Daniel Danis

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

|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

|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

|Mar 17, 2025
GA4GH Phenopacket-Driven Characterization of Genotype-Phenotype Correlations in Mendelian Disorders.

Lauren Rekerle, Daniel Danis, Filip Rehburg

|Mar 10, 2025
Consistent Performance of GPT-4o in Rare Disease Diagnosis Across Nine Languages and 4967 Cases.

Leonardo Chimirri, J Harry Caufield, Yasemin Bridges

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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