Roselli C, Surakka I, S Olesen M, Sveinbjornsson G, Marston N, Choi S
Nat Genet. 2025; 57(3):539-547.
PMID: 40050429
DOI: 10.1038/s41588-024-02072-3.
Sweat M, Pu W
NPJ Cardiovasc Health. 2025; 1.
PMID: 39867228
PMC: 11759492.
DOI: 10.1038/s44325-024-00035-5.
Leblanc F, Jin X, Kang K, Lee C, Xu J, Xuan L
iScience. 2024; 27(9):110660.
PMID: 39262787
PMC: 11388022.
DOI: 10.1016/j.isci.2024.110660.
Linna-Kuosmanen S, Vuori M, Kiviniemi T, Palmu J, Niiranen T
Eur Heart J Suppl. 2024; 26(Suppl 4):iv33-iv40.
PMID: 39099578
PMC: 11292413.
DOI: 10.1093/eurheartjsupp/suae072.
Goette A, Corradi D, Dobrev D, Aguinaga L, Cabrera J, Chugh S
Europace. 2024; 26(9).
PMID: 39077825
PMC: 11431804.
DOI: 10.1093/europace/euae204.
Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown-Rahman syndrome.
Zebrauskiene D, Sadauskiene E, Dapkunas J, Kairys V, Balciunas J, Konovalovas A
Clin Epigenetics. 2024; 16(1):76.
PMID: 38845031
PMC: 11157947.
DOI: 10.1186/s13148-024-01686-y.
The Long Non-Coding RNA MALAT1 Modulates NR4A1 Expression through a Downstream Regulatory Element in Specific Cancer Cell Types.
Wernig-Zorc S, Schwartz U, Martinez-Rodriguez P, Inalef J, Pavicic F, Ehrenfeld P
Int J Mol Sci. 2024; 25(10.
PMID: 38791553
PMC: 11121914.
DOI: 10.3390/ijms25105515.
Bone morphogenetic protein 10 and atrial fibrillation.
Liu L, Liang Y, Lan Q, Chen J, Wang R, Zhao J
Int J Cardiol Heart Vasc. 2024; 51:101376.
PMID: 38496259
PMC: 10943040.
DOI: 10.1016/j.ijcha.2024.101376.
Atrial fibrillation: pathophysiology, genetic and epigenetic mechanisms.
Vinciguerra M, Dobrev D, Nattel S
Lancet Reg Health Eur. 2024; 37:100785.
PMID: 38362554
PMC: 10866930.
DOI: 10.1016/j.lanepe.2023.100785.
Role of Genetic Variation in Transcriptional Regulatory Elements in Heart Rhythm.
Jonker T, Barnett P, Boink G, Christoffels V
Cells. 2024; 13(1).
PMID: 38201209
PMC: 10777909.
DOI: 10.3390/cells13010004.
The Imageable Genome.
Jane P, Xu X, Taelman V, Jane E, Gariani K, Dumont R
Nat Commun. 2023; 14(1):7329.
PMID: 37957176
PMC: 10643363.
DOI: 10.1038/s41467-023-43123-3.
Multimodal learning of noncoding variant effects using genome sequence and chromatin structure.
Tan W, Shen Y
Bioinformatics. 2023; 39(9).
PMID: 37669132
PMC: 10502240.
DOI: 10.1093/bioinformatics/btad541.
Single-cell genomics improves the discovery of risk variants and genes of atrial fibrillation.
Selewa A, Luo K, Wasney M, Smith L, Sun X, Tang C
Nat Commun. 2023; 14(1):4999.
PMID: 37591828
PMC: 10435551.
DOI: 10.1038/s41467-023-40505-5.
Genome and atrial fibrillation.
Nakano Y
J Arrhythm. 2023; 39(3):303-309.
PMID: 37324776
PMC: 10264727.
DOI: 10.1002/joa3.12847.
Association of bone morphogenetic protein 10 and recurrent atrial fibrillation after catheter ablation.
Hennings E, Aeschbacher S, Coslovsky M, Paladini R, Meyre P, Voellmin G
Europace. 2023; 25(6).
PMID: 37314197
PMC: 10265951.
DOI: 10.1093/europace/euad149.
Multiplatform modeling of atrial fibrillation identifies phospholamban as a central regulator of cardiac rhythm.
Kervadec A, Kezos J, Ni H, Yu M, Marchant J, Spiering S
Dis Model Mech. 2023; 16(7).
PMID: 37293707
PMC: 10387351.
DOI: 10.1242/dmm.049962.
An atrial fibrillation-associated regulatory region modulates cardiac levels and arrhythmia susceptibility.
Bosada F, van Duijvenboden K, Giovou A, Rivaud M, Uhm J, Verkerk A
Elife. 2023; 12.
PMID: 36715501
PMC: 9928424.
DOI: 10.7554/eLife.80317.
Global chromatin landscapes identify candidate noncoding modifiers of cardiac rhythm.
Bhattacharyya S, Kollipara R, Orquera-Tornakian G, Goetsch S, Zhang M, Perry C
J Clin Invest. 2022; 133(3).
PMID: 36454649
PMC: 9888383.
DOI: 10.1172/JCI153635.
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.
Levin M, Tsao N, Singhal P, Liu C, Vy H, Paranjpe I
Nat Commun. 2022; 13(1):6914.
PMID: 36376295
PMC: 9663424.
DOI: 10.1038/s41467-022-34216-6.
The Genetics and Epigenetics of Ventricular Arrhythmias in Patients Without Structural Heart Disease.
Wang M, Tu X
Front Cardiovasc Med. 2022; 9:891399.
PMID: 35783865
PMC: 9240357.
DOI: 10.3389/fcvm.2022.891399.