Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)

M. Ragan Hart; Barbara B. Biesecker; Carrie L. Blout; Kurt D. Christensen; Laura M. Amendola; Katie L. Bergstrom; Sawona Biswas; Kevin M. Bowling; Kyle B. Brothers; Laura K. Conlin; Greg M. Cooper; Matthew C. Dulik; Kelly M. East; Jessica N. Everett; Candice R. Finnila; Arezou A. Ghazani; Marian J. Gilmore; Katrina A.B. Goddard; Gail P. Jarvik; Jennifer J. Johnston; Tia L. Kauffman; Whitley V. Kelley; Joel B. Krier; Katie L. Lewis; Amy L. McGuire; Carmit McMullen; Jeffrey Ou; Sharon E. Plon; Heidi L. Rehm; C. Sue Richards; Edward J. Romasko; Ane Miren Sagardia; Nancy B. Spinner; Michelle L. Thompson; Erin Turbitt; Jason L. Vassy; Benjamin S. Wilfond; David L. Veenstra; Jonathan S. Berg; Robert C. Green; Leslie G. Biesecker; Lucia A. Hindorff

doi:10.1038/s41436-019-0440-2

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)

M. Ragan Hart, Barbara B. Biesecker, Carrie L. Blout, Kurt D. Christensen, Laura M. Amendola, Katie L. Bergstrom, Sawona Biswas, Kevin M. Bowling, Kyle B. Brothers, Laura K. Conlin, Greg M. Cooper, Matthew C. Dulik, Kelly M. East, Jessica N. Everett, Candice R. Finnila, Arezou A. Ghazani, Marian J. Gilmore, Katrina A.B. Goddard, Gail P. Jarvik, Jennifer J. JohnstonTia L. Kauffman, Whitley V. Kelley, Joel B. Krier, Katie L. Lewis, Amy L. McGuire, Carmit McMullen, Jeffrey Ou, Sharon E. Plon, Heidi L. Rehm, C. Sue Richards, Edward J. Romasko, Ane Miren Sagardia, Nancy B. Spinner, Michelle L. Thompson, Erin Turbitt, Jason L. Vassy, Benjamin S. Wilfond, David L. Veenstra, Jonathan S. Berg, Robert C. Green, Leslie G. Biesecker, Lucia A. Hindorff

Research output: Contribution to journal › Comment/debate

5 Scopus citations

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.

Original language	English
Pages (from-to)	1261-1262
Number of pages	2
Journal	Genetics in Medicine
Volume	21
Issue number	5
DOIs	https://doi.org/10.1038/s41436-019-0440-2
State	Published - May 1 2019

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Hart, M. R., Biesecker, B. B., Blout, C. L., Christensen, K. D., Amendola, L. M., Bergstrom, K. L., Biswas, S., Bowling, K. M., Brothers, K. B., Conlin, L. K., Cooper, G. M., Dulik, M. C., East, K. M., Everett, J. N., Finnila, C. R., Ghazani, A. A., Gilmore, M. J., Goddard, K. A. B., Jarvik, G. P., ... Hindorff, L. A. (2019). Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x). Genetics in Medicine, 21(5), 1261-1262. https://doi.org/10.1038/s41436-019-0440-2

Hart, M. Ragan ; Biesecker, Barbara B. ; Blout, Carrie L. et al. / Correction : Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x). In: Genetics in Medicine. 2019 ; Vol. 21, No. 5. pp. 1261-1262.

@article{9b154b3038e04cdf9d4cdaf8ab466130,

title = "Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)",

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.",

author = "Hart, \{M. Ragan\} and Biesecker, \{Barbara B.\} and Blout, \{Carrie L.\} and Christensen, \{Kurt D.\} and Amendola, \{Laura M.\} and Bergstrom, \{Katie L.\} and Sawona Biswas and Bowling, \{Kevin M.\} and Brothers, \{Kyle B.\} and Conlin, \{Laura K.\} and Cooper, \{Greg M.\} and Dulik, \{Matthew C.\} and East, \{Kelly M.\} and Everett, \{Jessica N.\} and Finnila, \{Candice R.\} and Ghazani, \{Arezou A.\} and Gilmore, \{Marian J.\} and Goddard, \{Katrina A.B.\} and Jarvik, \{Gail P.\} and Johnston, \{Jennifer J.\} and Kauffman, \{Tia L.\} and Kelley, \{Whitley V.\} and Krier, \{Joel B.\} and Lewis, \{Katie L.\} and McGuire, \{Amy L.\} and Carmit McMullen and Jeffrey Ou and Plon, \{Sharon E.\} and Rehm, \{Heidi L.\} and Richards, \{C. Sue\} and Romasko, \{Edward J.\} and Sagardia, \{Ane Miren\} and Spinner, \{Nancy B.\} and Thompson, \{Michelle L.\} and Erin Turbitt and Vassy, \{Jason L.\} and Wilfond, \{Benjamin S.\} and Veenstra, \{David L.\} and Berg, \{Jonathan S.\} and Green, \{Robert C.\} and Biesecker, \{Leslie G.\} and Hindorff, \{Lucia A.\}",

note = "Publisher Copyright: {\textcopyright} 2019, American College of Medical Genetics and Genomics.",

year = "2019",

month = may,

day = "1",

doi = "10.1038/s41436-019-0440-2",

language = "English",

volume = "21",

pages = "1261--1262",

journal = "Genetics in Medicine",

issn = "1098-3600",

number = "5",

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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, Sagardia, AM, Spinner, NB, Thompson, ML, Turbitt, E, Vassy, JL, Wilfond, BS, Veenstra, DL, Berg, JS, Green, RC, Biesecker, LG & Hindorff, LA 2019, 'Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)', Genetics in Medicine, vol. 21, no. 5, pp. 1261-1262. https://doi.org/10.1038/s41436-019-0440-2

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x). / Hart, M. Ragan; Biesecker, Barbara B.; Blout, Carrie L. et al.
In: Genetics in Medicine, Vol. 21, No. 5, 01.05.2019, p. 1261-1262.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Correction

T2 - Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)

AU - Hart, M. Ragan

AU - Biesecker, Barbara B.

AU - Blout, Carrie L.

AU - Christensen, Kurt D.

AU - Amendola, Laura M.

AU - Bergstrom, Katie L.

AU - Biswas, Sawona

AU - Bowling, Kevin M.

AU - Brothers, Kyle B.

AU - Conlin, Laura K.

AU - Cooper, Greg M.

AU - Dulik, Matthew C.

AU - East, Kelly M.

AU - Everett, Jessica N.

AU - Finnila, Candice R.

AU - Ghazani, Arezou A.

AU - Gilmore, Marian J.

AU - Goddard, Katrina A.B.

AU - Jarvik, Gail P.

AU - Johnston, Jennifer J.

AU - Kauffman, Tia L.

AU - Kelley, Whitley V.

AU - Krier, Joel B.

AU - Lewis, Katie L.

AU - McGuire, Amy L.

AU - McMullen, Carmit

AU - Ou, Jeffrey

AU - Plon, Sharon E.

AU - Rehm, Heidi L.

AU - Richards, C. Sue

AU - Romasko, Edward J.

AU - Sagardia, Ane Miren

AU - Spinner, Nancy B.

AU - Thompson, Michelle L.

AU - Turbitt, Erin

AU - Vassy, Jason L.

AU - Wilfond, Benjamin S.

AU - Veenstra, David L.

AU - Berg, Jonathan S.

AU - Green, Robert C.

AU - Biesecker, Leslie G.

AU - Hindorff, Lucia A.

PY - 2019/5/1

Y1 - 2019/5/1

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85060535694

U2 - 10.1038/s41436-019-0440-2

DO - 10.1038/s41436-019-0440-2

M3 - Comment/debate

C2 - 30670880

AN - SCOPUS:85060535694

SN - 1098-3600

VL - 21

SP - 1261

EP - 1262

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 5

ER -

Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL et al. Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x). Genetics in Medicine. 2019 May 1;21(5):1261-1262. doi: 10.1038/s41436-019-0440-2

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)

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