Daniel Danis

18PUBLICATIONS
325CO-AUTHORS
Deep learningGene expression (incl. microarray and other genome-wide approaches)Translational and applied bioinformaticsRecommender systemsEpigenetics (incl. genome methylation and epigenomics)
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Publications (18)

|Jun 16, 2026
In-depth Human Phenotype Ontology Curation Boosts Prioritization Performance for Netherton Syndrome.

|Feb 06, 2026
A Phenotypic Paradigm for Cerebral Palsy Genetics.

Adam S Arterbery, Michael A Gargano, Anita Bagley

|Dec 03, 2025
Performance of Information Theory Derived: Semantic Similarity Algorithms for Differential Diagnosis and Clustering.

Ben Coleman, Daniel Danis, Justin Reese

|Nov 18, 2025
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

|Jun 19, 2025
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses.

Steven Laurie, Wouter Steyaert, Elke de Boer

|May 19, 2025
Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperability.

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly

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Frequent Collaborators

17 joint publications

Peter Robinson

8 joint publications

Christopher J Mungall

7 joint publications

Justin T Reese

7 joint publications

Julius Ob Jacobsen