Detalhe da pesquisa
1.
How does genetic variation modify ND-CNV phenotypes?
Trends Genet
; 38(2): 140-151, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34364706
2.
Mendelian randomization analysis using GWAS and eQTL data to investigate the relationship between chronotype and neuropsychiatric disorders and their molecular basis.
Am J Med Genet B Neuropsychiatr Genet
; : e32980, 2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38549512
3.
Autism spectrum disorder genomics: The progress and potential of genomic technologies.
Genomics
; 112(6): 5136-5142, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32941983
4.
Genetic contributions to stability and change in intelligence from childhood to old age.
Nature
; 482(7384): 212-5, 2012 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22258510
5.
Seventy-five genetic loci influencing the human red blood cell.
Nature
; 492(7429): 369-75, 2012 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23222517
6.
New gene functions in megakaryopoiesis and platelet formation.
Nature
; 480(7376): 201-8, 2011 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-22139419
7.
Differential expression of the inflammation marker IL12p40 in the at-risk mental state for psychosis: a predictor of transition to psychotic disorder?
BMC Psychiatry
; 16(1): 326, 2016 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27650124
8.
Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels.
PLoS Genet
; 9(8): e1003585, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23990791
9.
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
PLoS Genet
; 9(9): e1003796, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068962
10.
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.
PLoS Genet
; 9(2): e1003266, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23408906
11.
Genes from a translational analysis support a multifactorial nature of white matter hyperintensities.
Stroke
; 46(2): 341-7, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25586835
12.
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
Am J Hum Genet
; 91(1): 152-62, 2012 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22703881
13.
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.
Am J Hum Genet
; 91(4): 744-53, 2012 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23022100
14.
Evidence of inbreeding depression on human height.
PLoS Genet
; 8(7): e1002655, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22829771
15.
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Circulation
; 128(12): 1310-24, 2013 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-23969696
16.
Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling.
Neuroimage
; 95: 136-50, 2014 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24657781
17.
Neuropsychiatric disorders, chronotype and sleep: A narrative review of GWAS findings and the application of Mendelian randomization to investigate causal relationships.
Genes Brain Behav
; 23(1): e12885, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38359178
18.
Circadian Variation in the Response to Vaccination: A Systematic Review and Evidence Appraisal.
J Biol Rhythms
; : 7487304241232447, 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38459699
19.
KNG1 Ile581Thr and susceptibility to venous thrombosis.
Blood
; 117(13): 3692-4, 2011 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-21270443
20.
ADRB2, brain white matter integrity and cognitive ageing in the Lothian Birth Cohort 1936.
Behav Genet
; 43(1): 13-23, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23229623