Judit Sándor

ORCID: 0000-0003-0134-4414
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About
Contact & Profiles
Research Areas
  • Biomedical Ethics and Regulation
  • Reproductive Health and Technologies
  • Patient Dignity and Privacy
  • Ethics in Clinical Research
  • Neuroethics, Human Enhancement, Biomedical Innovations
  • Ethics in medical practice
  • Ethics and Legal Issues in Pediatric Healthcare
  • CRISPR and Genetic Engineering
  • European and International Law Studies
  • Organ Donation and Transplantation
  • Law, AI, and Intellectual Property
  • Animal Genetics and Reproduction
  • European history and politics
  • BRCA gene mutations in cancer
  • Health, Medicine and Society
  • Intellectual Property and Patents
  • Global Security and Public Health
  • Healthcare, Law, Governance, and Management Studies
  • French Historical and Cultural Studies
  • Historical Studies on Reproduction, Gender, Health, and Societal Changes
  • Palliative Care and End-of-Life Issues
  • Psychology of Moral and Emotional Judgment
  • Privacy, Security, and Data Protection
  • Korean Peninsula Historical and Political Studies
  • Ovarian function and disorders

Central European University
2008-2023

Institute for Legal Studies
2017-2019

Ghent University
2016

European Commission
2016

Despite the increasing availability of direct-to-consumer (DTC) genetic testing, it is currently unclear how such services are regulated in Europe, due to lack EU or national legislation specifically addressing this issue. In article, we provide an overview laws that could potentially impact regulation DTC testing 26 European countries, namely Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg,...

10.1007/s12687-017-0344-2 article EN cc-by Journal of Community Genetics 2017-11-18

This article is concerned with the ultimate objectives of genetic biobanks set up to promote public interest—being sharing samples and data for medical research—and consequences personal privacy realising them. Our aim chart values, interests principles in play, consider challenges realizing biobanking on a global scale, propose viable ways forward that ensure, as far possible, access provisions remain fit purpose throughout entire life biobank, while adequately protecting at stake. It...

10.1177/096853321001000404 article EN Medical Law International 2010-09-01

Neuroenhancement involves the use of neurotechnologies to improve cognitive, affective or behavioural functioning, where these are not judged be clinically impaired. Questions about enhancement have become one key topics neuroethics over past decade. The current study draws on in-depth public engagement activities in ten European countries giving a bottom-up perspective ethics and desirability enhancement. This informed design an online contrastive vignette experiment that was administered...

10.1007/s12152-018-9366-7 article EN cc-by Neuroethics 2018-05-01

According to estimates more than 400 biobanks currently operate across Europe. The term 'biobank' indicates a specific field of genetic study that has quietly developed without any significant critical reflection European societies. Although scientists now routinely use this phrase, the wider public is still confused when word 'bank' being connected with collection their biological samples. There striking lack knowledge field. In recent Eurobarometer survey it was demonstrated even in 2010...

10.1136/jme.2010.041632 article EN Journal of Medical Ethics 2011-09-24

This report presents a comprehensive set of recommendations for protection human beings who are trafficked the purpose organ removal or targeted such trafficking. Developed by an interdisciplinary group international experts under auspices project Trafficking in Human Beings Purpose Organ Removal (also known as HOTT project), these grounded view that individual parts with money within illegal scheme is ipso facto victim and crime trafficking (THBOR) intersects organs. Consequently, victims...

10.1097/txd.0000000000000565 article EN cc-by-nc-nd Transplantation Direct 2016-01-05

Abstract Surveying the early responses to Covid‐19 pandemic among nation states, one finds a veritable babel of responses, some predictable and not. Would these results have been different half century or more ago, when smallpox was eradicated hopes were high that international cooperation would yield similar for other infectious diseases? Is this story about stability provided by bipolar postwar world, juxtaposed with complex geopolitical repositioning finally followed collapse Soviet...

10.1002/hast.1282 article EN The Hastings Center Report 2021-09-01

Abstract With the technical possibility of genome editing, we have reached a new phase transforming human beings and even altering our genetic legacy. Genome editing constitutes responsibilities in many fields. Science society never been as dependent on each other they are today. We must also learn from past episodes eugenics need to investigate fraudulent practices cases failure scientific research that often occurred due merciless competition, profit-seeking commercial interests, or...

10.1163/15718093-bja10081 article EN cc-by European Journal of Health Law 2022-04-08

The paper aims to understand the various legacies of eugenics in postwar period recognize both continuities and discontinuities with an approach which is conceptually sound historically correct. Building on earlier work Lene Koch, endeavours chart historical trajectory by examining how its definition those related or oppositional concepts have evolved within selected lexicon entries across stages century. inclusion publication a concept indicate significance, linguistic vitality, prevalence...

10.1007/s11019-024-10218-7 article EN cc-by Medicine Health Care and Philosophy 2024-07-16

State socialist Hungary undertook historically unparalleled action to satisfy the health needs of its population. To support efforts, it recognized in constitution protection as an essential state task and, later, a right health. Although formulated citizens, was not available enfranchise individual. Instead, expressed common social needs, well responsibility and institutional obligation take care those needs. This emphasis on over individual rights had crucial impact implementation...

10.5937/pravzap0-49493 article EN cc-by Pravni zapisi 2024-01-01

The analysis of the 2008 Hungarian law on human genetic data.

10.2139/ssrn.2295635 article EN SSRN Electronic Journal 2009-01-01

This paper is an overview and analysis of the relevant Greek laws on data protection, genetic research.

10.2139/ssrn.2295967 article EN SSRN Electronic Journal 2009-01-01

The law has struggled to justify the unilateral use of individual genomic data, as it could never quite fit either into narrower data protection or broader privacy frameworks. This article aims explore this tension by examining rights and interests biobank participants.This offers a legal analysis, looking at how model fits framework. Hungarian is primary focus but reference made international norms, well.The first biobanks were designed with purpose achieving collective goals providing...

10.1089/gtmb.2016.0400 article EN Genetic Testing and Molecular Biomarkers 2017-01-24
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