Emil Karl Gustavsson

University College London, London, United Kingdom 
"Emil Gustavsson"
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Göran Arnqvist research assistant Uppsala (Evolution Tree)
Klas Kullander research assistant Uppsala
Matthew Farrer grad student Univesity of British Columia (UBC)
John Hardy post-doc UCL
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Chen Z, Reynolds RH, Pardiñas AF, et al. (2023) The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. Neurobiology of Disease. 180: 106082
Chen Z, Tucci A, Cipriani V, et al. (2023) Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia. Brain : a Journal of Neurology
Krohn L, Heilbron K, Blauwendraat C, et al. (2022) Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nature Communications. 13: 7496
Johansen M, Joensen S, Restorff M, et al. (2022) Polygenic risk of Alzheimer's disease in the Faroe Islands. European Journal of Neurology
Birkeland NA, Carlsen VN, Gulati S, et al. (2022) Deep brain stimulation in a Parkinson's disease patient with calcifications and a mutation in the SLC20A2 gene. Parkinsonism & Related Disorders. 96: 88-90
Lai D, Alipanahi B, Fontanillas P, et al. (2021) Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology
Chen Z, Zhang D, Reynolds RH, et al. (2021) Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage. Nature Communications. 12: 2076
Chia R, Sabir MS, Bandres-Ciga S, et al. (2021) Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature Genetics
Nybø CJ, Gustavsson EK, Farrer MJ, et al. (2020) Neuropathological findings in PINK1-associated Parkinson's disease. Parkinsonism & Related Disorders. 78: 105-108
Gustavsson EK, Follett J, Farrer MJ, et al. (2019) A Family with Primary Periodic Paralysis and a Mutation in MCM3AP, a gene implicated in mRNA Transport. Muscle & Nerve
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