Detalhe da pesquisa
1.
Exploring the potential association among sleep disturbances, cognitive impairments, and immune activation in 22q11.2 deletion syndrome.
Am J Med Genet A;
182(3): 461-468, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31837200
2.
Pharmacogenetics of citalopram-related side effects in children with depression and/or anxiety disorders.
J Neural Transm (Vienna);
123(11): 1347-1354, 2016 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27324805
3.
Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome.
Pediatr Res;
77(4): 579-85, 2015 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25580739
4.
Lymphoblast transcriptome analysis in 22q11.2 deletion syndrome individuals with schizophrenia-spectrum disorder.
World J Biol Psychiatry;
25(4): 242-254, 2024 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38493364
5.
Genotype-phenotype correlation in 22q11.2 deletion syndrome.
BMC Med Genet;
13: 122, 2012 Dec 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23245648
6.
Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders.
World J Biol Psychiatry;
22(1): 46-57, 2021 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32212948
7.
Effectiveness and tolerability of citalopram for the treatment of depression and anxiety disorders in children and adolescents: an open-label study.
J Neural Transm (Vienna);
117(1): 139-45, 2010 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19851705
8.
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach.
Transl Psychiatry;
9(1): 15, 2019 01 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30710087
9.
Serotonin transporter polymorphism (5-HTTLPR) and citalopram effectiveness and side effects in children with depression and/or anxiety disorders.
J Child Adolesc Psychopharmacol;
17(6): 741-50, 2007 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18315446
10.
Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.
Psychiatr Genet;
27(5): 169-177, 2017 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28570395
11.
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.
Circ Cardiovasc Genet;
10(5)2017 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29025761
12.
The Relationship Between Plasma Cytokine Levels and Response to Selective Serotonin Reuptake Inhibitor Treatment in Children and Adolescents with Depression and/or Anxiety Disorders.
J Child Adolesc Psychopharmacol;
26(8): 727-732, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26771135
13.
Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome.
Eur Neuropsychopharmacol;
26(10): 1610-8, 2016 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27524298
14.
Hyperactive auditory processing in Williams syndrome: Evidence from auditory evoked potentials.
Psychophysiology;
52(6): 782-9, 2015 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25603839
15.
Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.
J Psychiatr Res;
56: 28-35, 2014 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24853458
16.
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Biol Psychiatry;
75(5): 406-13, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23992923
17.
Additive effects of 5-HTTLPR (serotonin transporter) and tryptophan hydroxylase 2 G-703T gene polymorphisms on the clinical response to citalopram among children and adolescents with depression and anxiety disorders.
J Child Adolesc Psychopharmacol;
23(2): 117-22, 2013 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23510446
18.
Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.
J Psychiatr Res;
47(11): 1623-9, 2013 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23910792
19.
Pharmacogenetics of selective serotonin reuptake inhibitors in pediatric depression and anxiety.
Pharmacogenomics;
9(11): 1725-36, 2008 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19018726
20.
Association between a common haplotype in the COMT gene region and psychiatric disorders in individuals with 22q11.2DS.
Int J Neuropsychopharmacol;
11(3): 351-63, 2008 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17949513