Detalhe da pesquisa
1.
Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease.
Cell
; 153(3): 707-20, 2013 Apr 25.
Artigo
Inglês
| MEDLINE | ID: mdl-23622250
2.
Proteomic associations with forced expiratory volume: a Mendelian randomisation study.
Respir Res
; 25(1): 44, 2024 Jan 18.
Artigo
Inglês
| MEDLINE | ID: mdl-38238732
3.
A proteomic analysis of atrial fibrillation in a prospective longitudinal cohort (AGES-Reykjavik study).
Europace
; 25(11)2023 11 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37967346
4.
The Proteomic Profile of Interstitial Lung Abnormalities.
Am J Respir Crit Care Med
; 206(3): 337-346, 2022 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35438610
5.
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature
; 533(7604): 539-42, 2016 05 26.
Artigo
Inglês
| MEDLINE | ID: mdl-27225129
6.
Molecular screening of familial hypercholesterolemia in Icelanders.
Scand J Clin Lab Invest
; 80(6): 508-514, 2020 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-32706999
7.
Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.
PLoS Genet
; 12(10): e1006327, 2016 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-27764101
8.
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.
Proc Natl Acad Sci U S A
; 111(38): 13790-4, 2014 Sep 23.
Artigo
Inglês
| MEDLINE | ID: mdl-25201988
9.
PLD3 variants in population studies.
Nature
; 520(7545): E2-3, 2015 Apr 02.
Artigo
Inglês
| MEDLINE | ID: mdl-25832410
10.
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution.
Nat Genet
; 39(2): 218-25, 2007 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17206141
11.
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
Nat Genet
; 39(6): 770-5, 2007 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-17460697
12.
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
Am J Hum Genet
; 91(1): 152-62, 2012 Jul 13.
Artigo
Inglês
| MEDLINE | ID: mdl-22703881
13.
Common dysregulation network in the human prefrontal cortex underlies two neurodegenerative diseases.
Mol Syst Biol
; 10: 743, 2014 Jul 30.
Artigo
Inglês
| MEDLINE | ID: mdl-25080494
14.
Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.
PLoS Genet
; 8(5): e1002705, 2012.
Artigo
Inglês
| MEDLINE | ID: mdl-22589742
15.
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.
Nat Genet
; 38(3): 320-3, 2006 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-16415884
16.
Synthesis of 53 tissue and cell line expression QTL datasets reveals master eQTLs.
BMC Genomics
; 15: 532, 2014 Jun 27.
Artigo
Inglês
| MEDLINE | ID: mdl-24973796
17.
Variations in DNA elucidate molecular networks that cause disease.
Nature
; 452(7186): 429-35, 2008 Mar 27.
Artigo
Inglês
| MEDLINE | ID: mdl-18344982
18.
Genetics of gene expression and its effect on disease.
Nature
; 452(7186): 423-8, 2008 Mar 27.
Artigo
Inglês
| MEDLINE | ID: mdl-18344981
19.
Proteomic prediction of incident heart failure and its main subtypes.
Eur J Heart Fail
; 26(1): 87-102, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-37936531
20.
Serum proteomics reveals APOE dependent and independent protein signatures in Alzheimer's disease.
Res Sq
; 2024 Jan 09.
Artigo
Inglês
| MEDLINE | ID: mdl-38260284