Peter M. Krawitz

Orcid: 0000-0002-3194-8625

According to our database1, Peter M. Krawitz authored at least 17 papers between 2009 and 2025.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of four.

Timeline

Legend:

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PhD thesis 
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Links

On csauthors.net:

Bibliography

2025
GANonymization: A GAN-Based Face Anonymization Framework for Preserving Emotional Expressions.
ACM Trans. Multim. Comput. Commun. Appl., January, 2025

2024
Approximating facial expression effects on diagnostic accuracy <i>via</i> generative AI in medical genetics.
Bioinform., 2024

2023
Multimodal Machine Learning Combining Facial Images and Clinical Texts Improves Diagnosis of Rare Genetic Diseases.
CoRR, 2023

Improving Deep Facial Phenotyping for Ultra-rare Disorder Verification Using Model Ensembles.
Proceedings of the IEEE/CVF Winter Conference on Applications of Computer Vision, 2023

Region-based Saliency Explanations on the Recognition of Facial Genetic Syndromes.
Proceedings of the Machine Learning for Healthcare Conference, 2023

Few-Shot Meta-Learning for Recognizing Facial Phenotypes of Genetic Disorders.
Proceedings of the Caring is Sharing - Exploiting the Value in Data for Health and Innovation - Proceedings of MIE 2023, Gothenburg, Sweden, 22, 2023

2022
GenRisk: a tool for comprehensive genetic risk modeling.
Bioinform., 2022

2021
Knowledge transfer to enhance the performance of deep learning models for automated classification of B cell neoplasms.
Patterns, 2021

DeepCNV: a deep learning approach for authenticating copy number variations.
Briefings Bioinform., 2021

2018
DeepGestalt - Identifying Rare Genetic Syndromes Using Deep Learning.
CoRR, 2018

2017
A likelihood ratio-based method to predict exact pedigrees for complex families from next-generation sequencing data.
Bioinform., 2017

2016
Challenges ahead for matchmaking.
it Inf. Technol., 2016

2015
Strategies to improve the performance of rare variant association studies by optimizing the selection of controls.
Bioinform., 2015

2012
GeneTalk: an expert exchange platform for assessing rare sequence variants in personal genomes.
Bioinform., 2012

2011
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders.
Bioinform., 2011

2010
Microindel detection in short-read sequence data.
Bioinform., 2010

2009
Boolean Modeling of Biological Networks.
Proceedings of the Encyclopedia of Complexity and Systems Science, 2009


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