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Author Details
Full Name
Michael Schuster
Affiliation
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
ORCID
Career Start Year
2005
Papers
49
H Index
29
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37342957
Systemic Inflammation and Normocytic Anemia in DOCK11 Deficiency.
N Engl J Med
2023
37587144
Pharmacological perturbation of the phase-separating protein SMNDC1.
Nat Commun
2023
37499656
Cell-autonomous regulation of complement C3 by factor H limits macrophage efferocytosis and exacerbates atherosclerosis.
Immunity
2023
37249233
Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis.
Blood
2023
35015307
PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms.
Am J Hematol
2022
36044849
SMNDC1 links chromatin remodeling and splicing to regulate pancreatic hormone expression.
Cell Rep
2022
35994477
A toolbox for class I HDACs reveals isoform specific roles in gene regulation and protein acetylation.
PLoS Genet
2022
33361811
RANK links thymic regulatory T cells to fetal loss and gestational diabetes in pregnancy.
Nature
2021
33761144
Hematopoietic expression of a chimeric murine-human CALR oncoprotein allows the assessment of anti-CALR antibody immunotherapies in vivo.
Am J Hematol
2021
33536639
SARS-CoV-2 infects and replicates in cells of the human endocrine and exocrine pancreas.
Nat Metab
2021
33589750
EZH2 inactivation in RAS-driven myeloid neoplasms hyperactivates RAS-signaling and increases MEK inhibitor sensitivity.
Leukemia
2021
33558760
Acute BAF perturbation causes immediate changes in chromatin accessibility.
Nat Genet
2021
34663987
Mutations and variants of ONECUT1 in diabetes.
Nat Med
2021
34333533
High-throughput drug screening identifies the ATR-CHK1 pathway as a therapeutic vulnerability of CALR mutated hematopoietic cells.
Blood Cancer J
2021
32318068
NCOR1 Orchestrates Transcriptional Landscapes and Effector Functions of CD4<sup>+</sup> T Cells.
Front Immunol
2020
33229462
Genomic epidemiology of superspreading events in Austria reveals mutational dynamics and transmission properties of SARS-CoV-2.
Sci Transl Med
2020
31133746
MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation.
Nat Genet
2019
31748746
Longitudinal molecular trajectories of diffuse glioma in adults.
Nature
2019
31219742
Mitochondria Are a Subset of Extracellular Vesicles Released by Activated Monocytes and Induce Type I IFN and TNF Responses in Endothelial Cells.
Circ Res
2019
31064751
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms.
Blood
2019
28964722
A T cell-specific deletion of HDAC1 protects against experimental autoimmune encephalomyelitis.
J Autoimmun
2018
27899802
Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia.
Leukemia
2017
28134926
DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma.
Nat Med
2017
29089570
Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia.
Nat Commun
2017
28530711
A combinatorial screen of the CLOUD uncovers a synergy targeting the androgen receptor.
Nat Chem Biol
2017
27072894
Comprehensive genome and epigenome characterization of CHO cells in response to evolutionary pressures and over time.
Biotechnol Bioeng
2016
26423830
Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms.
Blood
2016
27149854
A Comprehensive Analysis of the Dynamic Response to Aphidicolin-Mediated Replication Stress Uncovers Targets for ATM and ATMIN.
Cell Rep
2016
27143436
Familial early-onset dementia with complex neuropathologic phenotype and genomic background.
Neurobiol Aging
2016
27159579
Mapping the chemical chromatin reactivation landscape identifies BRD4-TAF1 cross-talk.
Nat Chem Biol
2016
27337980
The Ensembl gene annotation system.
Database (Oxford)
2016
25263445
NOTCH1 activation in breast cancer confers sensitivity to inhibition of SUMOylation.
Oncogene
2015
26083206
Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.
N Engl J Med
2015
25917266
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia.
Leukemia
2015
25704812
Epigenome mapping reveals distinct modes of gene regulation and widespread enhancer reprogramming by the oncogenic fusion protein EWS-FLI1.
Cell Rep
2015
25163811
A SAGE based approach to human glomerular endothelium: defining the transcriptome, finding a novel molecule and highlighting endothelial diversity.
BMC Genomics
2014
23203987
Ensembl 2013.
Nucleic Acids Res
2013
22086963
Ensembl 2012.
Nucleic Acids Res
2012
21045057
Ensembl 2011.
Nucleic Acids Res
2011
19906699
Ensembl's 10th year.
Nucleic Acids Res
2010
20521244
Using the ensembl genome server to browse genomic sequence data.
Curr Protoc Bioinformatics
2010
20459813
eHive: an artificial intelligence workflow system for genomic analysis.
BMC Bioinformatics
2010
19033362
Ensembl 2009.
Nucleic Acids Res
2009
19498102
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes.
Genome Res
2009
18000006
Ensembl 2008.
Nucleic Acids Res
2008
17148474
Ensembl 2007.
Nucleic Acids Res
2007
18428779
Using the Ensembl genome server to browse genomic sequence data.
Curr Protoc Bioinformatics
2007
16381931
Ensembl 2006.
Nucleic Acids Res
2006
15608235
Ensembl 2005.
Nucleic Acids Res
2005
1 - 49 of 49
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Elizabeth A Worthey
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Alistair R R Forrest
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Marco A Marra
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Winston Hide
Harvard Medical School
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Francisco M De La Vega
Stanford University School of Medicine
Career Start Year
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Sean M Grimmond
The University of Melbourne
Career Start Year
1990
Number of shared co-authors
8
David A Wheeler
Baylor College of Medicine
Career Start Year
1984
Number of shared co-authors
20
row(s) 1 - 30 of 30
Collaborators
Christoph Bock
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers
31
Stephen M J Searle
Wellcome Trust Sanger Institute
Co-authored papers
11
Stefan Kubicek
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers
10
Tim Hubbard
Co-authored papers
10
Ewan Birney
European Bioinformatics Institute
Co-authored papers
10
Paul Flicek
European Bioinformatics Institute
Co-authored papers
10
Richard Durbin
University of Cambridge
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Robert Kralovics
Medical University of Vienna
Co-authored papers
9
Fiona Cunningham
European Bioinformatics Institute
Co-authored papers
9
Damian Keefe
University of Adelaide
Co-authored papers
8
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers
6
Laura Clarke
Co-authored papers
6
Susan Fairley
European Bioinformatics Institute
Co-authored papers
6
Stefan Gr??f
Heart and Lung Research Institute, University of Cambridge
Co-authored papers
5
Arek Kasprzyk
European Bioinformatics Institute (EBI)
Co-authored papers
5
Abel Ureta-Vidal
Co-authored papers
5
J??rg Menche
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Co-authored papers
5
Karyn Megy
University of Cambridge
Co-authored papers
4
Ian Dunham
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers
4
Daniel Barrell
Oncology R&D
Co-authored papers
4
Thomas A Down
Co-authored papers
4
Jessica Severin
Center for Integrative Medical Sciences
Co-authored papers
4
Tim Cutts
Wellcome Trust Sanger Institute
Co-authored papers
4
Fiorella Schischlik
National Cancer Institute, National Institutes of Health
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Syed Haider
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Y Amy Tang
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Richard Holland
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1 - 30