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Daniel Danis

Showing results (1-10 of 44) with videos related to

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Biorxiv : the Preprint Server for Biology|December 3, 2025
Performance of Information Theory Derived: Semantic Similarity Algorithms for Differential Diagnosis and ClusteringBen Coleman, Daniel Danis, Justin Reese, et al.
BMC Medical Genetics|May 19, 2019
Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case reportLukas Varga, Daniel Danis, Martina Skopkova, et al.
Endocrine Regulations|May 2, 2018
Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patientsDaniel Danis, Katarina Brennerova, Martina Skopkova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2024
Leveraging clinical intuition to improve accuracy of phenotype-driven prioritizationMartha A Beckwith, Daniel Danis, Yasemin Bridges, et al.
NPJ Genomic Medicine|November 4, 2024
Alternative splicing is coupled to gene expression in a subset of variably expressed genesGuy Karlebach, Robin Steinhaus, Daniel Danis, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Alternative splicing is coupled to gene expression in a subset of variably expressed genesGuy Karlebach, Robin Steinhaus, Daniel Danis, et al.
Genome Biology|July 15, 2020
HBA-DEALS: accurate and simultaneous identification of differential expression and splicing using hierarchical Bayesian analysisGuy Karlebach, Peter Hansen, Diogo Ft Veiga, et al.
International Journal of Pediatric Otorhinolaryngology|November 25, 2020
Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndromeLukas Varga, Daniel Danis, Jakub Drsata, et al.
Diabetes Research and Clinical Practice|March 1, 2017
Congenital hyperinsulinism and glycogenosis-like phenotype due to a novel HNF4A mutationJuraj Stanik, Martina Skopkova, Katarina Brennerova, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
On the limitations of large language models in clinical diagnosisJustin T Reese, Daniel Danis, J Harry Caufield, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Biorxiv : the Preprint Server for Biology|December 3, 2025
Performance of Information Theory Derived: Semantic Similarity Algorithms for Differential Diagnosis and ClusteringBen Coleman, Daniel Danis, Justin Reese, et al.
BMC Medical Genetics|May 19, 2019
Novel EYA4 variant in Slovak family with late onset autosomal dominant hearing loss: a case reportLukas Varga, Daniel Danis, Martina Skopkova, et al.
Endocrine Regulations|May 2, 2018
Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patientsDaniel Danis, Katarina Brennerova, Martina Skopkova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2024
Leveraging clinical intuition to improve accuracy of phenotype-driven prioritizationMartha A Beckwith, Daniel Danis, Yasemin Bridges, et al.
NPJ Genomic Medicine|November 4, 2024
Alternative splicing is coupled to gene expression in a subset of variably expressed genesGuy Karlebach, Robin Steinhaus, Daniel Danis, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Alternative splicing is coupled to gene expression in a subset of variably expressed genesGuy Karlebach, Robin Steinhaus, Daniel Danis, et al.
Genome Biology|July 15, 2020
HBA-DEALS: accurate and simultaneous identification of differential expression and splicing using hierarchical Bayesian analysisGuy Karlebach, Peter Hansen, Diogo Ft Veiga, et al.
International Journal of Pediatric Otorhinolaryngology|November 25, 2020
Novel variants in EDNRB gene in Waardenburg syndrome type II and SOX10 gene in PCWH syndromeLukas Varga, Daniel Danis, Jakub Drsata, et al.
Diabetes Research and Clinical Practice|March 1, 2017
Congenital hyperinsulinism and glycogenosis-like phenotype due to a novel HNF4A mutationJuraj Stanik, Martina Skopkova, Katarina Brennerova, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
On the limitations of large language models in clinical diagnosisJustin T Reese, Daniel Danis, J Harry Caufield, et al.
Pageof 5