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dr hab. Jan Domaradzki
Employment
- assistant professor at Poznan University of Medical Sciences
- 2003 - present assistant professor at Chair of Social Sciences and Humanities
Research fields
- sociology of medicine
- sociology of genetics
- biotechnology elsi
- social aspects of gentics
- spiritual care
- rare genetic disease
- family caregivers
- social represeantations of biotechnology
- Rare genetic diseases
- social implications of a new genetics
- social aspects of biotechnology
- representations of biotechnology in the media
- ELSI
- medical sociology
Publications
Filters
total: 70
Catalog Publications
Year 2022
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“We are also here”—Spiritual Care Practitioners’ Experiences of the COVID-19 Pandemic: A Qualitative Study from Poland
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‘Who Else If Not We’. Medical Students’ Perception and Experiences with Volunteering during the COVID-19 Crisis in Poznan, Poland
Publication
Year 2021
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Are rare diseases overlooked by medical education? Awareness of rare diseases among physicians in Poland: an explanatory study
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Does Religion Influence the Motivations of Future Healthcare Professionals to Volunteer During the COVID-19 Pandemic in Poland? An Exploratory Study
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Knowledge and Attitudes of Future Healthcare Professionals Toward Rare Diseases
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Medical Students' Voluntary Service During the COVID-19 Pandemic in Poland
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The Werther Effect, the Papageno Effect or No Effect? A Literature Review
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Thomas Szasz: The Uncompromising Rebel and Critic of Psychiatry
Publication
Year 2020
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Needs assessment study of rare diseases education for nurses and nursing students in Poland
Publication
Year 2019
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Medical students' knowledge and opinions about rare diseases: A case study from Poland
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Public Attitudes toward Biobanking of Human Biological Material for Research Purposes: A Literature Review
Publication
Year 2018
Year 2017
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Definitions of health and disease among physicians and Społem PSS employees
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Medykalizacja a genetyzacja: ciągłość czy zmiana?
Publication
Year 2016
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Behavioural genetics in Polish print news media between 2000-2014
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Family caregivers’ experiences with healthcare services: a case of Huntington disease
Publication
Year 2015
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Caring for patients with Huntington disease – A survey of caregivers’ experiences and views
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DNA and its Metaphors
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Patient rights, risk, and responsibilities in the genetic era – a right to know, a right not to know, or a duty to know?
Publication -
The Impact of Huntington Disease on Family Carers: a Literature Overview
Publication
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