The ‘thousand-dollar genome’: an ethical exploration

Public Health Genomics and Genetic Test Evaluation: The Challenge of Conducting Behavioural Research on the Utility of Lifestyle-Genetic Tests

(2012) Saskia C. Sanderson et al.   Journal of Nutrigenetics and Nutrigenomics

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Ethical challenges in providing noninvasive prenatal diagnosis

(2010) Peter A Benn et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

Blurring lines

(2010) Heidi C Howard et al.   EMBO REPORTS

A novel custom resequencing array for dilated cardiomyopathy

(2010) Rebekah S Zimmerman et al.   GENETICS IN MEDICINE

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee 

(2010) J. Harper et al.   HUMAN REPRODUCTION

Challenges in the clinical application of whole-genome sequencing

(2010) Kelly E Ormond et al.   LANCET

The personal genome—the future of personalised medicine?

(2010) Nilesh J Samani et al.   LANCET

Clinical assessment incorporating a personal genome

(2010) Euan A Ashley et al.   LANCET

Let parents decide

(2010) Alan Handyside   NATURE

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

Comparison of Multiplex Ligation-Dependent Probe Amplification and Karyotyping in Prenatal Diagnosis

(2010) Elisabeth M. Boormans et al.   OBSTETRICS AND GYNECOLOGY

Increased nuchal translucency in euploid fetuses-what should we be telling the parents?

(2010) C.M. Bilardo et al.   PRENATAL DIAGNOSIS

Successful pregnancies after application of array-comparative genomic hybridization in PGS-aneuploidy screening

(2010) Ali Hellani et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Chasing a Disease to the Vanishing Point

(2010) J. Couzin-Frankel   SCIENCE

How Attitudes Research Contributes to Overoptimistic Expectations of Personal Genome Testing

(2009) Eline Bunnik et al.   AMERICAN JOURNAL OF BIOETHICS

Genetic research on stored tissue samples from minors: A systematic review of the ethical literature

(2009) Kristien Hens et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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

Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

(2009) Ron Hochstenbach et al.   European Journal of Medical Genetics

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate

(2009) E. Vanneste et al.   HUMAN REPRODUCTION

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

New challenges for informed consent through whole genome array testing

(2009) C Netzer et al.   JOURNAL OF MEDICAL GENETICS

Parents' Interest in Predictive Genetic Testing for Their Children When a Disease Has No Treatment

(2009) B. A. Tarini et al.   PEDIATRICS

Why Realistic Test Scenarios in Translational Genomics Research Remain Hypothetical

(2009) A.C.J.W. Janssens   Public Health Genomics

Children and Population Biobanks

(2009) D. Gurwitz et al.   SCIENCE

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

(2009) R. Drmanac et al.   SCIENCE

Genomic and personalized medicine: foundations and applications

(2009) Geoffrey S. Ginsburg et al.   Translational Research

THE MORAL OBLIGATION TO CREATE CHILDREN WITH THE BEST CHANCE OF THE BEST LIFE

(2008) JULIAN SAVULESCU et al.   BIOETHICS

Next-Generation Sequencing: The Race Is On

(2008) Andreas von Bubnoff   CELL

Genomic Medicine in Prenatal Diagnosis

(2008) SARAH T. SOUTH et al.   CLINICAL OBSTETRICS AND GYNECOLOGY

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

(2008) Sandra Darilek et al.   GENETICS IN MEDICINE

Generations of sequencing technologies

(2008) Erik Pettersson et al.   GENOMICS

Genome-based prediction of common diseases: advances and prospects

(2008) A. C. J.W. Janssens et al.   HUMAN MOLECULAR GENETICS

The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis

(2008) C. F. Wright et al.   HUMAN REPRODUCTION UPDATE

Comparing whole genomes using DNA microarrays

(2008) David Gresham et al.   NATURE REVIEWS GENETICS

Letting the Genome out of the Bottle — Will We Get Our Wish?

(2008) David J. Hunter et al.   NEW ENGLAND JOURNAL OF MEDICINE

Newborn screening

(2008) Bridget Wilcken et al.   PATHOLOGY

Current controversies in prenatal diagnosis 3: for prenatal diagnosis, should we offer less or more than metaphase karyotyping?

(2008) Caroline M. Ogilvie et al.   PRENATAL DIAGNOSIS

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

(2008) Ignatia B. Van den Veyver et al.   PRENATAL DIAGNOSIS

Genetic Mapping in Human Disease

(2008) D. Altshuler et al.   SCIENCE