Featured
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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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Article
| Open AccessSexual dimorphism in the genetic influence on human childlessness
- Renske M Verweij
- , Melinda C Mills
- & Harold Snieder
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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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Article |
From older to younger: intergenerational promotion of health behaviours in Portuguese families affected by familial amyloid polyneuropathy
- Carla Roma Oliveira
- , Alvaro Mendes
- & Liliana Sousa
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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 |
Psychosocial effects in parents and children 12 years after newborn genetic screening for type 1 diabetes
- Nicola J Kerruish
- , Dione M Healey
- & Andrew R Gray
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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
| Open AccessPsychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project
- Saskia C Sanderson
- , Michael D Linderman
- & Eric E Schadt
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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 |
Communicating microarray results of uncertain clinical significance in consultation summary letters and implications for practice
- Jean Lillian Paul
- , Rachel Pope-Couston
- & Tiong Yang Tan
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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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Book Review |
Genomics and society—Ethical, Legal, Cultural and Socioeconomic Implication
- Mats Hansson
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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
| Open AccessSupporting genetics in primary care: investigating how theory can inform professional education
- Brenda J Wilson
- , Rafat Islam
- & June C Carroll
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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
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Article
| Open AccessThe risk of re-identification versus the need to identify individuals in rare disease research
- Mats G Hansson
- , Hanns Lochmüller
- & Simon Woods
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Article |
‘You should at least ask’. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research
- Pauline McCormack
- , Anna Kole
- & Simon Woods
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Article
| Open AccessImproving the informed consent process in international collaborative rare disease research: effective consent for effective research
- Sabina Gainotti
- , Cathy Turner
- & Deborah Mascalzoni
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Clinical Utility Gene Card |
Clinical utility gene card for: Familial platelet disorder with associated myeloid malignancies
- Tim Ripperger
- , Kiran Tawana
- & Doris Steinemann
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Review |
A decision tool to guide the ethics review of a challenging breed of emerging genomic projects
- Yann Joly
- , Derek So
- & Bartha Knoppers
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Article |
Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals
- Melissa Hill
- , Jo-Ann Johnson
- & Lyn S Chitty
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Policy |
Big Data in medical research and EU data protection law: challenges to the consent or anonymise approach
- Menno Mostert
- , Annelien L Bredenoord
- & Johannes J M van Delden
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Article
| Open AccessDevelopment and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
- Celine Lewis
- , Melissa Hill
- & Lyn S Chitty
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Article |
Patient hopes for diagnostic genomic sequencing: roles of uncertainty and social status
- Cynthia M Khan
- , Elizabeth G Moore
- & Christine Rini