Detalhe da pesquisa
1.
Genetic determinants of mannose-binding lectin activity predispose to thromboembolic complications in critical COVID-19.
Nat Immunol
; 23(6): 861-864, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35624204
2.
The human genetic epidemiology of COVID-19.
Nat Rev Genet
; 23(9): 533-546, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501396
3.
Reduced reproductive success is associated with selective constraint on human genes.
Nature
; 603(7903): 858-863, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35322230
4.
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Nature
; 562(7726): 268-271, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30258228
5.
Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes.
Int J Mol Sci
; 24(17)2023 Aug 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37686257
6.
Prevalence and correlates of vitamin D deficiency in adults after traumatic brain injury.
Clin Endocrinol (Oxf)
; 85(4): 636-44, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26921561
7.
Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.
BMJ Open
; 12(10): e064695, 2022 10 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36198465
8.
Trait Expression and Environmental Responses of Pea (Pisum sativum L.) Genetic Resources Targeting Cultivation in the Arctic.
Front Plant Sci
; 12: 688067, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34394142
9.
The contribution of X-linked coding variation to severe developmental disorders.
Nat Commun
; 12(1): 627, 2021 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33504798
10.
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.
medRxiv
; 2021 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33758887
11.
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.
J Clin Invest
; 131(23)2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34597274
12.
Cognitive impairment and health-related quality of life following traumatic brain injury.
NeuroRehabilitation
; 44(3): 321-331, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31177238
13.
Quantifying the contribution of recessive coding variation to developmental disorders.
Science
; 362(6419): 1161-1164, 2018 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30409806
14.
Heart rate variability derived from exercise ECG in the detection of coronary artery disease.
Physiol Meas
; 28(10): 1189-200, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17906387
15.
Gendered use of experts in the media: Analysis of the gender gap in Finnish news journalism.
Public Underst Sci
; 26(3): 355-368, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26740547
16.
The p22phox C242T gene polymorphism is associated with a reduced risk of angiographically verified coronary artery disease in a high-risk Finnish Caucasian population. The Finnish Cardiovascular Study.
Am Heart J
; 152(3): 538-42, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16923427
17.
The Finnish Cardiovascular Study (FINCAVAS): characterising patients with high risk of cardiovascular morbidity and mortality.
BMC Cardiovasc Disord
; 6: 9, 2006 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-16515696
18.
Vascular endothelial growth factor-D expression in human atherosclerotic lesions.
Cardiovasc Res
; 59(4): 971-9, 2003 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-14553837
19.
Changes in gene expression in atherosclerotic plaques analyzed using DNA array.
Atherosclerosis
; 165(1): 23-32, 2002 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-12208467
20.
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population.
Ann Med
; 45(1): 85-90, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22462493