Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

Siddharth Srivastava; Jamie A Love-Nichols; Kira A Dies; David H Ledbetter; Christa L Martin; Wendy K Chung; Helen V Firth; Thomas Frazier; Robin L Hansen; Lisa Prock; Han Brunner; Ny Hoang; Stephen W Scherer; Mustafa Sahin; David T Miller; NDD Exome Scoping Review Work Group

doi:10.1038/s41436-020-0913-3

Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock, Han Brunner, Ny Hoang, Stephen W Scherer, Mustafa Sahin^*, David T Miller, NDD Exome Scoping Review Work Group

^*Corresponding author for this work

Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English
Pages (from-to)	1731-1732
Number of pages	2
Journal	Genetics in Medicine
Volume	22
Issue number	10
DOIs	https://doi.org/10.1038/s41436-020-0913-3
Publication status	Published - Oct 2020

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10.1038/s41436-020-0913-3

1 Review article

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Srivastava, S., Love-Nichols, J. A., Dies, K. A., Ledbetter, D. H., Martin, C. L., Chung, W. K., Firth, H., Frazier, T., Hansen, R. L., Prock, L., Brunner, H., Hoang, N., Scherer, S. W., Sahin, M., Miller, D. T., Restrepo, B., Shankar, S., Riggs, E. R., Constantinou, P., Reed-Weston, A., & 6 othersTong, R. S., Howe, J., Buchanan, J., Fisher, R., Mahida, S. & NDD Exome Scoping Review Work Group, Nov 2019, In: Genetics in Medicine. 21, 11, p. 2413-2421 9 p.
Research output: Contribution to journal › (Systematic) Review article › peer-review

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Cite this

Srivastava, S., Love-Nichols, J. A., Dies, K. A., Ledbetter, D. H., Martin, C. L., Chung, W. K., Firth, H. V., Frazier, T., Hansen, R. L., Prock, L., Brunner, H., Hoang, N., Scherer, S. W., Sahin, M., Miller, D. T., & NDD Exome Scoping Review Work Group (2020). Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. Genetics in Medicine, 22(10), 1731-1732. https://doi.org/10.1038/s41436-020-0913-3

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title = "Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "Siddharth Srivastava and Love-Nichols, {Jamie A} and Dies, {Kira A} and Ledbetter, {David H} and Martin, {Christa L} and Chung, {Wendy K} and Firth, {Helen V} and Thomas Frazier and Hansen, {Robin L} and Lisa Prock and Han Brunner and Ny Hoang and Scherer, {Stephen W} and Mustafa Sahin and Miller, {David T} and {NDD Exome Scoping Review Work Group}",

year = "2020",

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doi = "10.1038/s41436-020-0913-3",

language = "English",

volume = "22",

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Srivastava, S, Love-Nichols, JA, Dies, KA, Ledbetter, DH, Martin, CL, Chung, WK, Firth, HV, Frazier, T, Hansen, RL, Prock, L, Brunner, H, Hoang, N, Scherer, SW, Sahin, M, Miller, DT & NDD Exome Scoping Review Work Group 2020, 'Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders', Genetics in Medicine, vol. 22, no. 10, pp. 1731-1732. https://doi.org/10.1038/s41436-020-0913-3

Correction: Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders. / Srivastava, Siddharth; Love-Nichols, Jamie A; Dies, Kira A et al.

In: Genetics in Medicine, Vol. 22, No. 10, 10.2020, p. 1731-1732.

Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

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AU - Srivastava, Siddharth

AU - Love-Nichols, Jamie A

AU - Dies, Kira A

AU - Ledbetter, David H

AU - Martin, Christa L

AU - Chung, Wendy K

AU - Firth, Helen V

AU - Frazier, Thomas

AU - Hansen, Robin L

AU - Prock, Lisa

AU - Brunner, Han

AU - Hoang, Ny

AU - Scherer, Stephen W

AU - Sahin, Mustafa

AU - Miller, David T

AU - NDD Exome Scoping Review Work Group

PY - 2020/10

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N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

U2 - 10.1038/s41436-020-0913-3

DO - 10.1038/s41436-020-0913-3

M3 - Erratum / corrigendum / retractions

C2 - 32728138

VL - 22

SP - 1731

EP - 1732

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

IS - 10

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