Detalhe da pesquisa
1.
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.
Am J Hum Genet;
110(9): 1482-1495, 2023 09 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37652022
2.
Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy.
Eur Heart J;
44(48): 5146-5158, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37431535
3.
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions.
Genet Med;
23(1): 69-79, 2021 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33046849
4.
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies.
Genet Med;
23(5): 856-864, 2021 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33500567
5.
An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy.
Int J Mol Sci;
21(19)2020 Sep 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33003281
6.
New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy.
Circulation;
144(9): 754-757, 2021 08 31.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34460321
7.
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
Nat Cardiovasc Res;
2(11): 1078-1094, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38666070
8.
The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort.
NPJ Genom Med;
5: 46, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33110626
9.
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy.
Genome Med;
11(1): 5, 2019 01 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30696458
10.
NaNog: A pluripotency homeobox (master) molecule.
Glob Cardiol Sci Pract;
2015(3): 36, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26566529
11.
Reprogramming for cardiac regeneration.
Glob Cardiol Sci Pract;
2014(3): 309-29, 2014.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25763379