Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
出版年份 2018 全文链接
标题
Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics
作者
关键词
-
出版物
EUROPEAN JOURNAL OF HUMAN GENETICS
Volume 27, Issue 2, Pages 169-182
出版商
Springer Nature
发表日期
2018-10-11
DOI
10.1038/s41431-018-0285-1
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Recontacting Patients with Updated Genetic Testing Recommendations for Medullary Thyroid Carcinoma and Pheochromocytoma or Paraganglioma
- (2018) Minerva A. Romero Arenas et al. ANNALS OF SURGICAL ONCOLOGY
- Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives
- (2018) Gea Beunders et al. European Journal of Medical Genetics
- Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
- (2018) Danya F. Vears et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Points to consider for laboratories reporting results from diagnostic genomic sequencing
- (2017) D. F. Vears et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Recontacting in clinical practice: the views and expectations of patients in the United Kingdom
- (2017) Daniele Carrieri et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom
- (2017) Daniele Carrieri et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Recontacting in clinical genetics and genomic medicine? We need to talk about it
- (2017) Daniele Carrieri et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A 'joint venture' model of recontacting in clinical genomics: challenges for responsible implementation
- (2017) Sandi Dheensa et al. European Journal of Medical Genetics
- Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom
- (2016) Daniele Carrieri et al. GENETICS IN MEDICINE
- Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research
- (2016) Emmanuelle Souzeau et al. Translational Vision Science & Technology
- Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research
- (2015) Anna Middleton et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Guidelines for diagnostic next-generation sequencing
- (2015) Gert Matthijs et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature
- (2014) Ellen Otten et al. GENETICS IN MEDICINE
- Personal utility in genomic testing: is there such a thing?
- (2014) Eline M Bunnik et al. JOURNAL OF MEDICAL ETHICS
- Defining and managing incidental findings in genetic and genomic practice
- (2014) Shiri Shkedi-Rafid et al. JOURNAL OF MEDICAL GENETICS
- The Challenges of Genome Analysis in the Health Care Setting
- (2014) Anneke Lucassen et al. Genes
- Consent and confidentiality in clinical genetic practice: guidance on genetic testing and sharing genetic information
- (2013) A. Lucassen et al. CLINICAL MEDICINE
- The ‘thousand-dollar genome’: an ethical exploration
- (2013) Wybo J Dondorp et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Whole-genome sequencing in health care
- (2013) Carla G van El et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process
- (2013) Carmen Ayuso et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The Coming Explosion in Genetic Testing — Is There a Duty to Recontact?
- (2011) Reed E. Pyeritz NEW ENGLAND JOURNAL OF MEDICINE
- What Is Clinical Utility and Why Should We Care?
- (2010) L J Lesko et al. CLINICAL PHARMACOLOGY & THERAPEUTICS
- Mainstreaming Genetics: A Comparative Review of Clinical Services for Inherited Cardiovascular Conditions in the UK
- (2010) H. Burton et al. Public Health Genomics
- Evaluating the utility of personal genomic information
- (2009) Morris W Foster et al. GENETICS IN MEDICINE
- What process attributes of clinical genetics services could maximise patient benefits?
- (2008) Marion McAllister et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
- (2008) Elina Rantanen et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information
- (2008) Brian H Shirts et al. GENETICS IN MEDICINE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started