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Marie-Christine Chartier-Harlin

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Eugénie Mutez; Jordi Pérez-Tur; Christel Vanbesien-Mailliot; Nawal Waucquier; Luc Defebvre; Alain Destée; David Devos; Aurélie Duflot; Bernard Frigard; Dorota Hamalek; Jean-Pierre Kerckaert; Alexandre Kreisler; Lydie Larvor; frederic lepretre; Vincent Mouroux; Marie-Christine Chartier-Harlin
Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation.
Eugénie Mutez; frederic lepretre; Emilie Le Rhun; Lydie Larvor; Aurélie Duflot; Vincent Mouroux; Jean-Pierre Kerckaert; Martin Figeac; Kathy Dujardin; Alain Destée; Marie-Christine Chartier-Harlin
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.
Carles vilarino-guell; C Wider; A I Soto-Ortolaza; Stephanie A Cobb; Jennifer Kachergus; B H Keeling; J C Dachsel; Mary Hulihan; dennis dickson; Zbigniew K Wszolek; Ryan Uitti; Neill R Graff-Radford; Bradley Boeve; Keith A Josephs; Bruce L Miller; K B Boylan; Katrina Gwinn-Hardy; Charles H Adler; Jan Aasly; Faycal Hentati; Alain Destée; Anna Krygowska-Wajs; Marie-Christine Chartier-Harlin; Owen A Ross; Rosa Rademakers; Matthew J Farrer
Characterization of DCTN1 genetic variability in neurodegeneration.

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All Publications

2011: Eugénie Mutez; Jordi Pérez-Tur; Christel Vanbesien-Mailliot; Nawal Waucquier; Luc Defebvre; Alain Destée; David Devos; Aurélie Duflot; Bernard Frigard; Dorota Hamalek; Jean-Pierre Kerckaert; Alexandre Kreisler; Lydie Larvor; frederic lepretre; Vincent Mouroux; Marie-Christine Chartier-Harlin
Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation.
Neurobiology of aging 2011;32(10):1839-48.
2011: Eugénie Mutez; frederic lepretre; Emilie Le Rhun; Lydie Larvor; Aurélie Duflot; Vincent Mouroux; Jean-Pierre Kerckaert; Martin Figeac; Kathy Dujardin; Alain Destée; Marie-Christine Chartier-Harlin
SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes.
Human mutation 2011;32(4):E2079-90.
2009: Carles vilarino-guell; C Wider; A I Soto-Ortolaza; Stephanie A Cobb; Jennifer Kachergus; B H Keeling; J C Dachsel; Mary Hulihan; dennis dickson; Zbigniew K Wszolek; Ryan Uitti; Neill R Graff-Radford; Bradley Boeve; Keith A Josephs; Bruce L Miller; K B Boylan; Katrina Gwinn-Hardy; Charles H Adler; Jan Aasly; Faycal Hentati; Alain Destée; Anna Krygowska-Wajs; Marie-Christine Chartier-Harlin; Owen A Ross; Rosa Rademakers; Matthew J Farrer
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology 2009;72(23):2024-8.
2008: Owen A Ross; Adam T Braithwaite; Lisa Skipper; Jennifer Kachergus; Mary Hulihan; Frank A Middleton; Kenya Nishioka; Julia Fuchs; Thomas Gasser; Demetrius M Maraganore; Charles H Adler; Lydie Larvor; Marie-Christine Chartier-Harlin; Christer Nilsson; J William Langston; Katrina Gwinn-Hardy; Nobutaka Hattori; Matthew J Farrer
Genomic investigation of alpha-synuclein multiplication and parkinsonism.
Annals of neurology 2008;63(6):743-50.
2007: Christel C A Vanbesien-Mailliot; Isabelle Wolowczuk; Jérôme Mairesse; Odile Viltart; Myriam Delacre; Jamal Khalife; Marie-Christine Chartier-Harlin; Stefania Maccari
Prenatal stress has pro-inflammatory consequences on the immune system in adult rats.
Psychoneuroendocrinology 2007;32(2):114-24.
2006: Demetrius M Maraganore; Mariza de Andrade; Alexis Elbaz; Matthew J Farrer; John Ioannidis; Rejko Krüger; Walter A Rocca; Nicole K Schneider; Timothy G Lesnick; Sarah J Lincoln; Mary Hulihan; Jan Aasly; Tetsuo Ashizawa; Marie-Christine Chartier-Harlin; Harvey Checkoway; Carlo Ferrarese; Georgios M Hadjigeorgiou; Nobutaka Hattori; Hideshi Kawakami; jean-charles lambert; Timothy Lynch; George D Mellick; Spiridon Papapetropoulos; Abbas Parsian; Aldo Quattrone; Olaf Riess; Eng-King Tan; Christine Van Broeckhoven
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
JAMA : the journal of the American Medical Association 2006;296(6):661-70.
2005: Antonia Pritchard; Judith Harris; Colin W Pritchard; David St Clair; Helen Lemmon; jean-charles lambert; Marie-Christine Chartier-Harlin; Angela Hayes; Uma Thaker; Takeshi Iwatsubo; D M A Mann; Corinne Lendon
Association study and meta-analysis of low-density lipoprotein receptor related protein in Alzheimer's disease.
Neuroscience letters 2005;382(3):221-6.
2004: A Hayes; Elaine K Green; Antonia Pritchard; J M Harris; Y Zhang; jean-charles lambert; Marie-Christine Chartier-Harlin; Stuart Pickering-Brown; Corinne Lendon; D M A Mann
A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(10):1475-7.
2004: Marie-Christine Chartier-Harlin; Jennifer Kachergus; Christophe Roumier; Vincent Mouroux; Xavier Douay; Sarah J Lincoln; Clotilde Levecque; Lydie Larvor; Joris Andrieux; Mary Hulihan; Nawal Waucquier; Luc Defebvre; Philippe Amouyel; Matthew J Farrer; Alain Destée
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
Lancet 2004;364(9440):1167-9.
2004: Clotilde Levecque; Alain Destée; Vincent Mouroux; Philippe Amouyel; Marie-Christine Chartier-Harlin
Assessment of Nurr1 nucleotide variations in familial Parkinson's disease.
Neuroscience letters 2004;366(2):135-8.
2004: Yong Zhang; Angela Hayes; Antonia Pritchard; Uma Thaker; M Sayeed Haque; Helen Lemmon; Judith Harris; Alistair Cumming; jean-charles lambert; Marie-Christine Chartier-Harlin; David St Clair; Takeshi Iwatsubo; D M A Mann; Corinne Lendon
Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease.
Neuroscience letters 2004;362(2):99-102.
2004: Demetrius M Maraganore; Timothy G Lesnick; Alexis Elbaz; Marie-Christine Chartier-Harlin; Thomas Gasser; Rejko Krüger; Nobutaka Hattori; George D Mellick; Aldo Quattrone; Jun-Ichi Satoh; Tatsushi Toda; Jian Wang; John Ioannidis; Mariza de Andrade; Walter A Rocca; Taksushi Toda
UCHL1 is a Parkinson's disease susceptibility gene.
Annals of neurology 2004;55(4):512-21.
2004: Alexis Elbaz; Clotilde Levecque; Jacqueline Clavel; Jean-Sébastien Vidal; Florence Richard; Philippe Amouyel; Annick Alpérovitch; Marie-Christine Chartier-Harlin; Christophe Tzourio
CYP2D6 polymorphism, pesticide exposure, and Parkinson's disease.
Annals of neurology 2004;55(3):430-4.
2004: Clotilde Levecque; Alexis Elbaz; Jacqueline Clavel; Jean-Sébastien Vidal; Philippe Amouyel; Annick Alpérovitch; Christophe Tzourio; Marie-Christine Chartier-Harlin
Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(3):478-80.
2004: jean-charles lambert; D M A Mann; J Harris; L Araria-Goumidi; Marie-Christine Chartier-Harlin; D Cottel; Takeshi Iwatsubo; Philippe Amouyel; Corinne Lendon
Association study of Notch 4 polymorphisms with Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(3):377-81.
2004: Marie-Christine Chartier-Harlin; L Araria-Goumidi; jean-charles lambert
[Genetic complexity of Alzheimer's disease].
Revue neurologique 2004;160(2):251-5.
2004: Jinzhou Tian; Jing Shi; K Bailey; JM Harris; Antonia Pritchard; jean-charles lambert; Marie-Christine Chartier-Harlin; Stuart Pickering-Brown; Corinne Lendon; D M A Mann
A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease.
Neuroscience letters 2004;354(2):103-6.
2003: jean-charles lambert; Erin Luedecking-Zimmer; S Merrot; A Hayes; Uma Thaker; P Desai; A Houzet; Xavier Hermant; Dominique Cottel; Antonia Pritchard; Takeshi Iwatsubo; Florence Pasquier; Bernard Frigard; P M Conneally; Marie-Christine Chartier-Harlin; Steven T DeKosky; Corinne Lendon; D M A Mann; M Ilyas Kamboh; Philippe Amouyel
Association of 3'-UTR polymorphisms of the oxidised LDL receptor 1 (OLR1) gene with Alzheimer's disease.
Journal of medical genetics 2003;40(6):424-30.
2003: Alexis Elbaz; Clotilde Levecque; Jacqueline Clavel; Jean-Sébastien Vidal; Florence Richard; Jean-René Corrèze; Bernard Delemotte; Philippe Amouyel; Annick Alpérovitch; Marie-Christine Chartier-Harlin; Christophe Tzourio
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 2003;18(2):130-7.
2003: Clotilde Levecque; Alexis Elbaz; Jacqueline Clavel; Florence Richard; Jean-Sébastien Vidal; Philippe Amouyel; Christophe Tzourio; Annick Alpérovitch; Marie-Christine Chartier-Harlin
Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.
Human molecular genetics 2003;12(1):79-86.
2002: L Araria-Goumidi; jean-charles lambert; Dominique Cottel; Philippe Amouyel; Marie-Christine Chartier-Harlin
No association of the HLA-A2 allele with Alzheimer's disease.
Neuroscience letters 2002;335(2):75-8.
2002: Corinne Lendon; Uma Thaker; JM Harris; AM McDonagh; jean-charles lambert; Marie-Christine Chartier-Harlin; Takeshi Iwatsubo; Stuart Pickering-Brown; D M A Mann
The angiotensin 1-converting enzyme insertion (I)/deletion (D) polymorphism does not influence the extent of amyloid or tau pathology in patients with sporadic Alzheimer's disease.
Neuroscience letters 2002;328(3):314-8.
2002: L Araria-Goumidi; J B Huguet; jean-charles lambert; Bernard Frigard; Dominique Cottel; Philippe Amouyel; Marie-Christine Chartier-Harlin
No association of the -48CT polymorphism of the presenilin 1 gene with Alzheimer disease in a late-onset sporadic population.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(7-8):1023-7.
2002: L Araria-Goumidi; jean-charles lambert; D M A Mann; Corinne Lendon; Bernard Frigard; Takeshi Iwatsubo; D Cottel; Philippe Amouyel; Marie-Christine Chartier-Harlin
Association study of three polymorphisms of TGF-beta1 gene with Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 2002;73(1):62-4.
2002: Elaine K Green; JM Harris; Helen Lemmon; jean-charles lambert; Marie-Christine Chartier-Harlin; D St Clair; D M A Mann; Takeshi Iwatsubo; Corinne Lendon
Are interleukin-1 gene polymorphisms risk factors or disease modifiers in AD?
Neurology 2002;58(10):1566-8.
2002: Elaine K Green; Uma Thaker; AM McDonagh; Takeshi Iwatsubo; jean-charles lambert; Marie-Christine Chartier-Harlin; JM Harris; Stuart Pickering-Brown; Corinne Lendon; D M A Mann
A polymorphism within intron 11 of the tau gene is not increased in frequency in patients with sporadic Alzheimer's disease, nor does it influence the extent of tau pathology in the brain.
Neuroscience letters 2002;324(2):113-6.
2001: A Taylor; Mario Ezquerra; G Bagri; A Yip; L Goumidi; Dominique Cottel; Douglas Easton; John Grimley Evans; J Xuereb; Nigel J Cairns; Philippe Amouyel; Marie-Christine Chartier-Harlin; Carol Brayne; David C Rubinsztein
Alzheimer disease is not associated with polymorphisms in the angiotensinogen and renin genes.
American journal of medical genetics 2001;105(8):761-4.
2001: jean-charles lambert; D M A Mann; JM Harris; Marie-Christine Chartier-Harlin; Alistair Cumming; J Coates; Helen Lemmon; D StClair; Takeshi Iwatsubo; Corinne Lendon
The -48 C/T polymorphism in the presenilin 1 promoter is associated with an increased risk of developing Alzheimer's disease and an increased Abeta load in brain.
Journal of medical genetics 2001;38(6):353-5.
2001: Matthew J Farrer; Alain Destée; Clotilde Levecque; Andrew Singleton; Simone Engelender; E Becquet; Vincent Mouroux; Florence Richard; Luc Defebvre; Richard Crook; D Hernandez; Christopher A Ross; John Hardy; Philippe Amouyel; Marie-Christine Chartier-Harlin
Genetic analysis of synphilin-1 in familial Parkinson's disease.
Neurobiology of disease 2001;8(2):317-23.
2001: Claudine Berr; jean-charles lambert; Véronique Sazdovitch; Philippe Amouyel; Marie-Christine Chartier-Harlin; M Mohr; N Heldt; M Kiesmann; JEAN-JACQUES HAUW
Neuropathological epidemiology of cerebral aging: a study of two genetic polymorphisms.
Neurobiology of aging 2001;22(2):227-35.
2001: jean-charles lambert; D M A Mann; L Goumidi; J Harris; Philippe Amouyel; Takeshi Iwatsubo; Corinne Lendon; Marie-Christine Chartier-Harlin
Effect of the APOE promoter polymorphisms on cerebral amyloid peptide deposition in Alzheimer's disease.
Lancet 2001;357(9256):608-9.
2001: Clotilde Levecque; Alain Destée; Vincent Mouroux; E Becquet; Luc Defebvre; Philippe Amouyel; Marie-Christine Chartier-Harlin
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2001;108(8-9):979-84.
2000: Matthew J Farrer; T Destée; E Becquet; Fabienne Wavrant-De Vrièze; Vincent Mouroux; Florence Richard; Luc Defebvre; Sarah J Lincoln; John Hardy; Philippe Amouyel; Marie-Christine Chartier-Harlin
Linkage exclusion in French families with probable Parkinson' s disease.
Movement disorders : official journal of the Movement Disorder Society 2000;15(6):1075-83.
2000: jean-charles lambert; D M A Mann; L Goumidi; Judith Harris; Florence Pasquier; Bernard Frigard; Dominique Cottel; Corinne Lendon; Takeshi Iwatsubo; Philippe Amouyel; Marie-Christine Chartier-Harlin
A FE65 polymorphism associated with risk of developing sporadic late-onset alzheimer's disease but not with Abeta loading in brains.
Neuroscience letters 2000;293(1):29-32.
2000: jean-charles lambert; L Goumidi; F W Vrièze; Bernard Frigard; J M Harris; A Cummings; J Coates; Florence Pasquier; Dominique Cottel; M Gaillac; David St Clair; D M A Mann; John Hardy; Corinne Lendon; Philippe Amouyel; Marie-Christine Chartier-Harlin
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.
Human molecular genetics 2000;9(15):2275-80.
1999: Susanna Schraen-Maschke; S Brique; Marie-Christine Chartier-Harlin; E Brique; Alain Destée; Bernard Sablonnière
Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
American journal of medical genetics 1999;88(6):738-41.
1999: Sarah J Lincoln; Richard Crook; Marie-Christine Chartier-Harlin; Katrina Gwinn-Hardy; Matt Baker; Vincent Mouroux; Florence Richard; E Becquet; Philippe Amouyel; Alain Destée; John Hardy; Matthew J Farrer
No pathogenic mutations in the beta-synuclein gene in Parkinson's disease.
Neuroscience letters 1999;269(2):107-9.
1999: Fabienne Wavrant-De Vrièze; Richard Crook; Peter Holmans; Pat Kehoe; Michael J Owen; Julie Williams; K Roehl; D K Laliiri; Shantia Shears; Jeremy Booth; W Wu; Alison Goate; Marie-Christine Chartier-Harlin; John Hardy; Jordi Pérez-Tur
Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease.
Neuroscience letters 1999;269(2):67-70.
1999: F Wavrant-DeVrièze; jean-charles lambert; L Stas; Richard Crook; Dominique Cottel; Florence Pasquier; Bernard Frigard; M Lambrechts; Els Thiry; Philippe Amouyel; J P Tur; Marie-Christine Chartier-Harlin; John Hardy; Fred Van Leuven
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's disease.
Human genetics 1999;104(5):432-4.
1999: Varuni Rudrasingham; Fabienne Wavrant-De Vrièze; jean-charles lambert; S Chakraverty; Pat Kehoe; Richard Crook; Philippe Amouyel; W Wu; Frances Rice; Jordi Pérez-Tur; Bernard Frigard; John C Morris; S Carty; Ronald C. Petersen; Dominique Cottel; Nigel Tunstall; Peter Holmans; Simon Lovestone; Marie-Christine Chartier-Harlin; Alison Goate; John Hardy; Michael J Owen; Julie Williams
Alpha-2 macroglobulin gene and Alzheimer disease.
Nature genetics 1999;22(1):17-9; author reply 21-2.
1999: jean-charles lambert; Marie-Christine Chartier-Harlin; Dominique Cottel; F Richard; E Neuman; D Guez; Sylvie Legrain; Claudine Berr; Philippe Amouyel; Nicole Helbecque
Is the LDL receptor-related protein involved in Alzheimer's disease?
Neurogenetics 1999;2(2):109-13.
1999: F Wavrant-DeVrièze; Varuni Rudrasingham; jean-charles lambert; S Chakraverty; Pat Kehoe; Richard Crook; Philippe Amouyel; W Wu; Peter Holmans; Frances Rice; Jordi Pérez-Tur; Bernard Frigard; John C Morris; S Carty; Dominique Cottel; Nigel Tunstall; Simon Lovestone; Ronald C. Petersen; Marie-Christine Chartier-Harlin; Alison Goate; Michael J Owen; Julie Williams; John Hardy
No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.
Neuroscience letters 1999;262(2):137-9.
1999: S Brique; Alain Destée; jean-charles lambert; Vincent Mouroux; André Delacourte; Philippe Amouyel; Marie-Christine Chartier-Harlin
A new GTP-cyclohydrolase I mutation in an unusual dopa-responsive dystonia, familial form.
Neuroreport 1999;10(3):487-91.
1999: Pat Kehoe; Fabienne Wavrant De-Vrieze; Richard Crook; W S Wu; Peter Holmans; Iain Fenton; Gillian Spurlock; Nadine Norton; Hywel Williams; Nigel Williams; Simon Lovestone; Jordi Perez-Tur; Michael Hutton; Marie-Christine Chartier-Harlin; Shantia Shears; K Roehl; Jeremy Booth; W Van Voorst; Dzanan Ramic; Julie Williams; Alison Goate; John Hardy; Michael J Owen
A full genome scan for late onset Alzheimer's disease.
Human molecular genetics 1999;8(2):237-45.
1999: Sarah J Lincoln; Katrina Gwinn-Hardy; John Goudreau; Marie-Christine Chartier-Harlin; Matt Baker; Vincent Mouroux; Florence Richard; Alain Destée; E Becquet; Philippe Amouyel; Timothy Lynch; John Hardy; Matthew J Farrer
No pathogenic mutations in the persyn gene in Parkinson's disease.
Neuroscience letters 1999;259(1):65-6.
1998: jean-charles lambert; C Berr; Florence Pasquier; André Delacourte; Bernard Frigard; Dominique Cottel; Jordi Pérez-Tur; Vincent Mouroux; M Mohr; D Cécyre; Douglas Galasko; Corinne Lendon; J Poirier; John Hardy; D M A Mann; Philippe Amouyel; Marie-Christine Chartier-Harlin
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease.
Human molecular genetics 1998;7(9):1511-6.
1998: W S Wu; Peter Holmans; F Wavrant-DeVrièze; Shantia Shears; Pat Kehoe; Richard Crook; Jeremy Booth; Nigel Williams; Jordi Pérez-Tur; K Roehl; Iain Fenton; Marie-Christine Chartier-Harlin; Simon Lovestone; Julie Williams; Michael Hutton; John Hardy; Michael J Owen; Alison Goate
Genetic studies on chromosome 12 in late-onset Alzheimer disease.
JAMA : the journal of the American Medical Association 1998;280(7):619-22.
1998: jean-charles lambert; Fabienne Wavrant-De Vrièze; Philippe Amouyel; Marie-Christine Chartier-Harlin
Association at LRP gene locus with sporadic late-onset Alzheimer's disease.
Lancet 1998;351(9118):1787-8.
1998: jean-charles lambert; Florence Pasquier; Dominique Cottel; Bernard Frigard; Philippe Amouyel; Marie-Christine Chartier-Harlin
A new polymorphism in the APOE promoter associated with risk of developing Alzheimer's disease.
Human molecular genetics 1998;7(3):533-40.
1997: jean-charles lambert; Jordi Pérez-Tur; Marie-Joëlle Dupire; Douglas Galasko; D M A Mann; P Amouyel; John Hardy; André Delacourte; Marie-Christine Chartier-Harlin
Distortion of allelic expression of apolipoprotein E in Alzheimer's disease.
Human molecular genetics 1997;6(12):2151-4.
1997: F Wavrant-DeVrièze; Jordi Pérez-Tur; jean-charles lambert; Bernard Frigard; Florence Pasquier; André Delacourte; Philippe Amouyel; John Hardy; Marie-Christine Chartier-Harlin
Association between the low density lipoprotein receptor-related protein (LRP) and Alzheimer's disease.
Neuroscience letters 1997;227(1):68-70.
1997: H Bickeböller; Dominique Campion; Alexis Brice; Philippe Amouyel; Didier Hannequin; O Didierjean; C Penet; Cosette Martin; Jordi Pérez-Tur; A Michon; Bruno Dubois; F Ledoze; Catherine Thomas-Anterion; Florence Pasquier; Michèle Puel; Jean-Francois Demonet; Olivier Moreaud; Marie-Claude Babron; D Meulien; D Guez; Marie-Christine Chartier-Harlin; Thierry Frebourg; Yves Agid; M Martinez; Françoise Clerget-Darpoux
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.
American journal of human genetics 1997;60(2):439-46.
1996: jean-charles lambert; Jordi Pérez-Tur; M J Dupire; André Delacourte; Bernard Frigard; Marie-Christine Chartier-Harlin
Analysis of the APOE alleles impact in Down's syndrome.
Neuroscience letters 1996;220(1):57-60.
1996: Jordi Pérez-Tur; Fabienne Wavrant De-Vrieze; jean-charles lambert; Marie-Christine Chartier-Harlin
Presenilin-1 polymorphism and Alzheimer's disease. The Alzheimer's Study Group.
Lancet 1996;347(9014):1560-1.
1996: Luc BUEE; Jordi Pérez-Tur; B Leveugle; V Buée-Scherrer; Elliott J Mufson; A J Loerzel; Marie-Christine Chartier-Harlin; Daniel P Perl; André Delacourte; Patrick R Hof
Apolipoprotein E in Guamanian amyotrophic lateral sclerosis/parkinsonism-dementia complex: genotype analysis and relationships to neuropathological changes.
Acta neuropathologica 1996;91(3):247-53.
1995: Jordi Pérez-Tur; Dominique Campion; M Martinez; Alexis Brice; Sandrine Tardieu; Didier Hannequin; Yves Agid; André Delacourte; Françoise Clerget-Darpoux; Marie-Christine Chartier-Harlin
Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.
American journal of medical genetics 1995;60(6):550-3.
1995: Luc BUEE; B Permanne; Jordi Pérez-Tur; Marie-Christine Chartier-Harlin; André Delacourte
Alzheimer's disease: A beta or ApoE amyloidosis?
Lancet 1995;346(8966):59.
1994: Marie-Christine Chartier-Harlin; M Parfitt; S Legrain; Jordi Pérez-Tur; T Brousseau; A Evans; Claudine Berr; O Vidal; P Roques; V Gourlet
Apolipoprotein E, epsilon 4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: analysis of the 19q13.2 chromosomal region.
Human molecular genetics 1994;3(4):569-74.
1993: M Parfitt; Richard Crook; P Roques; Martin N Rossor; Marie-Christine Chartier-Harlin
The Cystatin-C gene is not linked to early onset familial Alzheimer's disease.
Neuroscience letters 1993;154(1-2):81-3.
1993: A M Kennedy; S Newman; Andrew McCaddon; J Ball; P Roques; Michael Mullan; John Hardy; Marie-Christine Chartier-Harlin; Richard S J Frackowiak; Elizabeth K Warrington
Familial Alzheimer's disease. A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine-->glycine).
Brain : a journal of neurology 1993;116 ( Pt 2)():309-24.
1992: Rosa Adroer; Marie-Christine Chartier-Harlin; Fiona Crawford; Rafael Oliva
Improved direct sequencing of Alzheimer's amyloid precursor protein (APP) exons 16 and 17.
Neuroscience letters 1992;141(1):69-71.
1992: L Fidani; K Rooke; Marie-Christine Chartier-Harlin; D Hughes; Rudolph E Tanzi; Michael Mullan; P Roques; Martin N Rossor; John Hardy; Alison Goate
Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.
Human molecular genetics 1992;1(3):165-8.
1992: Fiona Crawford; Marie-Christine Chartier-Harlin; Michael Mullan; John Hardy; André Delacourte; G Arnott
Alzheimer's--a correction.
Nature 1992;356(6368):390.
1992: John Hardy; Marie-Christine Chartier-Harlin; Michael Mullan
Alzheimer disease: the new agenda.
American journal of human genetics 1992;50(3):648-51.
1991: Fiona Crawford; John Hardy; Michael Mullan; Alison Goate; D Hughes; L Fidani; P Roques; Martin N Rossor; Marie-Christine Chartier-Harlin
Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence.
Neuroscience letters 1991;133(1):1-2.
1991: Marie-Christine Chartier-Harlin; Fiona Crawford; Henry Houlden; AC Warren; D Hughes; L Fidani; Alison Goate; Martin N Rossor; P Roques; John Hardy
Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene.
Nature 1991;353(6347):844-6.
1991: Marie-Christine Chartier-Harlin; Fiona Crawford; K Hamandi; Michael Mullan; Alison Goate; John Hardy; Hubert Backhovens; J J Martin; Christine Van Broeckhoven
Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.
Neuroscience letters 1991;129(1):134-5.
1991: Alison Goate; Marie-Christine Chartier-Harlin; Michael Mullan; J Brown; Fiona Crawford; L Fidani; L Giuffra; A Haynes; N Irving; L James
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.
Nature 1991;349(6311):704-6.