Detalhe da pesquisa
1.
Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function.
Hum Mol Genet;
31(18): 3095-3106, 2022 09 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35531971
2.
Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion.
Acta Neuropathol;
147(1): 64, 2024 Mar 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38556574
3.
Complement C3 and C3aR mediate different aspects of emotional behaviours; relevance to risk for psychiatric disorder.
Brain Behav Immun;
99: 70-82, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34543680
4.
Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by hemizygosity of the psychiatric risk gene Cacna1c.
Mol Psychiatry;
26(6): 1748-1760, 2021 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33597718
5.
Prader-Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT2CR-mediated response inhibition.
Hum Mol Genet;
28(18): 3013-3023, 2019 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31087031
6.
Dissociable effects of complement C3 and C3aR on survival and morphology of adult born hippocampal neurons, pattern separation, and cognitive flexibility in male mice.
Brain Behav Immun;
98: 136-150, 2021 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34403734
7.
Distinct physiological and behavioural functions for parental alleles of imprinted Grb10.
Nature;
469(7331): 534-8, 2011 Jan 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21270893
8.
Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.
Eur J Neurosci;
42(4): 2105-13, 2015 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26040449
9.
Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice.
Nat Genet;
37(6): 625-9, 2005 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15908950
10.
A mild impairment in reversal learning in a bowl-digging substrate deterministic task but not other cognitive tests in the Dlg2+/- rat model of genetic risk for psychiatric disorder.
Genes Brain Behav;
22(6): e12865, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37705179
11.
Genomic imprinting effects on brain development and function.
Nat Rev Neurosci;
8(11): 832-43, 2007 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17925812
12.
Complement Dependent Synaptic Reorganisation During Critical Periods of Brain Development and Risk for Psychiatric Disorder.
Front Neurosci;
16: 840266, 2022.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35600620
13.
Selective behavioural impairments in mice heterozygous for the cross disorder psychiatric risk gene DLG2.
Genes Brain Behav;
21(4): e12799, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35118804
14.
Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes.
Biol Psychiatry;
92(5): 341-361, 2022 09 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35659384
15.
Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder.
Genes Brain Behav;
21(4): e12797, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35075790
16.
Reduced expression of the psychiatric risk gene DLG2 (PSD93) impairs hippocampal synaptic integration and plasticity.
Neuropsychopharmacology;
47(7): 1367-1378, 2022 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35115661
17.
Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour.
Hum Mol Genet;
18(12): 2140-8, 2009 Jun 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19304781
18.
P-Rex2 regulates Purkinje cell dendrite morphology and motor coordination.
Proc Natl Acad Sci U S A;
105(11): 4483-8, 2008 Mar 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18334636
19.
Haploinsufficiency of the schizophrenia and autism risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanisms.
Transl Psychiatry;
11(1): 313, 2021 05 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34031371
20.
Analysis of Diffusion Tensor Imaging Data From the UK Biobank Confirms Dosage Effect of 15q11.2 Copy Number Variation on White Matter and Shows Association With Cognition.
Biol Psychiatry;
90(5): 307-316, 2021 09 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33931204