Detalhe da pesquisa
1.
Runs of Homozygosity: Association with Coronary Artery Disease and Gene Expression in Monocytes and Macrophages.
Am J Hum Genet
; 97(2): 228-37, 2015 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26166477
2.
Renal Mechanisms of Association between Fibroblast Growth Factor 1 and Blood Pressure.
J Am Soc Nephrol
; 26(12): 3151-60, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25918036
3.
Male-specific region of the Y chromosome and cardiovascular risk: phylogenetic analysis and gene expression studies.
Arterioscler Thromb Vasc Biol
; 33(7): 1722-7, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23640493
4.
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosome.
Lancet
; 379(9819): 915-922, 2012 Mar 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22325189
5.
Evaluating the clinical effectiveness of the NHS Health Check programme: a prospective analysis in the Genetics and Vascular Health Check (GENVASC) study.
BMJ Open
; 13(5): e068025, 2023 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37253489
6.
Elucidation of the genetic causes of bicuspid aortic valve disease.
Cardiovasc Res
; 119(3): 857-866, 2023 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35727948
7.
Pathway analysis shows association between FGFBP1 and hypertension.
J Am Soc Nephrol
; 22(5): 947-55, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21436287
8.
Contribution of NOTCH1 genetic variants to bicuspid aortic valve and other congenital lesions.
Heart
; 108(14): 1114-1120, 2022 06 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35288444
9.
Novel loss of function mutation in NOTCH1 in a family with bicuspid aortic valve, ventricular septal defect, thoracic aortic aneurysm, and aortic valve stenosis.
Mol Genet Genomic Med
; 8(10): e1437, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32720365
10.
Effects of the coronary artery disease associated LPA and 9p21 loci on risk of aortic valve stenosis.
Int J Cardiol
; 276: 212-217, 2019 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30482443
11.
Systematic Review of Studies That Have Evaluated Screening Tests in Relatives of Patients Affected by Nonsyndromic Thoracic Aortic Disease.
J Am Heart Assoc
; 7(15): e009302, 2018 08 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30371227
12.
Genetic Insights Into Bicuspid Aortic Valve Disease.
Cardiol Rev
; 25(4): 158-164, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28574935
13.
Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease.
PLoS One
; 10(2): e0117684, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25658981
14.
[Persistent left superior vena cava]. / Przetrwala zyla glówna górna lewa.
Kardiol Pol
; 61(12): 581-2, 2004 Dec.
Artigo
em Polonês
| MEDLINE | ID: mdl-15815760
15.
Coronary artery disease predisposing haplogroup I of the Y chromosome, aggression and sex steroids--genetic association analysis.
Atherosclerosis
; 233(1): 160-4, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24529138
16.
Urotensin-II system in genetic control of blood pressure and renal function.
PLoS One
; 8(12): e83137, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24391740
17.
Heritability of early repolarization: a population-based study.
Circ Cardiovasc Genet
; 4(2): 134-8, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21282333
18.
Large-scale candidate gene analysis of HDL particle features.
PLoS One
; 6(1): e14529, 2011 Jan 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21283740
19.
Genetic architecture of ambulatory blood pressure in the general population: insights from cardiovascular gene-centric array.
Hypertension
; 56(6): 1069-76, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21060006