Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

M Ragan Hart^{1

2}, Barbara B Biesecker³, Carrie L Blout⁴, Kurt D Christensen^{4

5}, Laura M Amendola^{6

7}, Katie L Bergstrom⁸, Sawona Biswas⁹, Kevin M Bowling¹⁰, Kyle B Brothers¹¹, Laura K Conlin^{12

13}, Greg M Cooper¹⁰, Matthew C Dulik^{12

13}, Kelly M East¹⁰, Jessica N Everett^{14

15}, Candice R Finnila¹⁰, Arezou A Ghazani¹⁶, Marian J Gilmore¹⁷, Katrina A B Goddard¹⁸, Gail P Jarvik^{6

7}, Jennifer J Johnston¹⁹, Tia L Kauffman¹⁸, Whitley V Kelley¹⁰, Joel B Krier⁴, Katie L Lewis¹⁹, Amy L McGuire²⁰, Carmit McMullen¹⁸, Jeffrey Ou⁷, Sharon E Plon⁸, Heidi L Rehm^{5

21

22}, C Sue Richards²³, Edward J Romasko¹², Ane Miren Sagardia³, Nancy B Spinner¹², Michelle L Thompson¹⁰, Erin Turbitt³, Jason L Vassy^{4

5

24}, Benjamin S Wilfond²⁵, David L Veenstra^#^{7

26}, Jonathan S Berg^#²⁷, Robert C Green^#^{4

5

22

28}, Leslie G Biesecker^#¹⁹, Lucia A Hindorff^#²⁹

Affiliations

¹ Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA. hartmr@uw.edu.
² Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA. hartmr@uw.edu.
³ Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
⁴ Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
⁵ Harvard Medical School, Boston, MA, USA.
⁶ Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA.
⁷ Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA.
⁸ Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX, USA.
⁹ Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
¹⁰ HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
¹¹ Department of Pediatrics, University of Louisville, Louisville, KY, USA.
¹² Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
¹³ Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
¹⁴ Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
¹⁵ Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, MI, USA.
¹⁶ Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
¹⁷ Department of Medical Genetics, Kaiser Permanente Northwest, Portland, OR, USA.
¹⁸ Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
¹⁹ Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
²⁰ Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX, USA.
²¹ Laboratory for Molecular Medicine, Partners HealthCare, Cambridge, MA, USA.
²² Broad Institute of MIT and Harvard, Cambridge, MA, USA.
²³ Knight Diagnostic Laboratories, Oregon Health Science University, Portland, OR, USA.
²⁴ VA Boston Healthcare System, Boston, MA, USA.
²⁵ Department of Pediatrics and Seattle Children's Research Institute, University of Washington, Seattle, WA, USA.
²⁶ Department of Pharmacy, University of Washington, Seattle, WA, USA.
²⁷ Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
²⁸ Partners Personalized Medicine, Boston, MA, USA.
²⁹ Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. hindorffl@mail.nih.gov.

^# Contributed equally.

PMID: 30670880
DOI: 10.1038/s41436-019-0440-2

Free article

Published Erratum

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

M Ragan Hart et al. Genet Med. 2019 May.

Free article

. 2019 May;21(5):1261-1262.

doi: 10.1038/s41436-019-0440-2.

Authors

Affiliations

¹ Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA. hartmr@uw.edu.
² Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA. hartmr@uw.edu.
³ Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
⁴ Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
⁵ Harvard Medical School, Boston, MA, USA.
⁶ Department of Medicine (Medical Genetics), University of Washington, Seattle, WA, USA.
⁷ Clinical Sequencing Exploratory Research Coordinating Center, University of Washington, Seattle, WA, USA.
⁸ Department of Pediatrics, Oncology Section, Baylor College of Medicine, Houston, TX, USA.
⁹ Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
¹⁰ HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
¹¹ Department of Pediatrics, University of Louisville, Louisville, KY, USA.
¹² Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital, Philadelphia, PA, USA.
¹³ Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
¹⁴ Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
¹⁵ Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, MI, USA.
¹⁶ Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
¹⁷ Department of Medical Genetics, Kaiser Permanente Northwest, Portland, OR, USA.
¹⁸ Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
¹⁹ Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
²⁰ Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX, USA.
²¹ Laboratory for Molecular Medicine, Partners HealthCare, Cambridge, MA, USA.
²² Broad Institute of MIT and Harvard, Cambridge, MA, USA.
²³ Knight Diagnostic Laboratories, Oregon Health Science University, Portland, OR, USA.
²⁴ VA Boston Healthcare System, Boston, MA, USA.
²⁵ Department of Pediatrics and Seattle Children's Research Institute, University of Washington, Seattle, WA, USA.
²⁶ Department of Pharmacy, University of Washington, Seattle, WA, USA.
²⁷ Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
²⁸ Partners Personalized Medicine, Boston, MA, USA.
²⁹ Division of Genomic Medicine, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. hindorffl@mail.nih.gov.

^# Contributed equally.

PMID: 30670880
DOI: 10.1038/s41436-019-0440-2

Abstract

The originally published version of this Article contained errors in Fig. 2. The numbers below the black arrowheads were incorrect; please see incorrect Figure in associated Correction. These errors have now been corrected in the PDF and HTML versions of the Article.

PubMed Disclaimer

Erratum for

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Miren Sagardia A, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA. Hart MR, et al. Genet Med. 2019 May;21(5):1100-1110. doi: 10.1038/s41436-018-0308-x. Epub 2018 Oct 5. Genet Med. 2019. PMID: 30287922 Free PMC article.

Publication types

Actions

LinkOut - more resources

Full Text Sources
- Elsevier Science

Save citation to file

Email citation

Add to Collections

Add to My Bibliography

Your saved search

Create a file for external citation management software

Your RSS Feed

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

Affiliations

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study

Authors

Affiliations

Abstract

Erratum for

Publication types

LinkOut - more resources

Full Text Sources