Author

Jasmin Blatterer

Medical University of Graz

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Research Focus:spatial domain detection· 1 Assay:spatial transcriptomics· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Alexandra AfenjariD· 1 shared Amin El HeliebiiD· 1 shared Annelise Yoo Mah-SomiD· 1 shared Antonia SyrniotiiD· 1 shared Benjamin C. CreekmoreiD· 1 shared Christin-Therese Müller· 1 shared Christina T. LamiD· 1 shared Christine Beichler· 1 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alexandra AfenjarORCID

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2 papers

Recent·Most cited

Tissue architecture and immune niches govern ctDNA release in colorectal cancer

Stefan Kühberger, Katja Sallinger, Christin-Therese Müller, Maria Escriva Conde, Sergio Marco Salas, Silvia Andaloro, Christine Beichler, Ricarda Graf, Karin Pankratz, Julia Enzi, Sarah Binder, Martina Scheiber, Lilli Bonstingl, Jasmin Blatterer, Stefan Uranitsch, , Ellen Heitzer

This study identifies tissue architecture and immune niches as key factors influencing ctDNA release in colorectal cancer by integrating spatial transcriptomics and in situ mutation detection.

bioRxiv · Nov 28, 2025 · PreprintCancer Biology

A Novel Autosomal Dominant Childhood-Onset Disorder Associated with Pathogenic Variants in VCP

Annelise Yoo Mah-Som, Jil Daw, Diana Huynh, Mengcheng Wu, Benjamin C. Creekmore, William Burns, Steven A. Skinner, Øystein L. Holla, Marie Falkenberg Smeland, Marc Planes, Kévin Uguen, Sylvia Redon, Tatjana Bierhals, Tasja Scholz, Jonas Denecke, , Marwan S. Shinawi

The paper identifies novel VCP variants causing a childhood-onset neurodevelopmental disorder through exome sequencing and functional analysis.

medRxiv · Jun 19, 2023 · PreprintGenetic & Genomic Medicine