Detalhe da pesquisa
1.
DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.
Clin Genet
; 105(2): 185-189, 2024 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37904629
2.
OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis.
RNA
; 25(6): 657-668, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30819774
3.
Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis.
Eur Heart J Suppl
; 22(Suppl C): C34-C45, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-32368197
4.
FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
Clin Genet
; 96(4): 317-329, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31245841
5.
Whole-Blood miRNA Sequencing Profiling for Vasospasm in Patients With Aneurysmal Subarachnoid Hemorrhage.
Stroke
; 49(9): 2220-2223, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30354977
6.
Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes.
Nephrol Dial Transplant
; 33(12): 2201-2207, 2018 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361146
7.
Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.
PLoS Genet
; 7(12): e1002367, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22144904
8.
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
Eur Heart J
; 32(9): 1065-76, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21459883
9.
Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians.
Mol Biol Rep
; 38(1): 495-501, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20376705
10.
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.
Genet Epidemiol
; 33(3): 237-46, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18979498
11.
Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population.
J Thromb Thrombolysis
; 29(1): 114-8, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19373437
12.
Changes in circulating miRNA19a-3p precede insulin resistance programmed by intra-uterine growth retardation in mice.
Mol Metab
; 42: 101083, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32956848
13.
Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells.
Sci Rep
; 10(1): 11404, 2020 07 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32647159
14.
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.
PLoS One
; 15(2): e0229472, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32059048
15.
P-selectin gene polymorphisms and risk of coronary heart disease among Tunisians.
J Thromb Thrombolysis
; 28(3): 314-9, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19082691
16.
Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage.
J Neurosurg
; : 1-5, 2019 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31783362
17.
Genetic susceptibilities in the association between maternal exposure to tobacco smoke and the risk of nonsyndromic oral cleft.
Am J Med Genet A
; 146A(18): 2396-406, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18698632
18.
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.
J Mol Med (Berl)
; 85(11): 1271-80, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17634906
19.
Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.
Sci Rep
; 7(1): 11207, 2017 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28894120
20.
Fibrogenic Potential of PW1/Peg3 Expressing Cardiac Stem Cells.
J Am Coll Cardiol
; 70(6): 728-741, 2017 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28774379