Detalhe da pesquisa
1.
Derepression of a neuronal inhibitor due to miRNA dysregulation in a schizophrenia-related microdeletion.
Cell;
152(1-2): 262-75, 2013 Jan 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23332760
2.
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.
Am J Hum Genet;
105(3): 493-508, 2019 09 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31447100
3.
Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion.
Proc Natl Acad Sci U S A;
114(30): E6127-E6136, 2017 07 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28696314
4.
Family history identifies sporadic schizoaffective disorder as a subtype for genetic studies.
S Afr J Psychiatr;
26: 1393, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32391182
5.
6.
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.
Nature;
471(7339): 499-503, 2011 Mar 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21346763
7.
Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism.
Proc Natl Acad Sci U S A;
111(1): 343-8, 2014 Jan 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24344280
8.
Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia.
Nature;
464(7289): 763-7, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20360742
9.
The BDNF Val66Met variant affects gene expression through miR-146b.
Neurobiol Dis;
77: 228-37, 2015 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25771167
10.
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.
Nat Rev Neurosci;
11(6): 402-16, 2010 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20485365
11.
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
Nat Genet;
38(5): 556-60, 2006 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16582909
12.
The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion.
J Neurosci;
33(37): 14825-39, 2013 Sep 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24027283
13.
The genetic architecture of schizophrenia: new mutations and emerging paradigms.
Annu Rev Med;
63: 63-80, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22034867
14.
Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.
Proc Natl Acad Sci U S A;
108(11): 4447-52, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21368174
15.
Altered axonal targeting and short-term plasticity in the hippocampus of Disc1 mutant mice.
Proc Natl Acad Sci U S A;
108(49): E1349-58, 2011 Dec 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22049344
16.
Convergent evidence for impaired AKT1-GSK3beta signaling in schizophrenia.
Nat Genet;
36(2): 131-7, 2004 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-14745448
17.
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
Nat Genet;
36(7): 725-31, 2004 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15184899
18.
MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction.
Neurobiol Dis;
46(2): 291-301, 2012 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22406400
19.
Genetic vs. pharmacological inactivation of COMT influences cannabinoid-induced expression of schizophrenia-related phenotypes.
Int J Neuropsychopharmacol;
15(9): 1331-42, 2012 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22074909
20.
Evidence for altered hippocampal function in a mouse model of the human 22q11.2 microdeletion.
Mol Cell Neurosci;
47(4): 293-305, 2011 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21635953