Detalhe da pesquisa
1.
The genetic landscape of Scotland and the Isles.
Proc Natl Acad Sci U S A
; 116(38): 19064-19070, 2019 09 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31481615
2.
Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans.
Hum Mol Genet
; 27(16): 2927-2939, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29860447
3.
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.
Hum Mol Genet
; 27(4): 742-756, 2018 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29309628
4.
A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts.
Hum Genomics
; 13(1): 6, 2019 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-30704525
5.
Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis.
PLoS Med
; 16(6): e1002828, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31211782
6.
Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
Hum Genomics
; 12(1): 24, 2018 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29695297
7.
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
8.
Collapsed methylation quantitative trait loci analysis for low frequency and rare variants.
Hum Mol Genet
; 25(19): 4339-4349, 2016 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27559110
9.
Prenatal and early life influences on epigenetic age in children: a study of mother-offspring pairs from two cohort studies.
Hum Mol Genet
; 25(1): 191-201, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26546615
10.
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
11.
Longitudinal analysis of DNA methylation associated with birth weight and gestational age.
Hum Mol Genet
; 24(13): 3752-63, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25869828
12.
Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC).
Hum Mol Genet
; 24(8): 2201-17, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25552657
13.
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Hum Mol Genet
; 24(4): 1155-68, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25281659
14.
TRPA1 gene polymorphisms and childhood asthma.
Pediatr Allergy Immunol
; 28(2): 191-198, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27779810
15.
Age at menarche and lung function: a Mendelian randomization study.
Eur J Epidemiol
; 32(8): 701-710, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28624884
16.
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.
J Med Genet
; 53(3): 163-71, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26660103
17.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
PLoS Genet
; 10(6): e1004423, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24945404
18.
Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin.
PLoS Genet
; 10(7): e1004474, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25010111
19.
Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
Am J Hum Genet
; 93(1): 19-28, 2013 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23746548
20.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS Genet
; 9(9): e1003751, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068947