Silke R. Sperling
Silke R. Sperling
Professor for Cardiovascular Genetics, Charité - University Medicine Berlin
Verified email at
Cited by
Cited by
The transcriptional landscape of the mammalian genome
P Carninci, T Kasukawa, S Katayama, J Gough, MC Frith, N Maeda, ...
science 309 (5740), 1559-1563, 2005
Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene
K Handschug, S Sperling, SJK Yoon, S Hennig, AJL Clark, A Huebner
Human Molecular Genetics 10 (3), 283-290, 2001
Regulation of muscle development by DPF3, a novel histone acetylation and methylation reader of the BAF chromatin remodeling complex
M Lange, B Kaynak, UB Forster, M Tönjes, JJ Fischer, C Grimm, ...
Genes & development 22 (17), 2370-2384, 2008
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
Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly
AV Postma, K Van Engelen, J Van De Meerakker, T Rahman, S Probst, ...
Circulation: Cardiovascular Genetics 4 (1), 43-50, 2011
Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology—a position statement of the development, anatomy, and pathology ESC Working Group
JM Pérez-Pomares, JL de La Pompa, D Franco, D Henderson, SY Ho, ...
Cardiovascular research 109 (2), 204-216, 2016
Identification and functional analysis of CITED2 mutations in patients with congenital heart defects
S Sperling, CH Grimm, I Dunkel, S Mebus, HP Sperling, A Ebner, R Galli, ...
Human mutation 26 (6), 575-582, 2005
The effect of micrococcal nuclease digestion on nucleosome positioning data
HR Chung, I Dunkel, F Heise, C Linke, S Krobitsch, ...
PloS one 5 (12), e15754, 2010
Genome-wide array analysis of normal and malformed human hearts
B Kaynak, A von Heydebreck, S Mebus, D Seelow, S Hennig, J Vogel, ...
Circulation 107 (19), 2467-2474, 2003
Identification of Y-box binding protein 1 as a core regulator of MEK/ERK pathway-dependent gene signatures in colorectal cancer cells
K Jürchott, RJ Kuban, T Krech, N Blüthgen, U Stein, W Walther, C Friese, ...
PLoS genetics 6 (12), e1001231, 2010
Combinatorial effects of four histone modifications in transcription and differentiation
JJ Fischer, J Toedling, T Krueger, M Schueler, W Huber, S Sperling
Genomics 91 (1), 41-51, 2008
Genomic organization of transcriptomes in mammals: Coregulation and cofunctionality
A Purmann, J Toedling, M Schueler, P Carninci, H Lehrach, ...
Genomics 89 (5), 580-587, 2007
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
CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities
RB Jehuda, B Eisen, Y Shemer, LN Mekies, A Szantai, I Reiter, H Cui, ...
Heart Rhythm 15 (2), 267-276, 2018
Characterization of TBX20 in human hearts and its regulation by TFAP2
S Hammer, M Toenjes, M Lange, JJ Fischer, I Dunkel, S Mebus, ...
Journal of cellular biochemistry 104 (3), 1022-1033, 2008
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
Systems biology approaches to heart development and congenital heart disease
SR Sperling
Cardiovascular research 91 (2), 269-278, 2011
MicroRazerS: rapid alignment of small RNA reads
AK Emde, M Grunert, D Weese, K Reinert, SR Sperling
Bioinformatics 26 (1), 123-124, 2010
Novel mutations in the sarcomeric protein myopalladin in patients with dilated cardiomyopathy
T Meyer, V Ruppert, S Ackermann, A Richter, A Perrot, SR Sperling, ...
European Journal of Human Genetics 21 (3), 294-300, 2013
Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7
K van Engelen, AV Postma, JBA Van De Meerakker, JW Roos-Hesselink, ...
Netherlands Heart Journal 21, 113-117, 2013
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