Detalhe da pesquisa
1.
A global in vivo Drosophila RNAi screen identifies NOT3 as a conserved regulator of heart function.
Cell
; 141(1): 142-53, 2010 Apr 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-20371351
2.
REduction of THRomboembolic EVents during Ablation using the laserballoon: The RETHREVA registry.
J Cardiovasc Electrophysiol
; 29(3): 365-374, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29315961
3.
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality.
J Am Soc Nephrol
; 28(8): 2311-2321, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28360221
4.
An enhancer polymorphism at the cardiomyocyte intercalated disc protein NOS1AP locus is a major regulator of the QT interval.
Am J Hum Genet
; 94(6): 854-69, 2014 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24857694
5.
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics.
Nat Methods
; 11(8): 868-74, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24952909
6.
Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations.
Pflugers Arch
; 468(8): 1375-87, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287068
7.
SNiPA: an interactive, genetic variant-centered annotation browser.
Bioinformatics
; 31(8): 1334-6, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25431330
8.
Candidate gene variants of the immune system and sudden infant death syndrome.
Int J Legal Med
; 130(4): 1025-1033, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26975745
9.
The cost-effectiveness of UGT1A1 genotyping before colorectal cancer treatment with irinotecan from the perspective of the German statutory health insurance.
Acta Oncol
; 55(3): 318-28, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26098842
10.
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
PLoS Genet
; 8(2): e1002490, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22359512
11.
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet
; 8(8): e1002793, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22876189
12.
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
Eur Heart J
; 35(16): 1069-77, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23853074
13.
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Nat Genet
; 38(6): 644-51, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16648850
14.
SNP prioritization using a Bayesian probability of association.
Genet Epidemiol
; 37(2): 214-21, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23280596
15.
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
Genet Epidemiol
; 37(2): 205-13, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23307621
16.
Genome-wide association studies of the PR interval in African Americans.
PLoS Genet
; 7(2): e1001304, 2011 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21347284
17.
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
PLoS Genet
; 6(8)2010 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-20700443
18.
Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.
BMC Genomics
; 13: 490, 2012 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22988944
19.
Mutations in the mitochondrial thioredoxin reductase gene TXNRD2 cause dilated cardiomyopathy.
Eur Heart J
; 32(9): 1121-33, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21247928
20.
Independent susceptibility markers for atrial fibrillation on chromosome 4q25.
Circulation
; 122(10): 976-84, 2010 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20733104