Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

SLALOM Consortium; PARALS Consortium; SLAGEN Consortium; SLAP Consortium; Wouter van Rheenen; Rick A. A. van der Spek; Mark K. Bakker; Joke J. F. A. van Vugt; Paul J. Hop; Ramona A. J. Zwamborn; Niek de Klein; Harm-Jan Westra; Olivier B. Bakker; Patrick Deelen; Gemma Shireby; Eilis Hannon; Matthieu Moisse; Denis Baird; Restuadi Restuadi; Egor Dolzhenko; Annelot M. Dekker; Klara Gawor; Henk-Jan Westeneng; Gijs H. P. Tazelaar; Kristel R. van Eijk; Maarten Kooyman; Ross P. Byrne; Mark Doherty; Mark Heverin; Ahmad Al Khleifat; Alfredo Iacoangeli; Aleksey Shatunov; Nicola Ticozzi; Johnathan Cooper-Knock; Bradley N. Smith; Marta Gromicho; Siddharthan Chandran; Suvankar Pal; Karen E. Morrison; Pamela J. Shaw; John Hardy; Richard W. Orrell; Michael Sendtner; Thomas Meyer; Nazli Basak; Anneke J. van der Kooi; Antonia Ratti; Isabella Fogh; Cinzia Gellera; Giuseppe Lauria; Stefania Corti; Julia Kraft; Lude Franke; Jan H. Veldink

doi:10.1038/s41588-022-01020-3

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, Wouter van Rheenen^*, Rick A. A. van der Spek, Mark K. Bakker, Joke J. F. A. van Vugt, Paul J. Hop, Ramona A. J. Zwamborn, Niek de Klein, Harm-Jan Westra, Olivier B. Bakker, Patrick Deelen, Gemma Shireby, Eilis Hannon, Matthieu Moisse, Denis Baird, Restuadi Restuadi, Egor DolzhenkoAnnelot M. Dekker, Klara Gawor, Henk-Jan Westeneng, Gijs H. P. Tazelaar, Kristel R. van Eijk, Maarten Kooyman, Ross P. Byrne, Mark Doherty, Mark Heverin, Ahmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, Nicola Ticozzi, Johnathan Cooper-Knock, Bradley N. Smith, Marta Gromicho, Siddharthan Chandran, Suvankar Pal, Karen E. Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Michael Sendtner, Thomas Meyer, Nazli Basak, Anneke J. van der Kooi, Antonia Ratti, Isabella Fogh, Cinzia Gellera, Giuseppe Lauria, Stefania Corti, Julia Kraft, Lude Franke, Jan H. Veldink

^*Corresponding author for this work

Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)

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Original language	English
Pages (from-to)	361-361
Number of pages	1
Journal	Nature genetics
Volume	54
Issue number	3
DOIs	https://doi.org/10.1038/s41588-022-01020-3
Publication status	Published - Mar-2022

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SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, van Rheenen, W., van der Spek, R. A. A., Bakker, M. K., van Vugt, J. J. F. A., Hop, P. J., Zwamborn, R. A. J., de Klein, N., Westra, H.-J., Bakker, O. B., Deelen, P., Shireby, G., Hannon, E., Moisse, M., Baird, D., Restuadi, R., ... Veldink, J. H. (2022). Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021). Nature genetics, 54(3), 361-361. https://doi.org/10.1038/s41588-022-01020-3

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title = "Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)",

author = "{SLALOM Consortium} and {PARALS Consortium} and {SLAGEN Consortium} and {SLAP Consortium} and {van Rheenen}, Wouter and {van der Spek}, {Rick A. A.} and Bakker, {Mark K.} and {van Vugt}, {Joke J. F. A.} and Hop, {Paul J.} and Zwamborn, {Ramona A. J.} and {de Klein}, Niek and Harm-Jan Westra and Bakker, {Olivier B.} and Patrick Deelen and Gemma Shireby and Eilis Hannon and Matthieu Moisse and Denis Baird and Restuadi Restuadi and Egor Dolzhenko and Dekker, {Annelot M.} and Klara Gawor and Henk-Jan Westeneng and Tazelaar, {Gijs H. P.} and {van Eijk}, {Kristel R.} and Maarten Kooyman and Byrne, {Ross P.} and Mark Doherty and Mark Heverin and {Al Khleifat}, Ahmad and Alfredo Iacoangeli and Aleksey Shatunov and Nicola Ticozzi and Johnathan Cooper-Knock and Smith, {Bradley N.} and Marta Gromicho and Siddharthan Chandran and Suvankar Pal and Morrison, {Karen E.} and Shaw, {Pamela J.} and John Hardy and Orrell, {Richard W.} and Michael Sendtner and Thomas Meyer and Nazli Basak and {van der Kooi}, {Anneke J.} and Antonia Ratti and Isabella Fogh and Cinzia Gellera and Giuseppe Lauria and Stefania Corti and Julia Kraft and Lude Franke and Veldink, {Jan H.}",

year = "2022",

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doi = "10.1038/s41588-022-01020-3",

language = "English",

volume = "54",

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issn = "1061-4036",

publisher = "Nature Publishing Group",

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SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, van Rheenen, W, van der Spek, RAA, Bakker, MK, van Vugt, JJFA, Hop, PJ, Zwamborn, RAJ, de Klein, N, Westra, H-J , Bakker, OB , Deelen, P, Shireby, G, Hannon, E, Moisse, M, Baird, D, Restuadi, R, Dolzhenko, E, Dekker, AM, Gawor, K, Westeneng, H-J, Tazelaar, GHP, van Eijk, KR, Kooyman, M, Byrne, RP, Doherty, M, Heverin, M, Al Khleifat, A, Iacoangeli, A, Shatunov, A, Ticozzi, N, Cooper-Knock, J, Smith, BN, Gromicho, M, Chandran, S, Pal, S, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Sendtner, M, Meyer, T, Basak, N, van der Kooi, AJ, Ratti, A, Fogh, I, Gellera, C, Lauria, G, Corti, S, Kraft, J, Franke, L & Veldink, JH 2022, 'Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)', Nature genetics, vol. 54, no. 3, pp. 361-361. https://doi.org/10.1038/s41588-022-01020-3

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021). / SLALOM Consortium; PARALS Consortium; SLAGEN Consortium et al.
In: Nature genetics, Vol. 54, No. 3, 03.2022, p. 361-361.

Research output: Contribution to journal › Erratum

TY - JOUR

T1 - Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

AU - SLALOM Consortium

AU - PARALS Consortium

AU - SLAGEN Consortium

AU - SLAP Consortium

AU - van Rheenen, Wouter

AU - van der Spek, Rick A. A.

AU - Bakker, Mark K.

AU - van Vugt, Joke J. F. A.

AU - Hop, Paul J.

AU - Zwamborn, Ramona A. J.

AU - de Klein, Niek

AU - Westra, Harm-Jan

AU - Bakker, Olivier B.

AU - Deelen, Patrick

AU - Shireby, Gemma

AU - Hannon, Eilis

AU - Moisse, Matthieu

AU - Baird, Denis

AU - Restuadi, Restuadi

AU - Dolzhenko, Egor

AU - Dekker, Annelot M.

AU - Gawor, Klara

AU - Westeneng, Henk-Jan

AU - Tazelaar, Gijs H. P.

AU - van Eijk, Kristel R.

AU - Kooyman, Maarten

AU - Byrne, Ross P.

AU - Doherty, Mark

AU - Heverin, Mark

AU - Al Khleifat, Ahmad

AU - Iacoangeli, Alfredo

AU - Shatunov, Aleksey

AU - Ticozzi, Nicola

AU - Cooper-Knock, Johnathan

AU - Smith, Bradley N.

AU - Gromicho, Marta

AU - Chandran, Siddharthan

AU - Pal, Suvankar

AU - Morrison, Karen E.

AU - Shaw, Pamela J.

AU - Hardy, John

AU - Orrell, Richard W.

AU - Sendtner, Michael

AU - Meyer, Thomas

AU - Basak, Nazli

AU - van der Kooi, Anneke J.

AU - Ratti, Antonia

AU - Fogh, Isabella

AU - Gellera, Cinzia

AU - Lauria, Giuseppe

AU - Corti, Stefania

AU - Kraft, Julia

AU - Franke, Lude

AU - Veldink, Jan H.

PY - 2022/3

Y1 - 2022/3

U2 - 10.1038/s41588-022-01020-3

DO - 10.1038/s41588-022-01020-3

M3 - Erratum

SN - 1061-4036

VL - 54

SP - 361

EP - 361

JO - Nature genetics

JF - Nature genetics

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SLALOM Consortium, PARALS Consortium, SLAGEN Consortium, SLAP Consortium, van Rheenen W, van der Spek RAA et al. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021). Nature genetics. 2022 Mar;54(3):361-361. doi: 10.1038/s41588-022-01020-3