Zeitschriftenartikel (90)
1.
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141 (10), S. 1105 - 1118 (2022)
RUNX1 isoform disequilibrium promotes the development of trisomy 21 associated myeloid leukemia. Blood 2.
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10 (12), 3148 (2022)
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models. Biomedicines 3.
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82 (6), S. 1930 - 1952 (2022)
Modularity Maximization for Graphons. SIAM Journal on Applied Mathematics 4.
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29 (12), S. 1277 - 1290 (2022)
A critical period of translational control during brain development at codon resolution. Nature Structural Molecular Biology 5.
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1, S. 1215 - 1229 (2022)
A single-cell comparison of adult and fetal humen epicardium defines the age-associated changes in epicardial activity. Nature Cardiovascular Research 6.
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31 (23), S. 4019 - 4033 (2022)
Comparative genomic analyses of multiple backcross mouse populations suggest SGCG as a novel potential obesity-modifier gene. Human Molecular Genetics 7.
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9 (11), 221131 (2022)
Quantifying the 'end of history' through a Bayesian Markov-chain approach. Royal Society Open Science 8.
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13 (1), S. 279 - 301 (2022)
Image analysis workflows to reveal the spatial organization of cell nuclei and chromosomes. Nucleus 9.
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140 (20), S. 2113 - 2126 (2022)
Deregulation and epigenetic modification of BCL2-family genes cause resistance to venetoclax in hematologic malignancies. Blood 10.
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9, 699 (2022)
Multi-omics HeCaToS dataset of repeated dose toxicity for cardiotoxic & hepatotoxic compounds. Scientific Data 11.
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13, 1030409 (2022)
In silico analysis of alternative splicing events implicated in intracellular trafficking during B-lymphocyte differentiation. Frontiers in Immunology 12.
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13 (1), 6570 (2022)
Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X. Nature Communications 13.
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54, S. 1664 - 1674 (2022)
Molecular map of chronic lymphocytic leukemia and its impact on outcome. Nature Genetics 14.
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191 (1), 107, S. 100 (2022)
A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies. American Journal of Medical Genetics Part A 15.
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13 (1), 6470 (2022)
Integration of Hi-C with short and long-read genome sequencing reveals the structure of germline rearranged genomes. Nature Communications 16.
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Co-option of the transcription factor SALL1 in mole ovotestis formation. bioRxiv, 514220 (2022)
17.
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12 (10), 1549 (2022)
Identification of Universally Applicable and Species-Specific Marker Peptides for Bacillus anthracis. Life 18.
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149 (20), dev200679 (2022)
Hypoxia induces an early primitive streak signature, enhancing spontaneous elongation and lineage representation in gastruloids. Development 19.
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24 (10), S. 1487 - 1498 (2022)
Single-cell atlas of human liver development reveals pathways directing hepatic cell fates. Nature Cell Biology 20.
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185 (20), S. 3689 - 3704 (2022)
Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes. Cell