About: Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal

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rdf:type	Item
description	article (en) ലേഖനം (ml) wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 2015 (uk) im März 2015 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56768446-98F6F80D-8C61-4A03-8D8C-3EC2D2620FBF
publication date	2015-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56768446-E038BF71-CA13-4428-8975-098801453C86
language of work or name	English
author name string	wds:Q56768446-06FE7DC1-B3D5-49C3-AD17-F3BF91F3D157 wds:Q56768446-280868DA-326A-4465-84B1-89415188E56E wds:Q56768446-38B607FF-3B8B-4331-98F5-96FA75FC2A1E wds:Q56768446-53CFF92C-9BFA-4854-8180-DB68568AA4A7 wds:Q56768446-598FDBD8-9FBD-4A6B-8CF5-12C79D424361 wds:Q56768446-831B509D-3907-4B29-B64B-9B7743C3F832 wds:Q56768446-BE0894D6-6AB5-4BE9-B357-186755EDB109 wds:Q56768446-EDEAFB63-AA2E-483D-B730-0FDFC4665B17 wds:Q56768446-F1CBF015-72C6-4BC8-8C20-0E50DF5CB5D2
author name string	Michael S Watson Adele Schneider Mary E Norton Anthony R Gregg Nancy C Rose Janice G Edwards Gerald Feldman James Goldberg Katie Stoll
rdfs:label	Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (en) Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (nl)
skos:prefLabel	Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (en) Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (nl)
name	Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (en) Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal (nl)
author	wds:Q56768446-B7CA1392-563C-4F60-959D-2E293AECDEA7
author	Ronald J Wapner
title	wds:Q56768446-625D0AB1-B025-455A-A141-A988F432C9E9
title	Expanded carrier screening in reproductive medicine-points to consider: a joint statement of the American College of Medical Genetics and Genomics, American College of Obstetricians and Gynecologists, National Society of Genetic Counselors, Perinatal Quality Foundation, and Society for Maternal-Fetal Medicine (en)
page(s)	wds:Q56768446-8EDAF0E2-7070-4032-8E30-6BC4BBE9990F
page(s)	653-662
instance of	wds:Q56768446-4006CF25-BAD1-4715-B3EB-CF9FA986F0F7 wds:Q56768446-8c0f91e6-23fd-45db-9400-1443c6654eff
instance of	editorial scholarly article
main subject	wds:Q56768446-245b60d1-cd87-4ab6-8057-9032643978c1 wds:Q56768446-2AF5FE7A-EB38-4DAC-A5D9-33BD06587DDB
main subject	medical genetics genomics
PubMed ID	wds:Q56768446-11691181-96BA-4836-836F-05DCEDB1AA67
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25730230
PubMed ID	25730230
published in	wds:Q56768446-65101FAE-FB23-4F30-AB79-0C1C057E3F11
published in	Obstetrics and Gynecology
issue	wds:Q56768446-98DBB370-64DD-4807-9525-E1C9BB547CF9
volume	wds:Q56768446-6D4F98AE-C2E8-447C-8F15-C9863519A5F8
issue	3
volume	125
DOI	wds:Q56768446-F06C82B9-9570-43F9-BD81-F8A59005A023
DOI	http://dx.doi.org/10.1097/AOG.0000000000000666
DOI	10.1097/AOG.0000000000000666
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56768446
is cites work of	Expanded carrier screening: A review of early implementation and literature Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives Responsible implementation of expanded carrier screening "It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare Obstetrician and Gynecologist Utilization of the Noninvasive Prenatal Testing Expanded Option Global genetic carrier testing: a vision for the future Recent advances in prenatal genetic screening and testing Swedish parents' interest in preconception genetic carrier screening Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics Experiences among Women with Positive Prenatal Expanded Carrier Screening Results Changing trends in carrier screening for genetic disease in the United States Pre- and post-testing counseling considerations for the provision of expanded carrier screening: exploration of European geneticists' views Business and Breakthrough: Framing (Expanded) Genetic Carrier Screening for the Public. A systematic analysis of online marketing materials used by providers of expanded carrier screening. Benefits and limitations of prenatal screening for Prader-Willi syndrome FMR1 premutation frequency in a large, ethnically diverse population referred for carrier testing. Connecting Gaucher and Parkinson Disease: Considerations for Clinical and Research Genetic Counseling Settings. Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus Population-based preconception carrier screening: how potential users from the general population view a test for 50 serious diseases. NGS-Based Assay for the Identification of Individuals Carrying Recessive Genetic Mutations in Reproductive Medicine Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape Genetic Counselors' Perspectives and Practices Regarding Expanded Carrier Screening after Initial Clinical Availability Swedish healthcare providers' perceptions of preconception expanded carrier screening (ECS)-a qualitative study Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for Governments Clinical Utility of Expanded Carrier Screening: Reproductive Behaviors of At-Risk Couples. Advantages of expanded universal carrier screening: what is at stake? Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing. Pregnant Women's Perspectives on Expanded Carrier Screening. Patient actions and reactions after receiving negative results from expanded carrier screening. Adopted Individuals' Views on the Utility and Value of Expanded Carrier Screening Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory The evolving landscape of expanded carrier screening: challenges and opportunities Recent developments in genetics and medically assisted reproduction: from research to clinical applications A data-driven evaluation of the size and content of expanded carrier screening panels Estimating yields of prenatal carrier screening and implications for design of expanded carrier screening panels Commentary: Expanded carrier screening: how much is too much?

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