The use of empirical research in bioethics: a survey of researchers in twelve European countries by Tenzin Wangmo, Veerle Provoost

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Acceptable objectives of empirical research in bioethics: a qualitative exploration of researchers’ views by Emilian Mihailov, Veerle Provoost, Tenzin Wangmo

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An invisible caregiver for visibly older parents: Experiences of (young) adults shared as comments to newspaper articles on advanced age parenthood. by Kato Verghote, Priya Satalkar-Götz, Guido Pennings, Veerle Provoost

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‘I feel that injustice is being done to me’: a qualitative study of women’s viewpoints on the (lack of) reimbursement for social egg freezing by Michiel De Proost, Gily Coene, Julie Nekkebroeck, Veerle Provoost

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“It was a foregone conclusion”: a qualitative study of women’s experiences and meaning-making of later-in-life abortion in Belgium by Kato Verghote, Nathalie Neeser, Tenzin Wangmo, Guido Pennings, Veerle Provoost

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“I’m not your grandpa”: Experiences of advanced age fathers raising their teenage children in Belgium, an interpretative phenomenological analysis by Steven R. Piek, Kato Verghote, Andrea Martani, Guido Pennings, Veerle Provoost

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The last vial. What it means to (aspiring) parents to use the same sperm donor for siblings by Sara Somers, Veerle Provoost, An Ravelingien, Ann Buysse, Guido Pennings, Petra De Sutter

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Correction to: ‘A radical operation’ – a thematic analysis of newspaper framing of bariatric surgery in adolescents by Sander Lefere, Kato Verghote, Ruth De Bruyne, Veerle Provoost, Priya P. Satalkar

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‘A radical operation’ – a thematic analysis of newspaper framing of bariatric surgery in adolescents by Sander Lefere, Kato Verghote, Ruth De Bruyne, Veerle Provoost, Priya P. Satalkar

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An update on the “empirical turn” in bioethics: analysis of empirical research in nine bioethics journals by Tenzin Wangmo, Sirin Hauri, Eloise Gennet, Evelyn Anane-Sarpong, Veerle Provoost, Bernice S. Elger

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Public and patient involvement in health data governance (DATAGov): protocol of a people-centred, mixed-methods study on data use and sharing for rare diseases care and research by Susana Silva, Alicia Renedo, Cláudia de Freitas, Mariana Amorim, Helena Machado, Elisa Leão Teles, Maria João Baptista, Veerle Provoost

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Standards of practice in empirical bioethics research: towards a consensus by Jonathan Ives, Michael Dunn, Bert Molewijk, Jan Schildmann, Kristine Bærøe, Lucy Frith, Richard Huxtable, Elleke Landeweer, Marcel Mertz, Veerle Provoost, Annette Rid, Sabine Salloch, Mark Sheehan, Daniel Strech, Martine de Vries, Guy Widdershoven

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