Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/183102
Title: Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis
Author: Al Khleifat, Ahmad
Iacoangeli, Alfredo
Vugt, Joke J. F. A. van
Bowles, Harry
Moisse, Matthieu
Zwamborn, Ramona A. J.
Spek, Rick A. A. van der
Shatunov, Aleksey
Cooper-Knock, Johnathan
Topp, Simon
Byrne, Ross
Gellera, Cinzia
López, Victoria
Jones, Ashley R.
Opie-Martin, Sarah
Vural, Atay
Campos, Yolanda
Rheenen, Wouter van
Kenna, Brendan
Eijk, Kristel R. van
Kenna, Kevin
Weber, Markus
Smith, Bradley
Fogh, Isabella
Silani, Vincenzo
Morrison, Karen E.
Dobson, Richard
Es, Michael A. van
Mclaughlin, Russell L.
Vourc’h, Patrick
Chio, Adriano
Corcia, Philippe
Carvalho, Mamede de
Gotkine, Marc
Panades, Monica P.
Mora, Jesus S.
Shaw, Pamela J.
Landers, John E.
Glass, Jonathan D.
Shaw, Christopher E.
Basak, Nazli
Hardiman, Orla
Robberecht, Wim
Damme, Philip van
Berg, Leonard H. van der
Veldink, Jan H.
Al Chalabi, Ammar
Keywords: Esclerosi lateral amiotròfica
Genètica humana
Amyotrophic lateral sclerosis
Human genetics
Issue Date: 28-Jan-2022
Publisher: Springer Science and Business Media LLC
Abstract: There is a strong genetic contribution to Amyotrophic lateral sclerosis (ALS) risk, with heritability estimates of up to 60%. Both Mendelian and small effect variants have been identified, but in common with other conditions, such variants only explain a little of the heritability. Genomic structural variation might account for some of this otherwise unexplained heritability. We therefore investigated association between structural variation in a set of 25 ALS genes, and ALS risk and phenotype. As expected, the repeat expansion in the C9orf72 gene was identified as associated with ALS. Two other ALS-associated structural variants were identified: inversion in the VCP gene and insertion in the ERBB4 gene. All three variants were associated both with increased risk of ALS and specific phenotypic patterns of disease expression. More than 70% of people with respiratory onset ALS harboured ERBB4 insertion compared with 25% of the general population, suggesting respiratory onset ALS may be a distinct genetic subtype.
Note: Reproducció del document publicat a: https://doi.org/10.1038/s41525-021-00267-9
It is part of: npj Genomic Medicine, 2022, vol 7, num 1
URI: http://hdl.handle.net/2445/183102
Related resource: https://doi.org/10.1038/s41525-021-00267-9
ISSN: 2056-7944
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Publicacions de projectes de recerca finançats per la UE

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