Detalhe da pesquisa
1.
DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis / chronic fatigue syndrome.
BMC Neurol
; 22(1): 269, 2022 Jul 19.
Artigo
Inglês
| MEDLINE | ID: mdl-35854226
2.
Genomic insights into the origin of farming in the ancient Near East.
Nature
; 536(7617): 419-24, 2016 08 25.
Artigo
Inglês
| MEDLINE | ID: mdl-27459054
3.
The genetic landscape of Scotland and the Isles.
Proc Natl Acad Sci U S A
; 116(38): 19064-19070, 2019 09 17.
Artigo
Inglês
| MEDLINE | ID: mdl-31481615
4.
Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions.
PLoS Genet
; 15(11): e1008480, 2019 11.
Artigo
Inglês
| MEDLINE | ID: mdl-31765389
5.
Balancing the local and the universal in maintaining ethical access to a genomics biobank.
BMC Med Ethics
; 18(1): 80, 2017 12 28.
Artigo
Inglês
| MEDLINE | ID: mdl-29282045
6.
Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based study.
BMC Med Genet
; 15: 70, 2014 Jun 23.
Artigo
Inglês
| MEDLINE | ID: mdl-24956927
7.
Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study.
Behav Genet
; 44(2): 91-6, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24554214
8.
Molecular genetic contributions to socioeconomic status and intelligence.
Intelligence
; 44(100): 26-32, 2014 May.
Artigo
Inglês
| MEDLINE | ID: mdl-24944428
9.
Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study.
BMC Med Genet
; 14: 38, 2013 Mar 22.
Artigo
Inglês
| MEDLINE | ID: mdl-23521772
10.
VIKING II, a worldwide observational cohort of volunteers with northern isles ancestry.
Int J Popul Data Sci
; 8(1): 2121, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37670955
11.
Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians.
Eur J Hum Genet
; 31(5): 588-595, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36927983
12.
A practical checklist for return of results from genomic research in the European context.
Eur J Hum Genet
; 31(6): 687-695, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36949262
13.
Typing myalgic encephalomyelitis by infection at onset: A DecodeME study.
NIHR Open Res
; 3: 20, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37881452
14.
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.
Nat Genet
; 55(3): 410-422, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36914875
15.
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung function.
Am J Respir Crit Care Med
; 184(7): 786-95, 2011 Oct 01.
Artigo
Inglês
| MEDLINE | ID: mdl-21965014
16.
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects.
Nat Genet
; 54(5): 581-592, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35534559
17.
Urinary peptides in heart failure: a link to molecular pathophysiology.
Eur J Heart Fail
; 23(11): 1875-1887, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-33881206
18.
Generation Scotland: Donor DNA Databank; A control DNA resource.
BMC Med Genet
; 11: 166, 2010 Nov 23.
Artigo
Inglês
| MEDLINE | ID: mdl-21092308
19.
Assessment of dried blood spots for DNA methylation profiling.
Wellcome Open Res
; 4: 44, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30984878
20.
An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort.
Sci Rep
; 9(1): 10964, 2019 07 29.
Artigo
Inglês
| MEDLINE | ID: mdl-31358886