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Fabian Praßer (1982-)

Informatiker

Name	Fabian Praßer
Time	1982- (Date of birth and death)
Place	Starnberg (Geburtsort) München (Wirkungsort) Berlin (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Prof. Dr.
Profession	Informatiker (characteristic profession) Hochschullehrer
Variant	Fabian Prasser
Related	Medizinische Informatik (Promotion und Habilitation) (Studienfach)
Further information	Habil. Fach Medizinische Informatik an der Techn. Univ. München; Professor für Medizininformatik an der Charité - Universitätsmedizin Berlin; Inhaber des Lehrstuhls für Medizininformatik am Berlin Institute of Health in der Charité - Universitätsmedizin Berlin
Source	AM
Record type	Person
GND-Identifier	1036892360
Record ID	1036892360
Involved in show all PROs als Kompass der intersektoralen onkologischen Versorgung – von der Praxis in das MTB und zurück Comparison of Three Anonymization Tools for a Health Fitness Study A quantitative analysis of the use of anonymization in biomedical research Parallel privacy preservation through partitioning (P4): a scalable data anonymization algorithm for health data Pseudonymization tools for medical research: a systematic review A scoping review of privacy and utility metrics in medical synthetic data Integrating the Patient Perspective into Healthcare and Real-World Evidence: The Multi-site, Cross-Disease, Patient-Centered Outcomes Research Project in the Medical Informatics Initiative (PCOR-MII) EasySMPC: a simple but powerful no-code tool for practical secure multiparty computation Secondary use of patient data within decentralized studies using the example of rare diseases in Germany: A data scientist's exploration of process and lessons learned Technological interventions to alleviate alarm fatigue in intensive care medicine : an IT systems approach Verbesserung des Record Linkage für die Gesundheitsforschung in Deutschland – wie können Defizite behoben werden? An interactive dashboard for analyzing user interaction patterns in the i2b2 clinical data warehouse Synthetic datasets for open software development in rare disease research Synthetic data generation for a longitudinal cohort study – evaluation, method extension and reproduction of published data analysis results Automatisierte Surveillance und Risikovorhersage mit dem Ziel einer risikostratifizierten Infektionskontrolle und -prävention (RISK Prediction for Risk-stratified Infection Control and Prevention) Arbeitsgruppe Interoperabilität: Kerndatensatz und Informationssysteme für Integration und Austausch von Daten in der Medizininformatik-Initiative Grundlagen für die wissenschaftliche Nutzung umfangreicher Versorgungsdaten in Deutschland – Ergebnisse der AG Data Sharing der Medizininformatik-Initiative National standardisierter Broad Consent in der Praxis: erste Erfahrungen, aktuelle Entwicklungen und kritische Betrachtungen An innovative technological infrastructure for managing SARS-CoV-2 data across different cohorts in compliance with General Data Protection Regulation Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease Secondary use of patient data within decentralized studies using the example of rare diseases in Germany: A data scientist's exploration of process and lessons learned The costs of anonymization: case study using clinical data The Costs of Anonymization: Case Study Using Clinical Data Sleep apnea healthcare management in dynamically changing times : Unlocking the potential of digitalization for better care of obstructive sleep apnea—in Germany and beyond Data integration and analysis for circadian medicine Enabling open science in medicine through data sharing: an overview and assessment of common approaches from the European perspective Structured, harmonized, and interoperable integration of clinical routine data to compute heart failure risk scores White Paper - Verbesserung des Record Linkage für die Gesundheitsforschung in Deutschland Statistical biases due to anonymization evaluated in an open clinical dataset from COVID-19 patients EasySMPC: a simple but powerful no-code tool for practical secure multiparty computation SARS-CoV-2 infection in chronic kidney disease patients with pre-existing dialysis: description across different pandemic intervals and effect on disease course (mortality) Das Modell der Datentreuhand in der medizinischen Forschung Privacy-preserving data sharing infrastructures for medical research: systematization and comparison Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease Die COVID-19 Pandemie als Herausforderung und Chance für Register in der Versorgungsforschung: Erfahrungen aus Lean European Open Survey on SARS-CoV-2 Infected Patients (LEOSS) NFDI4Health – Nationale Forschungsdateninfrastruktur für personenbezogene Gesundheitsdaten Agile and privacy preserving data warehousing for biomedical research All-cause mortality and disease progression in SARS-CoV-2-infected patients with or without antibiotic therapy: an analysis of the LEOSS cohort Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease Outcomes of SARS-CoV-2 infections in patients with neurodegenerative diseases in the LEOSS cohort Design and evaluation of a data anonymization pipeline to promote Open Science on COVID-19 The use of machine learning in rare diseases: a scoping review Towards a comprehensive and interoperable representation of consent-based data usage permissions in the German medical informatics initiative A comprehensive tool for creating and evaluating privacy-preserving biomedical prediction models Pseudonymization for research data collection: is the juice worth the squeeze? Data Integration for Future Medicine (DIFUTURE) : An Architectural and Methodological Overview Neue Methoden für die anonyme Verarbeitung sensibler medizinischer Forschungsdaten Efficient and effective pruning strategies for health data de-identification The Importance of Context: Risk-based De-identification of Biomedical Data A generic solution for web-based management of pseudonymized data Incremental ontology-based integration for translational medical research Incremental Ontology-Based Integration for Translational Medical Research Informatics and Translational Medical Research: Challenges and Developments

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Katalog der Deutschen Nationalbibliothek

Fabian Praßer (1982-)

PROs als Kompass der intersektoralen onkologischen Versorgung – von der Praxis in das MTB und zurück

Comparison of Three Anonymization Tools for a Health Fitness Study

A quantitative analysis of the use of anonymization in biomedical research

Parallel privacy preservation through partitioning (P4): a scalable data anonymization algorithm for health data

Pseudonymization tools for medical research: a systematic review

A scoping review of privacy and utility metrics in medical synthetic data

Integrating the Patient Perspective into Healthcare and Real-World Evidence: The Multi-site, Cross-Disease, Patient-Centered Outcomes Research Project in the Medical Informatics Initiative (PCOR-MII)

EasySMPC: a simple but powerful no-code tool for practical secure multiparty computation

Secondary use of patient data within decentralized studies using the example of rare diseases in Germany: A data scientist's exploration of process and lessons learned

Technological interventions to alleviate alarm fatigue in intensive care medicine : an IT systems approach

Verbesserung des Record Linkage für die Gesundheitsforschung in Deutschland – wie können Defizite behoben werden?

An interactive dashboard for analyzing user interaction patterns in the i2b2 clinical data warehouse

Synthetic datasets for open software development in rare disease research

Synthetic data generation for a longitudinal cohort study – evaluation, method extension and reproduction of published data analysis results

Automatisierte Surveillance und Risikovorhersage mit dem Ziel einer risikostratifizierten Infektionskontrolle und -prävention (RISK Prediction for Risk-stratified Infection Control and Prevention)

Arbeitsgruppe Interoperabilität: Kerndatensatz und Informationssysteme für Integration und Austausch von Daten in der Medizininformatik-Initiative

Grundlagen für die wissenschaftliche Nutzung umfangreicher Versorgungsdaten in Deutschland – Ergebnisse der AG Data Sharing der Medizininformatik-Initiative

National standardisierter Broad Consent in der Praxis: erste Erfahrungen, aktuelle Entwicklungen und kritische Betrachtungen

An innovative technological infrastructure for managing SARS-CoV-2 data across different cohorts in compliance with General Data Protection Regulation

Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease

Secondary use of patient data within decentralized studies using the example of rare diseases in Germany: A data scientist's exploration of process and lessons learned

The costs of anonymization: case study using clinical data

The Costs of Anonymization: Case Study Using Clinical Data

Sleep apnea healthcare management in dynamically changing times : Unlocking the potential of digitalization for better care of obstructive sleep apnea—in Germany and beyond

Data integration and analysis for circadian medicine

Enabling open science in medicine through data sharing: an overview and assessment of common approaches from the European perspective

Structured, harmonized, and interoperable integration of clinical routine data to compute heart failure risk scores

White Paper - Verbesserung des Record Linkage für die Gesundheitsforschung in Deutschland

Statistical biases due to anonymization evaluated in an open clinical dataset from COVID-19 patients

EasySMPC: a simple but powerful no-code tool for practical secure multiparty computation

SARS-CoV-2 infection in chronic kidney disease patients with pre-existing dialysis: description across different pandemic intervals and effect on disease course (mortality)

Das Modell der Datentreuhand in der medizinischen Forschung

Privacy-preserving data sharing infrastructures for medical research: systematization and comparison

Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease

Die COVID-19 Pandemie als Herausforderung und Chance für Register in der Versorgungsforschung: Erfahrungen aus Lean European Open Survey on SARS-CoV-2 Infected Patients (LEOSS)

NFDI4Health – Nationale Forschungsdateninfrastruktur für personenbezogene Gesundheitsdaten

Agile and privacy preserving data warehousing for biomedical research

All-cause mortality and disease progression in SARS-CoV-2-infected patients with or without antibiotic therapy: an analysis of the LEOSS cohort

Clinical course and predictive risk factors for fatal outcome of SARS-CoV-2 infection in patients with chronic kidney disease

Outcomes of SARS-CoV-2 infections in patients with neurodegenerative diseases in the LEOSS cohort

Design and evaluation of a data anonymization pipeline to promote Open Science on COVID-19

The use of machine learning in rare diseases: a scoping review

Towards a comprehensive and interoperable representation of consent-based data usage permissions in the German medical informatics initiative

A comprehensive tool for creating and evaluating privacy-preserving biomedical prediction models

Pseudonymization for research data collection: is the juice worth the squeeze?

Data Integration for Future Medicine (DIFUTURE) : An Architectural and Methodological Overview

Neue Methoden für die anonyme Verarbeitung sensibler medizinischer Forschungsdaten

Efficient and effective pruning strategies for health data de-identification

The Importance of Context: Risk-based De-identification of Biomedical Data

A generic solution for web-based management of pseudonymized data

Incremental ontology-based integration for translational medical research

Incremental Ontology-Based Integration for Translational Medical Research

Informatics and Translational Medical Research: Challenges and Developments