Expanding citizen engagement in the secondary use of health data: an opportunity for national health data access bodies to realise the intentions of the European Health Data Space by Marlies Saelaert, Louise Mathieu, Wannes Van Hoof, Brecht Devleesschauwer

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Criteria for reporting incidental findings in clinical exome sequencing – a focus group study on professional practices and perspectives in Belgian genetic centres by Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch

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Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study by Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch

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A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings by Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Caroline Van Cauwenbergh, Bart P. Leroy, Ignaas Devisch, Elfride De Baere

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Opportunities for a population-based cohort in Belgium by Nienke Schutte, Marlies Saelaert, Petronille Bogaert, Karin De Ridder, Herman Van Oyen, Johan Van der Heyden, Brecht Devleesschauwer

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