Author

Maximilian Deest

Medizinische Hochschule HannoverORCID 0000-0002-8759-8660Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Björn BrändliD· 2 shared Helge FrielingiD· 2 shared Alexandra Burkert· 1 shared Andreas LeffleriD· 1 shared Christian Karl EberleiniD· 1 shared Christian RohrandtiD· 1 shared Colin DavenportiD· 1 shared Frank Ulrich MülleriD· 1 shared

Activity by Year

2021-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Björn BrändlORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 18, 2022

Long-read nanopore sequencing reveals novel common genetic structural variants in Prader-Willi syndrome and associated psychosis

Maximilian Deest, Björn Brändl, Christian Rohrandt…·Helge Frieling

This study uses long-read sequencing to identify novel structural variants in Prader-Willi syndrome patients, linking them to psychiatric traits and challenging current genetic hypotheses.

DOI 10.1101/2022.07.18.22277235

humanwhole-genome sequencing

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Molecular BiologybioRxivPreprintSep 17, 2021

MinION nanopore sequencing provides similar methylation estimates to Sanger bisulfite sequencing in the TRPA1 promoter region

Sara Gombert, Kirsten Jahn, Hansi Pathak…·Helge Frieling

2 citations

DNA methylationstatistical model

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