Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (116)
61.
Journal Article
38 (12), e00599-17 (2018)
Loss of the hematopoietic stem cell factor GATA2 in the osteogenic lineage impairs trabecularization and mechanical strength of bone. Molecular and Cellular Biology (Washington, DC) 62.
Journal Article
70 (5), e3, pp. 881 - 893 (2018)
Structural Visualization of the Formation and Activation of the 50S Ribosomal Subunit during In Vitro Reconstitution. Molecular Cell 63.
Journal Article
20 (6), pp. 599 - 607 (2018)
Noncoding copy-number variations are associated with congenital limb malformation. GENETICS IN MEDICINE 64.
Journal Article
43 (2), pp. 115 - 124 (2018)
The social mind: Disentangling affective and cognitive routes to understanding others. Interdisciplinary Science Reviews 65.
Journal Article
23 (8), pp. 2509 - 2523 (2018)
Combining NGN2 Programming with Developmental Patterning Generates Human Excitatory Neurons with NMDAR-Mediated Synaptic Transmission. Cell Reports 66.
Journal Article
285 (1878), pii: 20180206 (2018)
Evolution of genomic variation in the burrowing owl in response to recent colonization of urban areas. Proceedings of the Royal Society of London. Series B: Biological Sciences (London) 67.
Journal Article
9 (1), 1925 (2018)
Assessment of Established Techniques to Determine Developmental and Malignant Potential of Human Pluripotent Stem Cells. Nature Communications 68.
Journal Article
10 (5), pp. 1537 - 1550 (2018)
X Chromosome Dosage Influences DNA Methylation Dynamics during Reprogramming to Mouse iPSCs. Stem Cell Reports 69.
Journal Article
50 (5), pp. 662 - 667 (2018)
Polymer physics predicts the effects of structural variants on chromatin architecture. Nature Genetics 70.
Journal Article
8 (5), pp. 600 - 615 (2018)
Genomic and Functional Fidelity of Small Cell Lung Cancer Patient-Derived Xenografts. Cancer Discovery 71.
Journal Article
41 (3), pp. 533 - 539 (2018)
Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism. Journal of Inherited Metabolic Disease 72.
Journal Article
10, 10:34 (2018)
Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes. Genome Medicine 73.
Journal Article
110 (7), pp. 587 - 597 (2018)
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research 74.
Journal Article
173 (3), pp. 624 - 633 (2018)
Cancer-Germline Antigen Expression Discriminates Clinical Outcome to CTLA-4 Blockade. Cell 75.
Journal Article
10, 13 (2018)
Neural correlates of socio-emotional perception in 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders 76.
Journal Article
23 (2), pp. 349 - 360 (2018)
Transcriptional Dysregulation of MYC Reveals Common Enhancer-Docking Mechanism. Cell Reports 77.
Journal Article
46 (6), pp. 2868 - 2882 (2018)
Genomic dissection of enhancers uncovers principles of combinatorial regulation and dynamic wiring of enhancer-promoter contacts. Nucleic Acids Research (London) 78.
Journal Article
22 (4), pp. 575 - 588 (2018)
A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development. Cell Stem Cell 79.
Journal Article
102 (4), pp. 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 80.
Journal Article
22, pp. 1 - 16 (2018)
Dissecting the Functional Consequences of De Novo DNA Methylation Dynamics in Human Motor Neuron Differentiation and Physiology. Cell Stem Cell