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Open Access
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| Open Access“Uninsurable because of a genetic test”: a qualitative study of consumer views about the use of genetic test results in Australian life insurance
- Cassandra Muller
- , Lyndon Gallacher
- & Jane Tiller
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Review Article
| Open AccessOvercoming barriers to single-cell RNA sequencing adoption in low- and middle-income countries
- Tracy Boakye Serebour
- , Adam P. Cribbs
- & Sarah J. B. Snelling
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| Open AccessSecondary use of genomic data: patients’ decisions at point of testing and perspectives to inform international data sharing
- Melissa Martyn
- , Emily Forbes
- & Clara Gaff
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| Open AccessPerceptions and preferences for genetic testing for sickle cell disease or trait: a qualitative study in Cameroon, Ghana and Tanzania
- Nchangwi Syntia Munung
- , Karen Kengne Kamga
- & Ambroise Wonkam
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| Open AccessThe interplay of ethics and genetic technologies in balancing the social valuation of the human genome in UNESCO declarations
- Hristina Gaydarska
- , Kayo Takashima
- & Jusaku Minari
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Review Article
| Open AccessEthical and social reflections on the proposed European Health Data Space
- Ciara Staunton
- , Mahsa Shabani
- & Santa Slokenberga
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Should non-invasive prenatal testing (NIPT) be used for fetal sex determination? Perspectives and experiences of healthcare professionals
- Zoë Claesen-Bengtson
- , Hilary Bowman-Smart
- & Pascal Borry
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| Open AccessGlowing gels and pipettes aplenty: how do commercial stock image banks portray genetic tests?
- Rachel Horton
- , Leah Boyle
- & Anneke Lucassen
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| Open AccessEthical considerations for genetic research in low-income countries: perceptions of informed consent, data sharing, and expectations in Nicaragua
- Iris S. Delgado
- , Abigail Outterson
- & Catharine Wang
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Viewpoint |
Advancing intercontinental collaboration in human genetics: success story of the African and European Young Investigator Forum
- Mohamed Zahir Alimohamed
- , Khuthala Mnika
- & Magdalena Mroczek
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Parents’ attitudes towards research involving genome sequencing of their healthy children: a qualitative study
- Christina Di Carlo
- , Chloe Mighton
- & Yvonne Bombard
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Viewpoint
| Open AccessA framework for evaluating long-term impact of newborn screening
- Shona Kalkman
- , Ron A. Wevers
- & Mariska M. G. Leeflang
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Article
| Open Access‘It’s a nightmare’: informed consent in paediatric genome-wide sequencing. A qualitative expert interview study from Germany and Switzerland
- Johanna Eichinger
- , Bettina Zimmermann
- & Insa Koné
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The reuse of genetic information in research and informed consent
- David Lorenzo
- , Montse Esquerda
- & Francesc Palau
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Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography
- Janneke M. L. Kuiper
- , Pascal Borry
- & Ine Van Hoyweghen
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No need for options for choice for unsolicited findings in informed consent for clinical genetic testing
- Eline M. Bunnik
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Comment |
Comment on Australian public perspectives on genomic data governance by Lynch et al. in the EJHG
- Elisa J. F. Houwink
- & Eric W. Klee
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Article
| Open AccessReconciling the biomedical data commons and the GDPR: three lessons from the EUCAN ELSI collaboratory
- Alexander Bernier
- , Fruzsina Molnár-Gábor
- & Lauren Maxwell
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Article
| Open AccessDirect notification by health professionals of relatives at-risk of genetic conditions (with patient consent): views of the Australian public
- Jane M. Tiller
- , Ami Stott
- & Margaret Otlowski
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Consanguineous couples’ experiences and views regarding expanded carrier screening: Barriers and facilitators in the decision-making process
- Sanne van der Hout
- , Anke J. Woudstra
- & Guido de Wert
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Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations
- Ileen Slegers
- , Kathelijn Keymolen
- & Maaike Fobelets
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| Open AccessCommunity concerns about genetic discrimination in life insurance persist in Australia: A survey of consumers offered genetic testing
- Jane Tiller
- , Andrew Bakshi
- & Paul Lacaze
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Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations
- Fiona Lynch
- , Yan Meng
- & Danya F. Vears
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Viewpoint |
Old and new challenges regarding comparable and viable data sharing in population-scale genomic research
- Aviad Raz
- , Jusaku Minari
- & Ruth Horn
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| Open AccessImmortal data: a qualitative exploration of patients’ understandings of genomic data
- Kate Lyle
- , Susie Weller
- & Anneke Lucassen
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| Open AccessA practical checklist for return of results from genomic research in the European context
- Danya F. Vears
- , Nina Hallowell
- & Isabelle Budin-Ljøsne
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Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores
- Maria Siermann
- , Ophelia Valcke
- & Pascal Borry
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Experiences of nonpregnant couples after receiving reproductive genetic carrier screening results in Belgium
- Eva Van Steijvoort
- , Hilde Peeters
- & Pascal Borry
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| Open AccessViews of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
- Lucinda Freeman
- , Martin B. Delatycki
- & Edwin P. Kirk
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Article
| Open AccessGBA/GBN-position on the feedback of incidental findings in biobank-based research: consensus-based workflow for hospital-based biobanks
- Joerg Geiger
- , Joerg Fuchs
- & Roland Jahns
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Review Article |
Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review
- Laurent Pasquier
- , Maryn Reyneke
- & Pascal Borry
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| Open AccessBalancing the safeguarding of privacy and data sharing: perceptions of genomic professionals on patient genomic data ownership in Australia
- Yuwan Malakar
- , Justine Lacey
- & Denis C. Bauer
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Article
| Open AccessParticipant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study
- Roberta Biasiotto
- , Maria Kösters
- & Deborah Mascalzoni
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| Open AccessNon-invasive prenatal testing in Germany: a unique ethical and policy landscape
- Hilary Bowman-Smart
- , Claudia Wiesemann
- & Ruth Horn
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| Open AccessExperiences of pregnant women with genome-wide non-invasive prenatal testing in a national screening program
- Karuna R. M. van der Meij
- , Qiu Ying. F. van de Pol
- & Elsbeth H. van Vliet-Lachotzki
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Comment
| Open AccessGenetic Counsellors play a key role in supporting ethically responsible expanded universal carrier screening
- Lisa Dive
- , Lucinda Freeman
- & Alison McEwen
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The role of the Genetic Counsellor in the multidisciplinary team: the perception of geneticists in Europe
- Francesca Catapano
- , Mohamed El Hachmi
- & Christophe Cordier
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Comment
| Open AccessGenetic discrimination still casts a large shadow in 2022
- Yann Joly
- & Gratien Dalpe
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Article
| Open AccessApproaching discussions about genetics with palliative patients and their families: a qualitative exploration with genetic health professionals
- Stephanie White
- , Erin Turbitt
- & Chris Jacobs
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| Open AccessTen years of dynamic consent in the CHRIS study: informed consent as a dynamic process
- Deborah Mascalzoni
- , Roberto Melotti
- & Roberta Biasiotto
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| Open AccessHealth professionals’ views and experiences of the Australian moratorium on genetic testing and life insurance: A qualitative study
- Grace Dowling
- , Jane Tiller
- & Paul Lacaze
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Views of Canadian healthcare professionals on the future uses of non-invasive prenatal testing: a mixed method study
- Hazar Haidar
- , Stanislav Birko
- & Vardit Ravitsky
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Review Article
| Open AccessEthical, legal and social/societal implications (ELSI) of recall-by-genotype (RbG) and genotype-driven-research (GDR) approaches: a scoping review
- Katharina Tschigg
- , Luca Consoli
- & Deborah Mascalzoni
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Comment
| Open AccessEthically robust reproductive genetic carrier screening needs to measure outcomes that matter to patients
- Lisa Dive
- & Ainsley J. Newson
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Changes in opinions about human germline gene editing as a result of the Dutch DNA-dialogue project
- Diewertje Houtman
- , Boy Vijlbrief
- & Sam Riedijk
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Review Article
| Open AccessReceiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research
- Faye Johnson
- , Fiona Ulph
- & Kevin W. Southern
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Review Article
| Open AccessExploring the ethics of genetic prioritisation for COVID-19 vaccines
- Jago Bruce
- & Stephanie B. Johnson