Ethical and Counseling Challenges in Prenatal Exome Sequencing (Q56517284)

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scientific article published on 11 September 2018

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English	Ethical and Counseling Challenges in Prenatal Exome Sequencing	scientific article published on 11 September 2018

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instance of

scholarly article

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Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

title

Ethical and counseling challenges in prenatal exome sequencing (English)

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stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

author

Sarah Harris

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1

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Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

Neeta L. Vora

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5

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Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

author name string

Kelly Gilmore

series ordinal

2

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Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

Emily Hardisty

series ordinal

3

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stated in

Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

Anne Drapkin Lyerly

series ordinal

4

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Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

language of work or name

English

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publication date

11 September 2018

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stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

published in

Prenatal Diagnosis

1 reference

stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

volume

38

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Europe PubMed Central

PMC publication ID

6370459

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

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20 April 2020

issue

12

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Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

page(s)

897-903

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Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

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12 December 2020

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12 December 2020

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Ethics of prenatal ultrasound

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The "right not to know" in the genomic era: time to break from tradition?

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12 December 2020

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How do research participants perceive "uncertainty" in genome sequencing?

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12 December 2020

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Anticipate and communicate: Ethical management of incidental and secondary findings in the clinical, research, and direct-to-consumer contexts (December 2013 report of the Presidential Commission for the Study of Bioethical Issues).

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Hope and persuasion by physicians during informed consent

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12 December 2020

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Reporting genomic secondary findings: ACMG members weigh in.

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12 December 2020

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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

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12 December 2020

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Illustrative case studies in the return of exome and genome sequencing results

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12 December 2020

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12 December 2020

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Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Concerns About Justification for Fetal Genome Sequencing

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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A Framework for Unrestricted Prenatal Whole-Genome Sequencing: Respecting and Enhancing the Autonomy of Prospective Parents

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Promises, pitfalls and practicalities of prenatal whole exome sequencing

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Opening Pandora's box?: ethical issues in prenatal whole genome and exome sequencing

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Supporting Women's Autonomy in Prenatal Testing

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12 December 2020

based on heuristic

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Whole exome sequencing as a diagnostic adjunct to clinical testing in a tertiary referral cohort of 3988 fetuses with structural abnormalities.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Parental experiences of prenatal whole exome sequencing (WES) in cases of ultrasound diagnosed fetal structural anomaly

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Joint Position Statement from the International Society of Prenatal Diagnosis (ISPD), the Society of Maternal Fetal Medicine (SMFM) and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis

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https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

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Importance of complete phenotyping in prenatal whole exome sequencing

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reference URL

https://pubmed.ncbi.nlm.nih.gov/30171820

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/PD.5353

1 reference

stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

PMC publication ID

6370459

1 reference

stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

PubMed publication ID

30171820

1 reference

stated in

Europe PubMed Central

PMC publication ID

6370459

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30171820%20AND%20SRC:MED&resulttype=core&format=json

retrieved

20 April 2020

 

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