Detalhe da pesquisa
1.
A genome-wide association study of corneal astigmatism: The CREAM Consortium.
Mol Vis
; 24: 127-142, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29422769
2.
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
Am J Hum Genet
; 93(2): 264-77, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24144296
3.
Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium.
Behav Genet
; 46(2): 170-82, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26362575
4.
A population-specific HTR2B stop codon predisposes to severe impulsivity.
Nature
; 468(7327): 1061-6, 2010 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-21179162
5.
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.
Hum Genet
; 134(2): 131-46, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25367360
6.
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error.
Commun Biol
; 6(1): 6, 2023 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36596879
7.
Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits.
Nicotine Tob Res
; 14(6): 720-33, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22241830
8.
The role of vision-related problems in fatal road accidents in Finland.
Acta Ophthalmol
; 99(4): 427-430, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32902159
9.
Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia.
Invest Ophthalmol Vis Sci
; 62(13): 24, 2021 10 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34698770
10.
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia.
JAMA Ophthalmol
; 139(6): 601-609, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33830181
11.
Fetal HLA-G mediated immune tolerance and interferon response in preeclampsia.
EBioMedicine
; 59: 102872, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32680723
12.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Commun Biol
; 3(1): 133, 2020 03 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32193507
13.
Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins.
Am J Med Genet B Neuropsychiatr Genet
; 150B(5): 683-92, 2009 Jul 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19051289
14.
Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene.
Am J Ophthalmol
; 188: 41-50, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29366613
15.
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.
Nat Genet
; 50(6): 834-848, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29808027
16.
Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2.
Sci Rep
; 6: 20092, 2016 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26833182
17.
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.
Nat Genet
; 48(8): 856-66, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27322543
18.
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.
Nat Commun
; 7: 11008, 2016 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-27020472
19.
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Nat Genet
; 48(6): 624-33, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27089181
20.
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.
JAMA Psychiatry
; 72(7): 642-50, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25993607