Detalhe da pesquisa
1.
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Mol Psychiatry;
25(3): 692-695, 2020 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30705424
2.
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Mol Psychiatry;
25(3): 584-602, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30283035
3.
Common variants conferring risk of schizophrenia.
Nature;
460(7256): 744-7, 2009 Aug 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19571808
4.
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.
Am J Hum Genet;
88(3): 372-81, 2011 Mar 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21353194
5.
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Hum Mol Genet;
20(18): 3699-709, 2011 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21665990
6.
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
Hum Mol Genet;
20(20): 4076-81, 2011 Oct 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21791550
7.
Disruption of the neurexin 1 gene is associated with schizophrenia.
Hum Mol Genet;
18(5): 988-96, 2009 Mar 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18945720
8.
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
Lancet;
376(9750): 1401-8, 2010 Oct 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20888040
9.
Association analysis of ANK3 gene variants in nordic bipolar disorder and schizophrenia case-control samples.
Am J Med Genet B Neuropsychiatr Genet;
156B(8): 969-74, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21972176
10.
Association analysis of PALB2 and BRCA2 in bipolar disorder and schizophrenia in a scandinavian case-control sample.
Am J Med Genet B Neuropsychiatr Genet;
153B(7): 1276-82, 2010 Oct 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20872766
11.
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
JAMA Psychiatry;
77(4): 420-430, 2020 04 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31665216
12.
Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Biol Psychiatry;
85(7): 563-572, 2019 04 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30583851
13.
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Transl Psychiatry;
9(1): 258, 2019 10 17.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31624239
14.
MAP1B mutations cause intellectual disability and extensive white matter deficit.
Nat Commun;
9(1): 3456, 2018 08 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30150678
15.
Reproductive fitness and genetic risk of psychiatric disorders in the general population.
Nat Commun;
8: 15833, 2017 06 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28607503
16.
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations.
NPJ Genom Med;
2: 24, 2017.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29263835
17.
A sequence variant associating with educational attainment also affects childhood cognition.
Sci Rep;
6: 36189, 2016 11 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27811963
18.
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder.
Biol Psychiatry;
72(8): 645-50, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22560537
19.
Copy number variations in affective disorders and meta-analysis.
Psychiatr Genet;
21(6): 319-22, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-21451435
20.
Candidate gene analysis of the human natural killer-1 carbohydrate pathway and perineuronal nets in schizophrenia: B3GAT2 is associated with disease risk and cortical surface area.
Biol Psychiatry;
69(1): 90-6, 2011 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20950796