapiro HM, Tassone F, Choudhary NS, Simon TJ.

Front Psychol. 2014 Jun 10;5:566. doi: 10.3389/fpsyg.2014.00566. eCollection 2014.

3.

Sex differences in COMT polymorphism effects on prefrontal inhibitory control in adolescence.

White TP, Loth E, Rubia K, Krabbendam L, Whelan R, Banaschewski T, Barker GJ, Bokde AL, Büchel C, Conrod P, Fauth-Bühler M, Flor H, Frouin V, Gallinat J, Garavan H, Gowland P, Heinz A, Ittermann B, Lawrence C, Mann K, Paillère ML, Nees F, Paus T, Pausova Z, Rietschel M, Robbins T, Smolka MN, Shergill SS, Schumann G; IMAGEN Consortium.

Neuropsychopharmacology. 2014 Oct;39(11):2560-9. doi: 10.1038/npp.2014.107. Epub 2014 May 13.

PMID:
24820538
4.

White matter abnormalities in 22q11.2 deletion syndrome: preliminary associations with the Nogo-66 receptor gene and symptoms of psychosis.

Perlstein MD, Chohan MR, Coman IL, Antshel KM, Fremont WP, Gnirke MH, Kikinis Z, Middleton FA, Radoeva PD, Shenton ME, Kates WR.

Schizophr Res. 2014 Jan;152(1):117-23. doi: 10.1016/j.schres.2013.11.015. Epub 2013 Dec 8.

5.

A cross-sectional analysis of the development of response inhibition in children with chromosome 22q11.2 deletion syndrome.

Shapiro HM, Wong LM, Simon TJ.

Front Psychiatry. 2013 Aug 7;4:81. doi: 10.3389/fpsyt.2013.00081. eCollection 2013.

6.

Selective overexpression of Comt in prefrontal cortex rescues schizophrenia-like phenotypes in a mouse model of 22q11 deletion syndrome.

Kimoto S, Muraki K, Toritsuka M, Mugikura S, Kajiwara K, Kishimoto T, Illingworth E, Tanigaki K.

Transl Psychiatry. 2012 Aug 7;2:e146. doi: 10.1038/tp.2012.70.

7.

No association of COMT (Val158Met) genotype with brain structure differences between men and women.

Barnes A, Isohanni M, Barnett JH, Pietiläinen O, Veijola J, Miettunen J, Paunio T, Tanskanen P, Ridler K, Suckling J, Bullmore ET, Murray GK, Jones PB.

PLoS One. 2012;7(3):e33964. doi: 10.1371/journal.pone.0033964. Epub 2012 Mar 30.

8.

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents.

Sundram F, Campbell LE, Azuma R, Daly E, Bloemen OJ, Barker GJ, Chitnis X, Jones DK, van Amelsvoort T, Murphy KC, Murphy DG.

J Neurodev Disord. 2010 Jun;2(2):77-92. doi: 10.1007/s11689-010-9043-6. Epub 2010 Mar 5.

9.

Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.

Philip N, Bassett A.

Behav Genet. 2011 May;41(3):403-12. doi: 10.1007/s10519-011-9468-z. Epub 2011 May 15. Review.

10.

Atypical development of the executive attention network in children with chromosome 22q11.2 deletion syndrome.

Stoddard J, Beckett L, Simon TJ.

J Neurodev Disord. 2011 Mar;3(1):76-85. doi: 10.1007/s11689-010-9070-3. Epub 2010 Dec 23.

11.

Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.

Kates WR, Bansal R, Fremont W, Antshel KM, Hao X, Higgins AM, Liu J, Shprintzen RJ, Peterson BS.

J Am Acad Child Adolesc Psychiatry. 2011 Mar;50(3):272-282.e2. doi: 10.1016/j.jaac.2010.12.002. Epub 2011 Jan 14.

12.

Neuroanatomic predictors to prodromal psychosis in velocardiofacial syndrome (22q11.2 deletion syndrome): a longitudinal study.

Kates WR, Antshel KM, Faraone SV, Fremont WP, Higgins AM, Shprintzen RJ, Botti JA, Kelchner L, McCarthy C.

Biol Psychiatry. 2011 May 15;69(10):945-52. doi: 10.1016/j.biopsych.2010.10.027. Epub 2010 Dec 31.

13.

Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome.

Gothelf D, Hoeft F, Ueno T, Sugiura L, Lee AD, Thompson P, Reiss AL.

J Psychiatr Res. 2011 Mar;45(3):322-31. doi: 10.1016/j.jpsychires.2010.07.008.

14.

Behavior, brain, and genome in genomic disorders: finding the correspondences.

Grigorenko EL, Urban AE, Mencl E.

J Dev Behav Pediatr. 2010 Sep;31(7):602-9. doi: 10.1097/DBP.0b013e3181f5a0a1.

15.

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. Epub 2010 May 20.

16.

Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.

Antshel KM, Shprintzen R, Fremont W, Higgins AM, Faraone SV, Kates WR.

J Am Acad Child Adolesc Psychiatry. 2010 Apr;49(4):333-44.

17.

The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study.

Coman IL, Gnirke MH, Middleton FA, Antshel KM, Fremont W, Higgins AM, Shprintzen RJ, Kates WR.

Neuroimage. 2010 Nov 15;53(3):1043-50. doi: 10.1016/j.neuroimage.2010.01.094. Epub 2010 Feb 1.

18.

Velo-Cardio-Facial Syndrome.

Gothelf D, Frisch A, Michaelovsky E, Weizman A, Shprintzen RJ.

J Ment Health Res Intellect Disabil. 2009 Apr;2(2):149-167.

19.

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.

20.

Impact of interacting functional variants in COMT on regional gray matter volume in human brain.

Honea R, Verchinski BA, Pezawas L, Kolachana BS, Callicott JH, Mattay VS, Weinberger DR, Meyer-Lindenberg A.

Neuroimage. 2009 Mar 1;45(1):44-51. doi: 10.1016/j.neuroimage.2008.10.064. Epub 2008 Nov 21.

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