| The cardiac transcription network modulated by Gata4, Mef2a, Nkx2. 5, Srf, histone modifications, and microRNAs J Schlesinger, M Schueler, M Grunert, JJ Fischer, Q Zhang, T Krueger, ... PLoS genetics 7 (2), e1001313, 2011 | 256 | 2011 |
| Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseases M Grunert, C Dorn, H Cui, I Dunkel, K Schulz, S Schoenhals, W Sun, ... Cardiovascular research 112 (1), 464-477, 2016 | 76 | 2016 |
| Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot M Grunert, C Dorn, M Schueler, I Dunkel, J Schlesinger, S Mebus, ... Human molecular genetics 23 (12), 3115-3128, 2014 | 60 | 2014 |
| MicroRazerS: rapid alignment of small RNA reads AK Emde, M Grunert, D Weese, K Reinert, SR Sperling Bioinformatics 26 (1), 123-124, 2010 | 50 | 2010 |
| Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart E Auxerre-Plantié, T Nielsen, M Grunert, O Olejniczak, A Perrot, C Özcelik, ... Disease models & mechanisms 13 (12), dmm045377, 2020 | 32 | 2020 |
| Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot V Bansal, C Dorn, M Grunert, S Klaassen, R Hetzer, F Berger, ... PloS one 9 (1), e85375, 2014 | 31 | 2014 |
| Altered microRNA and target gene expression related to Tetralogy of Fallot M Grunert, S Appelt, I Dunkel, F Berger, SR Sperling Scientific reports 9 (1), 19063, 2019 | 24 | 2019 |
| Application of high-throughput sequencing for studying genomic variations in congenital heart disease C Dorn, M Grunert, SR Sperling Briefings in functional genomics 13 (1), 51-65, 2014 | 24 | 2014 |
| Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiation M Grunert, S Appelt, S Schönhals, K Mika, H Cui, A Cooper, L Cyganek, ... Scientific Reports 10 (1), 10921, 2020 | 14 | 2020 |
| Muscle-relevant genes marked by stable H3K4me2/3 profiles and enriched MyoD binding during myogenic differentiation H Cui, V Bansal, M Grunert, B Malecova, A Dall'Agnese, L Latella, S Gatto, ... PloS one 12 (6), e0179464, 2017 | 14 | 2017 |
| The needle in the haystack—Searching for genetic and epigenetic differences in monozygotic twins discordant for tetralogy of fallot M Grunert, S Appelt, P Grossfeld, SR Sperling Journal of Cardiovascular Development and Disease 7 (4), 55, 2020 | 12 | 2020 |
| Cardiac transcription factors and regulatory networks M Grunert, C Dorn, S Rickert-Sperling Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2016 | 9 | 2016 |
| Technologies to study genetics and molecular pathways C Dorn, M Grunert, A Dopazo, F Sánchez-Cabo, A Gatto, J Vázquez, ... Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2016 | 2 | 2016 |
| Complex network interactions: cardiovascular systems biology M Grunert, A Perrot, S Rickert-Sperling The ESC Textbook of Cardiovascular Development, 343, 2018 | 1 | 2018 |
| Computational analysis of next-generation sequencing data in cardiac function and disease M Grunert | 1 | 2012 |
| Cardiac Transcription Factors and Regulatory Networks M Grunert, C Dorn, S Rickert-Sperling Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2024 | | 2024 |
| Human Genetics of Tetralogy of Fallot and Double-Outlet Right Ventricle C Dorn, A Perrot, M Grunert, S Rickert-Sperling Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2024 | | 2024 |
| Technologies to Study Genetics and Molecular Pathways M Grunert, C Dorn, A Dopazo, F Sánchez-Cabo, J Vázquez, ... Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2024 | | 2024 |
| Altered microRNA and target gene expression related to Tetralogy of Fallot M Grunert, S Appelt, S Rickert-Sperling EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 264-264, 2020 | | 2020 |
| Identification ofMYOM2as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot and its functional evaluation in theDrosophilaheart E Auxerre-Plantié, T Nielsen, M Grunert, O Olejniczak, A Perrot, C Özcelik, ... | | 2020 |
