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Items: 1 to 20 of 329

1.

A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.

Zarchi O, Diamond A, Weinberger R, Abbott D, Carmel M, Frisch A, Michaelovsky E, Gruber R, Green T, Weizman A, Gothelf D.

Eur Psychiatry. 2014 May;29(4):203-10. doi: 10.1016/j.eurpsy.2013.07.001. Epub 2013 Sep 17.

PMID:
24054518
2.

[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
3.

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. doi: 10.1016/j.euroneuro.2016.08.003. Epub 2016 Aug 12.

PMID:
27524298
4.

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
5.

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
6.

Mother-Child Interaction as a Window to a Unique Social Phenotype in 22q11.2 Deletion Syndrome and in Williams Syndrome.

Weisman O, Feldman R, Burg-Malki M, Keren M, Geva R, Diesendruck G, Gothelf D.

J Autism Dev Disord. 2015 Aug;45(8):2567-77. doi: 10.1007/s10803-015-2425-6.

PMID:
25791124
7.

Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Eisenberg DP, Jabbi M, Berman KF.

Neuroimage. 2010 Nov 15;53(3):857-69. doi: 10.1016/j.neuroimage.2010.02.070. Epub 2010 Mar 3. Review.

8.

Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.

Weisman O, Feldman R, Burg-Malki M, Keren M, Geva R, Diesendruck G, Gothelf D.

J Intellect Disabil Res. 2017 Dec;61(12):1083-1093. doi: 10.1111/jir.12424. Epub 2017 Oct 8.

PMID:
28990288
9.

Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome.

Schonherz Y, Davidov M, Knafo A, Zilkha H, Shoval G, Zalsman G, Frisch A, Weizman A, Gothelf D.

J Neurodev Disord. 2014 Feb 11;6(1):3. doi: 10.1186/1866-1955-6-3.

10.

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.

11.

Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology.

Sanders AF, Hobbs DA, Stephenson DD Jr, Laird RD, Beaton EA.

J Autism Dev Disord. 2017 Apr;47(4):992-1005. doi: 10.1007/s10803-016-3011-2.

PMID:
28083777
12.

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.

13.

Behavioral and Psychiatric Phenotypes in 22q11.2 Deletion Syndrome.

Tang KL, Antshel KM, Fremont WP, Kates WR.

J Dev Behav Pediatr. 2015 Oct;36(8):639-50. doi: 10.1097/DBP.0000000000000210. Review.

14.

Executive function in Williams and Down syndromes.

Carney DP, Brown JH, Henry LA.

Res Dev Disabil. 2013 Jan;34(1):46-55. doi: 10.1016/j.ridd.2012.07.013. Epub 2012 Aug 30.

PMID:
22940158
15.

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
16.

Phenotypic psychiatric characterization of children with Williams syndrome and response of those with ADHD to methylphenidate treatment.

Green T, Avda S, Dotan I, Zarchi O, Basel-Vanagaite L, Zalsman G, Weizman A, Gothelf D.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):13-20. doi: 10.1002/ajmg.b.31247. Epub 2011 Nov 3.

PMID:
22052570
17.

Multitasking Abilities in Adolescents With 22q11.2 Deletion Syndrome: Results From an Experimental Ecological Paradigm.

Schneider M, Eliez S, Birr J, Menghetti S, Debbané M, Van der Linden M.

Am J Intellect Dev Disabil. 2016 Mar;121(2):151-64. doi: 10.1352/1944-7558-121.2.151.

PMID:
26914469
18.

An examination of the relationship of anxiety and intelligence to adaptive functioning in children with chromosome 22q11.2 deletion syndrome.

Angkustsiri K, Leckliter I, Tartaglia N, Beaton EA, Enriquez J, Simon TJ.

J Dev Behav Pediatr. 2012 Nov-Dec;33(9):713-20. doi: 10.1097/DBP.0b013e318272dd24. Erratum in: J Dev Behav Pediatr. 2013 Jan;34(1):62.

19.

[Spectrum of neuropsychiatric features associated with velocardiofacial syndrome (Deletion 22q11.2)].

Sieberer M, Runte I, Wilkening A, Pabst B, Ziegenbein M, Haltenhof H.

Fortschr Neurol Psychiatr. 2006 May;74(5):263-74. Review. German.

PMID:
16758538
20.

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.

Van Aken K, Swillen A, Beirinckx M, Janssens L, Caeyenberghs K, Smits-Engelsman B.

Res Dev Disabil. 2010 May-Jun;31(3):634-41. doi: 10.1016/j.ridd.2010.01.002. Epub 2010 Feb 23.

PMID:
20181458

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