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Marie-Laure Yaspo

Marie-Laure Yaspo

D-Index & Metrics

Genetics

D-Index
62
Citations
60643
World Ranking
2926
National Ranking
204

Overview

Marie-Laure Yaspo is a researcher affiliated with the Max Planck Society in Germany. Their research primarily spans the fields of biochemistry, genetics, molecular biology, and medicine, with a focus on molecular biology, cancer research, oncology, hematology, and immunology.

The scientist's work covers several main topics, including:

  • Cancer Genomics and Diagnostics
  • Acute Myeloid Leukemia Research
  • RNA modifications and cancer
  • Protein Degradation and Inhibitors
  • Genetic factors in colorectal cancer
  • Cancer-related molecular mechanisms research
  • Acute Lymphoblastic Leukemia research

Marie-Laure Yaspo has collaborated frequently with a number of co-authors, such as Moritz Schütte, H Issa, R Bhayadia, Enikő Regényi, and Dirk Reinhardt.

The scientist has published in various recognized venues, with multiple papers appearing in the journals Blood, Klinische Pädiatrie, International Journal of Molecular Sciences, European Journal of Cancer, and Cancer Research.

Selected recent papers include:

  • "Dynamic Changes of Circulating Tumor DNA Predict Clinical Outcome in Patients With Advanced Non-Small-Cell Lung Cancer Treated With Immune Checkpoint Inhibitors," 2021, JCO Precision Oncology
  • "CD74 and CD44 Expression on CTCs in Cancer Patients with Brain Metastasis," 2021, International Journal of Molecular Sciences
  • "RUNX1 isoform disequilibrium promotes the development of trisomy 21-associated myeloid leukemia," 2022, Blood
  • "Support of a molecular tumour board by an evidence-based decision management system for precision oncology," 2020, European Journal of Cancer
  • "The megakaryocytic transcription factor ARID3A suppresses leukemia pathogenesis," 2021, Blood

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Pan-cancer analysis of whole genomes

    Peter J. Campbell;Gad Getz;Jan O. Korbel;Joshua M. Stuart

  • A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome

    Marc Sultan;Marcel H. Schulz;Marcel H. Schulz;Hugues Richard;Alon Magen

  • The DNA sequence of human chromosome 21

    M. Hattori;A. Fujiyama;T. D. Taylor;H. Watanabe

  • Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

    Biola M Javierre;Oliver S Burren;Steven P Wilder;Roman Kreuzhuber

  • An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

    Johanna Aaltonen;Petra Björses;Jaakko Perheentupa;Nina Horelli–Kuitunen

  • Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups

    Kristian W. Pajtler;Kristian W. Pajtler;Hendrik Witt;Martin Sill;David T.W. Jones

  • The whole-genome landscape of medulloblastoma subtypes

    Paul A. Northcott;Paul A. Northcott;Ivo Buchhalter;Ivo Buchhalter;A. Sorana Morrissy;Volker Hovestadt

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Patterns of somatic structural variation in human cancer genomes

    Yilong Li;Nicola D Roberts;Jeremiah A Wala;Jeremiah A Wala;Ofer Shapira;Ofer Shapira

  • Dissecting the genomic complexity underlying medulloblastoma

    David T. W. Jones;Natalie Jäger;Marcel Kool;Thomas Zichner

  • Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

    David T W Jones;Barbara Hutter;Natalie Jäger;Andrey Korshunov;Andrey Korshunov

  • Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

    Lu Chen;Lu Chen;Bing Ge;Francesco Paolo Casale;Louella Vasquez

  • Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma

    Paul A. Northcott;Catherine Lee;Catherine Lee;Thomas Zichner;Adrian M. Stütz

  • A high-resolution anatomical atlas of the transcriptome in the mouse embryo.

    Graciana Diez-Roux;Sandro Banfi;Marc Sultan;Lars Geffers

  • An endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell division

    Ralf Kittler;Gabriele Putz;Laurence Pelletier;Ina Poser

  • Decoding the regulatory landscape of medulloblastoma using DNA methylation sequencing

    Volker Hovestadt;David T.W. Jones;Simone Picelli;Wei Wang

  • Integrative Genomic Analyses Reveal an Androgen-Driven Somatic Alteration Landscape in Early-Onset Prostate Cancer

    Joachim Weischenfeldt;Ronald Simon;Lars Feuerbach;Karin Schlangen

  • Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules.

    Ute Nonhoff;Markus Ralser;Franziska Welzel;Ilaria Piccini

Frequent Co-Authors

Hans Lehrach
Hans Lehrach Max Planck Society
Roland Eils
Roland Eils Charité - University Medicine Berlin
Andrey Korshunov
Andrey Korshunov German Cancer Research Center
Stefan M. Pfister
Stefan M. Pfister German Cancer Research Center
Jan O. Korbel
Jan O. Korbel European Molecular Biology Laboratory
Peter Lichter
Peter Lichter German Cancer Research Center
David T. W. Jones
David T. W. Jones German Cancer Research Center
Marcel Kool
Marcel Kool German Cancer Research Center
Benedikt Brors
Benedikt Brors German Cancer Research Center
Paul Flicek
Paul Flicek The Jackson Laboratory

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