Detalhe da pesquisa
1.
Using implementation science to evaluate a population-wide genomic screening program: Findings from the first 20,000 In Our DNA SC participants.
Am J Hum Genet
; 111(3): 433-444, 2024 Mar 07.
Artigo
Inglês
| MEDLINE | ID: mdl-38307026
2.
Efficacy and Safety of Acoramidis in Transthyretin Amyloid Cardiomyopathy.
N Engl J Med
; 390(2): 132-142, 2024 Jan 11.
Artigo
Inglês
| MEDLINE | ID: mdl-38197816
3.
Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial.
Circulation
; 147(17): 1281-1290, 2023 04 25.
Artigo
Inglês
| MEDLINE | ID: mdl-36938756
4.
Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study.
Circulation
; 148(11): 872-881, 2023 09 12.
Artigo
Inglês
| MEDLINE | ID: mdl-37641966
5.
The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice.
Hum Mol Genet
; 29(21): 3504-3515, 2021 01 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33084860
6.
Impact of Donor Hemodynamics on Recipient Survival in Heart Transplantation.
J Card Fail
; 29(9): 1288-1295, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37230313
7.
Applying the R = MC2 implementation science heuristic to assess the impact of readiness on reach and implementation of a population-wide genomic screening program.
J Genet Couns
; 2023 Sep 21.
Artigo
Inglês
| MEDLINE | ID: mdl-37732417
8.
A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy.
Eur Heart J
; 43(32): e1-e9, 2022 08 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35441664
9.
Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
JAMA
; 330(5): 432-441, 2023 08 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37526719
10.
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
Circulation
; 144(1): 7-19, 2021 07 06.
Artigo
Inglês
| MEDLINE | ID: mdl-33947203
11.
Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy.
Circulation
; 143(19): 1852-1862, 2021 05 11.
Artigo
Inglês
| MEDLINE | ID: mdl-33874732
12.
Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants.
Circulation
; 144(20): 1600-1611, 2021 11 16.
Artigo
Inglês
| MEDLINE | ID: mdl-34587765
13.
Tnni3k alleles influence ventricular mononuclear diploid cardiomyocyte frequency.
PLoS Genet
; 15(10): e1008354, 2019 10.
Artigo
Inglês
| MEDLINE | ID: mdl-31589606
14.
Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.
JAMA
; 327(5): 454-463, 2022 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35103767
15.
Efficacy and Safety of Angiotensin Receptor Blockers in a Pre-Clinical Model of Arrhythmogenic Cardiomyopathy.
Int J Mol Sci
; 23(22)2022 Nov 11.
Artigo
Inglês
| MEDLINE | ID: mdl-36430389
16.
Hypermobile Ehlers-Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes.
Dev Dyn
; 250(3): 318-344, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-32629534
17.
Tafamidis Treatment for Patients with Transthyretin Amyloid Cardiomyopathy.
N Engl J Med
; 379(11): 1007-1016, 2018 Sep 13.
Artigo
Inglês
| MEDLINE | ID: mdl-30145929
18.
Management of heart failure in cardiac amyloidosis using an ambulatory diuresis clinic.
Am Heart J
; 233: 122-131, 2021 03.
Artigo
Inglês
| MEDLINE | ID: mdl-33352187
19.
FLNC truncations cause arrhythmogenic right ventricular cardiomyopathy.
J Med Genet
; 57(4): 254-257, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31924696
20.
Therapeutic Modulation of the Immune Response in Arrhythmogenic Cardiomyopathy.
Circulation
; 140(18): 1491-1505, 2019 10 29.
Artigo
Inglês
| MEDLINE | ID: mdl-31533459