Scientific Publications

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Articles published by our team : 

  • Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements.

By Pourchet O. et al. I.Cell Rep. 2021 Jan 19;34(3):108654.

https://pubmed.ncbi.nlm.nih.gov/33472083/

  • The supplementary motor area modulates interhemispheric interactions during movement preparation.

By Welniarz Q. et al. Hum Brain Mapp. 2019 May;40(7):2125-2142. https://www.ncbi.nlm.nih.gov/pubmed/30653778  

  • DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

By Marsh APL. et al. Hum Mutat. 2018 Jan;39(1):23-39. https://www.ncbi.nlm.nih.gov/pubmed/29068161  

  • Mutations in the netrin-1 gene cause congenital mirror movements.

By Méneret A. et al. J Clin Invest. 2017 Nov 1;127(11):3923-3936. https://www.ncbi.nlm.nih.gov/pubmed/28945198  

  • The corticospinal tract: Evolution, development, and human disorders.

By Welniarz Q. et al. Dev Neurobiol. 2017 Jul;77(7):810-829. https://www.ncbi.nlm.nih.gov/pubmed/27706924  

  • Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

By Marsh APL. et al. Nat Genet. 2017 Apr;49(4):511-514. https://www.ncbi.nlm.nih.gov/pubmed/28250454  

  • Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.

By Welniarz Q. et al. Sci Rep. 2017 Mar 24;7(1):410. https://www.ncbi.nlm.nih.gov/pubmed/28341853  

  • Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature.

By Trouillard O.et al. Tremor Other Hyperkinet Mov (N Y). 2016 Nov 3;6:424. https://www.ncbi.nlm.nih.gov/pubmed/27830107  

  • Congenital mirror movements caused by a mutation in the DCC gene.

By Méneret A. et al. Dev Med Child Neurol. 2015 Aug;57(8):776. https://www.ncbi.nlm.nih.gov/pubmed/26011025  

  • One hand clapping: lateralization of motor control.

By Welniarz Q. et al. Front Neuroanat. 2015 Jun 2;9:75. https://www.ncbi.nlm.nih.gov/pubmed/26082690  

  • Congenital Mirror Movements.

By Méneret A. et al. GeneReviews® . Seattle (WA): University of Washington, Seattle; 1993-2017. 2015 Mar 12. https://www.ncbi.nlm.nih.gov/books/NBK279760/  

  • Congenital mirror movements: from piano player to opera singer.

By Méneret A. et al. Neurology. 2015 Feb 24;84(8):860. doi: 10.1212/WNL.0000000000001290. http://www.neurology.org/content/84/8/860.long  

  • Congenital mirror movements: no mutation in DNAL4 in 17 index cases

By Méneret A. et al. J Neurol (2014) 261: 2030. https://www.ncbi.nlm.nih.gov/pubmed/25236653  

  • Reply: Congenital mirror movements: lack of decussation of pyramids Mirror movement: from physiopathology to treatment perspectives.

By Gallea C. et al. Brain. 2014 Aug;137(Pt 8):e293. https://www.ncbi.nlm.nih.gov/pubmed/24727566  

  • Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

By Méneret A. et al. Neurology. 2014 Jun 3; 82(22):1999-2002. https://www.ncbi.nlm.nih.gov/pubmed/24808016  

  • RAD51 deficiency disrupts the corticospinal lateralization of motor control.

By Gallea C. et al. Brain. 2013 Nov;136(Pt 11):3333-46. https://www.ncbi.nlm.nih.gov/pubmed/24056534  

  • RAD51 haploinsufficiency causes congenital mirror movements in humans.

By Depienne C. et al. Am J Hum Genet. 2012 Feb 10;90(2):301-7. https://www.ncbi.nlm.nih.gov/pubmed/22305526  

  • Congenital mirror movements: a clue to understanding bimanual motor control.

By Gallea C. et al. J Neurol. 2011 Nov; 258(11):1911-9. https://www.ncbi.nlm.nih.gov/pubmed/21633904  

  • A novel DCC mutation and genetic heterogeneity in congenital mirror movements.

By Depienne C. et al. Neurology. 2011 Jan 18;76(3):260-4. https://www.ncbi.nlm.nih.gov/pubmed/21242494