Journal Article (82)
61.
Journal Article
36 (6), pp. 1794 - 1796 (2016)
Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience 62.
Journal Article
14 (5), pp. 1246 - 1257 (2016)
Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs. Cell Reports 63.
Journal Article
530 (7588), pp. 57 - 62 (2016)
Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature 64.
Journal Article
2016, 15030 (2016)
The metabolic background is a global player in Saccharomyces gene expression epistasis. Nature Microbiology 65.
Journal Article
26 (2), pp. 183 - 191 (2016)
Exome Sequencing and CRISPR/Cas Genome Editing Identify Mutations of ZAK as a Cause of Limb Defects in Humans and Mice. Genome Research 66.
Journal Article
2016, pp. 1 - 8 (2016)
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Famillial Cancer 67.
Journal Article
8, 8:85 (2016)
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience 68.
Journal Article
575 (2 Pt 2), pp. 438 - 451 (2016)
Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 69.
Journal Article
13 (6), pp. 1183 - 1193 (2016)
Time-Dependent Gene Network Modelling by Sequential Monte Carlo. IEEE ACM Transactions on Computational Biology and Bioinformatics 70.
Journal Article
167 (5), e24, pp. 1398 - 1414 (2016)
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Cell 71.
Journal Article
12 (5), e1006022 (2016)
BOD1 Is Required for Cognitive Function in Humans and Drosophila. PLoS Genetics 72.
Journal Article
170 (1), pp. 94 - 102 (2016)
Tentative clinical diagnosis of Lujan-Fryns syndrome-A conglomeration of different genetic entities? American Journal of Medical Genetics Part A 73.
Journal Article
5, e16078 (2016)
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. eLife 74.
Journal Article
12 (12), e1005249 (2016)
Improved Prediction of Non-methylated Islands in Vertebrates Highlights Different Characteristic Sequence Patterns. PLoS Computational Biology 75.
Journal Article
17, 67 (2016)
sciReptor: analysis of single-cell level immunoglobulin repertoires. BMC Bioinformatics 76.
Journal Article
33 (1), pp. 185 - 200 (2016)
Evolution of DNA-Binding Sites of a Floral Master Regulatory Transcription Factor. Molecular Biology and Evolution 77.
Journal Article
89 (1), pp. 120 - 127 (2016)
New insights into Brunner syndrome and potential for targeted therapy. Clinical Genetics: an international journal of genetics in medicine 78.
Journal Article
33 (5), pp. 1231 - 1244 (2016)
Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa). Molecular Biology and Evolution 79.
Journal Article
7, 13784 (2016)
Corrigendum: Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications 80.
Journal Article
7, 12621 (2016)
Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications