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Year | Number of Results |
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2018 | 2 |
2019 | 4 |
2020 | 1 |
2024 | 0 |
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Page 1
Utility and implications of exome sequencing in early-onset Parkinson's disease.
Mov Disord. 2019 Jan;34(1):133-137. doi: 10.1002/mds.27559. Epub 2018 Dec 10.
Mov Disord. 2019.
PMID: 30537300
Free PMC article.
Novel NAXE variants as a cause for neurometabolic disorder: implications for treatment.
Trinh J, Imhoff S, Dulovic-Mahlow M, Kandaswamy KK, Tadic V, Schäfer J, Dobricic V, Nolte A, Werber M, Rolfs A, Münchau A, Klein C, Lohmann K, Brüggemann N.
Trinh J, et al. Among authors: imhoff s.
J Neurol. 2020 Mar;267(3):770-782. doi: 10.1007/s00415-019-09640-2. Epub 2019 Nov 20.
J Neurol. 2020.
PMID: 31745726
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The Role of Rare Coding Variants in Parkinson's Disease GWAS Loci.
Germer EL, Imhoff S, Vilariño-Güell C, Kasten M, Seibler P, Brüggemann N; International Parkinson’s Disease Genomics Consortium; Klein C, Trinh J.
Germer EL, et al. Among authors: imhoff s.
Front Neurol. 2019 Dec 13;10:1284. doi: 10.3389/fneur.2019.01284. eCollection 2019.
Front Neurol. 2019.
PMID: 31920912
Free PMC article.
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Variants in Miro1 Cause Alterations of ER-Mitochondria Contact Sites in Fibroblasts from Parkinson's Disease Patients.
Berenguer-Escuder C, Grossmann D, Massart F, Antony P, Burbulla LF, Glaab E, Imhoff S, Trinh J, Seibler P, Grünewald A, Krüger R.
Berenguer-Escuder C, et al. Among authors: imhoff s.
J Clin Med. 2019 Dec 16;8(12):2226. doi: 10.3390/jcm8122226.
J Clin Med. 2019.
PMID: 31888276
Free PMC article.
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A KAT6A variant in a family with autosomal dominantly inherited microcephaly and developmental delay.
Trinh J, Hüning I, Yüksel Z, Baalmann N, Imhoff S, Klein C, Rolfs A, Gillessen-Kaesbach G, Lohmann K.
Trinh J, et al. Among authors: imhoff s.
J Hum Genet. 2018 Sep;63(9):997-1001. doi: 10.1038/s10038-018-0469-0. Epub 2018 Jun 13.
J Hum Genet. 2018.
PMID: 29899504
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