Author

Martin Pavlov

Helmholtz Munich

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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Genetic & Genomic Medicine· 3

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Approach:benchmark study· 1 Research Focus:eQTL / molecular QTL mapping· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Holger ProkischiD· 2 shared Juliane WinkelmanniD· 2 shared Aiman Farzeen· 1 shared Alexander TeumeriD· 1 shared Annette PetersiD· 1 shared Arianna Vino· 1 shared Birgit LinkohriD· 1 shared Chao‐Jin XuiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Holger ProkischORCID

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3 papers

Recent·Most cited

RNA sequencing resolves cryptic pathogenic variants in mitochondrial disease

Z.H. Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chao‐Jin Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, T Y Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, , Fang Fang

This study uses RNA sequencing to identify pathogenic variants in mitochondrial disease patients who were undiagnosed by DNA sequencing, revealing cryptic splicing and regulatory events.

Annals of Clinical and Translational Neurology · Apr 25, 2026Peer-reviewedGenetic & Genomic Medicine

Novel and Known Genetic Players in Hypertension: From Gene Expression to Striking Insights

Aiman Farzeen, Riccardo Berutti, Martin Pavlov, Sapna Sharma, Markéta Fuchs, Nadine Lindemann, Birgit Linkohr, Moritz von Scheidt, Heribert Schunkert, Annette Peters, Harald Grallert, Mélanie Waldenberger, Juliane Winkelmann, Lars Mäegdefessel, Alexander Teumer, , Christian Gieger

This study identifies novel and known genetic contributors to hypertension using RNA-seq and eQTL analyses, highlighting potential drug targets and pathways.

medRxiv · Jul 1, 2025 · PreprintGenetic & Genomic Medicine

De novo protein-coding gene variants in developmental stuttering

Else Eising, Ivana Dzinovic, Arianna Vino, Lottie W. Stipdonk, Martin Pavlov, Juliane Winkelmann, Martin Sommer, Marie-Christine J. P. Franken, Konrad Oexle, Simon E. Fisher

The paper identifies de novo protein-coding gene variants in stuttering and highlights genetic links to neurodevelopmental disorders.

medRxiv · Nov 25, 2024 · PreprintGenetic & Genomic Medicine