Author

Marc Müller

Centre Hospitalier Régional et Universitaire de NancyORCID 0000-0001-6030-2164Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Marc Müller1 paper · ETH Zurich

Biology Disciplines

Click to filter author papers

Developmental Biology· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 3 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Assay:DNA methylation· 1

Frequent Co-Authors

Artur PirógiD· 1 shared Auke B.C. OtteniD· 1 shared Bartosz KaraszewskiiD· 1 shared Caroline Bonmati· 1 shared Clément Collignon· 1 shared Colin HercusiD· 1 shared David H. SpenceriD· 1 shared David Y. CheniD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperNeuroscience

Artur PirógORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintJul 29, 2026

Novel native serum peptidomics workflow enables the discovery of circulating subtype-specific peptide biomarkers in acute ischemic and haemorrhagic stroke

Sachin Kote, Jakub Faktor, Marc Müller…·Natalia-Marek Trzonkowska

This paper introduces a novel serum peptidomics workflow that improves peptide yield, throughput, and recovery, identifying subtype-specific peptide biomarkers for stroke subtypes.

DOI 10.64898/2026.07.26.740776

humanproteomics

𝕏 PostBluesky

GenomicsBlood Cancer JournalPeer-reviewedAug 13, 2025

Genomic and Immunogenomic Profiling of Extramedullary Acute Myeloid Leukemia Reveals Actionable Clonal Branching and Frequent Immune Editing

Clément Collignon, T H Hansen, Colin Hercus…·Francesca Ferraro

This study profiles genomic and immunogenomic features of eAML, finding clonal branching and immune editing, with FLT3 mutations in relapsed cases.

4 citations

humanwhole-exome sequencing

𝕏 PostBluesky

Developmental BiologyFrontiers in Cell and Developmental BiologyPeer-reviewedJun 12, 2020

Tfam knockdown results in reduction of mtDNA copy number, OXPHOS deficiency and abnormalities in zebrafish embryos

Auke B.C. Otten, Rick Kamps, Patrick J. Lindsey…·Hubert J.M. Smeets

This study shows that reducing Tfam in zebrafish embryos decreases mtDNA copy numbers, causes OXPHOS deficiency, and leads to developmental abnormalities.

49 citations

zebrafishbulk RNA-seq

𝕏 PostBluesky