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Author Details
Full Name
Marie-Laure Yaspo
Affiliation
Max Planck Institute for Molecular Genetics
ORCID
Career Start Year
1992
Papers
108
H Index
48
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36493345
RUNX1 isoform disequilibrium promotes the development of trisomy 21-associated myeloid leukemia.
Blood
2023
37766974
Myeloid leukemia vulnerabilities embedded in long noncoding RNA locus <i>MYNRL15</i>.
iScience
2023
37248468
A combined computational and functional approach identifies IGF2BP2 as a driver of chemoresistance in a wide array of pre-clinical models of colorectal cancer.
Mol Cancer
2023
37373474
Systemic Blood Proteome Patterns Reflect Disease Phenotypes in Neovascular Age-Related Macular Degeneration.
Int J Mol Sci
2023
35569281
Biomarker-driven therapies for metastatic uveal melanoma: A prospective precision oncology feasibility study.
Eur J Cancer
2022
35406521
Elevated MACC1 Expression in Colorectal Cancer Is Driven by Chromosomal Instability and Is Associated with Molecular Subtype and Worse Patient Survival.
Cancers (Basel)
2022
32703790
Cell type-specific novel long non-coding RNA and circular RNA in the BLUEPRINT hematopoietic transcriptomes atlas.
Haematologica
2021
34885128
Modeling of Personalized Treatments in Colon Cancer Based on Preclinical Genomic and Drug Sensitivity Data.
Cancers (Basel)
2021
34994642
Dynamic Changes of Circulating Tumor DNA Predict Clinical Outcome in Patients With Advanced Non-Small-Cell Lung Cancer Treated With Immune Checkpoint Inhibitors.
JCO Precis Oncol
2021
34209696
CD74 and CD44 Expression on CTCs in Cancer Patients with Brain Metastasis.
Int J Mol Sci
2021
34230613
Applicability of liquid biopsies to represent the mutational profile of tumor tissue from different cancer entities.
Oncogene
2021
32298052
Mass Cytometry-A Tool for the Curious: Networking in Berlin.
Cytometry A
2020
31982633
Support of a molecular tumour board by an evidence-based decision management system for precision oncology.
Eur J Cancer
2020
33115803
Endocytosis-Mediated Replenishment of Amino Acids Favors Cancer Cell Proliferation and Survival in Chromophobe Renal Cell Carcinoma.
Cancer Res
2020
33146701
Rational therapy with vigabatrin and a ketogenic diet in a patient with GAD1 deficiency.
Brain
2020
32853382
The hematopoietic stem cell marker VNN2 is associated with chemoresistance in pediatric B-cell precursor ALL.
Blood Adv
2020
30673601
Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes.
Cell Rep
2019
31735627
The Leukemogenic TCF3-HLF Complex Rewires Enhancers Driving Cellular Identity and Self-Renewal Conferring EP300 Vulnerability.
Cancer Cell
2019
31303423
Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.
Cancer Cell
2019
31526763
Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome.
Cancer Cell
2019
31594944
5-Fluorouracil treatment induces characteristic T>G mutations in human cancer.
Nat Commun
2019
28871137
C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation.
Leukemia
2018
30024899
Impact of congenital cytomegalovirus infection on transcriptomes from archived dried blood spots in relation to long-term clinical outcome.
PLoS One
2018
30184510
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils.
Cell Rep
2018
29876014
Multi-omics profiling reveals a distinctive epigenome signature for high-risk acute promyelocytic leukemia.
Oncotarget
2018
29876013
Combined HAT/EZH2 modulation leads to cancer-selective cell death.
Oncotarget
2018
30537516
Molecular Evolution of Early-Onset Prostate Cancer Identifies Molecular Risk Markers and Clinical Trajectories.
Cancer Cell
2018
29703216
Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes.
Genome Med
2018
29785028
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia.
Nat Med
2018
28595192
Cancer Precision Medicine: Why More Is More and DNA Is Not Enough.
Public Health Genomics
2017
28186126
Molecular dissection of colorectal cancer in pre-clinical models identifies biomarkers predicting sensitivity to EGFR inhibitors.
Nat Commun
2017
28726821
The whole-genome landscape of medulloblastoma subtypes.
Nature
2017
26814189
Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa).
Mol Biol Evol
2016
27863251
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.
Cell
2016
27543603
Impaired Planar Germ Cell Division in the Testis, Caused by Dissociation of RHAMM from the Spindle, Results in Hypofertility and Seminoma.
Cancer Res
2016
27058758
Medulloblastoma-associated DDX3 variant selectively alters the translational response to stress.
Oncotarget
2016
26814967
Active medulloblastoma enhancers reveal subgroup-specific cellular origins.
Nature
2016
25485837
BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence.
Nat Genet
2015
26546267
The direction of cross affects [corrected] obesity after puberty in male but not female offspring.
BMC Genomics
2015
26464088
Network and systems biology: essential steps in virtualising drug discovery and development.
Drug Discov Today Technol
2015
26621155
Erratum to: 'The direction of cross affects obesity after puberty in male but not female offspring'.
BMC Genomics
2015
26214592
Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options.
Nat Genet
2015
25875616
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
25965575
Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups.
Cancer Cell
2015
24920826
ARH-seq: identification of differential splicing in RNA-seq data.
Nucleic Acids Res
2014
25347188
Comparative analysis and modeling of the severity of steatohepatitis in DDC-treated mouse strains.
PLoS One
2014
25043047
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma.
Nature
2014
25113896
Influence of RNA extraction methods and library selection schemes on RNA-seq data.
BMC Genomics
2014
24799129
The nerve growth factor receptor CD271 is crucial to maintain tumorigenicity and stem-like properties of melanoma cells.
PLoS One
2014
24825921
Parallel profiling of the transcriptome, cistrome, and epigenome in the cellular response to ionizing radiation.
Sci Signal
2014
1 - 50 of 108
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row(s) 1 - 30 of 30
Collaborators
Hans-J??rg Warnatz
Max Planck Institute for Molecular Genetics
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25
Vyacheslav Amstislavskiy
Max-Planck-Institute for Molecular Genetics
Co-authored papers
18
Thomas Risch
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Co-authored papers
16
Roland Eils
Berlin Institute of Health (BIH) and Charite
Co-authored papers
10
Marcel Kool
Hopp Children's Cancer Center (KiTZ)
Co-authored papers
9
Peter Lichter
German Cancer Research Center (DKFZ)
Co-authored papers
9
David T W Jones
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers
9
Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
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9
Benedikt Brors
German Cancer Research Center (DKFZ)
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9
Stefan M Pfister
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers
9
Andrey Korshunov
Institute of Pathology, University Hospital Heidelberg
Co-authored papers
8
Michael D Taylor
The Hospital for Sick Children
Co-authored papers
8
Joost H A Martens
Co-authored papers
8
Paul A Northcott
St Jude Children's Research Hospital
Co-authored papers
8
Hendrik G Stunnenberg
Co-authored papers
8
Marina Ryzhova
N.N. Burdenko Neurosurgical Institute
Co-authored papers
7
Jan Koster
Amsterdam University Medical Centers location AMC
Co-authored papers
7
Natalie J??ger
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers
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Paul Flicek
European Bioinformatics Institute
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Chris Lawerenz
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Christof von Kalle
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