Genetic Pleiotropy < Genetic Predisposition to Disease < Genetic Research

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 52.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000009 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
000078 (1999)	S. Schraen-Maschke [France] ; S. Brique ; M C Chartier-Harlin ; E. Brique ; A. Destée ; B. Sablonnière	Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.
000157 (2000)	A. Elbaz [France] ; J M Manubens-Bertran ; M. Baldereschi ; M M Breteler ; F. Grigoletto ; S. Lopez-Pousa ; J F Dartigues ; A. Alpérovitch ; W A Rocca ; C. Tzourio	Parkinson's disease, smoking, and family history. EUROPARKINSON Study Group.
000222 (2001)	S. Thobois [France] ; S. Guillouet ; E. Broussolle	Contributions of PET and SPECT to the understanding of the pathophysiology of Parkinson's disease.
000299 (2003)	Clotilde Levecque [France] ; 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.
000369 (2003)	Christoph-Burkhard Lücking [France] ; Véronique Chesneau ; Ebba Lohmann ; Patrice Verpillat ; Cyprien Dulac ; Anne-Marie Bonnet ; Francesca Gasparini ; Yves Agid [France] ; Alexandra Dürr ; Alexis Brice	Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
000420 (2004)	C. Levecque ; A. Elbaz ; J. Clavel ; J. Vidal ; P. Amouyel ; A. Alperovitch ; C. Tzourio ; M. Chartier-Harlin	Association of polymorphisms in the Tau and Saitohin genes with Parkinson's disease
000424 (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.
000432 (2004)	O. Santt [France] ; H. Baranova ; E. Albuisson ; Y-J Bignon ; G. Lucotte	Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease.
000485 (2004)	M. Martinez ; A. Brice ; J. Vaughan ; A. Zimprich ; M. Breteler ; G. Meco ; A. Filla ; M. Farrer ; C. Betard ; J. Hardy ; G. De Michele ; V. Bonifati ; B. Oostra ; T. Gasser ; N. Wood ; A. Durr ; F. The	Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease
000558 (2005)	Suzanne Lesage ; Pablo Ibanez ; Ebba Lohmann ; Pierre Pollak ; François Tison ; Myriem Tazir ; Anne-Louise Leutenegger ; Joao Guimaraes ; Anne-Marie Bonnet ; Yves Agid [France] ; Alexandra Dürr ; Alexis Brice	G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
000643 (2006)	Anne-Louise Leutenegger [France] ; Mustafa A M. Salih ; Pablo Ibá Ez ; Maowia M. Mukhtar ; Suzanne Lesage ; Ali Arabi ; Ebba Lohmann ; Alexandra Dürr ; Ammar E M. Ahmed ; Alexis Brice	Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.
000664 (2006)	Alexis Elbaz ; Lorene M. Nelson ; Haydeh Payami ; John P A. Ioannidis ; Brian K. Fiske ; Grazia Annesi ; Andrea Carmine Belin ; Stewart A. Factor ; Carlo Ferrarese ; Georgios M. Hadjigeorgiou ; Donald S. Higgins ; Hideshi Kawakami ; Rejko Krüger ; Karen S. Marder ; Richard P. Mayeux ; George D. Mellick ; John G. Nutt ; Beate Ritz ; Ali Samii ; Caroline M. Tanner ; Christine Van Broeckhoven ; Stephen K. Van Den Eeden ; Karin Wirdefeldt ; Cyrus P. Zabetian ; Marie Dehem ; Jennifer S. Montimurro ; Audrey Southwick ; Richard M. Myers ; Thomas A. Trikalinos	Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson’s disease: a large-scale international study
000725 (2007)	Philippe Charron [France] ; Marc Genest ; Pascale Richard ; Michel Komajda ; Gilbert Pochmalicki	A familial form of conduction defect related to a mutation in the PRKAG2 gene.
000738 (2007)	P. Charles [France] ; A. Camuzat ; N. Benammar ; F. Sellal ; A. Destée ; A-M Bonnet ; S. Lesage ; I. Le Ber ; G. Stevanin ; A. Dürr ; A. Brice	Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
000762 (2008)	S. Lesage ; E. Lohmann ; F. Tison ; F. Durif ; A. Dürr ; A. Brice	Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls.
000891 (2009)	Ebba Lohmann [France] ; Laurence Leclere ; Francesca De Anna ; Suzanne Lesage ; Bruno Dubois ; Yves Agid [France] ; Alexandra Dürr ; Alexis Brice	A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.
000926 (2009)	E. Lohmann ; S. Thobois ; S. Lesage ; E. Broussolle ; S Tezenas Du Montcel ; M J. Ribeiro ; P. Remy ; A. Pelissolo ; B. Dubois ; L. Mallet ; P. Pollak ; Yves Agid [France] ; A. Brice	A multidisciplinary study of patients with early-onset PD with and without parkin mutations
000946 (2009)	Pablo Ibá Ez [France] ; Suzanne Lesage ; Sabine Janin ; Ebba Lohmann ; Frank Durif ; Alain Destée [France] ; Anne-Marie Bonnet ; Christine Brefel-Courbon ; Simon Heath ; Diana Zelenika ; Yves Agid [France] ; Alexandra Dürr ; Alexis Brice	Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.
000976 (2009)	Alexander Zimprich [Autriche] ; Claudia Schulte ; Eva Reinthaler ; Dietrich Haubenberger ; Jörg Balzar ; Peter Lichtner ; Salwa El Tawil ; S. Edris ; Thomas Foki ; Walter Pirker ; Regina Katzenschlager ; Gerhard Daniel ; Thomas Brücke ; Eduard Auff ; Thomas Gasser	PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease.
000983 (2009)	Suzanne Lesage [France] ; Alexis Brice	Parkinson's disease: from monogenic forms to genetic susceptibility factors.

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