Sua seleção (0)
Detalhe da pesquisa
1.
Genome-wide associations for birth weight and correlations with adult disease.
Nature;
538(7624): 248-252, 2016 10 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-27680694
2.
The in vivo endothelial cell translatome is highly heterogeneous across vascular beds.
Proc Natl Acad Sci U S A;
116(47): 23618-23624, 2019 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712416
3.
Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease.
Am J Hum Genet;
100(1): 21-30, 2017 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27939641
4.
Spontaneous Coronary Artery Dissection: Current State of the Science: A Scientific Statement From the American Heart Association.
Circulation;
137(19): e523-e557, 2018 May 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29472380
5.
First International Consensus on the diagnosis and management of fibromuscular dysplasia.
Vasc Med;
24(2): 164-189, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30648921
6.
The Association of Intracranial Aneurysms in Women with Renal Artery Aneurysms.
Ann Vasc Surg;
60: 147-155.e2, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31200039
7.
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
PLoS Genet;
12(10): e1006367, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792790
8.
Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE Study.
Am J Hematol;
2018 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29905378
9.
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
Genet Epidemiol;
40(6): 470-4, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229898
10.
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.
Am J Hum Genet;
94(3): 349-60, 2014 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24560520
11.
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.
Am J Hum Genet;
95(1): 49-65, 2014 Jul 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24975945
12.
Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.
Hum Mol Genet;
23(3): 782-95, 2014 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24057673
13.
No large-effect low-frequency coding variation found for myocardial infarction.
Hum Mol Genet;
23(17): 4721-8, 2014 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24728188
14.
Trans-ethnic meta-analysis of white blood cell phenotypes.
Hum Mol Genet;
23(25): 6944-60, 2014 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25096241
15.
Pediatric nonaortic arterial aneurysms.
J Vasc Surg;
63(2): 466-76.e1, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26804218
16.
A variational Bayes discrete mixture test for rare variant association.
Genet Epidemiol;
38(1): 21-30, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24482836
17.
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Hum Mol Genet;
22(8): 1663-78, 2013 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23303523
18.
Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.
Am J Hum Genet;
91(5): 794-808, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103231
19.
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-ß expression and connective tissue features.
FASEB J;
28(8): 3313-24, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24732132
20.
Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies.
Circ Res;
112(2): 318-26, 2013 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-23149595