Author

Michelle D. Runkel

University of Münster

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

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Adrian M. E. PilatziD· 1 shared Ann‐Kristin DickeiD· 1 shared Birgit StallmeyeriD· 1 shared Christian Ruckert· 1 shared Corinna FriedrichiD· 1 shared Daniela FietziD· 1 shared Frank TüttelmanniD· 1 shared Hans-Christian SchuppeiD· 1 shared

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2024-2024 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adrian M. E. PilatzORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMar 20, 2024

Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes

Nadja Rotte, Jessica E. M. Dunleavy, Michelle D. Runkel…·Corinna Friedrich

The paper identifies genotype-specific meiotic impairments in infertile men with loss-of-function variants in M1AP or ZZS genes, showing different recombination failures and reproductive outcomes.

DOI 10.1101/2024.03.20.24304490

humanDNA methylation

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