Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. - Wikidata - awgldk - TriplyDB

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

http://www.wikidata.org/entity/Q36184534

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Recent advances in prenatal genetic screening and testing Developing context-specific next-generation sequencing policy Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives.Qualifying choice: ethical reflection on the scope of prenatal screening.Has Noninvasive Prenatal Testing (NIPT) Come of Age?Circulating Cell-Free Tumour DNA in the Management of Cancer.Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications Prenatal screening for fetal aneuploidies with cell-free DNA in the general pregnancy population: a cost-effectiveness analysis Non-invasive Prenatal Testing (NIPT): Better Meet an Expert!: The Case of a Late Detected Trisomy 13 Reveals Structural Problems in NIPT Counselling and Highlights Substantial Risks for the Reproductive Autonomy.Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.Whole Genome Sequencing and Newborn Screening Responsible implementation of expanded carrier screening.Prenatal pharmacogenomics: a promising area for research.Technological advances in precision medicine and drug development.Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.Report on noninvasive prenatal testing: classical and alternative approaches.Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives."I think we've got too many tests!": Prenatal providers' reflections on ethical and clinical challenges in the practice integration of cell-free DNA screening.Genomic futures of prenatal screening: ethical reflection.Socioeconomic Differences in Informed Decisions About Down Syndrome Screening: A Systematic Review and Research Agenda.Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.The benefits and limitations of cell-free DNA screening for 22q11.2 deletion syndrome.Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.Canadian women's attitudes toward noninvasive prenatal testing of fetal DNA in maternal plasma (.).Decision-making for non-invasive prenatal testing for Down syndrome: Hong Kong Chinese women's preferences for individual vs relational autonomy.Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion.Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions.Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.Cost-effectiveness of cell-free DNA in maternal blood testing for prenatal detection of trisomy 21, 18 and 13: a systematic review.Informative priors on fetal fraction increase power of the noninvasive prenatal screen.Genetic Counseling for Couples Seeking Noninvasive Prenatal Testing in Japan: Experiences of Pregnant Women and their Partners.The Shifting Landscape of Prenatal Testing: Between Reproductive Autonomy and Public Health.Toward an Ethically Sensitive Implementation of Noninvasive Prenatal Screening in the Global Context.Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options.Fetal therapy for Down syndrome: an ethical exploration.Responsible innovation in human germline gene editing: Background document to the recommendations of ESHG and ESHRE.Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.Sex discordance identification following non-invasive prenatal testing.Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude?

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Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

http://www.wikidata.org/entity/Q36184534

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2015 nî lūn-bûn

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European Journal of Human Genetics

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Non-invasive prenatal testing ...... ovation in prenatal screening.

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Aad Tibben

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Alison Hall

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Anneke Lucassen

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Borut Peterlin

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Carla G van El

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Carsten Bergmann

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Diana W Bianchi

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Dragica Radojkovic

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European Society of Human Genetics

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Florence Fellmann

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P2860

Update on Procedure-Related Risks for Prenatal Diagnosis Techniques

Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

Disability rights critique of prenatal genetic testing: Reflections and recommendations

Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

Review: cell-free fetal DNA in the maternal circulation as an indication of placental health and disease

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma

Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

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10.1038/EJHG.2015.57

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11

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23

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Lidewij Henneman

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Martina C Cornel

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