Detalhe da pesquisa
1.
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.
Nat Genet
; 40(9): 1056-8, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18711365
2.
Homozygosity mapping of depressive disorder in a large family from Pakistan: significant linkage on chromosome 6 and 9.
Am J Med Genet B Neuropsychiatr Genet
; 162B(2): 157-62, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23281311
3.
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Am J Med Genet B Neuropsychiatr Genet
; 162B(8): 847-54, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24115684
4.
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression.
Am J Hum Genet
; 85(6): 833-46, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19944402
5.
Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages.
Hum Hered
; 66(3): 190-8, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18506107
6.
Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
Eur J Hum Genet
; 16(6): 750-8, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18322454
7.
ALG-2 interacting protein AIP1: a novel link between D1 and D3 signalling.
Eur J Neurosci
; 27(7): 1626-33, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18380665
8.
A genome-wide linkage study in families with major depression and co-morbid unexplained swelling.
Am J Med Genet B Neuropsychiatr Genet
; 147(3): 356-62, 2008 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-17955480
9.
Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing.
Am J Med Genet B Neuropsychiatr Genet
; 147B(6): 880-9, 2008 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18205168
10.
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness.
Mol Neuropsychiatry
; 1(3): 175-190, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27239468
11.
Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial.
Lancet Respir Med
; 3(9): 684-691, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26149841
12.
Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder.
PLoS One
; 6(4): e19011, 2011 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-21559497
13.
Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population.
Neurosci Lett
; 475(3): 169-73, 2010 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20371266
14.
Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder.
Neurosci Lett
; 478(1): 9-13, 2010 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20435087
15.
Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation.
Proc Natl Acad Sci U S A
; 104(8): 2709-14, 2007 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-17296936
16.
Targeted disruption of Huntingtin-associated protein-1 (Hap1) results in postnatal death due to depressed feeding behavior.
Hum Mol Genet
; 11(8): 945-59, 2002 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11971876