Detalhe da pesquisa
1.
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Cell
; 179(3): 589-603, 2019 10 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31607513
2.
Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium.
Proc Natl Acad Sci U S A
; 120(14): e2213880120, 2023 04 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36976765
3.
Connectome architecture shapes large-scale cortical alterations in schizophrenia: a worldwide ENIGMA study.
Mol Psychiatry
; 2024 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38336840
4.
Neurexins in autism and schizophrenia-a review of patient mutations, mouse models and potential future directions.
Mol Psychiatry
; 26(3): 747-760, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33191396
5.
Increased power by harmonizing structural MRI site differences with the ComBat batch adjustment method in ENIGMA.
Neuroimage
; 218: 116956, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32470572
6.
Wnt receptor gene FZD1 was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort.
Aust N Z J Psychiatry
; 54(9): 902-908, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31735061
7.
Stria terminalis, amygdala, and temporoparietal junction networks facilitate efficient emotion processing under expectations.
Hum Brain Mapp
; 40(18): 5382-5396, 2019 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31460690
8.
Is there a role for antibodies targeting muscarinic acetylcholine receptors in the pathogenesis of schizophrenia?
Aust N Z J Psychiatry
; 53(11): 1059-1069, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31347380
9.
No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
PLoS Genet
; 12(10): e1006343, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792727
10.
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Nat Genet
; 40(9): 1053-5, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18677311
11.
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent.
Am J Hum Genet
; 93(3): 463-70, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23954163
12.
Verbal Initiation, Suppression, and Strategy Use and the Relationship with Clinical Symptoms in Schizophrenia.
J Int Neuropsychol Soc
; 22(7): 735-43, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27329682
13.
Common variants on chromosome 6p22.1 are associated with schizophrenia.
Nature
; 460(7256): 753-7, 2009 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-19571809
14.
Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 168B(5): 374-82, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25943776
15.
Hybridization-based reconstruction of small non-coding RNA transcripts from deep sequencing data.
Nucleic Acids Res
; 40(16): 7633-43, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22705792
16.
DSM-IV "criterion A" schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization?
Cult Med Psychiatry
; 38(3): 408-26, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24981830
17.
Optimising the zebrafish Cre/Lox toolbox. Codon improved iCre, new gateway tools, Cre protein and guidelines.
Front Physiol
; 14: 1221310, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37601640
18.
Genetic interactions of schizophrenia using gene-based statistical epistasis exclusively identify nervous system-related pathways and key hub genes.
Front Genet
; 14: 1301150, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38259618
19.
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations.
Nat Genet
; 55(3): 369-376, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36914870
20.
Genetic influences on cost-efficient organization of human cortical functional networks.
J Neurosci
; 31(9): 3261-70, 2011 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21368038