Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

The SPARK Consortium

doi:10.1038/s41467-020-19289-5

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

The SPARK Consortium

Kennedy Krieger Institute

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

Abstract

The original version of this Article contained an error on page 5 of the Results section, which incorrectly read ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (10/7)’. The correct version states ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (7/10)’.

Original language	English (US)
Article number	5398
Journal	Nature communications
Volume	11
Issue number	1
DOIs	https://doi.org/10.1038/s41467-020-19289-5
State	Published - Dec 1 2020

ASJC Scopus subject areas

General Chemistry
General Biochemistry, Genetics and Molecular Biology
General Physics and Astronomy

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10.1038/s41467-020-19289-5

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@article{323af010292648459bd2975e0453a4e8,

title = "Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)",

abstract = "The original version of this Article contained an error on page 5 of the Results section, which incorrectly read {\textquoteleft}They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (10/7){\textquoteright}. The correct version states {\textquoteleft}They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (7/10){\textquoteright}.",

author = "{The SPARK Consortium} and Tianyun Wang and Kendra Hoekzema and Davide Vecchio and Huidan Wu and Arvis Sulovari and Coe, {Bradley P.} and Gillentine, {Madelyn A.} and Wilfert, {Amy B.} and Perez-Jurado, {Luis A.} and Malin Kvarnung and Yoeri Sleyp and Earl, {Rachel K.} and Rosenfeld, {Jill A.} and Geisheker, {Madeleine R.} and Lin Han and Bing Du and Chris Barnett and Elizabeth Thompson and Marie Shaw and Renee Carroll and Kathryn Friend and Rachael Catford and Palmer, {Elizabeth E.} and Xiaobing Zou and Jianjun Ou and Honghui Li and Hui Guo and Jennifer Gerdts and Emanuela Avola and Giuseppe Calabrese and Maurizio Elia and Donatella Greco and Anna Lindstrand and Ann Nordgren and Anderlid, {Britt Marie} and Geert Vandeweyer and {Van Dijck}, Anke and {Van der Aa}, Nathalie and Brooke McKenna and Miroslava Hancarova and Sarka Bendova and Marketa Havlovicova and Giovanni Malerba and Bernardina, {Bernardo Dalla} and Pierandrea Muglia and {van Haeringen}, Arie and Hoffer, {Mariette J.V.} and Ali Fatemi and Landa, {Rebecca J.} and Wodka, {Ericka L.}",

note = "Publisher Copyright: {\textcopyright} 2020, The Author(s).",

year = "2020",

month = dec,

day = "1",

doi = "10.1038/s41467-020-19289-5",

language = "English (US)",

volume = "11",

journal = "Nature communications",

issn = "2041-1723",

publisher = "Nature Publishing Group",

number = "1",

}

TY - JOUR

T1 - Author Correction

T2 - Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

AU - The SPARK Consortium

AU - Wang, Tianyun

AU - Hoekzema, Kendra

AU - Vecchio, Davide

AU - Wu, Huidan

AU - Sulovari, Arvis

AU - Coe, Bradley P.

AU - Gillentine, Madelyn A.

AU - Wilfert, Amy B.

AU - Perez-Jurado, Luis A.

AU - Kvarnung, Malin

AU - Sleyp, Yoeri

AU - Earl, Rachel K.

AU - Rosenfeld, Jill A.

AU - Geisheker, Madeleine R.

AU - Han, Lin

AU - Du, Bing

AU - Barnett, Chris

AU - Thompson, Elizabeth

AU - Shaw, Marie

AU - Carroll, Renee

AU - Friend, Kathryn

AU - Catford, Rachael

AU - Palmer, Elizabeth E.

AU - Zou, Xiaobing

AU - Ou, Jianjun

AU - Li, Honghui

AU - Guo, Hui

AU - Gerdts, Jennifer

AU - Avola, Emanuela

AU - Calabrese, Giuseppe

AU - Elia, Maurizio

AU - Greco, Donatella

AU - Lindstrand, Anna

AU - Nordgren, Ann

AU - Anderlid, Britt Marie

AU - Vandeweyer, Geert

AU - Van Dijck, Anke

AU - Van der Aa, Nathalie

AU - McKenna, Brooke

AU - Hancarova, Miroslava

AU - Bendova, Sarka

AU - Havlovicova, Marketa

AU - Malerba, Giovanni

AU - Bernardina, Bernardo Dalla

AU - Muglia, Pierandrea

AU - van Haeringen, Arie

AU - Hoffer, Mariette J.V.

AU - Fatemi, Ali

AU - Landa, Rebecca J.

AU - Wodka, Ericka L.

PY - 2020/12/1

Y1 - 2020/12/1

N2 - The original version of this Article contained an error on page 5 of the Results section, which incorrectly read ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (10/7)’. The correct version states ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (7/10)’.

AB - The original version of this Article contained an error on page 5 of the Results section, which incorrectly read ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (10/7)’. The correct version states ‘They are characterized by craniofacial dysmorphisms (9/10), thin vermillion border and lips (4/7), and feeding difficulties (6/11), and exhibit neonatal hypotonia (7/10)’.

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U2 - 10.1038/s41467-020-19289-5

DO - 10.1038/s41467-020-19289-5

M3 - Comment/debate

C2 - 33087701

AN - SCOPUS:85093103636

SN - 2041-1723

VL - 11

JO - Nature communications

JF - Nature communications

IS - 1

M1 - 5398

ER -

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders (Nature Communications, (2020), 11, 1, (4932), 10.1038/s41467-020-18723-y)

Abstract

ASJC Scopus subject areas

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