Emil Karl Gustavsson
Affiliations: | University College London, London, United Kingdom |
Area:
GeneticsGoogle:
"Emil Gustavsson"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| 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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Publications
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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 |