Correction:Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Erratum: Single-cell whole genome sequencing reveals no evidence for common aneuploidy in normal and Alzheimer's disease neurons

van den Bos, Hilda
Spierings, Diana C. J.
Taudt, Aaron
Bakker, Bjorn
Porubsky, David
Falconer, Ester
Novoa, Carolina
Halsema, Nancy
Kazemier, Hinke G.
Hoekstra-Wakker, Karina
Guryev, Victor
Dunnen, den, Wilfred
Foijer, Floris
Colome-Tatche, Maria
Boddeke, Hendrikus W. G. M.
Lansdorp, Peter M.

June 2016

After the publication of this work [1] it was noticed that there were errors in two author names.The...

Correction to: A systematic review of necrotising fasciitis in children from its first description in 1930 to 2018

Schroeder, Arne
Gerin, Aurelie
Firth, Gregory B.
Hoffmann, Kelly S.
Grieve, Andrew
von Sochaczewski, Christina Oetzmann

May 2019

After publication of the original article [1], we were notified that two of the author names were in...

Publisher Correction:Distinct patterns of within-host virus populations between two subgroups of human respiratory syncytial virus (Nature Communications, (2021), 12, 1, (5125), 10.1038/s41467-021-25265-4)

Lin, Gu Lung
Drysdale, Simon B.
Snape, Matthew D.
O’Connor, Daniel
Brown, Anthony
MacIntyre-Cockett, George
Mellado-Gomez, Esther
de Cesare, Mariateresa
Bonsall, David
Ansari, M. Azim
Öner, Deniz
Aerssens, Jeroen
Butler, Christopher
Bont, Louis
Openshaw, Peter
Martinón-Torres, Federico
Nair, Harish
Bowden, Rory
Golubchik, Tanya
Pollard, Andrew J.

December 2021

The original HTML version of this Article contained errors in the author affiliations, which were co...

Correction:Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article.</p

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article

Publisher Correction:Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

July 2019

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

Publisher Correction:Common brain disorders are associated with heritable patterns of apparent aging of the brain

Kaufmann, Tobias
van der Meer, Dennis
Doan, Nhat Trung
Schwarz, Emanuel
Lund, Martina J
Agartz, Ingrid
Alnæs, Dag
Barch, Deanna M
Baur-Streubel, Ramona
Bertolino, Alessandro
Bettella, Francesco
Beyer, Mona K
Bøen, Erlend
Borgwardt, Stefan
Brandt, Christine L
Buitelaar, Jan
Celius, Elisabeth G
Cervenka, Simon
Conzelmann, Annette
Córdova-Palomera, Aldo
Dale, Anders M
de Quervain, Dominique J F
Di Carlo, Pasquale
Djurovic, Srdjan
Dørum, Erlend S
Eisenacher, Sarah
Elvsåshagen, Torbjørn
Espeseth, Thomas
Fatouros-Bergman, Helena
Flyckt, Lena
Franke, Barbara
Frei, Oleksandr
Haatveit, Beathe
Håberg, Asta K
Harbo, Hanne F
Hartman, Catharina A
Heslenfeld, Dirk
Hoekstra, Pieter J
Høgestøl, Einar A
Jernigan, Terry L
Jonassen, Rune
Jönsson, Erik G
Kirsch, Peter
Kłoszewska, Iwona
Kolskår, Knut K
Landrø, Nils Inge
Le Hellard, Stephanie
Lesch, Klaus-Peter
Lovestone, Simon
Wang, Lei

February 2020

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

Correction: Dispelling myths about rare disease registry system development.

Bellgard, Matthew
Béroud, Christophe
Parkinson, Kay
Harris, Tess
Ayme, Segolene
Baynam, Gareth
Weeramanthri, Tarun
Dawkins, Hugh
Hunter, Adam

January 2014

International audience: Correction After publication of this work [1], we noted that we inadvertentl...

Author Correction:Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts (Nature Genetics, (2021), 53, 1, (86-99), 10.1038/s41588-020-00750-6)

Woo, Xing Yi
Giordano, Jessica
Srivastava, Anuj
Zhao, Zi Ming
Lloyd, Michael W.
de Bruijn, Roebi
Suh, Yun Suhk
Patidar, Rajesh
Chen, Li
Scherer, Sandra
Bailey, Matthew H.
Yang, Chieh Hsiang
Cortes-Sanchez, Emilio
Xi, Yuanxin
Wang, Jing
Wickramasinghe, Jayamanna
Kossenkov, Andrew V.
Rebecca, Vito W.
Sun, Hua
Mashl, R. Jay
Davies, Sherri R.
Jeon, Ryan
Frech, Christian
Randjelovic, Jelena
Rosains, Jacqueline
Galimi, Francesco
Bertotti, Andrea
Lafferty, Adam
O’Farrell, Alice C.
Modave, Elodie
Lambrechts, Diether
ter Brugge, Petra
Serra, Violeta
Marangoni, Elisabetta
El Botty, Rania
Kim, Hyunsoo
Kim, Jong Il
Yang, Han Kwang
Lee, Charles
Dean, Dennis A.
Davis-Dusenbery, Brandi
Evrard, Yvonne A.
Doroshow, James H.
Welm, Alana L.

May 2021

This paper was originally published without open access. As of the date of this correction, the pape...

Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x)

Surendran, Praveen
Feofanova, Elena V.
Lahrouchi, Najim
Ntalla, Ioanna
Karthikeyan, Savita
Cook, James
Chen, Lingyan
Mifsud, Borbala
Yao, Chen
Kraja, Aldi T.
Cartwright, James H.
Hellwege, Jacklyn N.
Giri, Ayush
Tragante, Vinicius
Thorleifsson, Gudmar
Liu, Dajiang J.
Prins, Bram P.
Stewart, Isobel D.
Cabrera, Claudia P.
Eales, James M.
Akbarov, Artur
Auer, Paul L.
Bielak, Lawrence F.
Bis, Joshua C.
Braithwaite, Vickie S.
Brody, Jennifer A.
Daw, E. Warwick
Warren, Helen R.
Drenos, Fotios
Nielsen, Sune Fallgaard
Faul, Jessica D.
Fauman, Eric B.
Fava, Cristiano
Ferreira, Teresa
Foley, Christopher N.
Franceschini, Nora
Smith, Albert V.
Zhao, Jing Hua
Zhao, Wei
Zhao, Wei
de Boer, Rudolf A.
van der Harst, Pim
van der Meer, Peter
Verweij, Niek

May 2021

In the version of this article originally published, the e-mail address of corresponding author Patr...

Erratum: Single-cell whole genome sequencing reveals no evidence for common aneuploidy in normal and Alzheimer's disease neurons

van den Bos, Hilda
Spierings, Diana C. J.
Taudt, Aaron
Bakker, Bjorn
Porubsky, David
Falconer, Ester
Novoa, Carolina
Halsema, Nancy
Kazemier, Hinke G.
Hoekstra-Wakker, Karina
Guryev, Victor
Dunnen, den, Wilfred
Foijer, Floris
Colome-Tatche, Maria
Boddeke, Hendrikus W. G. M.
Lansdorp, Peter M.

June 2016

After the publication of this work [1] it was noticed that there were errors in two author names.The...

Correction to: A systematic review of necrotising fasciitis in children from its first description in 1930 to 2018

Schroeder, Arne
Gerin, Aurelie
Firth, Gregory B.
Hoffmann, Kelly S.
Grieve, Andrew
von Sochaczewski, Christina Oetzmann

May 2019

After publication of the original article [1], we were notified that two of the author names were in...

Publisher Correction:Distinct patterns of within-host virus populations between two subgroups of human respiratory syncytial virus (Nature Communications, (2021), 12, 1, (5125), 10.1038/s41467-021-25265-4)

Lin, Gu Lung
Drysdale, Simon B.
Snape, Matthew D.
O’Connor, Daniel
Brown, Anthony
MacIntyre-Cockett, George
Mellado-Gomez, Esther
de Cesare, Mariateresa
Bonsall, David
Ansari, M. Azim
Öner, Deniz
Aerssens, Jeroen
Butler, Christopher
Bont, Louis
Openshaw, Peter
Martinón-Torres, Federico
Nair, Harish
Bowden, Rory
Golubchik, Tanya
Pollard, Andrew J.

December 2021

The original HTML version of this Article contained errors in the author affiliations, which were co...

Correction:Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article.</p

Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Schüle, Rebecca
Timmann, Dagmar
Erasmus, Corrie E.
Reichbauer, Jennifer
Wayand, Melanie
van de Warrenburg, Bart
Schöls, Ludger
Wilke, Carlo
Bevot, Andrea
Zuchner, Stephan
Beltran, Sergi
Laurie, Steven
Matalonga, Leslie
Graessner, Holm
Synofzik, Matthis

September 2021

In the original publication of the article, consortium author lists were missing in the article

Publisher Correction:Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

July 2019

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

Publisher Correction:Common brain disorders are associated with heritable patterns of apparent aging of the brain

Kaufmann, Tobias
van der Meer, Dennis
Doan, Nhat Trung
Schwarz, Emanuel
Lund, Martina J
Agartz, Ingrid
Alnæs, Dag
Barch, Deanna M
Baur-Streubel, Ramona
Bertolino, Alessandro
Bettella, Francesco
Beyer, Mona K
Bøen, Erlend
Borgwardt, Stefan
Brandt, Christine L
Buitelaar, Jan
Celius, Elisabeth G
Cervenka, Simon
Conzelmann, Annette
Córdova-Palomera, Aldo
Dale, Anders M
de Quervain, Dominique J F
Di Carlo, Pasquale
Djurovic, Srdjan
Dørum, Erlend S
Eisenacher, Sarah
Elvsåshagen, Torbjørn
Espeseth, Thomas
Fatouros-Bergman, Helena
Flyckt, Lena
Franke, Barbara
Frei, Oleksandr
Haatveit, Beathe
Håberg, Asta K
Harbo, Hanne F
Hartman, Catharina A
Heslenfeld, Dirk
Hoekstra, Pieter J
Høgestøl, Einar A
Jernigan, Terry L
Jonassen, Rune
Jönsson, Erik G
Kirsch, Peter
Kłoszewska, Iwona
Kolskår, Knut K
Landrø, Nils Inge
Le Hellard, Stephanie
Lesch, Klaus-Peter
Lovestone, Simon
Wang, Lei

February 2020

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

Correction: Dispelling myths about rare disease registry system development.

Bellgard, Matthew
Béroud, Christophe
Parkinson, Kay
Harris, Tess
Ayme, Segolene
Baynam, Gareth
Weeramanthri, Tarun
Dawkins, Hugh
Hunter, Adam

January 2014

International audience: Correction After publication of this work [1], we noted that we inadvertentl...

Author Correction:Conservation of copy number profiles during engraftment and passaging of patient-derived cancer xenografts (Nature Genetics, (2021), 53, 1, (86-99), 10.1038/s41588-020-00750-6)

Woo, Xing Yi
Giordano, Jessica
Srivastava, Anuj
Zhao, Zi Ming
Lloyd, Michael W.
de Bruijn, Roebi
Suh, Yun Suhk
Patidar, Rajesh
Chen, Li
Scherer, Sandra
Bailey, Matthew H.
Yang, Chieh Hsiang
Cortes-Sanchez, Emilio
Xi, Yuanxin
Wang, Jing
Wickramasinghe, Jayamanna
Kossenkov, Andrew V.
Rebecca, Vito W.
Sun, Hua
Mashl, R. Jay
Davies, Sherri R.
Jeon, Ryan
Frech, Christian
Randjelovic, Jelena
Rosains, Jacqueline
Galimi, Francesco
Bertotti, Andrea
Lafferty, Adam
O’Farrell, Alice C.
Modave, Elodie
Lambrechts, Diether
ter Brugge, Petra
Serra, Violeta
Marangoni, Elisabetta
El Botty, Rania
Kim, Hyunsoo
Kim, Jong Il
Yang, Han Kwang
Lee, Charles
Dean, Dennis A.
Davis-Dusenbery, Brandi
Evrard, Yvonne A.
Doroshow, James H.
Welm, Alana L.

May 2021

This paper was originally published without open access. As of the date of this correction, the pape...

Publisher Correction:Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x)

Surendran, Praveen
Feofanova, Elena V.
Lahrouchi, Najim
Ntalla, Ioanna
Karthikeyan, Savita
Cook, James
Chen, Lingyan
Mifsud, Borbala
Yao, Chen
Kraja, Aldi T.
Cartwright, James H.
Hellwege, Jacklyn N.
Giri, Ayush
Tragante, Vinicius
Thorleifsson, Gudmar
Liu, Dajiang J.
Prins, Bram P.
Stewart, Isobel D.
Cabrera, Claudia P.
Eales, James M.
Akbarov, Artur
Auer, Paul L.
Bielak, Lawrence F.
Bis, Joshua C.
Braithwaite, Vickie S.
Brody, Jennifer A.
Daw, E. Warwick
Warren, Helen R.
Drenos, Fotios
Nielsen, Sune Fallgaard
Faul, Jessica D.
Fauman, Eric B.
Fava, Cristiano
Ferreira, Teresa
Foley, Christopher N.
Franceschini, Nora
Smith, Albert V.
Zhao, Jing Hua
Zhao, Wei
Zhao, Wei
de Boer, Rudolf A.
van der Harst, Pim
van der Meer, Peter
Verweij, Niek

May 2021

In the version of this article originally published, the e-mail address of corresponding author Patr...

Erratum: Single-cell whole genome sequencing reveals no evidence for common aneuploidy in normal and Alzheimer's disease neurons

van den Bos, Hilda
Spierings, Diana C. J.
Taudt, Aaron
Bakker, Bjorn
Porubsky, David
Falconer, Ester
Novoa, Carolina
Halsema, Nancy
Kazemier, Hinke G.
Hoekstra-Wakker, Karina
Guryev, Victor
Dunnen, den, Wilfred
Foijer, Floris
Colome-Tatche, Maria
Boddeke, Hendrikus W. G. M.
Lansdorp, Peter M.

June 2016

After the publication of this work [1] it was noticed that there were errors in two author names.The...

Correction to: A systematic review of necrotising fasciitis in children from its first description in 1930 to 2018

Schroeder, Arne
Gerin, Aurelie
Firth, Gregory B.
Hoffmann, Kelly S.
Grieve, Andrew
von Sochaczewski, Christina Oetzmann

May 2019

After publication of the original article [1], we were notified that two of the author names were in...

Publisher Correction:Distinct patterns of within-host virus populations between two subgroups of human respiratory syncytial virus (Nature Communications, (2021), 12, 1, (5125), 10.1038/s41467-021-25265-4)

Lin, Gu Lung
Drysdale, Simon B.
Snape, Matthew D.
O’Connor, Daniel
Brown, Anthony
MacIntyre-Cockett, George
Mellado-Gomez, Esther
de Cesare, Mariateresa
Bonsall, David
Ansari, M. Azim
Öner, Deniz
Aerssens, Jeroen
Butler, Christopher
Bont, Louis
Openshaw, Peter
Martinón-Torres, Federico
Nair, Harish
Bowden, Rory
Golubchik, Tanya
Pollard, Andrew J.

December 2021

The original HTML version of this Article contained errors in the author affiliations, which were co...

Correction:Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Abstract

Extracted data

Correction:Solving unsolved rare neurological diseases—a Solve-RD viewpoint (European Journal of Human Genetics, (2021), 29, 9, (1332-1336), 10.1038/s41431-021-00901-1)

Abstract

Extracted data

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