Journal Article (87)
Journal Article
26 (5), pp. 350 - 360 (2019)
A symmetric toggle switch explains the onset of random X inactivation in different mammals. Nature Structural and Molecular Biology
Journal Article
14 (4), e0215618 (2019)
VarWatch-A stand-alone software tool for variant matching. PLoS One
Journal Article
10 (1), 1874 (2019)
Corrupted coordination of epigenetic modifications leads to diverging chromatin states and transcriptional heterogeneity in CLL. Nature Communications
Journal Article
47 (6), pp. 2981 - 2995 (2019)
Significant abundance of cis configurations of coding variants in diploid human genomes. Nucleic Acids Research
Journal Article
74 (1), pp. 143 - 157 (2019)
Structural Basis for the Action of an All-Purpose Transcription Anti-termination Factor. Molecular Cell
Journal Article
20 (1), 164 (2019)
Data and knowledge management in translational research: implementation of the eTRIKS platform for the IMI OncoTrack consortium. BMC Bioinformatics
Journal Article
33 (7-8), pp. 452 - 465 (2019)
The NSL complex-mediated nucleosome landscape is required to maintain transcription fidelity and suppression of transcription noise. Genes and Development
Journal Article
13, pp. 1 - 8 (2019)
eDetect: A Fast Error Detection and Correction Tool for Live Cell Imaging Data Analysis. iScience
Journal Article
20 (1), 157 (2019)
Predicting enhancers in mammalian genomes using supervised hidden Markov models. BMC Bioinformatics
Journal Article
35 (6), pp. 1009 - 1017 (2019)
The Distance Precision Matrix: computing networks from non-linear relationships. Bioinformatics
Journal Article
9 (9), 4641 (2019)
DMSO induces drastic changes in human cellular processes and epigenetic landscape in vitro. Scientific Reports
Journal Article
2 (2), e201800283 (2019)
Expanding the repertoire of glucocorticoid receptor target genes by engineering genomic response elements. Life Science Alliance
Journal Article
12, Article 60 (2019)
Mutation p.R356Q in the Collybistin Phosphoinositide Binding Site Is Associated With Mild Intellectual Disability. Frontiers in Molecular Neuroscience
Journal Article
4, 50 (2019)
Variant calling on the GRCh38 assembly with the data from phase three of the 1000 Genomes Project. Wellcome Open Research (open access publishing platform)
Journal Article
21 (2), pp. 198 - 213 (2019)
Combined Targeted Re-Sequencing of Cytosine DNA Methylation and Mutations of DNA Repair Genes with Potential Use for PARP1 Inhibitor Sensitivity Testing. The Journal of Molecular Diagnostics
Journal Article
39 (3), pp. 540 - 556 (2019)
Genetic determinants of steatosis and fibrosis progression in paediatric non‐alcoholic fatty liver disease. Liver International
Journal Article
21 (3), pp. 305 - 310 (2019)
Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations. Nature Cell Biology
Journal Article
15 (2), e1007964 (2019)
Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype. PLOS Genetics
Journal Article
12, pp. 27 - 40 (2019)
Tissue-Specific Chk1 Activation Determines Apoptosis by Regulating the Balance of p53 and p21. iScience
Journal Article
28 (4), pp. 598 - 614 (2019)
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation. Human Molecular Genetics