Detalhe da pesquisa
1.
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.
Circulation
; 147(10): 824-840, 2023 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36524479
2.
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
Hum Mol Genet
; 28(11): 1919-1929, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30715372
3.
Coagulation Gene Expression Profiling in Infants With Necrotizing Enterocolitis.
J Pediatr Gastroenterol Nutr
; 63(6): e169-e175, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27050058
4.
The genetics of pro-arrhythmic adverse drug reactions.
Br J Clin Pharmacol
; 77(4): 618-25, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23834499
5.
Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy.
Eur J Med Genet
; 60(9): 485-488, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28642161
6.
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Cardiovasc Res
; 106(3): 520-9, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25691538