Dávid Csercsik

Mr. Dávid Csercsik


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 January 2022 in PLOS Computational Biology
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Journal Article
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IRIstván Zoltán Reguly
István Zoltán Reguly
DCDávid Csercsik
Dávid Csercsik
JJJános Juhász
János Juhász
KTKálmán Tornai
Kálmán Tornai
ZBZsófia Bujtár
Zsófia Bujtár
ACAttila Csikász-Nagy
Attila Csikász-Nagy
Pandemic management requires reliable and efficient dynamical simulation to predict and control disease spreading. The COVID-19 (SARS-CoV-2) pandemic is mitigated by several non-pharmaceutical interventions, but it is hard to predict which of these are the most effective for a given population. We developed the computationally effective and scalable, agent-based microsimulation frameworkPanSim, allowing us to test control measures in multiple infection waves caused by the spread of a new virus variant in a city-sized societal environment using a unified framework fitted to realistic data. We show that vaccination strategies prioritising occupational risk groups minimise the number of infections but allow higher mortality while prioritising vulnerable groups minimises mortality but implies an increased infection rate. We also found that intensive vaccination along with non-pharmaceutical interventions can substantially suppress the spread of the virus, while low levels of vaccination, premature reopening may easily revert the epidemic to an uncontrolled state. Our analysis highlights that while vaccination protects the elderly from COVID-19, a large percentage of children will contract the virus, and we also show the benefits and limitations of various quarantine and testing scenarios. The uniquely detailed spatio-temporal resolution ofPanSimallows the design and testing of complex, specifically targeted interventions with a large number of agents under dynamically changing conditions.

7 April 2023 in IEEE Transactions on Wireless Communications
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Journal Article
Open access
DCDávid Csercsik
Dávid Csercsik
EJEduard A. Jorswieck
Eduard A. Jorswieck
We consider a general multi-connectivity framework, intended for ultra-reliable low-latency communications (URLLC) services, and propose a novel, preallocation-based combinatorial auction approach for the efficient allocation of channels. We compare the performance of the proposed method with several other state-of-the-art and alternative channel-allocation algorithms. The two proposed performance metrics are the capacity-based and the utility-based context. In the first case, every unit of additional capacity is regarded as beneficial for any tenant, independent of the already allocated quantity, and the main measure is the total throughput of the system. In the second case, we assume a minimal and maximal required capacity value for each tenant, and consider the implied utility values accordingly. In addition to the total system performance, we also analyze fairness and computational requirements in both contexts. We conclude that at the cost of higher but still plausible computational time, the fairness-enhanced version of the proposed preallocation based combinatorial auction algorithm outperforms every other considered method when one considers total system performance and fairness simultaneously, and performs especially well in the utility context. Therefore, the proposed algorithm may be regarded as candidate scheme for URLLC channel allocation problems, where minimal and maximal capacity requirements have to be considered.

3 December 2015 in Networks and Spatial Economics
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DCDávid Csercsik
Dávid Csercsik

1 June 2010 in BioSystems
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Journal Article
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DCDávid Csercsik
Dávid Csercsik
IFImre Farkas
Imre Farkas
GSGábor Szederkényi
Gábor Szederkényi
EHErik Hrabovszky
Erik Hrabovszky
ZLZsolt Liposits
Zsolt Liposits
KHKatalin Hangos
Katalin Hangos

18 September 2014 in Networks and Spatial Economics
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HHHelga Habis
Helga Habis
DCDávid Csercsik
Dávid Csercsik

3 January 2019 in Complexity
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Journal Article
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DCDávid Csercsik
Dávid Csercsik
Levente KovácsLevente Kovács
Levente Kovács
We formulate a dynamic model of vascular tumor growth, in which the interdependence of vascular dynamics with tumor volume is considered. The model describes the angiogenic switch; thus the inhibition of the vascularization process by antiangiogenic drugs may be taken into account explicitly. We validate the model against volume measurement data originating from experiments on mice and analyze the model behavior assuming different inputs corresponding to different therapies. Furthermore, we show that a simple extension of the model is capable of considering cytotoxic and antiangiogenic drugs as inputs simultaneously in qualitatively different ways.