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Open Access
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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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Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research
- Hadley Stevens Smith
- , Emily S. Bonkowski
- & Stacey Pereira
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Brief Communication
| Open AccessIs there a “pandemic effect” on individuals’ willingness to take genetic tests?
- Thibaud Deruelle
- , Veronika Kalouguina
- & Joël Wagner
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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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Review Article
| Open AccessHow does the genomic naive public perceive whole genomic testing for health purposes? A scoping review
- Isabella A. Sherburn
- , Keri Finlay
- & Stephanie Best
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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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Lessons learned during the process of reporting individual genomic results to participants of a population-based biobank
- Liis Leitsalu
- , Anu Reigo
- & Andres Metspalu
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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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Article
| 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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Article
| 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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A unique service: how an embedded psychology team can help patients and genetics clinicians within a clinical genetics service
- Clare Firth
- , Vishakha Tripathi
- & Charlotte Tomlinson
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Article
| Open AccessPerceptions of causal attribution and attitudes to genetic testing among people with schizophrenia and their first-degree relatives
- Melissa B. R. Cullen
- , Bettina Meiser
- & Rajneesh Kaur
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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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Article
| Open AccessParticipant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study
- Michelle Peter
- , Jennifer Hammond
- & Celine Lewis
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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
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Comment
| Open AccessComment on Informing relatives of their genetic risk: an examination of the Belgian context
- Aisling de Paor
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Comment |
Comment on Future trends in clinical genetic and genomic services by Borle et al.
- Elisa J. F. Houwink
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Viewpoint |
The Young Geneticists Network and the ESHG-Young committee, a forward-looking international community
- Florence Riccardi
- , Ruta Marcinkute
- & Can Ding
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Informing relatives of their genetic risk: an examination of the Belgian legal context
- Amicia Phillips
- , Thomas Bronselaer
- & Stefaan Callens
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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial
- Lieke M. van den Heuvel
- , Yvonne M. Hoedemaekers
- & Imke Christiaans
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Article
| Open AccessMotives for withdrawal of participation in biobanking and participants’ willingness to allow linkages of their data
- Reinder Broekstra
- , Judith L. Aris-Meijer
- & Sabine Otten
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Article
| Open AccessAttitudes among parents of persons with autism spectrum disorder towards information about genetic risk and future health
- Jarle Johannessen
- , Terje Nærland
- & Ole A. Andreassen
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Article
| Open AccessGenomic health data generation in the UK: a 360 view
- Elizabeth Ormondroyd
- , Peter Border
- & Andrew Papanikitas
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Article
| Open AccessThe ethical landscape(s) of non-invasive prenatal testing in England, France and Germany: findings from a comparative literature review
- Adeline Perrot
- & Ruth Horn
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Article
| Open AccessWhat is a ‘serious’ genetic condition? The perceptions of people living with genetic conditions
- Felicity K. Boardman
- & Corinna C. Clark
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Australian human research ethics committee members’ confidence in reviewing genomic research applications
- Ryan Pysar
- , Courtney K. Wallingford
- & Aideen M. McInerney-Leo
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Non-invasive prenatal testing (NIPT) and pregnant women’s views on good motherhood: a qualitative study
- Elisa Garcia
- , Lidewij Henneman
- & Danielle R. M. Timmermans
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Physicians’ perceptions of the factors influencing disclosure of secondary findings in tumour genomic profiling in Japan: a qualitative study
- Saki Shimada
- , Takahiro Yamada
- & Shinji Kosugi
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Article
| Open AccessRoutinization of prenatal screening with the non-invasive prenatal test: pregnant women’s perspectives
- Karuna R. M. van der Meij
- , Annabel Njio
- & Lidewij Henneman
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Review Article |
Establishing a second-generation artificial intelligence-based system for improving diagnosis, treatment, and monitoring of patients with rare diseases
- Noa Hurvitz
- , Henny Azmanov
- & Yaron Ilan
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Why do people seek out polygenic risk scores for complex disorders, and how do they understand and react to results?
- Larissa Peck
- , Kennedy Borle
- & Jehannine Austin
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Parent clinical trial priorities for fragile X syndrome: a best–worst scaling
- Erin Turbitt
- , Celeste D’Amanda
- & Barbara B. Biesecker
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Article
| Open AccessCouples’ experiences with expanded carrier screening: evaluation of a university hospital screening offer
- Ivy van Dijke
- , Phillis Lakeman
- & Lidewij Henneman
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Article
| Open AccessCascade screening for beta-thalassemia in Pakistan: development, feasibility and acceptability of a decision support intervention for relatives
- Shenaz Ahmed
- , Hussain Jafri
- & Mushtaq Ahmed
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Article
| Open AccessStakeholder engagement to ensure the sustainability of biobanks: a survey of potential users of biobank services
- Corinna Klingler
- , Magdaléna von Jagwitz-Biegnitz
- & Cornelia Specht
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Article
| Open AccessBalancing scientific interests and the rights of participants in designing a recall by genotype study
- Deborah Mascalzoni
- , Roberta Biasiotto
- & Andrew A. Hicks
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Article
| Open AccessInternational transfers of personal data for health research following Schrems II: a problem in need of a solution
- Dara Hallinan
- , Alexander Bernier
- & Stéphanie Rennes
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Article
| Open AccessHow do non-geneticist physicians deal with genetic tests? A qualitative analysis
- Laurent Pasquier
- , Guy Minguet
- & Grégoire Moutel
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Article
| Open AccessToward the diagnosis of rare childhood genetic diseases: what do parents value most?
- Samantha Pollard
- , Deirdre Weymann
- & Dean A. Regier
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Viewpoint
| Open AccessMoving somatic gene editing to the clinic: routes to market access and reimbursement in Europe
- Tessel Rigter
- , David Klein
- & Martina C. Cornel
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Article
| Open AccessWhat people really change after genetic testing (GT) performed in private labs: results from an Italian study
- Serena Oliveri
- , Clizia Cincidda
- & Gabriella Pravettoni
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The Ami and Yami aborigines of Taiwan and their genetic relationship to East Asian and Pacific populations
- Kai Tätte
- , Ene Metspalu
- & Rene J. Herrera
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The impact of unsolicited findings in clinical exome sequencing, a qualitative interview study
- Vyne van der Schoot
- , Simone J. Viellevoije
- & Anke J. M. Oerlemans