Detalhe da pesquisa
1.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature
; 627(8003): 347-357, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38374256
2.
Lifeday coverage of oral anticoagulants and one-year relative survival in patients with atrial fibrillation: a population-based study in Estonia.
BMC Cardiovasc Disord
; 23(1): 398, 2023 08 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37568101
3.
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms.
Proc Natl Acad Sci U S A
; 114(3): E327-E336, 2017 01 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28031487
4.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(2): 481-8, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486782
5.
Translating genotype data of 44,000 biobank participants into clinical pharmacogenetic recommendations: challenges and solutions.
Genet Med
; 21(6): 1345-1354, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30327539
6.
Recall by genotype and cascade screening for familial hypercholesterolemia in a population-based biobank from Estonia.
Genet Med
; 21(5): 1173-1180, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30270359
7.
Single base resolution analysis of 5-hydroxymethylcytosine in 188 human genes: implications for hepatic gene expression.
Nucleic Acids Res
; 44(14): 6756-69, 2016 08 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-27131363
8.
RegScan: a GWAS tool for quick estimation of allele effects on continuous traits and their combinations.
Brief Bioinform
; 16(1): 39-44, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24008273
9.
Exome analysis in an Estonian multiplex family with neural tube defects-a case report.
Childs Nerv Syst
; 33(9): 1575-1581, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28721594
10.
Whole-exome sequencing identifies de novo mutation in the COL1A1 gene to underlie the severe osteogenesis imperfecta.
Hum Genomics
; 9: 6, 2015 May 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-25958000
11.
Structured education can improve primary-care management of headache: the first empirical evidence, from a controlled interventional study.
J Headache Pain
; 17: 24, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26969188
12.
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.
Hum Genet
; 134(3): 291-303, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25543204
13.
In-solution hybrid capture of bisulfite-converted DNA for targeted bisulfite sequencing of 174 ADME genes.
Nucleic Acids Res
; 41(6): e72, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23325842
14.
Evidence of inbreeding depression on human height.
PLoS Genet
; 8(7): e1002655, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22829771
15.
Genetic and epigenetic regulation of gene expression in fetal and adult human livers.
BMC Genomics
; 15: 860, 2014 Oct 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25282492
16.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(3): 785, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588453
17.
Preoperative corticosteroid injections are associated with worse long-term outcome of surgical carpal tunnel release.
Acta Orthop
; 85(1): 102-6, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24286569
18.
Genetic determinants of plasma protein levels in the Estonian population.
Sci Rep
; 14(1): 7694, 2024 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38565889
19.
A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations.
medRxiv
; 2024 Mar 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38496537
20.
The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis.
PLoS Med
; 10(6): e1001474, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23824655