Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing-Reference-Cited by-同舟云学术

Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing

Published:2019-09-03 Issue:6 Volume:28 Page:1107-1118
ISSN:1059-7700
Container-title:Journal of Genetic Counseling
language:en
Short-container-title:Jrnl of Gene Coun

Author:

Reuter Chloe M.¹²,Kohler Jennefer N.¹²,Bonner Devon¹²,Zastrow Diane¹²,Fernandez Liliana¹²,Dries Annika¹²,Marwaha Shruti¹²,Davidson Jean¹²,Brokamp Elly³,Herzog Matthew⁴,Hong Joyce⁵,Macnamara Ellen⁶,Rosenfeld Jill A.⁷,Schoch Kelly⁸,Spillmann Rebecca⁸,Loscalzo Joseph⁵,Krier Joel⁵,Stoler Joan⁹,Sweetser David¹⁰,Palmer Christina G.S.⁴¹¹¹²,Phillips John A.³,Shashi Vandana⁸,Adams David A.⁶,Yang Yaping⁷,Ashley Euan A.¹²¹³,Fisher Paul G.¹¹⁴¹⁵,Mulvihill John J.¹⁶,Bernstein Jonathan A.¹¹⁵,Wheeler Matthew T.¹²,

Affiliation:

1. Center for Undiagnosed Diseases Stanford University School of Medicine Stanford CA

2. Division of Cardiovascular Medicine Stanford University School of Medicine Stanford CA

3. Department of Pediatrics Vanderbilt University Medical Center Nashville TN

4. Department of Human Genetics University of California Los Angeles Los Angeles CA

5. Department of Medicine Brigham and Women’s Hospital Boston MA

6. Undiagnosed Diseases Program National Human Genome Research Institute, National Institutes of Health Bethesda MD

7. Department of Molecular and Human Genetics Baylor College of Medicine Houston TX

8. Department of Pediatrics Duke University Medical Center Durham NC

9. Division of Genetics Boston Children’s Hospital Boston MA

10. Division of Medical Genetics and Metabolism, Department of Pediatrics Massachusetts General Hospital Boston MA

11. Psychiatry & Biobehavioral Sciences University of California Los Angeles Los Angeles CA

12. Institute for Society & Genetics University of California Los Angeles Los Angeles CA

13. Department of Genetics Stanford University School of Medicine Stanford CA

14. Department of Neurology and Neurological Sciences Stanford University School of Medicine Stanford CA

15. Department of Pediatrics Stanford University School of Medicine Stanford CA

16. Division of Genomic Medicine National Human Genome Research Institute Bethesda MD

Publisher

Wiley

Subject

Genetics (clinical)

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgc4.1161

Reference33 articles.

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2. Unsolved challenges of clinical whole‐exome sequencing: A systematic literature review of end‐users’ views;Bertier G.;BMC Medical Genomics,2016

3. Chromosomal microarray testing influences medical management

4. Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

5. Clinical Integration of Next Generation Sequencing: Coverage and Reimbursement Challenges

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