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Marcel Grunert
Marcel Grunert
Cardiovascular Genetics, ECRC, Charité Medical Faculty
Verified email at charite.de
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Cited by
Year
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
2512011
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
752016
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
582014
MicroRazerS: rapid alignment of small RNA reads
AK Emde, M Grunert, D Weese, K Reinert, SR Sperling
Bioinformatics 26 (1), 123-124, 2010
522010
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
302020
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
302014
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
242014
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
212019
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
132017
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
112020
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
112020
Cardiac transcription factors and regulatory networks
M Grunert, C Dorn, S Rickert-Sperling
Congenital Heart Diseases: The Broken Heart: Clinical Features, Human …, 2016
92016
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
22016
Computational analysis of next-generation sequencing data in cardiac function and disease
M Grunert
12012
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
Complex network interactions: cardiovascular systems biology
M Grunert, A Perrot, S Rickert-Sperling
The ESC Textbook of Cardiovascular Development, 343, 2018
2018
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