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Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, et al.Neurology. Genetics|April 28, 2020
Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutationMerel O Mol, Jeroen G J van Rooij, Esther Brusse, et al.Annals of Neurology|February 9, 2002
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent datasetVincenzo Bonifati, Guido J Breedveld, Ferdinando Squitieri, et al.Brain : a Journal of Neurology|March 16, 2007
TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutationsHarro Seelaar, H Jurgen Schelhaas, Asma Azmani, et al.Plos One|November 27, 2013
Resequencing three candidate genes for major depressive disorder in a Dutch cohortEva C Verbeek, Marianna R Bevova, Zoltán Bochdanovits, et al.Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
DJ-1 protects the nigrostriatal axis from the neurotoxin MPTP by modulation of the AKT pathwayHossein Aleyasin, Maxime W C Rousseaux, Paul C Marcogliese, et al.Cell Reports|March 23, 2026
The insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37Joana R Loureiro, Ana F Castro, Ana S Figueiredo, et al.Plos One|June 1, 2012
A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorderEva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, et al.Neuro-Oncology Advances|November 2, 2020
Experimental glioma with high bHLH expression harbor increased replicative stress and are sensitive toward ATR inhibitionMarilin Sophia Koch, Stefan Czemmel, Felix Lennartz, et al.Neurobiology of Aging|February 23, 2013
Regional differences in gene expression and promoter usage in aged human brainsLuba M Pardo, Patrizia Rizzu, Margherita Francescatto, et al.Pageof 7