Detalhe da pesquisa
1.
Common variation at 16p11.2 is associated with glycosuria in pregnancy: findings from a genome-wide association study in European women.
Hum Mol Genet
; 29(12): 2098-2106, 2020 07 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32227112
2.
Genomic analysis of diet composition finds novel loci and associations with health and lifestyle.
Mol Psychiatry
; 26(6): 2056-2069, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32393786
3.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Hum Mol Genet
; 27(11): 2025-2038, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29659830
4.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
Nature
; 514(7520): 92-97, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25231870
5.
Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males.
Hum Mol Genet
; 25(2): 382-8, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604150
6.
Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.
Am J Hum Genet
; 96(5): 695-708, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865494
7.
Using Genetic Variation to Explore the Causal Effect of Maternal Pregnancy Adiposity on Future Offspring Adiposity: A Mendelian Randomisation Study.
PLoS Med
; 14(1): e1002221, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28118352
8.
Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough.
Hum Mol Genet
; 24(20): 5930-9, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26231221
9.
Genome-wide association study of blood lead shows multiple associations near ALAD.
Hum Mol Genet
; 24(13): 3871-9, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25820613
10.
Smoking and caffeine consumption: a genetic analysis of their association.
Addict Biol
; 22(4): 1090-1102, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27027469
11.
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.
Proc Natl Acad Sci U S A
; 111(38): 13790-4, 2014 Sep 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25201988
12.
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.
Hum Mol Genet
; 23(16): 4452-64, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24770850
13.
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
14.
Mining the human phenome using allelic scores that index biological intermediates.
PLoS Genet
; 9(10): e1003919, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24204319
15.
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.
JAMA
; 315(11): 1129-40, 2016 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26978208
16.
A genome-wide approach to children's aggressive behavior: The EAGLE consortium.
Am J Med Genet B Neuropsychiatr Genet
; 171(5): 562-72, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26087016
17.
Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Hum Mol Genet
; 22(19): 3998-4006, 2013 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23720494
18.
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
19.
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.
Am J Hum Genet
; 90(3): 478-85, 2012 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22341974
20.
Assumption-free estimation of the genetic contribution to refractive error across childhood.
Mol Vis
; 21: 621-32, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26019481