Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)

Cristina E. Trevino; Aaron M. Holleman; Holly Corbitt; Cheryl L. Maslen; Tracie C. Rosser; David J. Cutler; H. Richard Johnston; Benjamin L. Rambo-Martin; Jai Oberoi; Kenneth J. Dooley; George T. Capone; Roger H. Reeves; Heather J. Cordell; Bernard D. Keavney; A. J. Agopian; Elizabeth Goldmuntz; Peter J. Gruber; James E. O’Brien; Douglas C. Bittel; Lalita Wadhwa; Clifford L. Cua; Ivan P. Moskowitz; Jennifer G. Mulle; Michael P. Epstein; Stephanie L. Sherman; Michael E. Zwick

doi:10.1038/s41598-021-94021-x

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)

Cristina E. Trevino, Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler, H. Richard Johnston, Benjamin L. Rambo-Martin, Jai Oberoi, Kenneth J. Dooley, George T. Capone, Roger H. Reeves, Heather J. Cordell, Bernard D. Keavney, A. J. Agopian, Elizabeth Goldmuntz, Peter J. Gruber, James E. O’Brien, Douglas C. Bittel, Lalita WadhwaClifford L. Cua, Ivan P. Moskowitz, Jennifer G. Mulle, Michael P. Epstein, Stephanie L. Sherman, Michael E. Zwick

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

Ivan P. Moskowitz was omitted from the author list in the original version of this Article.

Original language	English (US)
Article number	15164
Journal	Scientific Reports
Volume	11
Issue number	1
DOIs	https://doi.org/10.1038/s41598-021-94021-x
State	Published - Dec 2021
Externally published	Yes

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Trevino, C. E., Holleman, A. M., Corbitt, H., Maslen, C. L., Rosser, T. C., Cutler, D. J., Johnston, H. R., Rambo-Martin, B. L., Oberoi, J., Dooley, K. J., Capone, G. T., Reeves, R. H., Cordell, H. J., Keavney, B. D., Agopian, A. J., Goldmuntz, E., Gruber, P. J., O’Brien, J. E., Bittel, D. C., ... Zwick, M. E. (2021). Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4). Scientific Reports, 11(1), [15164]. https://doi.org/10.1038/s41598-021-94021-x

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4). / Trevino, Cristina E.; Holleman, Aaron M.; Corbitt, Holly et al.
In: Scientific Reports, Vol. 11, No. 1, 15164, 12.2021.

Research output: Contribution to journal › Comment/debate › peer-review

Trevino, CE, Holleman, AM, Corbitt, H, Maslen, CL, Rosser, TC, Cutler, DJ, Johnston, HR, Rambo-Martin, BL, Oberoi, J, Dooley, KJ, Capone, GT, Reeves, RH, Cordell, HJ, Keavney, BD, Agopian, AJ, Goldmuntz, E, Gruber, PJ, O’Brien, JE, Bittel, DC, Wadhwa, L, Cua, CL, Moskowitz, IP, Mulle, JG, Epstein, MP, Sherman, SL & Zwick, ME 2021, 'Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)', Scientific Reports, vol. 11, no. 1, 15164. https://doi.org/10.1038/s41598-021-94021-x

@article{382b200545de4b229303d7f408d7cdfc,

title = "Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)",

abstract = "Ivan P. Moskowitz was omitted from the author list in the original version of this Article.",

author = "Trevino, {Cristina E.} and Holleman, {Aaron M.} and Holly Corbitt and Maslen, {Cheryl L.} and Rosser, {Tracie C.} and Cutler, {David J.} and Johnston, {H. Richard} and Rambo-Martin, {Benjamin L.} and Jai Oberoi and Dooley, {Kenneth J.} and Capone, {George T.} and Reeves, {Roger H.} and Cordell, {Heather J.} and Keavney, {Bernard D.} and Agopian, {A. J.} and Elizabeth Goldmuntz and Gruber, {Peter J.} and O{\textquoteright}Brien, {James E.} and Bittel, {Douglas C.} and Lalita Wadhwa and Cua, {Clifford L.} and Moskowitz, {Ivan P.} and Mulle, {Jennifer G.} and Epstein, {Michael P.} and Sherman, {Stephanie L.} and Zwick, {Michael E.}",

note = "Funding Information: “First and foremost, we want to thank the families and individuals with Down syndrome for contributing their time and effort towards this project. The DS Heart Project (R.H.R.) was a collaborative project supported through several National Institutes of Health awards: R01 HL092981-01A1 (M.E.Z.) and R01 HL083300 (R.H.R.) from NIH/National Heart, Lung, and Blood Institute; R01 HD38979 (S.L.S.) from NIH/National Institute of Child Health and Human Development and GM117946 (M.P.E.) from NIH/National Institute of General Medical Sciences. Whole exome sequencing services that were done as part of the DSHP were provided by the University of Washington, Department of Genome Sciences under U.S. Federal Government contract number HHSN268201100037C (D. Nickerson). Whole genome sequencing services were supported by the Emory Integrated Genomics Core (EIGC) and the Emory Integrated Computational Core (EICC), which are subsidized by the Emory University School of Medicine and are part of the Emory Integrated Core Facilities. Partial support to M.E.Z was also provided by the Georgia Clinical & Translational Science Alliance which is funded by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award number UL1TR002378. The American Heart Association Western States Affiliate provided support to H. Corbitt (grant number 16PRE30190012). I.P. Moskowitz was supported by the following grants: R01 HL092153, R01 HL124836, and R01 HL126509. We thank Dr. Eleanor Feingold for providing the chromosome 21 genotype calls for the SNP Affymetrix dataset. We thank the Pediatric Cardiac Genomic Consortium (PCGC) for its contributions to this work, and recognize E.G. as sponsor of the PCGC-approved ancillary project. The PCGC provided samples for the WGS study which were collected under the auspices of the National Heart, Lung, and Blood Institute{\textquoteright}s Bench to Bassinet Program (https://benchtobassinet.com). Support for the PCGC is provided through grants from National Heart, Lung, and Blood Institute (U01-HL098188, U01-HL098147, U01-HL098153, U01-HL098163, U01-HL098123, U01-HL098162). We would like to thank Marianne S. Hird at the PCGC for her help on this project throughout its administration. The Agopian et al. (2017) GWAS discovery dataset used for the PRS analyses was generated with support from an Institutional Development Fund to The Center for Applied Genomics from The Children{\textquoteright}s Hospital of Philadelphia. Further support was provided by the National Heart, Lung, and Blood Institute P50-HL74731 (E.G.) and the National Center for Research Resources M01-RR-000240, RR024134 [now the National Center for Advancing Translational Sciences UL1TR000003) (E.G.). The Cordell et al. (2013) GWAS discovery data used for the PRS analyses were generated with support from the British Heart Foundation, Heart Research UK, Wellcome Trust and European Union. B.D.K. is supported by a British Heart Foundation Personal Chair. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.” Publisher Copyright: {\textcopyright} 2021, The Author(s).",

year = "2021",

month = dec,

doi = "10.1038/s41598-021-94021-x",

language = "English (US)",

volume = "11",

journal = "Scientific Reports",

issn = "2045-2322",

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T1 - Author Correction

T2 - Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)

AU - Trevino, Cristina E.

AU - Holleman, Aaron M.

AU - Corbitt, Holly

AU - Maslen, Cheryl L.

AU - Rosser, Tracie C.

AU - Cutler, David J.

AU - Johnston, H. Richard

AU - Rambo-Martin, Benjamin L.

AU - Oberoi, Jai

AU - Dooley, Kenneth J.

AU - Capone, George T.

AU - Reeves, Roger H.

AU - Cordell, Heather J.

AU - Keavney, Bernard D.

AU - Agopian, A. J.

AU - Goldmuntz, Elizabeth

AU - Gruber, Peter J.

AU - O’Brien, James E.

AU - Bittel, Douglas C.

AU - Wadhwa, Lalita

AU - Cua, Clifford L.

AU - Moskowitz, Ivan P.

AU - Mulle, Jennifer G.

AU - Epstein, Michael P.

AU - Sherman, Stephanie L.

AU - Zwick, Michael E.

N1 - Funding Information: “First and foremost, we want to thank the families and individuals with Down syndrome for contributing their time and effort towards this project. The DS Heart Project (R.H.R.) was a collaborative project supported through several National Institutes of Health awards: R01 HL092981-01A1 (M.E.Z.) and R01 HL083300 (R.H.R.) from NIH/National Heart, Lung, and Blood Institute; R01 HD38979 (S.L.S.) from NIH/National Institute of Child Health and Human Development and GM117946 (M.P.E.) from NIH/National Institute of General Medical Sciences. Whole exome sequencing services that were done as part of the DSHP were provided by the University of Washington, Department of Genome Sciences under U.S. Federal Government contract number HHSN268201100037C (D. Nickerson). Whole genome sequencing services were supported by the Emory Integrated Genomics Core (EIGC) and the Emory Integrated Computational Core (EICC), which are subsidized by the Emory University School of Medicine and are part of the Emory Integrated Core Facilities. Partial support to M.E.Z was also provided by the Georgia Clinical & Translational Science Alliance which is funded by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award number UL1TR002378. The American Heart Association Western States Affiliate provided support to H. Corbitt (grant number 16PRE30190012). I.P. Moskowitz was supported by the following grants: R01 HL092153, R01 HL124836, and R01 HL126509. We thank Dr. Eleanor Feingold for providing the chromosome 21 genotype calls for the SNP Affymetrix dataset. We thank the Pediatric Cardiac Genomic Consortium (PCGC) for its contributions to this work, and recognize E.G. as sponsor of the PCGC-approved ancillary project. The PCGC provided samples for the WGS study which were collected under the auspices of the National Heart, Lung, and Blood Institute’s Bench to Bassinet Program (https://benchtobassinet.com). Support for the PCGC is provided through grants from National Heart, Lung, and Blood Institute (U01-HL098188, U01-HL098147, U01-HL098153, U01-HL098163, U01-HL098123, U01-HL098162). We would like to thank Marianne S. Hird at the PCGC for her help on this project throughout its administration. The Agopian et al. (2017) GWAS discovery dataset used for the PRS analyses was generated with support from an Institutional Development Fund to The Center for Applied Genomics from The Children’s Hospital of Philadelphia. Further support was provided by the National Heart, Lung, and Blood Institute P50-HL74731 (E.G.) and the National Center for Research Resources M01-RR-000240, RR024134 [now the National Center for Advancing Translational Sciences UL1TR000003) (E.G.). The Cordell et al. (2013) GWAS discovery data used for the PRS analyses were generated with support from the British Heart Foundation, Heart Research UK, Wellcome Trust and European Union. B.D.K. is supported by a British Heart Foundation Personal Chair. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.” Publisher Copyright: © 2021, The Author(s).

PY - 2021/12

Y1 - 2021/12

N2 - Ivan P. Moskowitz was omitted from the author list in the original version of this Article.

AB - Ivan P. Moskowitz was omitted from the author list in the original version of this Article.

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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (Scientific Reports, (2020), 10, 1, (18051), 10.1038/s41598-020-74650-4)

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