Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

Francesco Vetrini; Shane McKee; Jill A. Rosenfeld; Mohnish Suri; Andrea M. Lewis; Kimberly Margaret Nugent; Elizabeth Roeder; Rebecca O. Littlejohn; Sue Holder; Wenmiao Zhu; Joseph T. Alaimo; Brett Graham; Jill M. Harris; James B. Gibson; Matthew Pastore; Kim L. McBride; Makanko Komara; Lihadh Al-Gazali; Aisha Al Shamsi; Elizabeth A. Fanning; Klaas J. Wierenga; Daryl A. Scott; Ziva Ben-Neriah; Vardiella Meiner; Hanoch Cassuto; Orly Elpeleg; J. Lloyd Holder; Lindsay C. Burrage; Laurie H. Seaver; Lionel Van Maldergem; Sonal Mahida; Janet S. Soul; Margaret Marlatt; Ludmila Matyakhina; Julie Vogt; June Anne Gold; Soo Mi Park; Vinod Varghese; Anne K. Lampe; Ajith Kumar; Melissa Lees; Muriel Holder-Espinasse; Vivienne McConnell; Birgitta Bernhard; Ed Blair; Victoria Harrison; Donna M. Muzny; Richard A. Gibbs; Sarah H. Elsea; Jennifer E. Posey; Weimin Bi; Seema Lalani; Fan Xia; Yaping Yang; Christine M. Eng; James R. Lupski; Pengfei Liu

doi:10.1186/s13073-019-0630-1

Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

Francesco Vetrini
, Shane McKee
, Jill A. Rosenfeld
, Mohnish Suri
, Andrea M. Lewis
, Kimberly Margaret Nugent
, Elizabeth Roeder
, Rebecca O. Littlejohn
, Sue Holder
, Wenmiao Zhu
, Joseph T. Alaimo
, Brett Graham
, Jill M. Harris
, James B. Gibson
, Matthew Pastore
, Kim L. McBride
, Makanko Komara
, Lihadh Al-Gazali
, Aisha Al Shamsi
, Elizabeth A. Fanning

Klaas J. Wierenga, Daryl A. Scott, Ziva Ben-Neriah, Vardiella Meiner, Hanoch Cassuto, Orly Elpeleg, J. Lloyd Holder, Lindsay C. Burrage, Laurie H. Seaver, Lionel Van Maldergem, Sonal Mahida, Janet S. Soul, Margaret Marlatt, Ludmila Matyakhina, Julie Vogt, June Anne Gold, Soo Mi Park, Vinod Varghese, Anne K. Lampe, Ajith Kumar, Melissa Lees, Muriel Holder-Espinasse, Vivienne McConnell, Birgitta Bernhard, Ed Blair, Victoria Harrison, Donna M. Muzny, Richard A. Gibbs, Sarah H. Elsea, Jennifer E. Posey, Weimin Bi, Seema Lalani, Fan Xia, Yaping Yang, Christine M. Eng, James R. Lupski, Pengfei Liu

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

2 Citations (Scopus)

Abstract

It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated. Correct statement: "Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS."

Original language	English
Article number	16
Journal	Genome Medicine
Volume	11
Issue number	1
DOIs	https://doi.org/10.1186/s13073-019-0630-1
Publication status	Published - Mar 25 2019

ASJC Scopus subject areas

Molecular Medicine
Molecular Biology
Genetics
Genetics(clinical)

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Dive into the research topics of 'Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)'. Together they form a unique fingerprint.

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Vetrini, F., McKee, S., Rosenfeld, J. A., Suri, M., Lewis, A. M., Nugent, K. M., Roeder, E., Littlejohn, R. O., Holder, S., Zhu, W., Alaimo, J. T., Graham, B., Harris, J. M., Gibson, J. B., Pastore, M., McBride, K. L., Komara, M., Al-Gazali, L., Al Shamsi, A., ... Liu, P. (2019). Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). Genome Medicine, 11(1), Article 16. https://doi.org/10.1186/s13073-019-0630-1

Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). / Vetrini, Francesco; McKee, Shane; Rosenfeld, Jill A. et al.
In: Genome Medicine, Vol. 11, No. 1, 16, 25.03.2019.

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

Vetrini, F, McKee, S, Rosenfeld, JA, Suri, M, Lewis, AM, Nugent, KM, Roeder, E, Littlejohn, RO, Holder, S, Zhu, W, Alaimo, JT, Graham, B, Harris, JM, Gibson, JB, Pastore, M, McBride, KL, Komara, M, Al-Gazali, L, Al Shamsi, A, Fanning, EA, Wierenga, KJ, Scott, DA, Ben-Neriah, Z, Meiner, V, Cassuto, H, Elpeleg, O, Lloyd Holder, J, Burrage, LC, Seaver, LH, Van Maldergem, L, Mahida, S, Soul, JS, Marlatt, M, Matyakhina, L, Vogt, J, Gold, JA, Park, SM, Varghese, V, Lampe, AK, Kumar, A, Lees, M, Holder-Espinasse, M, McConnell, V, Bernhard, B, Blair, E, Harrison, V, Muzny, DM, Gibbs, RA, Elsea, SH, Posey, JE, Bi, W, Lalani, S, Xia, F, Yang, Y, Eng, CM, Lupski, JR & Liu, P 2019, 'Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)', Genome Medicine, vol. 11, no. 1, 16. https://doi.org/10.1186/s13073-019-0630-1

Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM et al. Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). Genome Medicine. 2019 Mar 25;11(1):16. doi: 10.1186/s13073-019-0630-1

Vetrini, Francesco ; McKee, Shane ; Rosenfeld, Jill A. et al. / Correction : De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). In: Genome Medicine. 2019 ; Vol. 11, No. 1.

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title = "Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)",

abstract = "It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated. Correct statement: {"}Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS.{"}",

author = "Francesco Vetrini and Shane McKee and Rosenfeld, \{Jill A.\} and Mohnish Suri and Lewis, \{Andrea M.\} and Nugent, \{Kimberly Margaret\} and Elizabeth Roeder and Littlejohn, \{Rebecca O.\} and Sue Holder and Wenmiao Zhu and Alaimo, \{Joseph T.\} and Brett Graham and Harris, \{Jill M.\} and Gibson, \{James B.\} and Matthew Pastore and McBride, \{Kim L.\} and Makanko Komara and Lihadh Al-Gazali and \{Al Shamsi\}, Aisha and Fanning, \{Elizabeth A.\} and Wierenga, \{Klaas J.\} and Scott, \{Daryl A.\} and Ziva Ben-Neriah and Vardiella Meiner and Hanoch Cassuto and Orly Elpeleg and \{Lloyd Holder\}, J. and Burrage, \{Lindsay C.\} and Seaver, \{Laurie H.\} and \{Van Maldergem\}, Lionel and Sonal Mahida and Soul, \{Janet S.\} and Margaret Marlatt and Ludmila Matyakhina and Julie Vogt and Gold, \{June Anne\} and Park, \{Soo Mi\} and Vinod Varghese and Lampe, \{Anne K.\} and Ajith Kumar and Melissa Lees and Muriel Holder-Espinasse and Vivienne McConnell and Birgitta Bernhard and Ed Blair and Victoria Harrison and Muzny, \{Donna M.\} and Gibbs, \{Richard A.\} and Elsea, \{Sarah H.\} and Posey, \{Jennifer E.\} and Weimin Bi and Seema Lalani and Fan Xia and Yaping Yang and Eng, \{Christine M.\} and Lupski, \{James R.\} and Pengfei Liu",

note = "Publisher Copyright: {\textcopyright} 2019 The Author(s).",

year = "2019",

month = mar,

day = "25",

doi = "10.1186/s13073-019-0630-1",

language = "English",

volume = "11",

journal = "Genome Medicine",

issn = "1756-994X",

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number = "1",

}

TY - JOUR

T1 - Correction

T2 - De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

AU - Vetrini, Francesco

AU - McKee, Shane

AU - Rosenfeld, Jill A.

AU - Suri, Mohnish

AU - Lewis, Andrea M.

AU - Nugent, Kimberly Margaret

AU - Roeder, Elizabeth

AU - Littlejohn, Rebecca O.

AU - Holder, Sue

AU - Zhu, Wenmiao

AU - Alaimo, Joseph T.

AU - Graham, Brett

AU - Harris, Jill M.

AU - Gibson, James B.

AU - Pastore, Matthew

AU - McBride, Kim L.

AU - Komara, Makanko

AU - Al-Gazali, Lihadh

AU - Al Shamsi, Aisha

AU - Fanning, Elizabeth A.

AU - Wierenga, Klaas J.

AU - Scott, Daryl A.

AU - Ben-Neriah, Ziva

AU - Meiner, Vardiella

AU - Cassuto, Hanoch

AU - Elpeleg, Orly

AU - Lloyd Holder, J.

AU - Burrage, Lindsay C.

AU - Seaver, Laurie H.

AU - Van Maldergem, Lionel

AU - Mahida, Sonal

AU - Soul, Janet S.

AU - Marlatt, Margaret

AU - Matyakhina, Ludmila

AU - Vogt, Julie

AU - Gold, June Anne

AU - Park, Soo Mi

AU - Varghese, Vinod

AU - Lampe, Anne K.

AU - Kumar, Ajith

AU - Lees, Melissa

AU - Holder-Espinasse, Muriel

AU - McConnell, Vivienne

AU - Bernhard, Birgitta

AU - Blair, Ed

AU - Harrison, Victoria

AU - Muzny, Donna M.

AU - Gibbs, Richard A.

AU - Elsea, Sarah H.

AU - Posey, Jennifer E.

AU - Bi, Weimin

AU - Lalani, Seema

AU - Xia, Fan

AU - Yang, Yaping

AU - Eng, Christine M.

AU - Lupski, James R.

AU - Liu, Pengfei

PY - 2019/3/25

Y1 - 2019/3/25

N2 - It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated. Correct statement: "Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS."

AB - It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated. Correct statement: "Of note, subject 17 of our cohort presented with mild delayed motor milestones, generalized hypotonia, and, in particular, dysmorphic features including midface hypoplasia, tented upper lips, along with sleep issues, ASD, food-seeking behavior, and aggressive behavior; these clinical features are similar to those reported in SMS."

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UR - https://www.scopus.com/pages/publications/85063593384#tab=citedBy

U2 - 10.1186/s13073-019-0630-1

DO - 10.1186/s13073-019-0630-1

M3 - Comment/debate

C2 - 30909959

AN - SCOPUS:85063593384

SN - 1756-994X

VL - 11

JO - Genome Medicine

JF - Genome Medicine

IS - 1

M1 - 16

ER -

Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

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