Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)

Salim Megat; Natalia Mora; Jason Sanogo; Olga Roman; Alberto Catanese; Najwa Ouali Alami; Axel Freischmidt; Xhuljana Mingaj; Hortense De Calbiac; François Muratet; Sylvie Dirrig-Grosch; Stéphane Dieterle; Nick Van Bakel; Kathrin Müller; Kirsten Sieverding; Jochen Weishaupt; Peter Munch Andersen; Markus Weber; Christoph Neuwirth; Markus Margelisch; Andreas Sommacal; Kristel R. Van Eijk; Jan H. Veldink; Géraldine Lautrette; Philippe Couratier; Agnès Camuzat; Isabelle Le Ber; Maurizio Grassano; Adriano Chio; Tobias Boeckers; Albert C. Ludolph; Francesco Roselli; Deniz Yilmazer-Hanke; Stéphanie Millecamps; Edor Kabashi; Erik Storkebaum; Chantal Sellier; Luc Dupuis

doi:10.1038/s41467-023-43710-4

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)

Salim Megat^*
, Natalia Mora
, Jason Sanogo
, Olga Roman
, Alberto Catanese
, Najwa Ouali Alami
, Axel Freischmidt
, Xhuljana Mingaj
, Hortense De Calbiac
, François Muratet
, Sylvie Dirrig-Grosch
, Stéphane Dieterle
, Nick Van Bakel
, Kathrin Müller
, Kirsten Sieverding
, Jochen Weishaupt
, Peter Munch Andersen
, Markus Weber
, Christoph Neuwirth
, Markus Margelisch

Andreas Sommacal, Kristel R. Van Eijk, Jan H. Veldink, Géraldine Lautrette, Philippe Couratier, Agnès Camuzat, Isabelle Le Ber, Maurizio Grassano, Adriano Chio, Tobias Boeckers, Albert C. Ludolph, Francesco Roselli, Deniz Yilmazer-Hanke, Stéphanie Millecamps, Edor Kabashi, Erik Storkebaum, Chantal Sellier, Luc Dupuis^*,

^*Corresponding author for this work

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

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Abstract

Correction to: Nature Communications, published online 20 January 2023 The original version of this article contained errors in Table 2 in the variant_location, cDNA_change, protein_change and dbSNPid columns. The correct version of Table 2 is: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.87 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Glu20Gly 4.2e-06 3 0 0.84 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.73 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.75 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113949 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45574313C>G c.535C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45580471C>T c.1342C>T p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 which replaces the previous incorrect version: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.88 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Gln20Cys 4.2e-06 3 0 0.86 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.74 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.76 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113943 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45178432C>G c.734C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45184590C>T c.1734C>G p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 In addition, the original version of Fig. 3c showed one variant (Lys275Glu) in an incorrect location and another variant (Arg448Trp) was missing. The correct version of Fig. 3 is: (Figure presented.) which replaces the previous incorrect version: (Figure presented.) This has been corrected in both the PDF and HTML versions of the Article.

Original language	English
Article number	8026
Journal	Nature Communications
Volume	14
Issue number	1
DOIs	https://doi.org/10.1038/s41467-023-43710-4
Publication status	Published - Dec 2023

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Megat, S., Mora, N., Sanogo, J., Roman, O., Catanese, A., Alami, N. O., Freischmidt, A., Mingaj, X., De Calbiac, H., Muratet, F., Dirrig-Grosch, S., Dieterle, S., Van Bakel, N., Müller, K., Sieverding, K., Weishaupt, J., Andersen, P. M., Weber, M., Neuwirth, C. (2023). Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1). Nature Communications, 14(1), Article 8026. https://doi.org/10.1038/s41467-023-43710-4

@article{892bb1ae2b8b443792b97d0949427322,

title = "Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)",

abstract = "Correction to: Nature Communications, published online 20 January 2023 The original version of this article contained errors in Table 2 in the variant\_location, cDNA\_change, protein\_change and dbSNPid columns. The correct version of Table 2 is: (Table presented.) variant\_type variant\_location cDNA\_change protein\_change gnomAD\_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense\_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.87 26.5 rs200329756 frameshift\_variant 22:g.45564091dupATAGGAATTG c.35\_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Glu20Gly 4.2e-06 3 0 0.84 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense\_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice\_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.73 24.2 rs148003438 missense\_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.75 23 rs779406443 missense\_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113949 splice\_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense\_variant 22:g.45574313C>G c.535C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense\_variant 22:g.45580471C>T c.1342C>T p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 which replaces the previous incorrect version: (Table presented.) variant\_type variant\_location cDNA\_change protein\_change gnomAD\_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense\_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.88 26.5 rs200329756 frameshift\_variant 22:g.45564091dupATAGGAATTG c.35\_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Gln20Cys 4.2e-06 3 0 0.86 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense\_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice\_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.74 24.2 rs148003438 missense\_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.76 23 rs779406443 missense\_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113943 splice\_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense\_variant 22:g.45178432C>G c.734C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense\_variant 22:g.45184590C>T c.1734C>G p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 In addition, the original version of Fig. 3c showed one variant (Lys275Glu) in an incorrect location and another variant (Arg448Trp) was missing. The correct version of Fig. 3 is: (Figure presented.) which replaces the previous incorrect version: (Figure presented.) This has been corrected in both the PDF and HTML versions of the Article.",

author = "Salim Megat and Natalia Mora and Jason Sanogo and Olga Roman and Alberto Catanese and Alami, \{Najwa Ouali\} and Axel Freischmidt and Xhuljana Mingaj and \{De Calbiac\}, Hortense and Fran{\c c}ois Muratet and Sylvie Dirrig-Grosch and St{\'e}phane Dieterle and \{Van Bakel\}, Nick and Kathrin M{\"u}ller and Kirsten Sieverding and Jochen Weishaupt and Andersen, \{Peter Munch\} and Markus Weber and Christoph Neuwirth and Markus Margelisch and Andreas Sommacal and \{Van Eijk\}, \{Kristel R.\} and Veldink, \{Jan H.\} and G{\'e}raldine Lautrette and Philippe Couratier and Agn{\`e}s Camuzat and \{Le Ber\}, Isabelle and Maurizio Grassano and Adriano Chio and Tobias Boeckers and Ludolph, \{Albert C.\} and Francesco Roselli and Deniz Yilmazer-Hanke and St{\'e}phanie Millecamps and Edor Kabashi and Erik Storkebaum and Chantal Sellier and Luc Dupuis",

note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",

year = "2023",

month = dec,

doi = "10.1038/s41467-023-43710-4",

language = "English",

volume = "14",

journal = "Nature Communications",

issn = "2041-1723",

publisher = "Nature Research",

number = "1",

}

Megat, S, Mora, N, Sanogo, J, Roman, O, Catanese, A, Alami, NO, Freischmidt, A, Mingaj, X, De Calbiac, H, Muratet, F, Dirrig-Grosch, S, Dieterle, S, Van Bakel, N, Müller, K, Sieverding, K, Weishaupt, J, Andersen, PM, Weber, M, Neuwirth, C, Margelisch, M, Sommacal, A, Van Eijk, KR, Veldink, JH, Lautrette, G, Couratier, P, Camuzat, A, Le Ber, I, Grassano, M, Chio, A, Boeckers, T, Ludolph, AC, Roselli, F, Yilmazer-Hanke, D, Millecamps, S, Kabashi, E, Storkebaum, E, Sellier, C, Dupuis, L 2023, 'Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)', Nature Communications, vol. 14, no. 1, 8026. https://doi.org/10.1038/s41467-023-43710-4

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1). / Megat, Salim; Mora, Natalia; Sanogo, Jason et al.
In: Nature Communications, Vol. 14, No. 1, 8026, 12.2023.

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

TY - JOUR

T1 - Author Correction

T2 - Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)

AU - Megat, Salim

AU - Mora, Natalia

AU - Sanogo, Jason

AU - Roman, Olga

AU - Catanese, Alberto

AU - Alami, Najwa Ouali

AU - Freischmidt, Axel

AU - Mingaj, Xhuljana

AU - De Calbiac, Hortense

AU - Muratet, François

AU - Dirrig-Grosch, Sylvie

AU - Dieterle, Stéphane

AU - Van Bakel, Nick

AU - Müller, Kathrin

AU - Sieverding, Kirsten

AU - Weishaupt, Jochen

AU - Andersen, Peter Munch

AU - Weber, Markus

AU - Neuwirth, Christoph

AU - Margelisch, Markus

AU - Sommacal, Andreas

AU - Van Eijk, Kristel R.

AU - Veldink, Jan H.

AU - Lautrette, Géraldine

AU - Couratier, Philippe

AU - Camuzat, Agnès

AU - Le Ber, Isabelle

AU - Grassano, Maurizio

AU - Chio, Adriano

AU - Boeckers, Tobias

AU - Ludolph, Albert C.

AU - Roselli, Francesco

AU - Yilmazer-Hanke, Deniz

AU - Millecamps, Stéphanie

AU - Kabashi, Edor

AU - Storkebaum, Erik

AU - Sellier, Chantal

AU - Dupuis, Luc

PY - 2023/12

Y1 - 2023/12

N2 - Correction to: Nature Communications, published online 20 January 2023 The original version of this article contained errors in Table 2 in the variant_location, cDNA_change, protein_change and dbSNPid columns. The correct version of Table 2 is: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.87 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Glu20Gly 4.2e-06 3 0 0.84 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.73 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.75 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113949 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45574313C>G c.535C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45580471C>T c.1342C>T p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 which replaces the previous incorrect version: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.88 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Gln20Cys 4.2e-06 3 0 0.86 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.74 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.76 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113943 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45178432C>G c.734C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45184590C>T c.1734C>G p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 In addition, the original version of Fig. 3c showed one variant (Lys275Glu) in an incorrect location and another variant (Arg448Trp) was missing. The correct version of Fig. 3 is: (Figure presented.) which replaces the previous incorrect version: (Figure presented.) This has been corrected in both the PDF and HTML versions of the Article.

AB - Correction to: Nature Communications, published online 20 January 2023 The original version of this article contained errors in Table 2 in the variant_location, cDNA_change, protein_change and dbSNPid columns. The correct version of Table 2 is: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.87 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Glu20Gly 4.2e-06 3 0 0.84 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.73 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.75 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113949 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45574313C>G c.535C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45580471C>T c.1342C>T p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 which replaces the previous incorrect version: (Table presented.) variant_type variant_location cDNA_change protein_change gnomAD_AF ALS cases (n = 9390) Control (n = 4594) MVP CADD dbSNPid missense_variant 22:g.45564104G>A c.46G>A p.Asp16Asn 0.000322851 11 2 0.88 26.5 rs200329756 frameshift_variant 22:g.45564091dupATAGGAATTG c.35_45dupATAGGAATTGG p.Asp16fs NA 1 0 NA NA NA structural 22:g.45564117A>G c.59A>G p.Gln20Cys 4.2e-06 3 0 0.86 26.3 rs1200142847 structural 22:g.45567544C>T c.133C>T p.Arg45Cys 9.68367e-05 9 0 0.89 28.1 rs113634721 missense_variant 22:g.45571835C>T c.214C>T p.Arg72Cys 3.23018e-05 1 0 0.81 23.6 rs781273344 splice_variant 22:g.45574119G>A c.341G>A p.Gly114Asp 0.000419897 3 0 0.74 24.2 rs148003438 missense_variant 22:g.45574245A>G c.467A>G p.Tyr156Cys 2.88367e-05 1 0 0.76 23 rs779406443 missense_variant 22:g.45574601A>G c.823A>G p.Lys275Glu 3.22768e-05 2 0 0.71 23.5 rs753113943 splice_acceptor 22:g.45567480G>C c.70-1G>C NA 3.9-06 1 0 NA 32 rs770658454 missense_variant 22:g.45178432C>G c.734C>G p.Pro179Ala 6.52768e-06 1 0 0.81 22.4 rs763689432 missense_variant 22:g.45184590C>T c.1734C>G p.Arg448Trp 6.52768e-05 1 0 0.91 24 rs777952476 In addition, the original version of Fig. 3c showed one variant (Lys275Glu) in an incorrect location and another variant (Arg448Trp) was missing. The correct version of Fig. 3 is: (Figure presented.) which replaces the previous incorrect version: (Figure presented.) This has been corrected in both the PDF and HTML versions of the Article.

UR - https://www.scopus.com/pages/publications/85178467904

U2 - 10.1038/s41467-023-43710-4

DO - 10.1038/s41467-023-43710-4

M3 - Comment/Letter to the editor

C2 - 38049418

AN - SCOPUS:85178467904

SN - 2041-1723

VL - 14

JO - Nature Communications

JF - Nature Communications

IS - 1

M1 - 8026

ER -

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes (Nature Communications, (2023), 14, 1, (342), 10.1038/s41467-022-35724-1)

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes

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