Publications
The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.
Publications by the Yaspo Lab
Preprints
2019
10, Article 4571, p. 1 (2019)
5-Fluorouracil treatment induces characteristic T>G mutations in human cancer. Nature Communications Published
2025
14 (1), pp. 1 - 7 (2025)
Inhibiting H3K27 Demethylases Downregulates CREB-CREBBP, Overcoming Resistance in Relapsed Acute Lymphoblastic Leukemia. Cancer Medicine 2024
15 (1), Article 9864 (2024)
Base-excision repair pathway shapes 5-methylcytosine deamination signatures in pan-cancer genomes. Nature Communications 262 (11), pp. 3567 - 3575 (2024)
AI-driven discovery of blood xenobiotic biomarkers in neovascular age-related macular degeneration using iterative random forests. Graefe's Archive for Clinical and Experimental Ophthalmology 65 (7), Article 213, (2024)
From the Human Blood Metabolome to an Interventional Murine CNV Model: Unveiling Saccharin's Protective Effect on Neovascular AMD. 2024 ARVO Annual Meeting, Seattle, WA, May 05, 2024 - May 09, 2024. Investigative Ophthalmology and Visual Science 236 (03), Article 203, (2024)
Reverse engineering BCP-ALL signaling with large knock-out screens. 35. Jahrestagung der Kind-Philipp-Stiftung für pädiatrisch onkologische Forschung, Wilsede, June 05, 2024 - June 08, 2024. Klinische Pädiatrie 236 (03), Article 211, (2024)
The testicular niche – heterogeneity in leukemic cell adaptation to the new immunemicroenvironment. 35. Jahrestagung der Kind-Philipp-Stiftung für pädiatrisch onkologische Forschung, Wilsede, June 05, 2024 - June 08, 2024. Klinische Pädiatrie 65 (4), Article 5 (2024)
Exploring the Impact of Saccharin on Neovascular Age-Related Macular Degeneration: A Comprehensive Study in Patients and Mice. Investigative Ophthalmology and Visual Science 2023
19 (11), e11510 (2023)
Modeling unveils sex differences of signaling networks in mouse embryonic stem cells. Molecular Systems Biology 26 (10), 107844 (2023)
Myeloid leukemia vulnerabilities embedded in long noncoding RNA locus MYNRL15. iScience 2022
141 (10), pp. 1105 - 1118 (2022)
RUNX1 isoform disequilibrium promotes the development of trisomy 21 associated myeloid leukemia. Blood 169, pp. 146 - 155 (2022)
Biomarker-driven therapies for metastatic uveal melanoma: A prospective precision oncology feasibility study. European Journal of Cancer 21, 126 (2022)
Mutations in ALK signaling pathways conferring resistance to ALK inhibitor treatment lead to collateral vulnerabilities in neuroblastoma cells. Molecular Cancer 14 (7), 1749 (2022)
Elevated MACC1 Expression in Colorectal Cancer Is Driven by Chromosomal Instability and Is Associated with Molecular Subtype and Worse Patient Survival. Cancers / Molecular Diversity Preservation International (MDPI) 139 (5), pp. 651 - 665 (2022)
The megakaryocytic transcription factor ARID3A suppresses leukemia pathogenesis. Blood 2021
13 (23), 6018 (2021)
Modeling of Personalized Treatments in Colon Cancer Based on Preclinical Genomic and Drug Sensitivity Data. Cancers 2020
80, pp. 5491 - 5501 (2020)
Endocytosis-mediated replenishment of amino acids favors cancer cell proliferation and survival in chromophobe renal cell carcinoma. Cancer research: an official organ of the American Association for Cancer Research 4 (17), pp. 4052 - 4064 (2020)
The hematopoietic stem cell marker VNN2 is associated with chemoresistance in pediatric B-cell precursor ALL. Blood Advances 97 (8), pp. 764 - 767 (2020)
Mass Cytometry-A Tool for the Curious: Networking in Berlin. Cytometry Part A 66 (1), pp. 149 - 160 (2020)
Multicenter Evaluation of Circulating Cell-Free DNA Extraction and Downstream Analyses for the Development of Standardized (Pre)analytical Work Flows. Clinical Chemistry: International Journal of Molecular Diagnostics and Laboratory Medicine 2019
36 (6), pp. 630 - 644 (2019)
The Leukemogenic TCF3-HLF Complex Rewires Enhancers Driving Cellular Identity and Self-Renewal Conferring EP300 Vulnerability. Cancer Cell 10, Article 4571, p. 1 (2019)
5-Fluorouracil treatment induces characteristic T>G mutations in human cancer. Nature Communications 25 (Suppl. 2), pp. S132 - S137 (2019)
A data- and model-driven approach for cancer treatment. Der Onkologe 36 (2), pp. 123 - 138 (2019)
Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome. Cancer Cell 25 (Suppl. 1), pp. S109 - S115 (2019)
Ein daten- und modellgesteuerter Ansatz zur Behandlung maligner Tumoren. Der Onkologe 26 (4), pp. 1059 - 1069 (2019)
Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes. Cell Reports 2018
34 (6), pp. 996 - 1011 (2018)
Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories. Cancer Cell 24 (10), pp. 2784 - 2794 (2018)
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils. Cell Reports 10, 10:34 (2018)
Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes. Genome Medicine 2017
2017, pp. 1 - 9 (2017)
C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation. Leukemia: the Journal of Normal and Malignant Hemopoiese ; Official Journal of the Leukemia Research Fund U.K. 547 (7663), pp. 311 - 317 (2017)
The whole-genome landscape of medulloblastoma subtypes. Nature 20 (2), pp. 70 - 80 (2017)
Cancer Precision Medicine: Why More Is More and DNA Is Not Enough. Public Health Genomics 8, 8:14262 (2017)
Molecular dissection of colorectal cancer in pre-clinical models identifies biomarkers predicting sensitivity to EGFR inhibitors. Nature Communications 2016
76 (21), pp. 6382 - 6395 (2016)
Impaired Planar Germ Cell Division in the Testis, Caused by Dissociation of RHAMM from the Spindle, Results in Hypofertility and Seminoma. Cancer research: an official organ of the American Association for Cancer Research 48 (6), pp. 593 - 599 (2016)
Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nature Genetics 7 (19), pp. 28169 - 28182 (2016)
Medulloblastoma-associated DDX3 variant selectively alters the translational response to stress. Oncotarget 530 (7588), pp. 57 - 62 (2016)
Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature 167 (5), e24, pp. 1398 - 1414 (2016)
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Cell 33 (5), pp. 1231 - 1244 (2016)
Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa). Molecular Biology and Evolution 2015
16, p. 1018 - 1018 (2015)
Erratum. BMC Genomics 16, p. 904 (2015)
The direction of cross affects [corrected] obesity after puberty in male but not female offspring. BMC Genomics 526 (7571), pp. 68 - 74 (2015)
A global reference for human genetic variation. Nature 47 (9), pp. 1020 - 1029 (2015)
Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options. Nature Genetics 15, pp. 33 - 40 (2015)
Network and systems biology: essential steps in virtualising drug discovery and development. Drug Discovery Today: Technology 27 (5), pp. 728 - 743 (2015)
Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups. Cancer Cell 9 (5), e92596 (2015)
The nerve growth factor receptor CD271 is crucial to maintain tumorigenicity and stem-like properties of melanoma cells. PLoS One 10 (4), e0122518 (2015)
ChIP-Seq and RNA-Seq analyses identify components of the Wnt and Fgf signaling pathways as Prep1 target genes in mouse embryonic stem cells. PLoS One
ChIP-Seq and RNA-Seq Analyses Identify Components of the Wnt and Fgf Signaling Pathways as Prep1 Target Genes in Mouse Embryonic Stem Cells. PLoS One (2015)
47 (1), pp. 22 - 30 (2015)
BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence. Nature Genetics 16 (1), 16:1018 (2015)
Erratum to: 'The direction of cross affects obesity after puberty in male but not female offspring'. BMC Genomics 2014
9 (10), e111006 (2014)
Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains. PLoS One 9 (9), pp. 1104 - 1114 (2014)
Personalized medicine approaches for colon cancer driven by genomics and systems biology: OncoTrack. Biotechnology Journal 15, 15:675 (2014)
Influence of RNA extraction methods and library selection schemes on RNA-seq data. BMC Genomics 511 (7510), pp. 428 - 434 (2014)
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma. Nature 15 (6), R88 (2014)
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 510 (7506), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 5, 5:3934 (2014)
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel. Nature Communications 26 (510), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 7 (325), rs3 (2014)
Parallel profiling of the transcriptome, cistrome, and epigenome in the cellular response to ionizing radiation. Science Signaling 2013
342 (6154), p. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 2012
335 (6070), pp. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 2015
16, p. 1018 - 1018 (2015)
Erratum. BMC Genomics 16, p. 904 (2015)
The direction of cross affects [corrected] obesity after puberty in male but not female offspring. BMC Genomics 2014
9 (10), e111006 (2014)
Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains. PLoS One 15, 15:675 (2014)
Influence of RNA extraction methods and library selection schemes on RNA-seq data. BMC Genomics 42 (14), e110 (2014)
ARH-seq: identification of differential splicing in RNA-seq data. Nucleic Acids Research (London) 511 (7510), pp. 428 - 434 (2014)
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma. Nature 9 (7), e101154 (2014)
Exome sequencing from nanogram amounts of starting DNA: comparing three approaches. PLoS One 15 (6), R88 (2014)
Human genomic regions with exceptionally high levels of population differentiation identified from 911 whole-genome sequences. Genome Biology: Biology for the Post-Genomic Era 510 (7506), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 26 (510), pp. 537 - 541 (2014)
Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing. Nature 7 (325), rs3 (2014)
Parallel profiling of the transcriptome, cistrome, and epigenome in the cellular response to ionizing radiation. Science Signaling 2013
15, p. 144 - 144. 4th Quadrennial Meeting of the World Federation of Neuro-Oncology held in conjunction with the 18th Annual SNO Scientific Meeting and Eucation Day, San Francisco, November 21, 2013 - November 24, 2013. (2013)
The Medulloblastoma Methylome Reveals New Epigenetic Regulatory Mechanisms. In: Neuro-Oncology, Vol. 342 (6154), p. 1235587 - 1235587 (2013)
Integrative annotation of variants from 1092 humans: application to cancer genomics. Science 29 (13), pp. 1600 - 1606 (2013)
Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 155 (3), pp. 567 - 81 (2013)
Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 45 (8), pp. 927 - 32 (2013)
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma. Nature Genetics 501 (7468), pp. 506 - 511 (2013)
Transcriptome and genome sequencing uncovers functional variation in humans. Nature 3 (4), pp. 1321 - 33 (2013)
Analysis of the DNA-binding profile and function of TALE homeoproteins reveals their specialization and specific interactions with Hox genes/proteins. Cell Reports 23 (2), pp. 159 - 70 (2013)
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancer. Cancer Cell 2012
491 (7422), pp. 56 - 65 (2012)
An integrated map of genetic variation from 1,092 human genomes. Nature 422 (4), pp. 643 - 646 (2012)
A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods. Biochemical and Biophysical Research Communications 9 (5), pp. 459 - 462 (2012)
The 1000 Genomes Project: data management and community access. Nature methods 488 (7409), pp. 100 - 105 (2012)
Dissecting the genomic complexity underlying medulloblastoma. Nature 2011
500, pp. 79 - 98 (2011)
A strand-specific library preparation protocol for RNA sequencing. Methods in Enzymology 9 (1), p. e1000582 (2011)
A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biol 9 (1), p. e1000582 (2011)
A high-resolution anatomical atlas of the transcriptome in the mouse embryo. PLoS Biology
Biotin-basiertes de-enrichment von low-copy Vektorsequenzen in humanen genomischen Fosmidbanken für die Next Generation Sequenzierung. Bachelor, Humboldt Universität, Berlin (2011)
6 (8), p. e23882 (2011)
Matrin 3 binds and stabilizes mRNA. PLoS ONE 48 (1), pp. 24 - 31 (2011)
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia. J Med Genet 286 (26), pp. 23521 - 32 (2011)
The BTB and CNC homology 1 (BACH1) target genes are involved in the oxidative stress response and in control of the cell cycle. The Journal of Biological Chemistry 2010
38 (18), pp. 6112 - 6123 (2010)
Functional analysis and identification of cis-regulatory elements of human chromosome 21 gene promoters. Nucleic Acids Research 38 (10), p. e112 - e112 (2010)
Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments. Nucleic Acids Research 464 (7289), pp. 757 - 762 (2010)
The genome of a songbird. Nature 450 (1-2), pp. 48 - 54 (2010)
Screening of human gene promoter activities using transfected-cell arrays. Gene 2009
37 (18), p. e123 - e123 (2009)
Transcriptome analysis by strand-specific sequencing of complementary DNA. Nucleic Acids Research 37 (18), p. e123 - e123 (2009)
Transcriptome analysis by strand-specific sequencing of complementary DNA. Nucleic Acids Research
Systematic cloning and functional analysis of the proteins encoded on human chromosome 21. Dissertation, Freie Universität Berlin, Berlin (2009)
2008
321 (5891), pp. 956 - 960 (2008)
A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome. Science 9, p. 68 - 68 (2008)
High-throughput mammalian two-hybrid screening for protein-protein interactions using transfected cell arrays. BMC Genomics 2007
9 (3), pp. 307 - 314 (2007)
Quantitative PCR based expression analysis on a nanoliter scale using polymer nano-well chips. Biomedical Microdevices 8 (5), p. R91 - R91 (2007)
Gene expression variation in Down's syndrome mice allows prioritization of candidate genes. Genome Biology 18 (4), pp. 1385 - 1396 (2007)
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules. Molecular Biology of the Cell
Taking a functional genomic approach to the study of down syndrome pathogenesos. Dissertation, Freie Universität, Berlin (2007)
2006
347 (3), pp. 747 - 751 (2006)
An efficient and economic enhancer mix for PCR. Biochemical and Biophysical Research Communications (Orlando, FL) 7, p. 155 - 155 (2006)
Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins. BMC Genomics 2005
23 (10), pp. 1514 - 1525 (2005)
Primary differentiation in the human blastocyst: comparative molecular portraits of inner cell mass and trophectoderm cells. Stem Cells 2004
432 (7020), pp. 1036 - 1040 (2004)
An endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell division. Nature 18 (16), pp. 1821 - 1829 (2004)
Multiplexed hybridizations of positively charge-tagged peptide nucleic acids detected by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Rapid Communications in Mass Spectrometry 14 (7), pp. 1258 - 1267 (2004)
Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of Down Syndrome. Genome Research 114 (6), pp. 541 - 552 (2004)
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 114 (6), pp. 541 - 552 (2004)
Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 2003
13 (12), pp. 2736 - 2746 (2003)
Generation, annotation, evolutionary analysis, and database integration of 20,000 unique sea urchin EST clusters. Genome Research 24 (1-2), pp. 111 - 117 (2003)
Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: Challenging the gene dosage effect hypothesis (Part I). Amino Acids 2002
420 (6917), pp. 586 - 590 (2002)
A gene expression map of human chromosome 21 orthologues in the mouse. Nature 295 (5552), pp. 131 - 134 (2002)
Construction and Analysis of a Human-Chimpanzee Comparative Clone Map. Science