Marie-Christine Chartier-Harlin

Team "Early Stages of Parkinson's Disease" of the Jean-Pierre Aubert Research Center, INSERM UMR-S1172, CHRU Lille, University of Lille 1 and Lille 2

Affiliated withINSERM UMR-S1172, CHRU Lille, University of Lille 1 and Lille 2

Research Area

Biology

Biography

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 2	2015

Other Publications

Article	Year
Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study. Human molecular genetics\| PubMed ID: 12490535	2003
S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 12539205	2003
CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease. Annals of neurology\| PubMed ID: 14991823	2004
UCHL1 is a Parkinson's disease susceptibility gene. Annals of neurology\| PubMed ID: 15048890	2004
Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease. Neuroscience letters\| PubMed ID: 15193763	2004
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease. Lancet\| PubMed ID: 15451224	2004
Association study and meta-analysis of low-density lipoprotein receptor related protein in Alzheimer's disease. Neuroscience letters\| PubMed ID: 15925094	2005
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease. JAMA : the journal of the American Medical Association\| PubMed ID: 16896109	2006
Prenatal stress has pro-inflammatory consequences on the immune system in adult rats. Psychoneuroendocrinology\| PubMed ID: 17240075	2007
Genomic investigation of alpha-synuclein multiplication and parkinsonism. Annals of neurology\| PubMed ID: 18571778	2008
Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation. Neurobiology of aging\| PubMed ID: 20096956	2011
Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of neurology\| PubMed ID: 21391235	2011
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes. Human mutation\| PubMed ID: 21412942	2011
Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of aging\| PubMed ID: 21782285	2011
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet neurology\| PubMed ID: 21885347	2011
Translation initiator EIF4G1 mutations in familial Parkinson disease. American journal of human genetics\| PubMed ID: 21907011	2011
Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 23913756	2013
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants. Neurobiology of aging\| PubMed ID: 23962496	2014
Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease. Neurobiology of disease\| PubMed ID: 24269915	2014
Alpha-synuclein repeat variants and survival in Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 24578302	2014
Deregulation of protein translation control, a potential game-changing hypothesis for Parkinson's disease pathogenesis. Trends in molecular medicine\| PubMed ID: 26091824	2015