Rudi Balling

Drug-target identification in COVID-19 disease mechanisms using computational systems biology approaches

Early-to-mid stage idiopathic Parkinson’s disease shows enhanced cytotoxicity and differentiation in CD8 T-cells in females

An action plan for pan-European defence against new SARS-CoV-2 variants

Deep sequencing of sncRNAs reveals hallmarks and regulatory modules of the transcriptome during Parkinson’s disease progression

Towards a European strategy to address the COVID-19 pandemic

Towards a European health research and innovation cloud (HRIC)

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy

MIC‐MAC: An automated pipeline for high‐throughput characterization and classification of three‐dimensional microglia morphologies in mouse and human postmortem brain samples

Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish

From hype to reality: data science enabling personalized medicine

Single‐cell transcriptomics reveals distinct inflammation‐induced microglia signatures

Systems medicine disease maps: community-driven comprehensive representation of disease mechanisms

Community-driven roadmap for integrated disease maps

Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic Features

The P4 Health Spectrum – A Predictive, Preventive, Personalized and Participatory Continuum for Promoting Healthspan

Making sense of big data in health research: Towards an EU action plan

The P4 Health Spectrum – A Predictive, Preventive, Personalized and Participatory Continuum for Promoting Healthspan

MINERVA—a platform for visualization and curation of molecular interaction networks

Loss of SYNJ1 dual phosphatase activity leads to early onset refractory seizures and progressive neurological decline

Erratum to: Making sense of big data in health research: towards an EU action plan

The phenotypic spectrum of <i>SCN8A</i> encephalopathy

Global implementation of genomic medicine: We are not alone

Recessive mutations in<i>SLC13A5</i>result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia

Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes

Systems Medicine Approaches for the Definition of Complex Phenotypes in Chronic Diseases and Ageing. From Concept to Implementation and Policies

Dynamic modelling of ROS management and ROS-induced mitophagy

Design principles study of ROS management and ROS-induced mitophagy with a kinetic model