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Rare variants in β-Amyloid precursor protein (APP) and Parkinson's disease.
Schulte EC, Fukumori A, Mollenhauer B, Hor H, Arzberger T, Perneczky R, Kurz A, Diehl-Schmid J, Hüll M, Lichtner P, Eckstein G, Zimprich A, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Lorenzo-Betancor O, Pastor P, Peters A, Gieger C, Estivill X, Meitinger T, Kretzschmar HA, Trenkwalder C, Haass C, Winkelmann J. Schulte EC, et al. Among authors: molnar mj. Eur J Hum Genet. 2015 Oct;23(10):1328-33. doi: 10.1038/ejhg.2014.300. Epub 2015 Jan 21. Eur J Hum Genet. 2015. PMID: 25604855 Free PMC article.
Rare variants in PLXNA4 and Parkinson's disease.
Schulte EC, Stahl I, Czamara D, Ellwanger DC, Eck S, Graf E, Mollenhauer B, Zimprich A, Lichtner P, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Peters A, Gieger C, Müller-Myhsok B, Trenkwalder C, Winkelmann J. Schulte EC, et al. Among authors: molnar mj. PLoS One. 2013 Nov 11;8(11):e79145. doi: 10.1371/journal.pone.0079145. eCollection 2013. PLoS One. 2013. PMID: 24244438 Free PMC article. Clinical Trial.
Mitochondrial DNA mutations and cognition: a case-series report.
Inczedy-Farkas G, Trampush JW, Perczel Forintos D, Beech D, Andrejkovics M, Varga Z, Remenyi V, Bereznai B, Gal A, Molnar MJ. Inczedy-Farkas G, et al. Among authors: molnar mj. Arch Clin Neuropsychol. 2014 Jun;29(4):315-21. doi: 10.1093/arclin/acu016. Epub 2014 Apr 28. Arch Clin Neuropsychol. 2014. PMID: 24777554
The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population.
Márki S, Göblös A, Szlávicz E, Török N, Balicza P, Bereznai B, Takáts A, Engelhardt J, Klivényi P, Vécsei L, Molnár MJ, Nagy N, Széll M. Márki S, et al. Among authors: molnar mj. Parkinsons Dis. 2018 Apr 3;2018:9351598. doi: 10.1155/2018/9351598. eCollection 2018. Parkinsons Dis. 2018. PMID: 29850016 Free PMC article.
178 results