| Tet inactivation disrupts YY1 binding and long-range chromatin interactions during embryonic heart development S Fang, J Li, Y Xiao, M Lee, L Guo, W Han, T Li, MC Hill, T Hong, W Mo, ... Nature communications 10 (1), 4297, 2019 | 72 | 2019 |
| Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects C Liu, R Cao, Y Xu, T Li, F Li, S Chen, R Xu, K Sun Genome Medicine 10, 1-13, 2018 | 51 | 2018 |
| A combination strategy targeting enhancer plasticity exerts synergistic lethality against BETi-resistant leukemia cells L Guo, J Li, H Zeng, AG Guzman, T Li, M Lee, Y Zhou, MA Goodell, ... Nature communications 11 (1), 740, 2020 | 40 | 2020 |
| Sinus node dysfunction: Current understanding and future directions P Manoj, JA Kim, S Kim, T Li, M Sewani, MG Chelu, N Li American Journal of Physiology-Heart and Circulatory Physiology 324 (3 …, 2023 | 19 | 2023 |
| Copy number variants and exome sequencing analysis in six pairs of Chinese monozygotic twins discordant for congenital heart disease Y Xu, T Li, T Pu, R Cao, F Long, S Chen, K Sun, R Xu Twin Research and Human Genetics 20 (6), 521-532, 2017 | 13 | 2017 |
| Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation X Jiang, T Li, S Liu, Q Fu, F Li, S Chen, K Sun, R Xu, Y Xu Orphanet Journal of Rare Diseases 16, 1-14, 2021 | 12 | 2021 |
| SOX7 suppresses endothelial-to-mesenchymal transitions by enhancing VE-cadherin expression during outflow tract development X Jiang, T Li, B Li, W Wei, F Li, S Chen, R Xu, K Sun Clinical Science 135 (6), 829-846, 2021 | 12 | 2021 |
| Identification and analysis of KLF13 variants in patients with congenital heart disease W Li, B Li, T Li, E Zhang, Q Wang, S Chen, K Sun BMC Medical Genetics 21, 1-8, 2020 | 12 | 2020 |
| Identification of candidate genes for congenital heart defects on proximal chromosome 8p T Li, C Liu, Y Xu, Q Guo, S Chen, K Sun, R Xu Scientific Reports 6 (1), 36133, 2016 | 8 | 2016 |
| LOF variants identifying candidate genes of laterality defects patients with congenital heart disease S Liu, W Wei, P Wang, C Liu, X Jiang, T Li, F Li, Y Wu, S Chen, K Sun, ... PLoS Genetics 18 (12), e1010530, 2022 | 5 | 2022 |
| Genetic and functional analyses detect one pathological NFATC1 mutation in a Chinese tricuspid atresia family. B Li, T Li, T Pu, C Liu, S Chen, K Sun, R Xu Molecular Genetics & Genomic Medicine 9 (9), e1771, 2021 | 3 | 2021 |
| A High-Protein Diet Promotes Atrial Arrhythmogenesis via Absent-in-Melanoma 2 Inflammasome J Song, J Wu, DJ Robichaux, T Li, S Wang, MJ Arredondo Sancristobal, ... Cells 13 (2), 108, 2024 | 2 | 2024 |
| Cardiac conduction diseases: understanding the molecular mechanisms to uncover targets for future treatments T Li, Q Marashly, JA Kim, N Li, MG Chelu Expert Opinion on Therapeutic Targets, 1-16, 2024 | | 2024 |
| PO-01-170 A NOVEL LMNA MUTANT (R225X) LEADS TO CARDIAC CONDUCTION DISORDERS T Li, X Wang, J Song, L Li, Y Yuan, N Li, MG Chelu Heart Rhythm 21 (5), S171-S172, 2024 | | 2024 |
| Moderate cold exposure contributes to the extension of lifespan by alleviating the aggregation of disease-related proteins T Li, Y Yuan Frigid Zone Medicine 3 (3), 129-130, 2023 | | 2023 |
| In Silico Analyses Reveal the Relationship Between ROCK2 Mutations and Laterality Defects P Wang, S Liu, T Li, S Chen, F Li, K Sun, R Xu | | 2022 |
| Tet2 Deficiency in Macrophages Undermines Heart Repair after Infarction S Fang, Y Xiao, J Li, T Li, H Zeng, W Han, Y Zhou, D Sun, JM Martin, ... Blood 132, 2394, 2018 | | 2018 |
