Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/51061
Título: Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis
Autor: Al Khleifat, Ahmad
Iacoangeli, Alfredo
van Vugt, Joke J. F. A.
Bowles, Harry
Moisse, Matthieu
Zwamborn, Ramona A. J.
van der Spek, Rick A. A.
Shatunov, Aleksey
Cooper-Knock, Johnathan
Topp, Simon
Byrne, Ross
Gellera, Cinzia
López, Victoria
Jones, Ashley R.
Opie-Martin, Sarah
Vural, Atay
Campos, Yolanda
van Rheenen, Wouter
Kenna, Brendan
Van Eijk, Kristel R.
Kenna, Kevin
Weber, Markus
Smith, Bradley
Fogh, Isabella
Silani, Vincenzo
Morrison, Karen E.
Dobson, Richard
van Es, Michael A.
McLaughlin, Russell L.
Vourc’h, Patrick
Chio, Adriano
Corcia, Philippe
Carvalho, Mamede
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
Van Damme, Philip
van den Berg, Leonard H.
Veldink, Jan H.
Al-Chalabi, Ammar
Data: 2022
Editora: Springer Nature
Citação: npj Genomic Medicine (2022) 7:8
Resumo: 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.
Descrição: © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Peer review: yes
URI: http://hdl.handle.net/10451/51061
DOI: 10.1038/s41525-021-00267-9
Versão do Editor: https://www.nature.com/npjgenmed/
Aparece nas colecções:IMM - Artigos em Revistas Internacionais
FM - Artigos em Revistas Internacionais

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