Detalhe da pesquisa
1.
The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy.
Circ Res
; 128(10): 1514-1532, 2021 05 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33983834
2.
Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
JAMA
; 330(5): 432-441, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37526719
3.
Genetic and functional analyses of ZIC3 variants in congenital heart disease.
Hum Mutat
; 35(1): 66-75, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24123890
4.
Return of genetic results in the familial dilated cardiomyopathy research project.
J Genet Couns
; 22(2): 164-74, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22886719
5.
Maternal smoking at first prenatal visit as a marker of risk for adverse pregnancy outcomes in the Qikiqtaaluk (Baffin) Region.
Rural Remote Health
; 10(3): 1484, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20818840
6.
SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy.
Circ Genom Precis Med
; 13(4): e002892, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603605
7.
Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain.
Am J Med Genet A
; 164A(7): 1860-2, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24700809
8.
Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations.
Congest Heart Fail
; 14(2): 97-105, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18401220
9.
Family history: an essential tool for cardiovascular genetic medicine.
Congest Heart Fail
; 14(1): 37-45, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18256568
10.
Transcriptomics and Beyond in Dilated Cardiomyopathy.
JACC Basic Transl Sci
; 8(4): 419-421, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37138804
11.
Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees.
Circ Genom Precis Med
; 11(7): e002038, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30012837
12.
Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects.
Philos Trans R Soc Lond B Biol Sci
; 371(1710)2016 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-27821535
13.
Genetics and genetic testing in congenital heart disease.
Clin Perinatol
; 42(2): 373-93, ix, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26042910
14.
The family history as a tool to identify patients at risk for dilated cardiomyopathy.
Prog Cardiovasc Nurs
; 23(1): 41-4, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18326985
15.
Is Left Ventricular Noncompaction a Trait, Phenotype, or Disease? The Evidence Points to Phenotype.
Circ Cardiovasc Genet
; 10(6)2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29212902
16.
Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
Circ Cardiovasc Genet
; 3(1): 6-14, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20160190
17.
Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Circ Heart Fail
; 2(3): 253-61, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19808347
18.
Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
Circ Cardiovasc Genet
; 2(4): 306-13, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20031601