| Year |
Citation |
Score |
| 2023 |
Chen Z, Reynolds RH, Pardiñas AF, Gagliano Taliun SA, van Rheenen W, Lin K, Shatunov A, Gustavsson EK, Fogh I, Jones AR, Robberecht W, Corcia P, Chiò A, Shaw PJ, Morrison KE, et al. The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. Neurobiology of Disease. 180: 106082. PMID 36925053 DOI: 10.1016/j.nbd.2023.106082 |
0.614 |
|
| 2023 |
Chen Z, Tucci A, Cipriani V, Gustavsson EK, Ibañez K, Reynolds RH, Zhang D, Vestito L, Cisterna García A, Sethi S, Brenton JW, García-Ruiz S, Fairbrother-Browne A, Gil-Martinez AL, Hardy JA, et al. Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia. Brain : a Journal of Neurology. PMID 36624280 DOI: 10.1093/brain/awad009 |
0.507 |
|
| 2022 |
Krohn L, Heilbron K, Blauwendraat C, Reynolds RH, Yu E, Senkevich K, Rudakou U, Estiar MA, Gustavsson EK, Brolin K, Ruskey JA, Freeman K, Asayesh F, Chia R, Arnulf I, et al. Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Nature Communications. 13: 7496. PMID 36470867 DOI: 10.1038/s41467-022-34732-5 |
0.389 |
|
| 2022 |
Johansen M, Joensen S, Restorff M, Stórá T, Christy D, Gustavsson EK, Bian J, Guo Y, Farrer MJ, Petersen MS. Polygenic risk of Alzheimer's disease in the Faroe Islands. European Journal of Neurology. PMID 35384166 DOI: 10.1111/ene.15351 |
0.585 |
|
| 2022 |
Birkeland NA, Carlsen VN, Gulati S, Gustavsson EK, Aasly JO. Deep brain stimulation in a Parkinson's disease patient with calcifications and a mutation in the SLC20A2 gene. Parkinsonism & Related Disorders. 96: 88-90. PMID 35248831 DOI: 10.1016/j.parkreldis.2022.01.019 |
0.417 |
|
| 2021 |
Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, ... ... Gustavsson E, et al. Genome-wide association studies of LRRK2 modifiers of Parkinson's disease. Annals of Neurology. PMID 33938021 DOI: 10.1002/ana.26094 |
0.728 |
|
| 2021 |
Chen Z, Zhang D, Reynolds RH, Gustavsson EK, García-Ruiz S, D'Sa K, Fairbrother-Browne A, Vandrovcova J, Hardy J, Houlden H, Gagliano Taliun SA, Botía J, Ryten M. Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage. Nature Communications. 12: 2076. PMID 33824317 DOI: 10.1038/s41467-021-22262-5 |
0.507 |
|
| 2021 |
Chia R, Sabir MS, Bandres-Ciga S, Saez-Atienzar S, Reynolds RH, Gustavsson E, Walton RL, Ahmed S, Viollet C, Ding J, Makarious MB, Diez-Fairen M, Portley MK, Shah Z, Abramzon Y, et al. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Nature Genetics. PMID 33589841 DOI: 10.1038/s41588-021-00785-3 |
0.675 |
|
| 2020 |
Nybø CJ, Gustavsson EK, Farrer MJ, Aasly JO. Neuropathological findings in PINK1-associated Parkinson's disease. Parkinsonism & Related Disorders. 78: 105-108. PMID 32814227 DOI: 10.1016/j.parkreldis.2020.07.023 |
0.684 |
|
| 2019 |
Gustavsson EK, Follett J, Farrer MJ, Aasly JO. A Family with Primary Periodic Paralysis and a Mutation in MCM3AP, a gene implicated in mRNA Transport. Muscle & Nerve. PMID 31241196 DOI: 10.1002/mus.26622 |
0.599 |
|
| 2019 |
Follett J, Fox JD, Gustavsson EK, Kadgien C, Munsie LN, Cao LP, Tatarnikov I, Milnerwood AJ, Farrer MJ. DNAJC13 p.Asn855Ser, implicated in familial parkinsonism, alters membrane dynamics of Sorting Nexin 1. Neuroscience Letters. PMID 31082451 DOI: 10.1016/J.Neulet.2019.04.043 |
0.714 |
|
| 2018 |
Cataldi S, Follett J, Fox JD, Tatarnikov I, Kadgien C, Gustavsson EK, Khinda J, Milnerwood AJ, Farrer MJ. Altered dopamine release and monoamine transporters in Vps35 p.D620N knock-in mice. Npj Parkinson's Disease. 4: 27. PMID 30155515 DOI: 10.1038/S41531-018-0063-3 |
0.677 |
|
| 2018 |
Johansen KK, Torp SH, Farrer MJ, Gustavsson EK, Aasly JO. A Case of Parkinson's Disease with No Lewy Body Pathology due to a Homozygous Exon Deletion in . Case Reports in Neurological Medicine. 2018: 6838965. PMID 30050705 DOI: 10.1155/2018/6838965 |
0.646 |
|
| 2017 |
Gustavsson EK, Trinh J, McKenzie M, Bortnick S, Petersen MS, Farrer MJ, Aasly JO. Genetic Identification in Early Onset Parkinsonism among Norwegian Patients. Movement Disorders Clinical Practice. 4: 499-508. PMID 30363439 DOI: 10.1002/mdc3.12501 |
0.665 |
|
| 2016 |
Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, et al. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology. PMID 27692902 DOI: 10.1016/S1474-4422(16)30203-4 |
0.65 |
|
| 2016 |
Gustavsson EK, Trinh J, Guella I, Szu-Tu C, Khinda J, Lin CH, Wu RM, Stoessl J, Appel-Cresswell S, McKeown M, Rajput A, Rajput AH, Petersen MS, Jeon BS, Aasly JO, et al. DCTN1 p.K56R in progressive supranuclear palsy. Parkinsonism & Related Disorders. PMID 27132499 DOI: 10.1016/J.Parkreldis.2016.04.025 |
0.628 |
|
| 2015 |
Trinh J, Guella I, McKenzie M, Gustavsson EK, Szu-Tu C, Petersen MS, Rajput A, Rajput AH, McKeown M, Jeon BS, Aasly JO, Bardien S, Farrer MJ. Novel LRRK2 mutations in Parkinsonism. Parkinsonism & Related Disorders. PMID 26213354 DOI: 10.1016/J.Parkreldis.2015.07.011 |
0.65 |
|
| 2015 |
Gustavsson EK, Guella I, Trinh J, Szu-Tu C, Rajput A, Rajput AH, Steele JC, McKeown M, Jeon BS, Aasly JO, Farrer MJ. Genetic variability of the retromer cargo recognition complex in parkinsonism. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 580-4. PMID 25475142 DOI: 10.1002/Mds.26104 |
0.681 |
|
| 2015 |
Petersen MS, Guella I, Bech S, Gustavsson E, Farrer MJ. Parkinson's disease, genetic variability and the Faroe Islands. Parkinsonism & Related Disorders. 21: 75-8. PMID 25466404 DOI: 10.1016/j.parkreldis.2014.10.027 |
0.652 |
|
| 2015 |
Gustavsson EK, Trinh J, Guella I, Vilariño-Güell C, Appel-Cresswell S, Stoessl AJ, Tsui JK, McKeown M, Rajput A, Rajput AH, Aasly JO, Farrer MJ. DNAJC13 genetic variants in parkinsonism. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 273-8. PMID 25393719 DOI: 10.1002/Mds.26064 |
0.678 |
|
| 2014 |
Løvlie H, Immonen E, Gustavsson E, Kazancioğlu E, Arnqvist G. The influence of mitonuclear genetic variation on personality in seed beetles. Proceedings. Biological Sciences / the Royal Society. 281: 20141039. PMID 25320161 DOI: 10.1098/Rspb.2014.1039 |
0.52 |
|
| 2014 |
Trinh J, Amouri R, Duda JE, Morley JF, Read M, Donald A, Vilariño-Güell C, Thompson C, Szu Tu C, Gustavsson EK, Ben Sassi S, Hentati E, Zouari M, Farhat E, Nabli F, et al. Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism. Neurobiology of Aging. 35: 1125-31. PMID 24355527 DOI: 10.1016/j.neurobiolaging.2013.11.015 |
0.675 |
|
| 2014 |
Vilariño-Güell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, Yu I, Encarnacion M, Munsie LN, Tapia L, Gustavsson EK, Chou P, Tatarnikov I, Evans DM, Pishotta FT, et al. DNAJC13 mutations in Parkinson disease. Human Molecular Genetics. 23: 1794-801. PMID 24218364 DOI: 10.1093/Hmg/Ddt570 |
0.748 |
|
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