Literature DB >> 15184637

Absence of NR4A2 exon 1 mutations in 108 families with autosomal dominant Parkinson disease.

P Ibáñez1, E Lohmann, P Pollak, F Durif, C Tranchant, Y Agid, A Dürr, A Brice.   

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Year:  2004        PMID： 15184637     DOI： 10.1212/01.wnl.0000127496.23198.75

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

1.  A fast algorithm for functional mapping of complex traits.

Authors:  Wei Zhao; Rongling Wu; Chang-Xing Ma; George Casella
Journal:  Genetics       Date:  2004-08       Impact factor: 4.562

2.  Characterisation of a novel NR4A2 mutation in Parkinson's disease brain.

Authors:  P M A Sleiman; D G Healy; M M K Muqit; Y X Yang; M Van Der Brug; J L Holton; T Revesz; N P Quinn; K Bhatia; J K J Diss; A J Lees; M R Cookson; D S Latchman; N W Wood
Journal:  Neurosci Lett       Date:  2009-03-11       Impact factor: 3.046

3.  Efficient and biologically relevant consensus strategy for Parkinson's disease gene prioritization.

Authors:  Maykel Cruz-Monteagudo; Fernanda Borges; Cesar Paz-Y-Miño; M Natália D S Cordeiro; Irene Rebelo; Yunierkis Perez-Castillo; Aliuska Morales Helguera; Aminael Sánchez-Rodríguez; Eduardo Tejera
Journal:  BMC Med Genomics       Date:  2016-03-09       Impact factor: 3.063

Review 4.  Synaptic dysfunction in neurodegenerative and neurodevelopmental diseases: an overview of induced pluripotent stem-cell-based disease models.

Authors:  Era Taoufik; Georgia Kouroupi; Ourania Zygogianni; Rebecca Matsas
Journal:  Open Biol       Date:  2018-09       Impact factor: 6.411
  4 in total

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