Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)

Dana E. Layo-Carris; Emily E. Lubin; Annabel K. Sangree; Kelly J. Clark; Emily L. Durham; Elizabeth M. Gonzalez; Sarina Smith; Rajesh Angireddy; Xiao Min Wang; Erin Weiss; Annick Toutain; Roberto Mendoza-Londono; Lucie Dupuis; Nadirah Damseh; Danita Velasco; Irene Valenzuela; Marta Codina-Solà; Catherine Ziats; Jaclyn Have; Katie Clarkson; Dora Steel; Manju Kurian; Katy Barwick; Diana Carrasco; Aditi I. Dagli; M. J.M. Nowaczyk; Miroslava Hančárová; Šárka Bendová; Darina Prchalova; Zdeněk Sedláček; Alica Baxová; Catherine Bearce Nowak; Jessica Douglas; Wendy K. Chung; Nicola Longo; Konrad Platzer; Chiara Klöckner; Luisa Averdunk; Dagmar Wieczorek; Ilona Krey; Christiane Zweier; Andre Reis; Tugce Balci; Marleen Simon; Hester Y. Kroes; Antje Wiesener; Georgia Vasileiou; Nikolaos M. Marinakis; Danai Veltra; Christalena Sofocleous; Konstantina Kosma; Joanne Traeger Synodinos; Konstantinos A. Voudris; Marie Laure Vuillaume; Paul Gueguen; Nicolas Derive; Estelle Colin; Clarisse Battault; Billie Au; Martin Delatycki; Mathew Wallis; Lyndon Gallacher; Fatma Majdoub; Noor Smal; Sarah Weckhuysen; An Sofie Schoonjans; R. Frank Kooy; Marije Meuwissen; Benjamin T. Cocanougher; Kathryn Taylor; Carolyn E. Pizoli; Marie T. McDonald; Philip James; Elizabeth R. Roeder; Rebecca Littlejohn; Nicholas A. Borja; Willa Thorson; Kristine King; Radka Stoeva; Manon Suerink; Esther Nibbeling; Stephanie Baskin; Gwenaël L.E. Guyader; Julie Kaplan; Candace Muss; Deanna Alexis Carere; Elizabeth J.K. Bhoj; Laura M. Bryant

doi:10.1038/s41431-024-01659-y

Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)

Dana E. Layo-Carris
, Emily E. Lubin
, Annabel K. Sangree
, Kelly J. Clark
, Emily L. Durham
, Elizabeth M. Gonzalez
, Sarina Smith
, Rajesh Angireddy
, Xiao Min Wang
, Erin Weiss
, Annick Toutain
, Roberto Mendoza-Londono
, Lucie Dupuis
, Nadirah Damseh
, Danita Velasco
, Irene Valenzuela
, Marta Codina-Solà
, Catherine Ziats
, Jaclyn Have
, Katie Clarkson

Dora Steel, Manju Kurian, Katy Barwick, Diana Carrasco, Aditi I. Dagli, M. J.M. Nowaczyk, Miroslava Hančárová, Šárka Bendová, Darina Prchalova, Zdeněk Sedláček, Alica Baxová, Catherine Bearce Nowak, Jessica Douglas, Wendy K. Chung, Nicola Longo, Konrad Platzer, Chiara Klöckner, Luisa Averdunk, Dagmar Wieczorek, Ilona Krey, Christiane Zweier, Andre Reis, Tugce Balci, Marleen Simon, Hester Y. Kroes, Antje Wiesener, Georgia Vasileiou, Nikolaos M. Marinakis, Danai Veltra, Christalena Sofocleous, Konstantina Kosma, Joanne Traeger Synodinos, Konstantinos A. Voudris, Marie Laure Vuillaume, Paul Gueguen, Nicolas Derive, Estelle Colin, Clarisse Battault, Billie Au, Martin Delatycki, Mathew Wallis, Lyndon Gallacher, Fatma Majdoub, Noor Smal, Sarah Weckhuysen, An Sofie Schoonjans, R. Frank Kooy, Marije Meuwissen, Benjamin T. Cocanougher, Kathryn Taylor, Carolyn E. Pizoli, Marie T. McDonald, Philip James, Elizabeth R. Roeder, Rebecca Littlejohn, Nicholas A. Borja, Willa Thorson, Kristine King, Radka Stoeva, Manon Suerink, Esther Nibbeling, Stephanie Baskin, Gwenaël L.E. Guyader, Julie Kaplan, Candace Muss, Deanna Alexis Carere, Elizabeth J.K. Bhoj^*, Laura M. Bryant

^*Corresponding author for this work

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

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Abstract

An author was not named. The missing author is: “Annick Toutain” Her affiliation is: 27 Service de Génétique, CHU de Tours, Tours, France. 28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.

Original language	English
Article number	1032
Number of pages	1
Journal	European Journal of Human Genetics
Volume	32
Issue number	8
DOIs	https://doi.org/10.1038/s41431-024-01659-y
Publication status	Published - Aug 2024

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Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Layo-Carris, D. E., Lubin, E. E., Sangree, A. K., Clark, K. J., Durham, E. L., Gonzalez, E. M., Smith, S., Angireddy, R., Wang, X. M., Weiss, E., Mendoza-Londono, R., Dupuis, L., Damseh, N., Velasco, D., Valenzuela, I., Codina-Solà, M., Ziats, C., Have, J., Clarkson, K. & Steel, D. & 67 others, Kurian, M., Barwick, K., Carrasco, D., Dagli, A. I., Nowaczyk, M. J. M., Hančárová, M., Bendová, Š., Prchalova, D., Sedláček, Z., Baxová, A., Nowak, C. B., Douglas, J., Chung, W. K., Longo, N., Platzer, K., Klöckner, C., Averdunk, L., Wieczorek, D., Krey, I., Zweier, C., Reis, A., Balci, T., Simon, M., Kroes, H. Y., Wiesener, A., Vasileiou, G., Marinakis, N. M., Veltra, D., Sofocleous, C., Kosma, K., Traeger Synodinos, J., Voudris, K. A., Vuillaume, M.-L., Gueguen, P., Derive, N., Colin, E., Battault, C., Au, B., Delatycki, M., Wallis, M., Gallacher, L., Majdoub, F., Smal, N., Weckhuysen, S., Schoonjans, A.-S., Kooy, R. F., Meuwissen, M., Cocanougher, B. T., Taylor, K., Pizoli, C. E., McDonald, M. T., James, P., Roeder, E. R., Littlejohn, R., Borja, N. A., Thorson, W., King, K., Stoeva, R., Suerink, M., Nibbeling, E., Baskin, S., L E Guyader, G., Kaplan, J., Muss, C., Carere, D. A., Bhoj, E. J. K. & Bryant, L. M., 2024, In: European Journal of Human Genetics. 32, 8, p. 928–937 10 p.
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Layo-Carris, D. E., Lubin, E. E., Sangree, A. K., Clark, K. J., Durham, E. L., Gonzalez, E. M., Smith, S., Angireddy, R., Wang, X. M., Weiss, E., Toutain, A., Mendoza-Londono, R., Dupuis, L., Damseh, N., Velasco, D., Valenzuela, I., Codina-Solà, M., Ziats, C., Have, J., ... Bryant, L. M. (2024). Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1). European Journal of Human Genetics, 32(8), Article 1032. https://doi.org/10.1038/s41431-024-01659-y

Layo-Carris, Dana E. ; Lubin, Emily E. ; Sangree, Annabel K. et al. / Correction : Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1). In: European Journal of Human Genetics. 2024 ; Vol. 32, No. 8.

@article{4dc64299520e4fa1b4fca7af214958cf,

title = "Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)",

abstract = "An author was not named. The missing author is: “Annick Toutain” Her affiliation is: 27 Service de G{\'e}n{\'e}tique, CHU de Tours, Tours, France. 28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.",

author = "Layo-Carris, \{Dana E.\} and Lubin, \{Emily E.\} and Sangree, \{Annabel K.\} and Clark, \{Kelly J.\} and Durham, \{Emily L.\} and Gonzalez, \{Elizabeth M.\} and Sarina Smith and Rajesh Angireddy and Wang, \{Xiao Min\} and Erin Weiss and Annick Toutain and Roberto Mendoza-Londono and Lucie Dupuis and Nadirah Damseh and Danita Velasco and Irene Valenzuela and Marta Codina-Sol{\`a} and Catherine Ziats and Jaclyn Have and Katie Clarkson and Dora Steel and Manju Kurian and Katy Barwick and Diana Carrasco and Dagli, \{Aditi I.\} and Nowaczyk, \{M. J.M.\} and Miroslava Han{\v c}{\'a}rov{\'a} and {\v S}{\'a}rka Bendov{\'a} and Darina Prchalova and Zden{\v e}k Sedl{\'a}{\v c}ek and Alica Baxov{\'a} and Nowak, \{Catherine Bearce\} and Jessica Douglas and Chung, \{Wendy K.\} and Nicola Longo and Konrad Platzer and Chiara Kl{\"o}ckner and Luisa Averdunk and Dagmar Wieczorek and Ilona Krey and Christiane Zweier and Andre Reis and Tugce Balci and Marleen Simon and Kroes, \{Hester Y.\} and Antje Wiesener and Georgia Vasileiou and Marinakis, \{Nikolaos M.\} and Danai Veltra and Christalena Sofocleous and Konstantina Kosma and Synodinos, \{Joanne Traeger\} and Voudris, \{Konstantinos A.\} and Vuillaume, \{Marie Laure\} and Paul Gueguen and Nicolas Derive and Estelle Colin and Clarisse Battault and Billie Au and Martin Delatycki and Mathew Wallis and Lyndon Gallacher and Fatma Majdoub and Noor Smal and Sarah Weckhuysen and Schoonjans, \{An Sofie\} and Kooy, \{R. Frank\} and Marije Meuwissen and Cocanougher, \{Benjamin T.\} and Kathryn Taylor and Pizoli, \{Carolyn E.\} and McDonald, \{Marie T.\} and Philip James and Roeder, \{Elizabeth R.\} and Rebecca Littlejohn and Borja, \{Nicholas A.\} and Willa Thorson and Kristine King and Radka Stoeva and Manon Suerink and Esther Nibbeling and Stephanie Baskin and Guyader, \{Gwena{\"e}l L.E.\} and Julie Kaplan and Candace Muss and Carere, \{Deanna Alexis\} and Bhoj, \{Elizabeth J.K.\} and Bryant, \{Laura M.\}",

note = "Publisher Copyright: {\textcopyright} The Author(s) 2024.",

year = "2024",

month = aug,

doi = "10.1038/s41431-024-01659-y",

language = "English",

volume = "32",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Springer Nature",

number = "8",

}

Layo-Carris, DE, Lubin, EE, Sangree, AK, Clark, KJ, Durham, EL, Gonzalez, EM, Smith, S, Angireddy, R, Wang, XM, Weiss, E, Toutain, A, Mendoza-Londono, R, Dupuis, L, Damseh, N, Velasco, D, Valenzuela, I, Codina-Solà, M, Ziats, C, Have, J, Clarkson, K, Steel, D, Kurian, M, Barwick, K, Carrasco, D, Dagli, AI, Nowaczyk, MJM, Hančárová, M, Bendová, Š, Prchalova, D, Sedláček, Z, Baxová, A, Nowak, CB, Douglas, J, Chung, WK, Longo, N, Platzer, K, Klöckner, C, Averdunk, L, Wieczorek, D, Krey, I, Zweier, C, Reis, A, Balci, T, Simon, M, Kroes, HY, Wiesener, A, Vasileiou, G, Marinakis, NM, Veltra, D, Sofocleous, C, Kosma, K, Synodinos, JT, Voudris, KA, Vuillaume, ML, Gueguen, P, Derive, N, Colin, E, Battault, C, Au, B, Delatycki, M, Wallis, M, Gallacher, L, Majdoub, F, Smal, N, Weckhuysen, S, Schoonjans, AS, Kooy, RF, Meuwissen, M, Cocanougher, BT, Taylor, K, Pizoli, CE, McDonald, MT, James, P, Roeder, ER, Littlejohn, R, Borja, NA, Thorson, W, King, K, Stoeva, R, Suerink, M, Nibbeling, E, Baskin, S, Guyader, GLE, Kaplan, J, Muss, C, Carere, DA, Bhoj, EJK & Bryant, LM 2024, 'Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)', European Journal of Human Genetics, vol. 32, no. 8, 1032. https://doi.org/10.1038/s41431-024-01659-y

Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1). / Layo-Carris, Dana E.; Lubin, Emily E.; Sangree, Annabel K. et al.
In: European Journal of Human Genetics, Vol. 32, No. 8, 1032, 08.2024.

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

TY - JOUR

T1 - Correction

T2 - Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)

AU - Layo-Carris, Dana E.

AU - Lubin, Emily E.

AU - Sangree, Annabel K.

AU - Clark, Kelly J.

AU - Durham, Emily L.

AU - Gonzalez, Elizabeth M.

AU - Smith, Sarina

AU - Angireddy, Rajesh

AU - Wang, Xiao Min

AU - Weiss, Erin

AU - Toutain, Annick

AU - Mendoza-Londono, Roberto

AU - Dupuis, Lucie

AU - Damseh, Nadirah

AU - Velasco, Danita

AU - Valenzuela, Irene

AU - Codina-Solà, Marta

AU - Ziats, Catherine

AU - Have, Jaclyn

AU - Clarkson, Katie

AU - Steel, Dora

AU - Kurian, Manju

AU - Barwick, Katy

AU - Carrasco, Diana

AU - Dagli, Aditi I.

AU - Nowaczyk, M. J.M.

AU - Hančárová, Miroslava

AU - Bendová, Šárka

AU - Prchalova, Darina

AU - Sedláček, Zdeněk

AU - Baxová, Alica

AU - Nowak, Catherine Bearce

AU - Douglas, Jessica

AU - Chung, Wendy K.

AU - Longo, Nicola

AU - Platzer, Konrad

AU - Klöckner, Chiara

AU - Averdunk, Luisa

AU - Wieczorek, Dagmar

AU - Krey, Ilona

AU - Zweier, Christiane

AU - Reis, Andre

AU - Balci, Tugce

AU - Simon, Marleen

AU - Kroes, Hester Y.

AU - Wiesener, Antje

AU - Vasileiou, Georgia

AU - Marinakis, Nikolaos M.

AU - Veltra, Danai

AU - Sofocleous, Christalena

AU - Kosma, Konstantina

AU - Synodinos, Joanne Traeger

AU - Voudris, Konstantinos A.

AU - Vuillaume, Marie Laure

AU - Gueguen, Paul

AU - Derive, Nicolas

AU - Colin, Estelle

AU - Battault, Clarisse

AU - Au, Billie

AU - Delatycki, Martin

AU - Wallis, Mathew

AU - Gallacher, Lyndon

AU - Majdoub, Fatma

AU - Smal, Noor

AU - Weckhuysen, Sarah

AU - Schoonjans, An Sofie

AU - Kooy, R. Frank

AU - Meuwissen, Marije

AU - Cocanougher, Benjamin T.

AU - Taylor, Kathryn

AU - Pizoli, Carolyn E.

AU - McDonald, Marie T.

AU - James, Philip

AU - Roeder, Elizabeth R.

AU - Littlejohn, Rebecca

AU - Borja, Nicholas A.

AU - Thorson, Willa

AU - King, Kristine

AU - Stoeva, Radka

AU - Suerink, Manon

AU - Nibbeling, Esther

AU - Baskin, Stephanie

AU - Guyader, Gwenaël L.E.

AU - Kaplan, Julie

AU - Muss, Candace

AU - Carere, Deanna Alexis

AU - Bhoj, Elizabeth J.K.

AU - Bryant, Laura M.

PY - 2024/8

Y1 - 2024/8

N2 - An author was not named. The missing author is: “Annick Toutain” Her affiliation is: 27 Service de Génétique, CHU de Tours, Tours, France. 28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.

AB - An author was not named. The missing author is: “Annick Toutain” Her affiliation is: 27 Service de Génétique, CHU de Tours, Tours, France. 28 UMR1253, iBrain, Inserm, University of Tours, Tours, France.

UR - https://www.scopus.com/pages/publications/85199631647

U2 - 10.1038/s41431-024-01659-y

DO - 10.1038/s41431-024-01659-y

M3 - Comment/Letter to the editor

C2 - 39060653

AN - SCOPUS:85199631647

SN - 1018-4813

VL - 32

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 8

M1 - 1032

ER -

Layo-Carris DE, Lubin EE, Sangree AK, Clark KJ, Durham EL, Gonzalez EM et al. Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1). European Journal of Human Genetics. 2024 Aug;32(8):1032. doi: 10.1038/s41431-024-01659-y

Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)

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Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals

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