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.
A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins.
Hum Mol Genet
; 21(15): 3374-86, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22547224
3.
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
4.
GRIK4/KA1 protein expression in human brain and correlation with bipolar disorder risk variant status.
Am J Med Genet B Neuropsychiatr Genet
; 159B(1): 21-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22052594
5.
Confirmed rare copy number variants implicate novel genes in schizophrenia.
Biochem Soc Trans
; 38(2): 445-51, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20298200
6.
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset.
Am J Med Genet B Neuropsychiatr Genet
; 153B(8): 1425-33, 2010 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20886542
7.
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
8.
Disrupted-in-Schizophrenia-1.
Curr Psychiatry Rep
; 10(2): 140-7, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18474207
9.
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
10.
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
11.
Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorder.
Biol Psychiatry
; 61(6): 797-805, 2007 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16996484
12.
The PDE4B gene confers sex-specific protection against schizophrenia.
Psychiatr Genet
; 17(3): 129-33, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17417055
13.
Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? Evidence from DISC1, GRIK4 and NRG1.
Neurotox Res
; 11(1): 73-83, 2007 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17449450
14.
SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis.
Nucleic Acids Res
; 30(15): e74, 2002 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-12140336
15.
Candidate psychiatric illness genes identified in patients with pericentric inversions of chromosome 18.
Psychiatr Genet
; 15(1): 37-44, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15722956
16.
Borderline personality disorder characteristics in young adults with recurrent mood disorders: a comparison of bipolar and unipolar depression.
J Affect Disord
; 87(1): 17-23, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15967232
17.
High harm avoidance and low self-directedness in euthymic young adults with recurrent, early-onset depression.
J Affect Disord
; 87(1): 83-9, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15967233
18.
A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation.
BMC Med Genet
; 5: 21, 2004 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-15310400
19.
Is borderline personality disorder part of the bipolar spectrum?
Harv Rev Psychiatry
; 12(3): 133-9, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15371067
20.
A novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: altered l-serine level associated with disruption of PSAT1 gene expression.
Neurosci Res
; 69(2): 154-60, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20955740