Whole-genome sequencing in health care

Whole-genome sequencing and the physician

(2012) A Thorogood et al.   CLINICAL GENETICS

The changing landscape of genetic testing and its impact on clinical and laboratory services and research in Europe

(2012) Ros Hastings et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Developing a policy for paediatric biobanks: principles for good practice

(2012) Kristien Hens et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent

(2012) Wybo Dondorp et al.   HUMAN MUTATION

The use of arrays to detect copy-number variations in clinical practice

(2012) Birgit Sikkema-Raddatz et al.   HUMAN MUTATION

Genome-wide arrays: Quality criteria and platforms to be used in routine diagnostics

(2012) Joris R. Vermeesch et al.   HUMAN MUTATION

Diagnostic interpretation of array data using public databases and internet sources

(2012) Nicole de Leeuw et al.   HUMAN MUTATION

The Ethical Hazards and Programmatic Challenges of Genomic Newborn Screening

(2012) Aaron J. Goldenberg et al.   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

De novo mutations in human genetic disease

(2012) Joris A. Veltman et al.   NATURE REVIEWS GENETICS

Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

(2012) Marco Gerlinger et al.   NEW ENGLAND JOURNAL OF MEDICINE

Incidental Medical Information in Whole-Exome Sequencing

(2012) B. D. Solomon et al.   PEDIATRICS

Between hype and hope: whole-genome sequencing in clinical medicine

(2012) Iris Schrijver et al.   Personalized Medicine

Noninvasive Whole-Genome Sequencing of a Human Fetus

(2012) J. O. Kitzman et al.   Science Translational Medicine

The Predictive Capacity of Personal Genome Sequencing

(2012) N. J. Roberts et al.   Science Translational Medicine

Rapid Whole-Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units

(2012) C. J. Saunders et al.   Science Translational Medicine

Genetic testing and common disorders in a public health framework

(2011) Carla G van El et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time

(2011) Jonathan S Berg et al.   GENETICS IN MEDICINE

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

(2011) P. Borry et al.   HUMAN REPRODUCTION

Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing

(2011) C. J. Bell et al.   Science Translational Medicine

Communication of biobanks' research results: What do (potential) participants want?

(2010) Tineke M. Meulenkamp et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Statement of the ESHG on direct-to-consumer genetic testing for health-related purposes

(2010)   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical assessment incorporating a personal genome

(2010) Euan A Ashley et al.   LANCET

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

A de novo paradigm for mental retardation

(2010) Lisenka E L M Vissers et al.   NATURE GENETICS

Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

(2010) James R. Lupski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing

(2010) J. C. Roach et al.   SCIENCE

Disclosure of individual genetic data to research participants: the debate reconsidered

(2010) Annelien L. Bredenoord et al.   TRENDS IN GENETICS

Non-invasive prenatal testing: ethical issues explored

(2009) Antina de Jong et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic testing in asymptomatic minors: recommendations of the European Society of Human Genetics

(2009)   EUROPEAN JOURNAL OF HUMAN GENETICS

Predictive diagnosis of the cancer prone Li-Fraumeni syndrome by accident: new challenges through whole genome array testing

(2009) T Schwarzbraun et al.   JOURNAL OF MEDICAL GENETICS

Exome sequencing identifies the cause of a mendelian disorder

(2009) Sarah B Ng et al.   NATURE GENETICS

The complete genome of an individual by massively parallel DNA sequencing

(2008) David A. Wheeler et al.   NATURE