Zeitschriftenartikel (90)
61.
Zeitschriftenartikel
22 (4), S. 575 - 588 (2018)
A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development. Cell Stem Cell 62.
Zeitschriftenartikel
102 (4), S. 557 - 573 (2018)
Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. American Journal of Human Genetics 63.
Zeitschriftenartikel
22, S. 1 - 16 (2018)
Dissecting the Functional Consequences of De Novo DNA Methylation Dynamics in Human Motor Neuron Differentiation and Physiology. Cell Stem Cell 64.
Zeitschriftenartikel
25 (4), S. 327 - 332 (2018)
Global delay in nascent strand DNA methylation. Nature Structural and Molecular Biology 65.
Zeitschriftenartikel
25 (4), S. 355 (2018)
Author Correction: Global delay in nascent strand DNA methylation. Nature Structural and Molecular Biology 66.
Zeitschriftenartikel
145 (7), dev161208 (2018)
Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors. Development 67.
Zeitschriftenartikel
14 (3), e1007254 (2018)
Large scale variation in the rate of germ-line de novo mutation, base composition, divergence and diversity in humans. PLoS Genetics 68.
Zeitschriftenartikel
9 (1), 1048 (2018)
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors. Nature Communications 69.
Zeitschriftenartikel
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype. Neurogenetics, S. 1 - 11 (2018)
70.
Zeitschriftenartikel
22 (3), S. 369 - 383 (2018)
The Transcriptionally Permissive Chromatin State of Embryonic Stem Cells Is Acutely Tuned to Translational Output. Cell Stem Cell 71.
Zeitschriftenartikel
176 (3), S. 668 - 675 (2018)
Cutis Laxa and Excessive Bone Growth due to de novo mutations in PTDSS1. American Journal of Medical Genetics Part A 72.
Zeitschriftenartikel
9 (1), 9:10 (2018)
X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells. Biology of Sex Differences 73.
Zeitschriftenartikel
7 (2), S. 443 - 451 (2018)
Spatiotemporal Control of TGF-β Signaling with Light. ACS Synthetic Biology 74.
Zeitschriftenartikel
27 (4), S. 589 - 600 (2018)
FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis. Human Molecular Genetics 75.
Zeitschriftenartikel
9, 597 (2018)
Genome-wide tracking of dCas9-methyltransferase footprints. Nature Communications 76.
Zeitschriftenartikel
9 (5), S. 1279 - 1288 (2018)
A modular synthetic route to size-defined immunogenic Haemophilus influenzae b antigens is key to the identification of an octasaccharide lead vaccine candidate. Chemical Science 77.
Zeitschriftenartikel
3 (1), e00219-17 (2018)
Zika Virus Alters DNA Methylation of Neural Genes in an Organoid Model of the Developing Human Brain. mSystems 78.
Zeitschriftenartikel
50 (2), S. 250 - 258 (2018)
Genetic determinants and epigenetic effects of pioneer-factor occupancy. Nature Genetics 79.
Zeitschriftenartikel
23 (2), S. 222 - 230 (2018)
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. Molecular Psychiatry 80.
Zeitschriftenartikel
7 (1), bio.028498 (2018)
A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model. Biology Open