Featured
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Comment |
Expanded reproductive carrier screening—how can we do the most good and cause the least harm?
- Martin B. Delatycki
- , Nigel Laing
- & Edwin Kirk
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Article
| Open AccessFeasibility of couple-based expanded carrier screening offered by general practitioners
- Juliette Schuurmans
- , Erwin Birnie
- & Irene M. van Langen
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Article |
Autonomous decision-making for antenatal screening in Pakistan: views held by women, men and health professionals in a low–middle income country
- Shenaz Ahmed
- , Hussain Jafri
- & Mushtaq Ahmed
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Article |
Motivations for data sharing—views of research participants from four European countries: A DIRECT study
- Nisha Shah
- , Victoria Coathup
- & Jane Kaye
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Article
| Open AccessAustralians’ views and experience of personal genomic testing: survey findings from the Genioz study
- Jacqueline Savard
- , Chriselle Hickerton
- & Sylvia A. Metcalfe
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Article
| Open AccessNewborn dried blood spot samples in Denmark: the hidden figures of secondary use and research participation
- Francisca Nordfalk
- & Claus Thorn Ekstrøm
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Article |
Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
- Danya F. Vears
- , Emilia Niemiec
- & Pascal Borry
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Article |
Current practices for access, compensation, and prioritization in biobanks. Results from an interview study
- Holger Langhof
- , Hannes Kahrass
- & Daniel Strech
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Article |
Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate
- Marlies Saelaert
- , Heidi Mertes
- & Ignaas Devisch
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Viewpoint |
The FAIR guiding principles for data stewardship: fair enough?
- Martin Boeckhout
- , Gerhard A. Zielhuis
- & Annelien L. Bredenoord
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Article
| Open AccessUsing a genetic test result in the care of family members: how does the duty of confidentiality apply?
- Michael Parker
- & Anneke Lucassen
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Article |
Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe
- Fabio Sirchia
- , Daniele Carrieri
- & Susan E. Kelly
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Article |
Genetic diseases and information to relatives: practical and ethical issues for professionals after introduction of a legal framework in France
- Diane d’Audiffret Van Haecke
- & Sandrine de Montgolfier
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Article |
A randomized controlled study of a consent intervention for participating in an NIH genome sequencing study
- Erin Turbitt
- , Paola P Chrysostomou
- & Barbara B Biesecker
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Article
| Open AccessViews of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study
- Michael P Mackley
- , Edward Blair
- & Elizabeth Ormondroyd
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Article
| Open AccessThe RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers
- Sabina Gainotti
- , Paola Torreri
- & Domenica Taruscio
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Article |
Interpretations of autonomous decision-making in antenatal genetic screening among women in China, Hong Kong and Pakistan
- Shenaz Ahmed
- , Huso Yi
- & Mushtaq Ahmed
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Article |
Effect of deliberation on the public’s attitudes toward consent policies for biobank research
- Tom Tomlinson
- , Raymond G. De Vries
- & Scott Y. H. Kim
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Policy
| Open AccessHuman germline gene editing: Recommendations of ESHG and ESHRE
- Guido de Wert
- , Guido Pennings
- & Martina C. Cornel
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Policy
| Open AccessResponsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE
- Guido De Wert
- , Björn Heindryckx
- & Martina C. Cornel
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Review Article
| Open AccessRecent developments in genetics and medically assisted reproduction: from research to clinical applications
- J. C. Harper
- , K. Aittomäki
- & M. Macek Jr.
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Policy
| Open AccessOne small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans
- Heidi C. Howard
- , Carla G. van El
- & Martina C. Cornel
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Review Article |
Rules for processing genetic data for research purposes in view of the new EU General Data Protection Regulation
- Mahsa Shabani
- & Pascal Borry
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Article |
Points to consider for laboratories reporting results from diagnostic genomic sequencing
- D. F. Vears
- , K. Sénécal
- & P. Borry
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Review |
Third party interpretation of raw genetic data: an ethical exploration
- Lauren Badalato
- , Louiza Kalokairinou
- & Pascal Borry
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Article
| Open AccessRecontacting in clinical practice: the views and expectations of patients in the United Kingdom
- Daniele Carrieri
- , Sandi Dheensa
- & Susan E Kelly
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Article |
Acceptable applications of preimplantation genetic diagnosis (PGD) among Israeli PGD users
- Shachar Zuckerman
- , David A Zeevi
- & Gheona Altarescu
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Viewpoint |
Uninformed consent in nutrigenomic research
- A Cecile JW Janssens
- , Eline M Bunnik
- & Maartje HN Schermer
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Article
| Open AccessThe European Society of Human Genetics: beginnings, early history and development over its first 25 years
- Peter S Harper
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Article
| Open AccessThe RUDY study: using digital technologies to enable a research partnership
- Harriet J A Teare
- , Joanna Hogg
- & M Kassim Javaid
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Review |
Personal utility in genomic testing: a systematic literature review
- Jennefer N Kohler
- , Erin Turbitt
- & Barbara B Biesecker
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Short Report |
Paternity testing under the cloak of recreational genetics
- Nathalie Moray
- , Katherina E Pink
- & Maarten HD Larmuseau
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Letter |
Recontacting in clinical genetics and genomic medicine? We need to talk about it
- Daniele Carrieri
- , Sandi Dheensa
- & Susan E Kelly
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Article
| Open AccessRecontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom
- Daniele Carrieri
- , Sandi Dheensa
- & Susan E Kelly
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Article |
Access policies in biobank research: what criteria do they include and how publicly available are they? A cross-sectional study
- Holger Langhof
- , Hannes Kahrass
- & Daniel Strech
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Letter |
The Dutch legal approach regarding health care decisions involving minors in the NGS days
- Elcke J Kranendonk
- , Raoul C Hennekam
- & Martine Corrette Ploem
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Article |
Biobank attributes associated with higher patient participation: a randomized study
- Angèle Gayet-Ageron
- , Sandrine Rudaz
- & Thomas Perneger
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Article
| Open AccessRegistered access: a ‘Triple-A’ approach
- Stephanie O M Dyke
- , Emily Kirby
- & Bartha M Knoppers
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Article |
Advantages of expanded universal carrier screening: what is at stake?
- Sanne van der Hout
- , Kim CA Holtkamp
- & Wybo J Dondorp
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Article |
Who should have access to genomic data and how should they be held accountable? Perspectives of Data Access Committee members and experts
- Mahsa Shabani
- , Adrian Thorogood
- & Pascal Borry
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Article |
Whole-exome sequencing in pediatrics: parents’ considerations toward return of unsolicited findings for their child
- Candice Cornelis
- , Aad Tibben
- & Marieke van Summeren
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Article |
Return of individual genomic research results: what do consent forms tell participants?
- Stacey Pereira
- , Jill Oliver Robinson
- & Amy L McGuire
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Article |
Consent for newborn screening: parents’ and health-care professionals’ experiences of consent in practice
- Holly Etchegary
- , Stuart G Nicholls
- & Brenda Wilson
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Article
| Open AccessLegal approaches regarding health-care decisions involving minors: implications for next-generation sequencing
- Karine Sénécal
- , Kristof Thys
- & Pascal Borry