Author

Ashley R. Jones

King's College London

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 2 Bioinformatics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 2 Research Focus:GWAS / association mapping· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Aleksey ShatunoviD· 3 shared Ammar Al‐ChalabiiD· 3 shared Ahmad Al KhleifatiD· 2 shared Alfredo IacoangeliiD· 2 shared Isabella FoghiD· 2 shared Jan Herman VeldinkiD· 2 shared Leonard H. van den BergiD· 2 shared Pamela J. ShawiD· 2 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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3 shared papersNeuroscience

Aleksey ShatunovORCID

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Author profile →

3 papers

Recent·Most cited

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases

Zhongbo Chen, Regina Hertfelder Reynolds, Antonio F. Pardiñas, Sarah A. Gagliano Taliun, Wouter van Rheenen, Kuang Lin, Aleksey Shatunov, Emil Karl Gustavsson, Isabella Fogh, Ashley R. Jones, Wim Robberecht, Philippe Corcia, Adriano Chiò, Pamela J. Shaw, Karen E. Morrison, , Ammar Al‐Chalabi

This study investigates the role of Neanderthal introgression and natural selection in the heritability of neurodegenerative diseases and finds no significant contribution from either.

Neurobiology of Disease · Mar 14, 2023Peer-reviewedNeuroscience

Non-Coding Genetic Analysis Implicates Interleukin 18 Receptor Accessory Protein 3'UTR in Amyotrophic Lateral Sclerosis

Chen Eitan, Aviad Siany, Elad Barkan, Tsviya Olender, Kristel R. van Eijk, Matthieu Moisse, Sali M.K. Farhan, Yehuda Matan Danino, Eran Yanowski, Hagai Marmor-Kollet, Natalia Rivkin, Nancy‐Sarah Yacovzada, Shu‐Ting Hung, Johnathan Cooper‐Knock, Chien‐Hsiung Yu, , Eran Hornstein

The paper identifies non-coding variants in the IL18RAP 3'UTR that reduce ALS risk by modulating neuro-inflammation through NF-κB signaling in microglia.

bioRxiv · Jun 3, 2021 · PreprintNeuroscience

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA NGS data of ALS patients

Alfredo Iacoangeli, Ahmad Al Khleifat, William Sproviero, Aleksey Shatunov, Ashley R. Jones, Sarah Opie-Martin, Ersilia Naselli, Simon D. Topp, Isabella Fogh, Angela Hodges, Richard Dobson, Stephen Newhouse, Ammar Al‐Chalabi

ALSgeneScanner is a tool that provides automated, detailed reports on ALS-related gene variants from whole genome or exome sequencing data, aiding non-specialists in interpretation.

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · Mar 5, 2019Peer-reviewedBioinformatics