Detalhe da pesquisa
1.
Motivations for (non)participation in population-based health studies among the elderly - comparison of participants and nonparticipants of a prospective study on influenza vaccination.
BMC Med Res Methodol
; 17(1): 18, 2017 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28148221
2.
ImmunoChip study implicates antigen presentation to T cells in narcolepsy.
PLoS Genet
; 9(2): e1003270, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23459209
3.
Predicting sudden cardiac death using common genetic risk variants for coronary artery disease.
Eur Heart J
; 36(26): 1669-75, 2015 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25908775
4.
Polymorphisms related to ORMDL3 are associated with asthma susceptibility, alterations in transcriptional regulation of ORMDL3, and changes in TH2 cytokine levels.
J Allergy Clin Immunol
; 136(4): 893-903.e14, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25930191
5.
[Centralized biobanks: a basis for medical research]. / Zentralisierte Biobanken als Grundlage für die medizinische Forschung.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz
; 59(3): 336-43, 2016 Mar.
Artigo
em Alemão
| MEDLINE | ID: mdl-26830106
6.
A genome-wide expression quantitative trait loci analysis of proprotein convertase subtilisin/kexin enzymes identifies a novel regulatory gene variant for FURIN expression and blood pressure.
Hum Genet
; 134(6): 627-36, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25813623
7.
Rationale, design and objectives of ARegPKD, a European ARPKD registry study.
BMC Nephrol
; 16: 22, 2015 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886171
8.
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Hum Mol Genet
; 21(8): 1897-906, 2012 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22210626
9.
Genome-wide meta-analysis of common variant differences between men and women.
Hum Mol Genet
; 21(21): 4805-15, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22843499
10.
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.
Am J Hum Genet
; 88(5): 664-73, 2011 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21565293
11.
A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease.
Am J Hum Genet
; 89(1): 168-75, 2011 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21763483
12.
Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height.
Am J Hum Genet
; 88(1): 6-18, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21194676
13.
Wnt signaling and Dupuytren's disease.
N Engl J Med
; 365(4): 307-17, 2011 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-21732829
14.
Effects of Repeated Freeze and Thaw Cycles on the Genome-Wide DNA Methylation Profile of Isolated Genomic DNA.
Biopreserv Biobank
; 22(2): 110-114, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37074140
15.
Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils.
Am J Respir Cell Mol Biol
; 48(1): 71-7, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23043087
16.
PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.
Genet Epidemiol
; 36(3): 244-52, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22714936
17.
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.
Hum Mol Genet
; 20(6): 1241-51, 2011 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21216879
18.
Umbilical cord PUFA are determined by maternal and child fatty acid desaturase (FADS) genetic variants in the Avon Longitudinal Study of Parents and Children (ALSPAC).
Br J Nutr
; 109(7): 1196-210, 2013 Apr 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22877655
19.
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy.
PLoS Genet
; 6(10): e1001167, 2010 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20975947
20.
The Changing Epidemiology of Viral Hepatitis in a Post-Soviet Country-The Case of Kyrgyzstan.
Pathogens
; 12(8)2023 Jul 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37623949