Author Correction : CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z)

Taskesen, E
Mishra, A
van der Sluis, S
Ferrari, R
Veldink, J H
van Es, M A
Smit, A B
Posthuma, D
Pijnenburg, Y
Hernandez, DG
Nalls. MA
Rohrer JD
Ramasamy, A
Kwok, JBJ
Dobson-Stone, C
Schofield, PR
Halliday, GM
Hodges, JR
Piguet, O
Bartley, L
Thompson, E
Haan, E
Hernández, I
Ruiz, A
Boada, M
Borroni, B
Padovani, A
Cruchaga, C
Cairns, NJ
Benussi, L
Binetti G
Ghidoni, R
Forloni, G
Albani, D
Galimberti, D
Fenoglio, C
Serp
Wassermann EM
Baborie A
Jaros E
Tierney MC
Pastor P
Razquin C
Ortega-Cubero S
Alonso E
Perneczky R
Diehl-Schmid J
Alexopoulos P
Kurz A
Rainero I
Rubino E
Pinessi L
Rogaeva E
George-Hyslop PS
Rossi G
Tagliavini F
Giaccone G
Rowe JB
Schlachetzki JCM
Uphill J
Collinge J
Mead S
Danek A
Van Deerlin VM
Grossman M
Trojanowski JQ
van der Zee J
Van Broeckhoven C
Cappa SF
Leber I
Hannequin D
Golfier V
Vercelletto M
Brice A
Nacmias B
Sorbi S
Bagnoli S
Piaceri I
Nielsen JE
Hjermind LE
Riemenschneider M
Mayhaus M
Ibach B
Gasparoni G
Pichler S
Gu W
Rossor MN
Fox NC
Warren JD
Spillantini MG
Morris HR
Rizzu P
Heutink P
Snowden JS
Rollinson S
Richardson A
Gerhard A
Bruni AC
Maletta R
Frangipane F
Cupidi C
Bernardi L
Anfossi M
Gallo M
Conidi ME
Smirne N
Rademakers R
Baker M
Dickson DW
Graff-Radford NR
Petersen RC
Knopman D
Josephs KA
Boeve BF
Parisi JE
Seeley WW
Miller BL
Karydas AM
Rosen H
van Swieten JC
Dopper EGP
Seelaar H
Scheltens P
Logroscino G
Capozzo R
Novelli V
Puca AA
Franceschi M
Postiglione A
Milan G
Sorrentino P
Kristiansen M
Chiang HH
Graff C
Pasquier F
Rollin A
Deramecourt V
Lebouvier T
Kapogiannis D
Ferrucci L
Pickering-Brown S
Singleton AB
Hardy J
Momeni P.

January 2018

International FTD-Genomics Consortium was omitted from the author list in the original version of th...

Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation (Communications Biology, (2021), 4, 1, (666), 10.1038/s42003-021-02114-0).

Stavsky, A.
Stoler, O.
Kostic, M.
Katoshevsky, T.
Assali, E.A.
Savic, I.
Amitai, Y.
Prokisch, H.
Leiz, S.
Daumer-Haas, C.
Fleidervish, I.A.
Perocchi, F.
Gitler, D.
Sekler, I.

January 2021

The original version of this Article contained an error in the spelling of the author Fabiana Perocc...

Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899))

January 2018

A correction to this article has been published and is linked from the HTML and PDF versions of this...

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Blok, LS
Rousseau, J
Twist, J
Ehresmann, S
Takaku, M
Venselaar, H
Rodan, LH
Nowak, CB
Douglas, J
Swoboda, KJ
Steeves, MA
Sahai, I
Stumpel, CTRM
Stegmann, APA
Wheeler, P
Willing, M
Fiala, E
Kochhar, A
Gibson, WT
Cohen, ASA
Agbahovbe, R
Innes, AM
Au, PYB
Rankin, J
Anderson, IJ
Skinner, SA
Louie, RJ
Warren, HE
Afenjar, A
Keren, B
Nava, C
Buratti, J
Isapof, A
Rodriguez, D
Lewandowski, R
Propst, J
van Essen, T
Choi, M
Lee, S
Chae, JH
Price, S
Schnur, RE
Douglas, G
Wentzensen, IM
Zweier, C
Reis, A
Bialer, MG
Moore, C
Koopmans, M
Brilstra, EH
Monroe, GR
van Gassen, KLI
van Binsbergen, E
Newbury-Ecob, R
Bownass, L
Bader, I
Mayr, JA
Wortmann, SB
Jakielski, KJ
Strand, EA
Kloth, K
Bierhals, T
The DDD Study
Roberts, JD
Petrovich, RM
Machida, S
Kurumizaka, H
Lelieveld, S
Pfundt, R
Jansen, S
Deriziotis, P
Faivre, L
Thevenon, J
Assoum, M
Shriberg, L
Kleefstra, T
Brunner, HG
Wade, PA
Fisher, SE
Campeau, PM

May 2019

Correction to: Nature Communications https://doi.org/10.1038/s41467-018-06014-6, published online 05...

Correction to: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

Blok, Lot Snijders
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H.
Nowak, Catherine B.
Douglas, Jessica
Swoboda, Kathryn J.
Steeves, Marcie A.
Sahai, Inderneel
Stumpel, Connie T.R.M.
Stegmann, Alexander P.A.
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T.
Cohen, Ana S.A.
Agbahovbe, Ruky
Innes, A. Micheil
Au, P.Y.Billie
Rankin, Julia
Anderson, Ilse J.
Skinner, Steven A.
Louie, Raymond J.
Warren, Hannah E.
Afenjar, Alexandra
Keren, Boris
Jones, Philip
Jones, Wendy D.
King, Daniel
Baralle, Diana
Blyth, Moira
Foulds, Nicola
Green, Andrew
Harrison, Rachel
Hewitt, Sarah
Jackson, Andrew
Jones, Elizabeth
Lachlan, Katherine
Miles, Emma
Patel, Chirag
Roberts, Paul
Temple, I. Karen
Turner, Claire
Wellesley, Diana
Wilkinson, Emily
Wright, Caroline F.
The DDD study

February 2019

The original version of this Article contained an error in the spelling of the author Laurence Faivr...

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018).

Snijders Blok, L.
Rousseau, J.
Twist, J.
Ehresmann, S.
Takaku, M.
Venselaar, H.
Rodan, L.H.
Nowak, C.B.
Douglas, J.
Swoboda, K.J.
Steeves, M.A.
Sahai, I.
Stumpel, C.T.R.M.
Stegmann, A.P.A.
Wheeler, P.
Willing, M.
Fiala, E.
Kochhar, A.
Gibson, W.T.
Cohen, A.S.A.
Agbahovbe, R.
Innes, A.M.
Au, P.Y.B.
Rankin, J.
Anderson, I.J.
Skinner, S.A.
Louie, R.J.
Warren, H.E.
Afenjar, A.
Keren, B.
Nava, C.
Buratti, J.
Isapof, A.
Rodriguez, D.
Lewandowski, R.
Propst, J.
van Essen, T.
Choi, M.
Lee, S.
Chae, J.H.
Price, S.
Schnur, R.E.
Douglas, G.
Wentzensen, I.M.
Zweier, C.
Reis, A.
Bialer, M.G.
Moore, C.
Koopmans, M.
Brilstra, E.H.
Monroe, G.R.
van Gassen, K.L.I.
van Binsbergen, E.
Newbury-Ecob, R.
Bownass, L.
Bader, I.
Mayr, J.A.
Wortmann, S.B.
Jakielski, K.J.
Strand, E.A.
Kloth, K.
Bierhals, T.
Roberts, J.D.
Petrovich, R.M.
Machida, S.
Kurumizaka, H.
Lelieveld, S.
Pfundt, R.
Jansen, S.
Deriziotis, P.
Faivre, L.
Thevenon, J.
Assoum, M.
Shriberg, L.
Kleefstra, T.
Brunner, H.G.
Wade, P.A.
Fisher, S.E.
Campeau, P.M.

January 2019

The HTML and PDF versions of this Article were updated after publication to remove images of one ind...

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Blok, L. S.
Rousseau, J.
Twist, J.
Ehresmann, S.
Takaku, M.
Venselaar, H.
Rodan, L. H.
Bialer, M. G.
Moore, C.
Blyth, M.
+90 additional authors

January 2019

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

DDD Study

November 2018

An Author Correction to this article was published on 15 February 2019 An Author Correction to this ...

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Wang, Tianyun
Hoekzema, Kendra
Vecchio, Davide
Wu, Huidan
Sulovari, Arvis
Coe, Bradley P
Gillentine, Madelyn A
Wilfert, Amy B
Perez-Jurado, Luis A
Kvarnung, Malin
Sleyp, Yoeri
Earl, Rachel K
Rosenfeld, Jill A
Geisheker, Madeleine R
Han, Lin
Du, Bing
Barnett, Chris
Thompson, Elizabeth
Shaw, Marie
Carroll, Renee
Friend, Kathryn
Catford, Rachael
Palmer, Elizabeth E
Zou, Xiaobing
Ou, Jianjun
Li, Honghui
Guo, Hui
Gerdts, Jennifer
Avola, Emanuela
Calabrese, Giuseppe
Elia, Maurizio
Greco, Donatella
Lindstrand, Anna
Nordgren, Ann
Anderlid, Britt-Marie
Vandeweyer, Geert
Van Dijck, Anke
Van der Aa, Nathalie
McKenna, Brooke
Hancarova, Miroslava
Bendova, Sarka
Havlovicova, Marketa
Malerba, Giovanni
Bernardina, Bernardo Dalla
Muglia, Pierandrea
van Haeringen, Arie
Hoffer, Mariette JV
Franke, Barbara
Cappuccio, Gerarda
Delatycki, Martin
Lockhart, Paul J
Manning, Melanie A
Liu, Pengfei
Scheffer, Ingrid E
Brunetti-Pierri, Nicola
Rommelse, Nanda
Amaral, David G
Santen, Gijs WE
Trabetti, Elisabetta
Sedláček, Zdeněk
Michaelson, Jacob J
Pierce, Karen
Courchesne, Eric
Kooy, R Frank
Nordenskjöld, Magnus
Romano, Corrado
Peeters, Hilde
Bernier, Raphael A
Gecz, Jozef
Xia, Kun
Eichler, Evan E

January 2020

An amendment to this paper has been published and can be accessed via a link at the top of the paper

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre
Sorlin, Arthur
Kholmanskikh, Stanislav S.
Demeer, Bénédicte
St Onge, Judith
Duffourd, Yannis
Kuentz, Paul
Courcet, Jean-Benoît
Carmignac, Virginie
Garret, Philippine
Bessis, Didier
Boute, Odile
Bron, Alain
Captier, Guillaume
Carmi, Esther
Devauchelle, Bernard
Geneviève, David
Gondry Jouet, Catherine
Guibaud, Laurent
Lafon, Arnaud
Mathieu Dramard, Michèle
Thevenon, Julien
Dobyns, William B.
Bernard, Geneviève
Polubothu, Satyamaanasa
Faravelli, Francesca
Kinsler, Veronica A.
Thauvin, Christel
Faivre, Laurence
Ross, Elizabeth M.
Rivière, Jean-Baptiste

January 2019

Published Erratum: Correction to: Nature Genetics 51: 1438–1441 https://doi.org/10.1038/s41588-019-0...

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology (Nature Communications, (2020), 11, 1, (4589), 10.1038/s41467-020-18146-9)

Elouej, Sahar
Harhouri, Karim
Mao, Morgane Le
Baujat, Genevieve
Nampoothiri, Sheela
Kayserili, H. lya
Menabawy, Nihal Al
Selim, Laila
Paneque, Arianne Llamos
Kubisch, Christian
Lessel, Davor
Rubinsztajn, Robert
Charar, Chayki
Bartoli, Catherine
Airault, Coraline
Deleuze, Jean-François
Rötig, Agnes
Bauer, Peter
Pereira, Catarina
Loh, Abigail
Escande-Beillard, Nathalie
Muchir, Antoine
Martino, Lisa
Gruenbaum, Yosef
Lee, Song-Hua
Manivet, Philippe
Lenaers, Guy
Reversade, Bruno
Lévy, Nicolas
de Sandre-Giovannoli, Annachiara

December 2020

The original version of this Article contained errors in the author affiliations. The affiliations o...

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z)

Taskesen, E
Mishra, A
van der Sluis, S
Ferrari, R
Veldink, J H
van Es, M A
Smit, A B
Posthuma, D
Pijnenburg, Y
Hernandez, DG
Nalls. MA
Rohrer JD
Ramasamy, A
Kwok, JBJ
Dobson-Stone, C
Schofield, PR
Halliday, GM
Hodges, JR
Piguet, O
Bartley, L
Thompson, E
Haan, E
Hernández, I
Ruiz, A
Boada, M
Borroni, B
Padovani, A
Cruchaga, C
Cairns, NJ
Benussi, L
Binetti G
Ghidoni, R
Forloni, G
Albani, D
Galimberti, D
Fenoglio, C
Serp
Wassermann EM
Baborie A
Jaros E
Tierney MC
Pastor P
Razquin C
Ortega-Cubero S
Alonso E
Perneczky R
Diehl-Schmid J
Alexopoulos P
Kurz A
Rainero I
Rubino E
Pinessi L
Rogaeva E
George-Hyslop PS
Rossi G
Tagliavini F
Giaccone G
Rowe JB
Schlachetzki JCM
Uphill J
Collinge J
Mead S
Danek A
Van Deerlin VM
Grossman M
Trojanowski JQ
van der Zee J
Van Broeckhoven C
Cappa SF
Leber I
Hannequin D
Golfier V
Vercelletto M
Brice A
Nacmias B
Sorbi S
Bagnoli S
Piaceri I
Nielsen JE
Hjermind LE
Riemenschneider M
Mayhaus M
Ibach B
Gasparoni G
Pichler S
Gu W
Rossor MN
Fox NC
Warren JD
Spillantini MG
Morris HR
Rizzu P
Heutink P
Snowden JS
Rollinson S
Richardson A
Gerhard A
Bruni AC
Maletta R
Frangipane F
Cupidi C
Bernardi L
Anfossi M
Gallo M
Conidi ME
Smirne N
Rademakers R
Baker M
Dickson DW
Graff-Radford NR
Petersen RC
Knopman D
Josephs KA
Boeve BF
Parisi JE
Seeley WW
Miller BL
Karydas AM
Rosen H
van Swieten JC
Dopper EGP
Seelaar H
Scheltens P
Logroscino G
Capozzo R
Novelli V
Puca AA
Franceschi M
Postiglione A
Milan G
Sorrentino P
Kristiansen M
Chiang HH
Graff C
Pasquier F
Rollin A
Deramecourt V
Lebouvier T
Kapogiannis D
Ferrucci L
Pickering-Brown S
Singleton AB
Hardy J
Momeni P.

January 2018

International FTD-Genomics Consortium was omitted from the author list in the original version of th...

Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation (Communications Biology, (2021), 4, 1, (666), 10.1038/s42003-021-02114-0).

Stavsky, A.
Stoler, O.
Kostic, M.
Katoshevsky, T.
Assali, E.A.
Savic, I.
Amitai, Y.
Prokisch, H.
Leiz, S.
Daumer-Haas, C.
Fleidervish, I.A.
Perocchi, F.
Gitler, D.
Sekler, I.

January 2021

The original version of this Article contained an error in the spelling of the author Fabiana Perocc...

Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899))

January 2018

A correction to this article has been published and is linked from the HTML and PDF versions of this...

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Blok, LS
Rousseau, J
Twist, J
Ehresmann, S
Takaku, M
Venselaar, H
Rodan, LH
Nowak, CB
Douglas, J
Swoboda, KJ
Steeves, MA
Sahai, I
Stumpel, CTRM
Stegmann, APA
Wheeler, P
Willing, M
Fiala, E
Kochhar, A
Gibson, WT
Cohen, ASA
Agbahovbe, R
Innes, AM
Au, PYB
Rankin, J
Anderson, IJ
Skinner, SA
Louie, RJ
Warren, HE
Afenjar, A
Keren, B
Nava, C
Buratti, J
Isapof, A
Rodriguez, D
Lewandowski, R
Propst, J
van Essen, T
Choi, M
Lee, S
Chae, JH
Price, S
Schnur, RE
Douglas, G
Wentzensen, IM
Zweier, C
Reis, A
Bialer, MG
Moore, C
Koopmans, M
Brilstra, EH
Monroe, GR
van Gassen, KLI
van Binsbergen, E
Newbury-Ecob, R
Bownass, L
Bader, I
Mayr, JA
Wortmann, SB
Jakielski, KJ
Strand, EA
Kloth, K
Bierhals, T
The DDD Study
Roberts, JD
Petrovich, RM
Machida, S
Kurumizaka, H
Lelieveld, S
Pfundt, R
Jansen, S
Deriziotis, P
Faivre, L
Thevenon, J
Assoum, M
Shriberg, L
Kleefstra, T
Brunner, HG
Wade, PA
Fisher, SE
Campeau, PM

May 2019

Correction to: Nature Communications https://doi.org/10.1038/s41467-018-06014-6, published online 05...

Correction to: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

Blok, Lot Snijders
Rousseau, Justine
Twist, Joanna
Ehresmann, Sophie
Takaku, Motoki
Venselaar, Hanka
Rodan, Lance H.
Nowak, Catherine B.
Douglas, Jessica
Swoboda, Kathryn J.
Steeves, Marcie A.
Sahai, Inderneel
Stumpel, Connie T.R.M.
Stegmann, Alexander P.A.
Wheeler, Patricia
Willing, Marcia
Fiala, Elise
Kochhar, Aaina
Gibson, William T.
Cohen, Ana S.A.
Agbahovbe, Ruky
Innes, A. Micheil
Au, P.Y.Billie
Rankin, Julia
Anderson, Ilse J.
Skinner, Steven A.
Louie, Raymond J.
Warren, Hannah E.
Afenjar, Alexandra
Keren, Boris
Jones, Philip
Jones, Wendy D.
King, Daniel
Baralle, Diana
Blyth, Moira
Foulds, Nicola
Green, Andrew
Harrison, Rachel
Hewitt, Sarah
Jackson, Andrew
Jones, Elizabeth
Lachlan, Katherine
Miles, Emma
Patel, Chirag
Roberts, Paul
Temple, I. Karen
Turner, Claire
Wellesley, Diana
Wilkinson, Emily
Wright, Caroline F.
The DDD study

February 2019

The original version of this Article contained an error in the spelling of the author Laurence Faivr...

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018).

Snijders Blok, L.
Rousseau, J.
Twist, J.
Ehresmann, S.
Takaku, M.
Venselaar, H.
Rodan, L.H.
Nowak, C.B.
Douglas, J.
Swoboda, K.J.
Steeves, M.A.
Sahai, I.
Stumpel, C.T.R.M.
Stegmann, A.P.A.
Wheeler, P.
Willing, M.
Fiala, E.
Kochhar, A.
Gibson, W.T.
Cohen, A.S.A.
Agbahovbe, R.
Innes, A.M.
Au, P.Y.B.
Rankin, J.
Anderson, I.J.
Skinner, S.A.
Louie, R.J.
Warren, H.E.
Afenjar, A.
Keren, B.
Nava, C.
Buratti, J.
Isapof, A.
Rodriguez, D.
Lewandowski, R.
Propst, J.
van Essen, T.
Choi, M.
Lee, S.
Chae, J.H.
Price, S.
Schnur, R.E.
Douglas, G.
Wentzensen, I.M.
Zweier, C.
Reis, A.
Bialer, M.G.
Moore, C.
Koopmans, M.
Brilstra, E.H.
Monroe, G.R.
van Gassen, K.L.I.
van Binsbergen, E.
Newbury-Ecob, R.
Bownass, L.
Bader, I.
Mayr, J.A.
Wortmann, S.B.
Jakielski, K.J.
Strand, E.A.
Kloth, K.
Bierhals, T.
Roberts, J.D.
Petrovich, R.M.
Machida, S.
Kurumizaka, H.
Lelieveld, S.
Pfundt, R.
Jansen, S.
Deriziotis, P.
Faivre, L.
Thevenon, J.
Assoum, M.
Shriberg, L.
Kleefstra, T.
Brunner, H.G.
Wade, P.A.
Fisher, S.E.
Campeau, P.M.

January 2019

The HTML and PDF versions of this Article were updated after publication to remove images of one ind...

Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Blok, L. S.
Rousseau, J.
Twist, J.
Ehresmann, S.
Takaku, M.
Venselaar, H.
Rodan, L. H.
Bialer, M. G.
Moore, C.
Blyth, M.
+90 additional authors

January 2019

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (vol 9, 4619, 2018)

DDD Study

November 2018

An Author Correction to this article was published on 15 February 2019 An Author Correction to this ...

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Wang, Tianyun
Hoekzema, Kendra
Vecchio, Davide
Wu, Huidan
Sulovari, Arvis
Coe, Bradley P
Gillentine, Madelyn A
Wilfert, Amy B
Perez-Jurado, Luis A
Kvarnung, Malin
Sleyp, Yoeri
Earl, Rachel K
Rosenfeld, Jill A
Geisheker, Madeleine R
Han, Lin
Du, Bing
Barnett, Chris
Thompson, Elizabeth
Shaw, Marie
Carroll, Renee
Friend, Kathryn
Catford, Rachael
Palmer, Elizabeth E
Zou, Xiaobing
Ou, Jianjun
Li, Honghui
Guo, Hui
Gerdts, Jennifer
Avola, Emanuela
Calabrese, Giuseppe
Elia, Maurizio
Greco, Donatella
Lindstrand, Anna
Nordgren, Ann
Anderlid, Britt-Marie
Vandeweyer, Geert
Van Dijck, Anke
Van der Aa, Nathalie
McKenna, Brooke
Hancarova, Miroslava
Bendova, Sarka
Havlovicova, Marketa
Malerba, Giovanni
Bernardina, Bernardo Dalla
Muglia, Pierandrea
van Haeringen, Arie
Hoffer, Mariette JV
Franke, Barbara
Cappuccio, Gerarda
Delatycki, Martin
Lockhart, Paul J
Manning, Melanie A
Liu, Pengfei
Scheffer, Ingrid E
Brunetti-Pierri, Nicola
Rommelse, Nanda
Amaral, David G
Santen, Gijs WE
Trabetti, Elisabetta
Sedláček, Zdeněk
Michaelson, Jacob J
Pierce, Karen
Courchesne, Eric
Kooy, R Frank
Nordenskjöld, Magnus
Romano, Corrado
Peeters, Hilde
Bernier, Raphael A
Gecz, Jozef
Xia, Kun
Eichler, Evan E

January 2020

An amendment to this paper has been published and can be accessed via a link at the top of the paper

Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome

Vabres, Pierre
Sorlin, Arthur
Kholmanskikh, Stanislav S.
Demeer, Bénédicte
St Onge, Judith
Duffourd, Yannis
Kuentz, Paul
Courcet, Jean-Benoît
Carmignac, Virginie
Garret, Philippine
Bessis, Didier
Boute, Odile
Bron, Alain
Captier, Guillaume
Carmi, Esther
Devauchelle, Bernard
Geneviève, David
Gondry Jouet, Catherine
Guibaud, Laurent
Lafon, Arnaud
Mathieu Dramard, Michèle
Thevenon, Julien
Dobyns, William B.
Bernard, Geneviève
Polubothu, Satyamaanasa
Faravelli, Francesca
Kinsler, Veronica A.
Thauvin, Christel
Faivre, Laurence
Ross, Elizabeth M.
Rivière, Jean-Baptiste

January 2019

Published Erratum: Correction to: Nature Genetics 51: 1438–1441 https://doi.org/10.1038/s41588-019-0...

Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology (Nature Communications, (2020), 11, 1, (4589), 10.1038/s41467-020-18146-9)

Elouej, Sahar
Harhouri, Karim
Mao, Morgane Le
Baujat, Genevieve
Nampoothiri, Sheela
Kayserili, H. lya
Menabawy, Nihal Al
Selim, Laila
Paneque, Arianne Llamos
Kubisch, Christian
Lessel, Davor
Rubinsztajn, Robert
Charar, Chayki
Bartoli, Catherine
Airault, Coraline
Deleuze, Jean-François
Rötig, Agnes
Bauer, Peter
Pereira, Catarina
Loh, Abigail
Escande-Beillard, Nathalie
Muchir, Antoine
Martino, Lisa
Gruenbaum, Yosef
Lee, Song-Hua
Manivet, Philippe
Lenaers, Guy
Reversade, Bruno
Lévy, Nicolas
de Sandre-Giovannoli, Annachiara

December 2020

The original version of this Article contained errors in the author affiliations. The affiliations o...

Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific Reports (2017) DOI: 10.1038/s41598-017-09320-z)

Taskesen, E
Mishra, A
van der Sluis, S
Ferrari, R
Veldink, J H
van Es, M A
Smit, A B
Posthuma, D
Pijnenburg, Y
Hernandez, DG
Nalls. MA
Rohrer JD
Ramasamy, A
Kwok, JBJ
Dobson-Stone, C
Schofield, PR
Halliday, GM
Hodges, JR
Piguet, O
Bartley, L
Thompson, E
Haan, E
Hernández, I
Ruiz, A
Boada, M
Borroni, B
Padovani, A
Cruchaga, C
Cairns, NJ
Benussi, L
Binetti G
Ghidoni, R
Forloni, G
Albani, D
Galimberti, D
Fenoglio, C
Serp
Wassermann EM
Baborie A
Jaros E
Tierney MC
Pastor P
Razquin C
Ortega-Cubero S
Alonso E
Perneczky R
Diehl-Schmid J
Alexopoulos P
Kurz A
Rainero I
Rubino E
Pinessi L
Rogaeva E
George-Hyslop PS
Rossi G
Tagliavini F
Giaccone G
Rowe JB
Schlachetzki JCM
Uphill J
Collinge J
Mead S
Danek A
Van Deerlin VM
Grossman M
Trojanowski JQ
van der Zee J
Van Broeckhoven C
Cappa SF
Leber I
Hannequin D
Golfier V
Vercelletto M
Brice A
Nacmias B
Sorbi S
Bagnoli S
Piaceri I
Nielsen JE
Hjermind LE
Riemenschneider M
Mayhaus M
Ibach B
Gasparoni G
Pichler S
Gu W
Rossor MN
Fox NC
Warren JD
Spillantini MG
Morris HR
Rizzu P
Heutink P
Snowden JS
Rollinson S
Richardson A
Gerhard A
Bruni AC
Maletta R
Frangipane F
Cupidi C
Bernardi L
Anfossi M
Gallo M
Conidi ME
Smirne N
Rademakers R
Baker M
Dickson DW
Graff-Radford NR
Petersen RC
Knopman D
Josephs KA
Boeve BF
Parisi JE
Seeley WW
Miller BL
Karydas AM
Rosen H
van Swieten JC
Dopper EGP
Seelaar H
Scheltens P
Logroscino G
Capozzo R
Novelli V
Puca AA
Franceschi M
Postiglione A
Milan G
Sorrentino P
Kristiansen M
Chiang HH
Graff C
Pasquier F
Rollin A
Deramecourt V
Lebouvier T
Kapogiannis D
Ferrucci L
Pickering-Brown S
Singleton AB
Hardy J
Momeni P.

January 2018

International FTD-Genomics Consortium was omitted from the author list in the original version of th...

Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation (Communications Biology, (2021), 4, 1, (666), 10.1038/s42003-021-02114-0).

Stavsky, A.
Stoler, O.
Kostic, M.
Katoshevsky, T.
Assali, E.A.
Savic, I.
Amitai, Y.
Prokisch, H.
Leiz, S.
Daumer-Haas, C.
Fleidervish, I.A.
Perocchi, F.
Gitler, D.
Sekler, I.

January 2021

The original version of this Article contained an error in the spelling of the author Fabiana Perocc...

Erratum: Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS (Scientific reports (2017) 7 1 (8899))

January 2018

A correction to this article has been published and is linked from the HTML and PDF versions of this...

Author Correction : CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

Abstract

Extracted data

Author Correction : CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6)

Abstract

Extracted data

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