Detalhe da pesquisa
1.
Examining cognition across the bipolar/schizophrenia diagnostic spectrum.
J Psychiatry Neurosci
; 43(4): 245-253, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29947606
2.
Examining cognition across the bipolar/schizophrenia diagnostic spectrum.
J Psychiatry Neurosci
; 43(3): 170076, 2018 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29620518
3.
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
4.
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
5.
Neurocognitive abilities in the general population and composite genetic risk scores for attention-deficit hyperactivity disorder.
J Child Psychol Psychiatry
; 56(6): 648-56, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25280069
6.
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
7.
Autistic traits in children with ADHD index clinical and cognitive problems.
Eur Child Adolesc Psychiatry
; 23(1): 23-34, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23616179
8.
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries.
Hum Mol Genet
; 20(2): 387-91, 2011 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21037240
9.
Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia.
Br J Psychiatry
; 203(2): 107-11, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703318
10.
Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
; 156B(8): 929-40, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21960518
11.
Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
; 156B(3): 370-8, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21305692
12.
Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder.
Am J Med Genet B Neuropsychiatr Genet
; 153B(7): 1347-9, 2010 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20583128
13.
Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs.
BMC Med Genet
; 10: 122, 2009 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19951422
14.
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
Bipolar Disord
; 11(6): 610-20, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19689503
15.
Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Nat Genet
; 51(7): 1193, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31160808
16.
Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin.
Nat Genet
; 36(8): 783-4; author reply 784-5, 2004 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-15284840
17.
Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?
Am J Med Genet B Neuropsychiatr Genet
; 147B(6): 778-83, 2008 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-18161859
18.
Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder.
JAMA Psychiatry
; 75(1): 28-35, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29167880
19.
An InDel in Phospholipase-C-B-1 Is Linked with Euthyroid Multinodular Goiter.
Thyroid
; 28(7): 891-901, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29897006
20.
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Nat Genet
; 50(3): 381-389, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29483656