Author

Lukas Ramlow

Berlin Institute of Health at Charité - Universitätsmedizin BerlinORCID 0000-0001-6089-0613Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Organism:human· 1 Research Focus:software / tool· 1

Frequent Co-Authors

Daniel DanisiD· 2 shared Peter N. RobinsoniD· 2 shared Adam S. ArterberyiD· 1 shared Adam S.L. GraefeiD· 1 shared Ana Laura Arenas-Díaz· 1 shared Anita M BagleyiD· 1 shared Anxhela Gjyshi GustafsoniD· 1 shared Damian P. SmedleyiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Daniel DanisORCID

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Author profile →

2 papers

Recent·Most cited

A Phenotypic Paradigm for Cerebral Palsy Genetics

Adam S. Arterbery, Michael A. Gargano, Anita M Bagley, Jagadish Chandrabose Sundaramurthi, Lauren Rekerle, Thania Ordaz‐Robles, Daniel Danis, Adam S.L. Graefe, Ana Laura Arenas-Díaz, Jeremy Bauer, Hannah Blau, Leigh Carmody, Kristen L. Carroll, Janice Davis, Philip F. Giampietro, , Peter N. Robinson

The paper identifies pathogenic variants in 15.8% of CP patients and finds only 16 of 60 genes have significant CP association.

The American Journal of Human Genetics · Sep 1, 2026Peer-reviewedGenetic & Genomic Medicine

Ontologizer 3: a cross-platform desktop application for frequentist and Bayesian GO enrichment analysis

Lukas Ramlow, Jasmin Scholtes, Daniel Daniš, Peter N. Robinson

Ontologizer 3 provides a desktop tool for GO enrichment analysis using frequentist and Bayesian methods, showing higher precision with the Bayesian approach on simulated data.

bioRxiv · Jun 6, 2026 · PreprintBioinformatics