| A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance E van Rooij, D Quiat, BA Johnson, LB Sutherland, X Qi, JA Richardson, ... Developmental cell 17 (5), 662-673, 2009 | 1127 | 2009 |
| MicroRNAs in cardiovascular disease: from pathogenesis to prevention and treatment D Quiat, EN Olson The Journal of clinical investigation 123 (1), 11-18, 2013 | 326 | 2013 |
| Concerted regulation of myofiber-specific gene expression and muscle performance by the transcriptional repressor Sox6 D Quiat, KA Voelker, J Pei, NV Grishin, RW Grange, R Bassel-Duby, ... Proceedings of the National Academy of Sciences 108 (25), 10196-10201, 2011 | 169 | 2011 |
| Genomic frontiers in congenital heart disease SU Morton, D Quiat, JG Seidman, CE Seidman Nature Reviews Cardiology 19 (1), 26-42, 2022 | 135 | 2022 |
| Association of damaging variants in genes with increased cancer risk among patients with congenital heart disease SU Morton, A Shimamura, PE Newburger, AR Opotowsky, D Quiat, ... JAMA cardiology 6 (4), 457-462, 2021 | 40 | 2021 |
| Retrospective analysis of clinical genetic testing in pediatric primary dilated cardiomyopathy: testing outcomes and the effects of variant reclassification D Quiat, L Witkowski, H Zouk, KP Daly, AE Roberts Journal of the American Heart Association 9 (11), e016195, 2020 | 36 | 2020 |
| Discordant clinical features of identical hypertrophic cardiomyopathy twins GG Repetti, Y Kim, AC Pereira, J Ingles, MW Russell, NK Lakdawala, ... Proceedings of the National Academy of Sciences 118 (10), e2021717118, 2021 | 30 | 2021 |
| High-throughput screening of Kawasaki disease sera for antiviral antibodies D Quiat, T Kula, C Shimizu, JT Kanegaye, AH Tremoulet, Z Pitkowsky, ... The Journal of Infectious Diseases 222 (11), 1853-1857, 2020 | 15 | 2020 |
| Genome-wide de novo variants in congenital heart disease are not associated with maternal diabetes or obesity SU Morton, AC Pereira, D Quiat, F Richter, A Kitaygorodsky, J Hagen, ... Circulation: Genomic and Precision Medicine 15 (2), e003500, 2022 | 12 | 2022 |
| Damaging variants in FOXI3 cause microtia and craniofacial microsomia D Quiat, AT Timberlake, JJ Curran, ML Cunningham, B McDonough, ... Genetics in Medicine 25 (1), 143-150, 2023 | 10 | 2023 |
| Population prevalence of premature truncating variants in plakophilin-2 and association with arrhythmogenic right ventricular cardiomyopathy: a UK Biobank analysis RJ Hylind, AC Pereira, D Quiat, SF Chandler, TM Roston, WT Pu, ... Circulation: Genomic and Precision Medicine 15 (3), e003507, 2022 | 10 | 2022 |
| An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populations D Quiat, SW Kim, Q Zhang, SU Morton, AC Pereira, SR DePalma, ... Proceedings of the National Academy of Sciences 119 (21), e2203928119, 2022 | 6 | 2022 |
| Neither cardiac mitochondrial DNA variation nor copy number contribute to congenital heart disease risk JAL Willcox, JT Geiger, SU Morton, D McKean, D Quiat, JM Gorham, ... The American Journal of Human Genetics 109 (5), 961-966, 2022 | 4 | 2022 |
| Micro-rna regulation in ischemia and ischemia-reperfusion injury EN Olson, E Van Rooij, D Quiat US Patent App. 13/516,189, 2013 | 4 | 2013 |
| Left ventricular outflow tract gradient is associated with coronary artery obstruction in children with Williams-Beuren syndrome AYJ Tan, D Quiat, SJ Ghelani, K Yuki Journal of cardiothoracic and vascular anesthesia 35 (12), 3677-3680, 2021 | 2 | 2021 |
| Cardiomyopathies JC Garbern, D Quiat Nadas' Pediatric Cardiology, 592-606, 2025 | 1 | 2025 |
| Unbiased Screening of Kawasaki Disease Sera for Viral Antigen Exposure D Quiat, T Kula, C Shimizu, JT Kanegaye, AH Tremoulet, Z Pitkowsky, ... Open Forum Infectious Diseases 4 (Suppl 1), S684, 2017 | 1 | 2017 |
| Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes DM McKean, Q Zhang, P Narayan, SU Morton, V Strohmenger, VT Tang, ... The Journal of Clinical Investigation 134 (11), 2024 | | 2024 |
| Longitudinal Distance of Mitral Annular Disjunction by CMR Is Associated with Risk for Arrhythmia and Death in Children with Connective Tissue Disorder D Castellanos, S Barfuss, DBH Isabel, BAI DiBiasio-Hudson, G Lee, ... Journal of Cardiovascular Magnetic Resonance 26, 2024 | | 2024 |
| Genetic diagnosis of facioscapulohumeral muscular dystrophy type 1 using rare-variant linkage analysis and long-read genome sequencing K Li, D Quiat, F She, Y Liu, R He, A Haghighi, F Liu, R Zhang, ... Genetics in Medicine Open 2, 101817, 2024 | | 2024 |
