Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies-Reference-Cited by-同舟云学术

Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies

Published:2022-05-04 Issue:7 Volume:42 Page:947-954
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Kernie Catherine G.¹^ORCID,Wynn Julia²,Rosenbaum Allison¹,de Voest Jessica³,Galloway Stephanie⁴,Giordano Jessica⁴^ORCID,Stover Samantha⁵,Westerfield Lauren⁵,Gilmore Kelly⁶,Wapner Ronald J.⁴,Van den Veyver Ignatia B.⁵^ORCID,Vora Neeta L.⁶^ORCID,Clifton Rebecca G.³,Caughey Aaron B.⁷,Chung Wendy K.²⁸

Affiliation:

1. Columbia University Vagelos College of Physicians & Surgeons New York New York USA

2. Department of Pediatrics Columbia University Irving Medical Center New York New York USA

3. George Washington University Biostatistics Center Washington District of Columbia USA

4. Department of Obstetrics and Gynecology Columbia University Irving Medical Center New York New York USA

5. Department of Obstetrics & Gynecology and Molecular & Human Genetics Baylor College of Medicine, and Texas Children's Hospital Houston Texas USA

6. Department of Obstetrics & Gynecology University of North Carolina Chapel Hill Chapel Hill North Carolina USA

7. Department of Obstetrics & Gynecology Oregon Health & Science University Portland Oregon USA

8. Department of Medicine Columbia University Irving Medical Center New York New York USA

Funder

National Institute of Child Health and Human Development

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6153

Reference28 articles.

1. Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

2. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

3. Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact

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1. ‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service;Prenatal Diagnosis;2024-03-05

2. Improving prenatal diagnosis through standards and aggregation;Prenatal Diagnosis;2024-01-19

3. Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US;Prenatal Diagnosis;2023-09-26