Bastian Pfeifer

Orcid: 0000-0001-7035-9535

According to our database1, Bastian Pfeifer authored at least 31 papers between 2015 and 2024.

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Bibliography

2024
Correction to: Effective signal reconstruction from multiple ranked lists via convex optimization.
Data Min. Knowl. Discov., May, 2024

Effective signal reconstruction from multiple ranked lists via convex optimization.
Data Min. Knowl. Discov., May, 2024

CLARUS: An interactive explainable AI platform for manual counterfactuals in graph neural networks.
J. Biomed. Informatics, 2024

Feature graphs for interpretable unsupervised tree ensembles: centrality, interaction, and application in disease subtyping.
CoRR, 2024

Federated unsupervised random forest for privacy-preserving patient stratification.
CoRR, 2024

2023
Embedding-based terminology expansion via secondary use of large clinical real-world datasets.
J. Biomed. Informatics, November, 2023

Ensemble-GNN: federated ensemble learning with graph neural networks for disease module discovery and classification.
Bioinform., October, 2023


<i>Parea</i>: Multi-view ensemble clustering for cancer subtype discovery.
J. Biomed. Informatics, 2023

Be Careful When Evaluating Explanations Regarding Ground Truth.
CoRR, 2023

Explainable AI with counterfactual paths.
CoRR, 2023

Bayesian post-hoc regularization of random forests.
CoRR, 2023

Data-Driven Identification of Clinical Real-World Expressions Linked to ICD.
Proceedings of the Caring is Sharing - Exploiting the Value in Data for Health and Innovation - Proceedings of MIE 2023, Gothenburg, Sweden, 22, 2023

Secondary Use of Clinical Problem List Entries for Neural Network-Based Disease Code Assignment.
Proceedings of the Caring is Sharing - Exploiting the Value in Data for Health and Innovation - Proceedings of MIE 2023, Gothenburg, Sweden, 22, 2023

Human-in-the-Loop Integration with Domain-Knowledge Graphs for Explainable Federated Deep Learning.
Proceedings of the Machine Learning and Knowledge Extraction, 2023

2022
Actionable Explainable AI (AxAI): A Practical Example with Aggregation Functions for Adaptive Classification and Textual Explanations for Interpretable Machine Learning.
Mach. Learn. Knowl. Extr., December, 2022

Generating Explanations for Conceptual Validation of Graph Neural Networks: An Investigation of Symbolic Predicates Learned on Relevance-Ranked Sub-Graphs.
Künstliche Intell., 2022

Parea: multi-view ensemble clustering for cancer subtype discovery.
CoRR, 2022

Robust Random Forest-Based All-Relevant Feature Ranks for Trustworthy AI.
Proceedings of the Challenges of Trustable AI and Added-Value on Health, 2022

Terminology Expansion via Co-occurrence Analysis of Large Clinical Real-World Datasets.
Proceedings of the 10th IEEE International Conference on Healthcare Informatics, 2022

2021
A hierarchical clustering and data fusion approach for disease subtype discovery.
J. Biomed. Informatics, 2021

Towards multi-modal causability with Graph Neural Networks enabling information fusion for explainable AI.
Inf. Fusion, 2021

Network Module Detection from Multi-Modal Node Features with a Greedy Decision Forest for Actionable Explainable AI.
CoRR, 2021

Integrative hierarchical ensemble clustering for improved disease subtype discovery.
Proceedings of the IEEE International Conference on Bioinformatics and Biomedicine, 2021

2019
EHR problem list clustering for improved topic-space navigation.
BMC Medical Informatics Decis. Mak., 2019

Estimates of introgression as a function of pairwise distances.
BMC Bioinform., 2019

2018
BlockFeST: Bayesian calculation of region-specific FST to detect local adaptation.
Bioinform., 2018

Problem List Clustering for Improved Patient-Based Disease Perception.
Proceedings of the IEEE International Conference on Healthcare Informatics Workshops, 2018

EHR Text Categorization for Enhanced Patient-Based Document Navigation.
Proceedings of the Health Informatics Meets eHealth - Biomedical Meets eHealth - From Sensors to Decisions, 2018

2015
Whole-genome population genomic analyses.
PhD thesis, 2015

WhopGenome: high-speed access to whole-genome variation and sequence data in R.
Bioinform., 2015


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