Zeitschriftenartikel (90)
41.
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29 (7), S. 1643 - 1651 (2018)
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2. Osteoporosis International 42.
Zeitschriftenartikel
19 (7), S. 453 - 467 (2018)
Structural variation in the 3D genome. Nature Reviews Genetics 43.
Zeitschriftenartikel
6, 70 (2018)
Designing miRNA-Based Synthetic Cell Classifier Circuits Using Answer Set Programming. Frontiers in Bioengineering and Biotechnology 44.
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9 , 9:2386 (2018)
HEPATOKIN1 is a biochemistry-based model of liver metabolism for applications in medicine and pharmacology. Nature Communications 45.
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23 (12), S. 3429 - 3437 (2018)
Transient N-6-Methyladenosine Transcriptome Sequencing Reveals a Regulatory Role of m6A in Splicing Efficiency. Cell Reports 46.
Zeitschriftenartikel
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) 47.
Zeitschriftenartikel
70 (5), e3, S. 881 - 893 (2018)
Structural Visualization of the Formation and Activation of the 50S Ribosomal Subunit during In Vitro Reconstitution. Molecular Cell 48.
Zeitschriftenartikel
20 (6), S. 599 - 607 (2018)
Noncoding copy-number variations are associated with congenital limb malformation. GENETICS IN MEDICINE 49.
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23 (8), S. 2509 - 2523 (2018)
Combining NGN2 Programming with Developmental Patterning Generates Human Excitatory Neurons with NMDAR-Mediated Synaptic Transmission. Cell Reports 50.
Zeitschriftenartikel
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) 51.
Zeitschriftenartikel
9 (1), 1925 (2018)
Assessment of Established Techniques to Determine Developmental and Malignant Potential of Human Pluripotent Stem Cells. Nature Communications 52.
Zeitschriftenartikel
10 (5), S. 1537 - 1550 (2018)
X Chromosome Dosage Influences DNA Methylation Dynamics during Reprogramming to Mouse iPSCs. Stem Cell Reports 53.
Zeitschriftenartikel
50 (5), S. 662 - 667 (2018)
Polymer physics predicts the effects of structural variants on chromatin architecture. Nature Genetics 54.
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8 (5), S. 600 - 615 (2018)
Genomic and Functional Fidelity of Small Cell Lung Cancer Patient-Derived Xenografts. Cancer Discovery 55.
Zeitschriftenartikel
41 (3), S. 533 - 539 (2018)
Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism. Journal of Inherited Metabolic Disease 56.
Zeitschriftenartikel
10, 10:34 (2018)
Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes. Genome Medicine 57.
Zeitschriftenartikel
110 (7), S. 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 58.
Zeitschriftenartikel
173 (3), S. 624 - 633 (2018)
Cancer-Germline Antigen Expression Discriminates Clinical Outcome to CTLA-4 Blockade. Cell 59.
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23 (2), S. 349 - 360 (2018)
Transcriptional Dysregulation of MYC Reveals Common Enhancer-Docking Mechanism. Cell Reports 60.
Zeitschriftenartikel
46 (6), S. 2868 - 2882 (2018)
Genomic dissection of enhancers uncovers principles of combinatorial regulation and dynamic wiring of enhancer-promoter contacts. Nucleic Acids Research (London)