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A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Pihlstrøm L, Blauwendraat C, Cappelletti C, Berge-Seidl V, Langmyhr M, Henriksen SP, van de Berg WDJ, Gibbs JR, Cookson MR; International Parkinson Disease Genomics Consortium; North American Brain Expression Consortium; Singleton AB, Nalls MA, Toft M. Pihlstrøm L, et al. Among authors: henriksen sp. Ann Neurol. 2018 Jul;84(1):117-129. doi: 10.1002/ana.25274. Epub 2018 Aug 26. Ann Neurol. 2018. PMID: 30146727 Free PMC article.
Rare variants in dementia genes and Parkinson's disease.
Iqbal Z, Pihlstrøm L, Rengmark A, Henriksen SP, Linder J, Forsgren L, Toft M. Iqbal Z, et al. Among authors: henriksen sp. Eur J Hum Genet. 2016 Dec;24(12):1661-1662. doi: 10.1038/ejhg.2016.79. Epub 2016 Jun 22. Eur J Hum Genet. 2016. PMID: 27329738 Free PMC article. No abstract available.
Missense mutations in DYT-TOR1A dystonia.
Iqbal Z, Koht J, Pihlstrøm L, Henriksen SP, Cappelletti C, Russel MB, Norberto de Souza O, Skogseid IM, Toft M. Iqbal Z, et al. Among authors: henriksen sp. Neurol Genet. 2019 Jun 6;5(4):e343. doi: 10.1212/NXG.0000000000000343. eCollection 2019 Aug. Neurol Genet. 2019. PMID: 31321303 Free PMC article. No abstract available.
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia.
Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CM, Toft M. Iqbal Z, et al. Among authors: henriksen sp. PLoS One. 2017 Mar 31;12(3):e0174667. doi: 10.1371/journal.pone.0174667. eCollection 2017. PLoS One. 2017. PMID: 28362824 Free PMC article.
11 results