Zeitschriftenartikel (90)
Zeitschriftenartikel
115 (51), S. 13021 - 13026 (2018)
Mutation in LBX1/Lbx1 precludes transcription factor cooperativity and causes congenital hypoventilation in humans and mice. Proceedings of the National Academy of Sciences of the United States of America
Zeitschriftenartikel
34 (6), S. 996 - 1011 (2018)
Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell
Zeitschriftenartikel
23 (6), S. 900 - 904 (2018)
Esrrb Unlocks Silenced Enhancers for Reprogramming to Naive Pluripotency - Correction. Cell Stem Cell
Zeitschriftenartikel
25 (10), e7, S. 2676 - 2688 (2018)
tRNA Translocation by the Eukaryotic 80S Ribosome and the Impact of GTP Hydrolysis. Cell Reports
Zeitschriftenartikel
177 (8), S. 691 - 699 (2018)
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Am J Med Genet B Neuropsychiatr Genet
Zeitschriftenartikel
33, S. 20 - 24 (2018)
Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. Stem Cell Research
Zeitschriftenartikel
210 (4), S. 1527 - 1542 (2018)
Identification of two novel candidate genes for insulin secretion by comparative genomics of multiple backcross populations. Genetics
Zeitschriftenartikel
33, S. 120 - 124 (2018)
Generation of two human isogenic iPSC lines from fetal dermal fibroblasts. Stem Cell Research
Zeitschriftenartikel
7, e40757 (2018)
Targets and genomic constraints of ectopic Dnmt3b expression. eLife
Zeitschriftenartikel
145 (22), pii: dev168617 (2018)
Comparative genomic analysis of embryonic, lineage-converted and stem cell-derived motor neurons. Development
Zeitschriftenartikel
563 (7731), S. 325 (2018)
Paying PIs from grants blocks talent and diversity. Nature
Zeitschriftenartikel
16 (1), 138 (2018)
Classifying human promoters by occupancy patterns identifies recurring sequence elements, combinatorial binding, and spatial interactions. BMC Biology
Zeitschriftenartikel
14 (11), e1007793 (2018)
Synthetic STARR-seq reveals how DNA shape and sequence modulate transcriptional output and noise. PLoS Genetics
Zeitschriftenartikel
10 (466), eaau7137 (2018)
Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand. Science Translational Medicine
Zeitschriftenartikel
20, S. 1481 - 1482 (2018)
Response to Peron et al. GENETICS IN MEDICINE
Zeitschriftenartikel
103 (5), S. 512 - 521 (2018)
Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis. Calcified Tissue International
Zeitschriftenartikel
9, 9:484 (2018)
Network and Pathway Analysis of Toxicogenomics Data. Frontiers in Genetics
Zeitschriftenartikel
8 (1), 14611 (2018)
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation. Scientific Reports
Zeitschriftenartikel
50 (10), S. 1442 - 1451 (2018)
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature Genetics
Zeitschriftenartikel
50 (10), S. 1463 - 1473 (2018)
Dynamic 3D chromatin architecture determines enhancer specificity and morphogenetic identity in limb development. Nature Genetics