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Items: 1 to 20 of 92

1.

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion.

Vorstman JA, Breetvelt EJ, Thode KI, Chow EW, Bassett AS.

Schizophr Res. 2013 Jan;143(1):55-9. doi: 10.1016/j.schres.2012.10.010. Epub 2012 Nov 13.

PMID:
23153825
2.

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening.

Wenger TL, Miller JS, DePolo LM, de Marchena AB, Clements CC, Emanuel BS, Zackai EH, McDonald-McGinn DM, Schultz RT.

Mol Autism. 2016 May 6;7:27. doi: 10.1186/s13229-016-0090-z. eCollection 2016. Erratum in: Mol Autism. 2016;7:34.

3.

Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome.

Monks S, Niarchou M, Davies AR, Walters JT, Williams N, Owen MJ, van den Bree MB, Murphy KC.

Schizophr Res. 2014 Mar;153(1-3):231-6. doi: 10.1016/j.schres.2014.01.020. Epub 2014 Feb 15.

PMID:
24534796
4.

Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome.

Yuen T, Chow EW, Silversides CK, Bassett AS.

Schizophr Res. 2013 Dec;151(1-3):221-5. doi: 10.1016/j.schres.2013.10.041. Epub 2013 Nov 19.

PMID:
24262682
5.

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. Epub 2013 Aug 28.

6.

[Neurocognitive and psychiatric management of the 22q11.2 deletion syndrome].

Demily C, Rossi M, Schneider M, Edery P, Leleu A, d'Amato T, Franck N, Eliez S.

Encephale. 2015 Jun;41(3):266-73. doi: 10.1016/j.encep.2014.10.005. Epub 2014 Dec 16. Review. French.

PMID:
25523123
7.

Risk factors and the evolution of psychosis in 22q11.2 deletion syndrome: a longitudinal 2-site study.

Gothelf D, Schneider M, Green T, Debbané M, Frisch A, Glaser B, Zilkha H, Schaer M, Weizman A, Eliez S.

J Am Acad Child Adolesc Psychiatry. 2013 Nov;52(11):1192-1203.e3. doi: 10.1016/j.jaac.2013.08.008. Epub 2013 Aug 29.

PMID:
24157393
8.

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Jonas RK, Montojo CA, Bearden CE.

Biol Psychiatry. 2014 Mar 1;75(5):351-60. doi: 10.1016/j.biopsych.2013.07.019. Epub 2013 Aug 28. Review.

9.

Developmental trajectories in 22q11.2 deletion.

Swillen A, McDonald-McGinn D.

Am J Med Genet C Semin Med Genet. 2015 Jun;169(2):172-81. doi: 10.1002/ajmg.c.31435. Epub 2015 May 18. Review.

10.

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.

Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW.

Hum Mol Genet. 2008 Dec 15;17(24):4045-53. doi: 10.1093/hmg/ddn307. Epub 2008 Sep 20. Erratum in: Hum Mol Genet. 2009 May 1;18(9):1717.

11.

Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcome.

Schneider M, Van der Linden M, Menghetti S, Glaser B, Debbané M, Eliez S.

J Psychiatr Res. 2014 Jan;48(1):86-93. doi: 10.1016/j.jpsychires.2013.10.010. Epub 2013 Oct 25.

PMID:
24189154
12.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
13.

Social impairments in chromosome 22q11.2 deletion syndrome (22q11.2DS): autism spectrum disorder or a different endophenotype?

Angkustsiri K, Goodlin-Jones B, Deprey L, Brahmbhatt K, Harris S, Simon TJ.

J Autism Dev Disord. 2014 Apr;44(4):739-46. doi: 10.1007/s10803-013-1920-x.

14.

Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.

Prasad S, Katina S, Hennessy RJ, Murphy KC, Bowman AW, Waddington JL.

Am J Med Genet A. 2015 Mar;167A(3):529-36. doi: 10.1002/ajmg.a.36893.

15.

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. Epub 2014 May 9.

PMID:
24853458
16.

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. Epub 2007 Sep 4.

17.

The feasibility and safety of S-adenosyl-L-methionine (SAMe) for the treatment of neuropsychiatric symptoms in 22q11.2 deletion syndrome: a double-blind placebo-controlled trial.

Green T, Steingart L, Frisch A, Zarchi O, Weizman A, Gothelf D.

J Neural Transm (Vienna). 2012 Nov;119(11):1417-23. doi: 10.1007/s00702-012-0831-x. Epub 2012 Jun 8.

PMID:
22678699
18.

Perceived burden and neuropsychiatric morbidities in adults with 22q11.2 deletion syndrome.

Karas DJ, Costain G, Chow EW, Bassett AS.

J Intellect Disabil Res. 2014 Feb;58(2):198-210. doi: 10.1111/j.1365-2788.2012.01639.x. Epub 2012 Oct 29.

19.

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.

Schneider M, Debbané M, Bassett AS, Chow EW, Fung WL, van den Bree M, Owen M, Murphy KC, Niarchou M, Kates WR, Antshel KM, Fremont W, McDonald-McGinn DM, Gur RE, Zackai EH, Vorstman J, Duijff SN, Klaassen PW, Swillen A, Gothelf D, Green T, Weizman A, Van Amelsvoort T, Evers L, Boot E, Shashi V, Hooper SR, Bearden CE, Jalbrzikowski M, Armando M, Vicari S, Murphy DG, Ousley O, Campbell LE, Simon TJ, Eliez S; International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome..

Am J Psychiatry. 2014 Jun;171(6):627-39. Review.

20.

Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia?

Demily C, Franck N.

Eur J Med Genet. 2016 Nov;59(11):596-603. doi: 10.1016/j.ejmg.2016.09.007. Epub 2016 Sep 14.

PMID:
27639442

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