Detalhe da pesquisa
1.
Loss of epigenetic information as a cause of mammalian aging.
Cell
; 186(2): 305-326.e27, 2023 01 19.
Artigo
Inglês
| MEDLINE | ID: mdl-36638792
2.
Transcription factor protein interactomes reveal genetic determinants in heart disease.
Cell
; 185(5): 794-814.e30, 2022 03 03.
Artigo
Inglês
| MEDLINE | ID: mdl-35182466
3.
Loss of epigenetic information as a cause of mammalian aging.
Cell
; 187(5): 1312-1313, 2024 Feb 29.
Artigo
Inglês
| MEDLINE | ID: mdl-38428398
4.
Bedside Back to Bench: Building Bridges between Basic and Clinical Genomic Research.
Cell
; 169(1): 6-12, 2017 03 23.
Artigo
Inglês
| MEDLINE | ID: mdl-28340351
5.
Macrophages Facilitate Electrical Conduction in the Heart.
Cell
; 169(3): 510-522.e20, 2017 04 20.
Artigo
Inglês
| MEDLINE | ID: mdl-28431249
6.
A Tension-Based Model Distinguishes Hypertrophic versus Dilated Cardiomyopathy.
Cell
; 165(5): 1147-1159, 2016 May 19.
Artigo
Inglês
| MEDLINE | ID: mdl-27114035
7.
CHD4 and SMYD1 repress common transcriptional programs in the developing heart.
Development
; 151(8)2024 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-38619323
8.
The H2Bub1-deposition complex is required for human and mouse cardiogenesis.
Development
; 150(23)2023 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38038666
9.
Molecular and Spatial Signatures of Mouse Embryonic Endothelial Cells at Single-Cell Resolution.
Circ Res
; 134(5): 529-546, 2024 03.
Artigo
Inglês
| MEDLINE | ID: mdl-38348657
10.
Complement genes contribute sex-biased vulnerability in diverse disorders.
Nature
; 582(7813): 577-581, 2020 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32499649
11.
Cells of the adult human heart.
Nature
; 588(7838): 466-472, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32971526
12.
Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk.
Am J Hum Genet
; 109(5): 961-966, 2022 05 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35397206
13.
Missense Mutation in Human CHD4 Causes Ventricular Noncompaction by Repressing ADAMTS1.
Circ Res
; 133(1): 48-67, 2023 06 23.
Artigo
Inglês
| MEDLINE | ID: mdl-37254794
14.
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations.
Proc Natl Acad Sci U S A
; 119(21): e2203928119, 2022 05 24.
Artigo
Inglês
| MEDLINE | ID: mdl-35584116
15.
Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model.
Proc Natl Acad Sci U S A
; 119(28): e2204174119, 2022 07 12.
Artigo
Inglês
| MEDLINE | ID: mdl-35787042
16.
Discordant clinical features of identical hypertrophic cardiomyopathy twins.
Proc Natl Acad Sci U S A
; 118(10)2021 03 09.
Artigo
Inglês
| MEDLINE | ID: mdl-33658374
17.
Pathogenesis of Cardiomyopathy Caused by Variants in ALPK3, an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere.
Circulation
; 146(22): 1674-1693, 2022 11 29.
Artigo
Inglês
| MEDLINE | ID: mdl-36321451
18.
Damaging variants in FOXI3 cause microtia and craniofacial microsomia.
Genet Med
; 25(1): 143-150, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36260083
19.
Filamin C Cardiomyopathy Variants Cause Protein and Lysosome Accumulation.
Circ Res
; 129(7): 751-766, 2021 09 17.
Artigo
Inglês
| MEDLINE | ID: mdl-34405687
20.
CalTrack: High-Throughput Automated Calcium Transient Analysis in Cardiomyocytes.
Circ Res
; 129(2): 326-341, 2021 07 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34018815