Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

Erfan Aref-Eshghi; Jennifer Kerkhof; Victor P. Pedro; Groupe D. I. France; Mouna Barat-Houari; Nathalie Ruiz-Pallares; Jean-Christophe Andrau; Didier Lacombe; Julien van-Gils; Patricia Fergelot; Christéle Dubourg; Valerie Cormier-Daire; Sophie Rondeau; François Lecoquierre; Pascale Saugier-Veber; Gaël Nicolas; Gaetan Lesca; Nicolas Chatron; Damien Sanlaville; Antonio Vitobello; Laurence Faivre; Christel Thauvin-Robinet; Frederic Laumonnier; Martine Raynaud; Mariëlle Alders; Marcel Mannens; Peter Henneman; Raoul C. Hennekam; Guillaume Velasco; Claire Francastel; Damien Ulveling; Andrea Ciolfi; Simone Pizzi; Marco Tartaglia; Solveig Heide; Delphine Héron; Cyril Mignot; Boris Keren; Sandra Whalen; Alexandra Afenjar; Thierry Bienvenu; Philippe M. Campeau; Justine Rousseau; Michael A. Levy; Lauren Brick; Mariya Kozenko; Tugce B. Balci; Victoria Mok Siu; Alan Stuart; Mike Kadour; Jennifer Masters; Kyoko Takano; Tjitske Kleefstra; Nicole de Leeuw; Michael Field; Marie Shaw; Jozef Gecz; Peter J. Ainsworth; Hanxin Lin; David I. Rodenhiser; Michael J. Friez; Matt Tedder; Jennifer A. Lee; Barbara R. DuPont; Roger E. Stevenson; Steven A. Skinner; Charles E. Schwartz; David Genevieve; Bekim Sadikovic

doi:https://doi.org/10.1016/j.ajhg.2021.04.022

Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

Erfan Aref-Eshghi, Jennifer Kerkhof, Victor P. Pedro, Groupe D. I. France, Mouna Barat-Houari, Nathalie Ruiz-Pallares, Jean-Christophe Andrau, Didier Lacombe, Julien van-Gils, Patricia Fergelot, Christéle Dubourg, Valerie Cormier-Daire, Sophie Rondeau, François Lecoquierre, Pascale Saugier-Veber, Gaël Nicolas, Gaetan Lesca, Nicolas Chatron, Damien Sanlaville, Antonio VitobelloLaurence Faivre, Christel Thauvin-Robinet, Frederic Laumonnier, Martine Raynaud, Mariëlle Alders, Marcel Mannens, Peter Henneman, Raoul C. Hennekam, Guillaume Velasco, Claire Francastel, Damien Ulveling, Andrea Ciolfi, Simone Pizzi, Marco Tartaglia, Solveig Heide, Delphine Héron, Cyril Mignot, Boris Keren, Sandra Whalen, Alexandra Afenjar, Thierry Bienvenu, Philippe M. Campeau, Justine Rousseau, Michael A. Levy, Lauren Brick, Mariya Kozenko, Tugce B. Balci, Victoria Mok Siu, Alan Stuart, Mike Kadour, Jennifer Masters, Kyoko Takano, Tjitske Kleefstra, Nicole de Leeuw, Michael Field, Marie Shaw, Jozef Gecz, Peter J. Ainsworth, Hanxin Lin, David I. Rodenhiser, Michael J. Friez, Matt Tedder, Jennifer A. Lee, Barbara R. DuPont, Roger E. Stevenson, Steven A. Skinner, Charles E. Schwartz, David Genevieve, Bekim Sadikovic

Research output: Contribution to journal › Comment/Letter to the editor › Academic

10 Citations (Scopus)

Abstract

(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.

Original language	English
Pages (from-to)	1161-1163
Number of pages	3
Journal	American journal of human genetics
Volume	108
Issue number	6
DOIs	https://doi.org/10.1016/j.ajhg.2021.04.022
Publication status	Published - 3 Jun 2021

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https://doi.org/10.1016/j.ajhg.2021.04.022

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Aref-Eshghi, E., Kerkhof, J., Pedro, V. P., France, G. D. I., Barat-Houari, M., Ruiz-Pallares, N., Andrau, J.-C., Lacombe, D., van-Gils, J., Fergelot, P., Dubourg, C., Cormier-Daire, V., Rondeau, S., Lecoquierre, F., Saugier-Veber, P., Nicolas, G., Lesca, G., Chatron, N., Sanlaville, D., ... Sadikovic, B. (2021). Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019)). American journal of human genetics, 108(6), 1161-1163. https://doi.org/10.1016/j.ajhg.2021.04.022

Aref-Eshghi, Erfan ; Kerkhof, Jennifer ; Pedro, Victor P. et al. / Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019)). In: American journal of human genetics. 2021 ; Vol. 108, No. 6. pp. 1161-1163.

@article{cdb0867e2c894acebf7c719b012236d1,

title = "Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))",

abstract = "(The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.",

author = "Erfan Aref-Eshghi and Jennifer Kerkhof and Pedro, {Victor P.} and France, {Groupe D. I.} and Mouna Barat-Houari and Nathalie Ruiz-Pallares and Jean-Christophe Andrau and Didier Lacombe and Julien van-Gils and Patricia Fergelot and Christ{\'e}le Dubourg and Valerie Cormier-Daire and Sophie Rondeau and Fran{\c c}ois Lecoquierre and Pascale Saugier-Veber and Ga{\"e}l Nicolas and Gaetan Lesca and Nicolas Chatron and Damien Sanlaville and Antonio Vitobello and Laurence Faivre and Christel Thauvin-Robinet and Frederic Laumonnier and Martine Raynaud and Mari{\"e}lle Alders and Marcel Mannens and Peter Henneman and Hennekam, {Raoul C.} and Guillaume Velasco and Claire Francastel and Damien Ulveling and Andrea Ciolfi and Simone Pizzi and Marco Tartaglia and Solveig Heide and Delphine H{\'e}ron and Cyril Mignot and Boris Keren and Sandra Whalen and Alexandra Afenjar and Thierry Bienvenu and Campeau, {Philippe M.} and Justine Rousseau and Levy, {Michael A.} and Lauren Brick and Mariya Kozenko and Balci, {Tugce B.} and Siu, {Victoria Mok} and Alan Stuart and Mike Kadour and Jennifer Masters and Kyoko Takano and Tjitske Kleefstra and {de Leeuw}, Nicole and Michael Field and Marie Shaw and Jozef Gecz and Ainsworth, {Peter J.} and Hanxin Lin and Rodenhiser, {David I.} and Friez, {Michael J.} and Matt Tedder and Lee, {Jennifer A.} and DuPont, {Barbara R.} and Stevenson, {Roger E.} and Skinner, {Steven A.} and Schwartz, {Charles E.} and David Genevieve and Bekim Sadikovic",

note = "Publisher Copyright: {\textcopyright} 2021 American Society of Human Genetics",

year = "2021",

month = jun,

day = "3",

doi = "https://doi.org/10.1016/j.ajhg.2021.04.022",

language = "English",

volume = "108",

pages = "1161--1163",

journal = "American journal of human genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "6",

}

Aref-Eshghi, E, Kerkhof, J, Pedro, VP, France, GDI, Barat-Houari, M, Ruiz-Pallares, N, Andrau, J-C, Lacombe, D, van-Gils, J, Fergelot, P, Dubourg, C, Cormier-Daire, V, Rondeau, S, Lecoquierre, F, Saugier-Veber, P, Nicolas, G, Lesca, G, Chatron, N, Sanlaville, D, Vitobello, A, Faivre, L, Thauvin-Robinet, C, Laumonnier, F, Raynaud, M, Alders, M , Mannens, M , Henneman, P , Hennekam, RC, Velasco, G, Francastel, C, Ulveling, D, Ciolfi, A, Pizzi, S, Tartaglia, M, Heide, S, Héron, D, Mignot, C, Keren, B, Whalen, S, Afenjar, A, Bienvenu, T, Campeau, PM, Rousseau, J, Levy, MA, Brick, L, Kozenko, M, Balci, TB, Siu, VM, Stuart, A, Kadour, M, Masters, J, Takano, K, Kleefstra, T, de Leeuw, N, Field, M, Shaw, M, Gecz, J, Ainsworth, PJ, Lin, H, Rodenhiser, DI, Friez, MJ, Tedder, M, Lee, JA, DuPont, BR, Stevenson, RE, Skinner, SA, Schwartz, CE, Genevieve, D & Sadikovic, B 2021, 'Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))', American journal of human genetics, vol. 108, no. 6, pp. 1161-1163. https://doi.org/10.1016/j.ajhg.2021.04.022

Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019)). / Aref-Eshghi, Erfan; Kerkhof, Jennifer; Pedro, Victor P. et al.
In: American journal of human genetics, Vol. 108, No. 6, 03.06.2021, p. 1161-1163.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

AU - Aref-Eshghi, Erfan

AU - Kerkhof, Jennifer

AU - Pedro, Victor P.

AU - France, Groupe D. I.

AU - Barat-Houari, Mouna

AU - Ruiz-Pallares, Nathalie

AU - Andrau, Jean-Christophe

AU - Lacombe, Didier

AU - van-Gils, Julien

AU - Fergelot, Patricia

AU - Dubourg, Christéle

AU - Cormier-Daire, Valerie

AU - Rondeau, Sophie

AU - Lecoquierre, François

AU - Saugier-Veber, Pascale

AU - Nicolas, Gaël

AU - Lesca, Gaetan

AU - Chatron, Nicolas

AU - Sanlaville, Damien

AU - Vitobello, Antonio

AU - Faivre, Laurence

AU - Thauvin-Robinet, Christel

AU - Laumonnier, Frederic

AU - Raynaud, Martine

AU - Alders, Mariëlle

AU - Mannens, Marcel

AU - Henneman, Peter

AU - Hennekam, Raoul C.

AU - Velasco, Guillaume

AU - Francastel, Claire

AU - Ulveling, Damien

AU - Ciolfi, Andrea

AU - Pizzi, Simone

AU - Tartaglia, Marco

AU - Heide, Solveig

AU - Héron, Delphine

AU - Mignot, Cyril

AU - Keren, Boris

AU - Whalen, Sandra

AU - Afenjar, Alexandra

AU - Bienvenu, Thierry

AU - Campeau, Philippe M.

AU - Rousseau, Justine

AU - Levy, Michael A.

AU - Brick, Lauren

AU - Kozenko, Mariya

AU - Balci, Tugce B.

AU - Siu, Victoria Mok

AU - Stuart, Alan

AU - Kadour, Mike

AU - Masters, Jennifer

AU - Takano, Kyoko

AU - Kleefstra, Tjitske

AU - de Leeuw, Nicole

AU - Field, Michael

AU - Shaw, Marie

AU - Gecz, Jozef

AU - Ainsworth, Peter J.

AU - Lin, Hanxin

AU - Rodenhiser, David I.

AU - Friez, Michael J.

AU - Tedder, Matt

AU - Lee, Jennifer A.

AU - DuPont, Barbara R.

AU - Stevenson, Roger E.

AU - Skinner, Steven A.

AU - Schwartz, Charles E.

AU - Genevieve, David

AU - Sadikovic, Bekim

PY - 2021/6/3

Y1 - 2021/6/3

N2 - (The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.

AB - (The American Journal of Human Genetics 106, 356–370; March 5, 2020) In the version of this paper originally published, the underlying cause for Hunter McAlpine syndrome was incorrectly described in Table 1. The relevant description has been changed to read “Chr5q35-qter duplication involving NSD1” in the updated Table 1 reflected here. The authors apologize for this error.

UR - http://www.scopus.com/inward/record.url?scp=85107089857&partnerID=8YFLogxK

U2 - https://doi.org/10.1016/j.ajhg.2021.04.022

DO - https://doi.org/10.1016/j.ajhg.2021.04.022

M3 - Comment/Letter to the editor

C2 - 34087165

SN - 0002-9297

VL - 108

SP - 1161

EP - 1163

JO - American journal of human genetics

JF - American journal of human genetics

IS - 6

ER -

Aref-Eshghi E, Kerkhof J, Pedro VP, France GDI, Barat-Houari M, Ruiz-Pallares N et al. Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019)). American journal of human genetics. 2021 Jun 3;108(6):1161-1163. doi: https://doi.org/10.1016/j.ajhg.2021.04.022

Erratum: Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders (The American Journal of Human Genetics (2020) 106(3) (356–370), (S0002929720300197), (10.1016/j.ajhg.2020.01.019))

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