Detalhe da pesquisa
1.
Vaginal bacterial load in the second trimester is associated with early preterm birth recurrence: a nested case-control study.
BJOG
; 128(13): 2061-2072, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34139060
2.
The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders.
Mol Psychiatry
; 23(2): 400-412, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28070120
3.
Should phenotype of previous preterm birth influence management of women with short cervix in subsequent pregnancy? Comparison of vaginal progesterone and Arabin pessary.
Ultrasound Obstet Gynecol
; 53(4): 529-534, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29920812
4.
Familiality and SNP heritability of age at onset and episodicity in major depressive disorder.
Psychol Med
; 45(10): 2215-25, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25698070
5.
Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.
Mol Psychiatry
; 19(4): 452-61, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23568192
6.
Discriminating metastasised from non-metastasised seminoma based on transcriptional changes in primary tumours using NGS.
Br J Cancer
; 110(11): 2738-46, 2014 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-24786602
7.
A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.
Mol Psychiatry
; 18(1): 122-32, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22105623
8.
Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders.
Psychol Med
; 43(6): 1207-17, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22225676
9.
Estimating the heritability of reporting stressful life events captured by common genetic variants.
Psychol Med
; 43(9): 1965-71, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23237013
10.
A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
Nat Genet
; 18(3): 262-5, 1998 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9500549
11.
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.
Nat Genet
; 29(1): 66-9, 2001 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-11528394
12.
Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-ß therapy in multiple sclerosis patients.
Pharmacogenomics J
; 12(3): 238-45, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21502966
13.
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Mol Psychiatry
; 16(1): 97-107, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19786962
14.
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies.
Mol Psychiatry
; 16(6): 647-63, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20368705
15.
Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression.
Mol Psychiatry
; 15(7): 736-47, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19125159
16.
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways.
Mol Psychiatry
; 15(7): 702-11, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19139748
17.
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.
Mol Psychiatry
; 15(6): 589-601, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19107115
18.
Somatization in major depression--clinical features and genetic associations.
Acta Psychiatr Scand
; 124(4): 317-28, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21838737
19.
More CLEC16A gene variants associated with multiple sclerosis.
Acta Neurol Scand
; 123(6): 400-6, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20849399
20.
An extensive comparison of quantitative trait Loci mapping methods.
Hum Hered
; 69(3): 202-11, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20203525