Found: 8

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  • α-2 macroglobulin gene and Alzheimer disease.

    Published in:
    Nature Genetics, 1999, v. 22, n. 1, p. 17, doi. 10.1038/8726
    By:
    • Rudrasingham, Varuni;
    • Wavrant-De Vrièze, Fabienne;
    • Lambert, Jean-Charles;
    • Chakraverty, Sumi;
    • Kehoe, Patrick;
    • Crook, Richard;
    • Amouyel, Philippe;
    • Wu, William;
    • Rice, Frances;
    • Pérez-Tur, Jordi;
    • Frigard, Bernard;
    • Morris, John C.;
    • Carty, Stephanie;
    • Petersen, Ronald;
    • Cottel, Dominique;
    • Tunstall, Nigel;
    • Holmans, Peter;
    • Lovestone, Simon;
    • Chartier-Harlin, Marie-Christine
    Publication type:
    Article

  • Cholesterol 25-Hydroxylase on Chromosome 10q Is a Susceptibility Gene for Sporadic Alzheimer’s Disease.

    Published in:
    Neurodegenerative Diseases, 2005, v. 2, n. 5, p. 233, doi. 10.1159/000090362
    By:
    • Papassotiropoulos, Andreas;
    • Lamber, Jean-Charles;
    • Wavrant-De Vrièze, Fabienne;
    • Wollmer, M. Axel;
    • von der Kammer, Heinz;
    • Streffer, Johannes R.;
    • Maddalena, Alessia;
    • Kim-Dung Huynh;
    • Wolleb, Sibylle;
    • Lütjohann, Dieter;
    • Schneider, Brigitte;
    • Thal, Dietmar R.;
    • Grimaldi, Luigi M. E.;
    • Tsolaki, Magdalini;
    • Kapaki, Elisabeth;
    • Ravid, Rivka;
    • Konietzko, Uwe;
    • Hegi, Thomas;
    • Pasch, Thomas;
    • Jung, Hans
    Publication type:
    Article

  • Linkage and Association Analyses of Type 2 Diabetes/Impaired Glucose Metabolism and Adiponectin Serum Levels in Japanese Americans From Hawaii.

    Published in:
    Diabetes, 2007, v. 56, n. 2, p. 537, doi. 10.2337/db06-0443
    By:
    • Kovac, Ilija P.;
    • Havlik, Richard J.;
    • Foley, Daniel;
    • Peila, Rita;
    • Hernandez, Dena;
    • Wavrant-De Vrièze, Fabienne;
    • Singleton, Andrew;
    • Egan, Josephine;
    • Taub, Dennis;
    • Rodriguez, Beatriz;
    • Masaki, Kamal;
    • Curb, J. David;
    • Fujimoto, Wilfred Y.;
    • Wilson, Alexander F.
    Publication type:
    Article

  • Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 22, p. 2703, doi. 10.1093/hmg/ddm224
    By:
    • Hamshere, Marian L.;
    • Holmans, Peter A.;
    • Avramopoulos, Dimitrios;
    • Bassett, Susan S.;
    • Blacker, Deborah;
    • Bertram, Lars;
    • Wiener, Howard;
    • Rochberg, Nan;
    • Tanzi, Rudolph E.;
    • Myers, Amanda;
    • Wavrant-De Vrièze, Fabienne;
    • Go, Rodney;
    • Fallin, Daniele;
    • Lovestone, Simon;
    • Hardy, John;
    • Goate, Alison;
    • O'Donovan, Michael;
    • Williams, Julie;
    • Owen, Michael J.
    Publication type:
    Article

  • DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.

    Published in:
    Human Molecular Genetics, 2006, v. 15, n. 17, p. 2560, doi. 10.1093/hmg/ddl178
    By:
    • Li, Yonghong;
    • Grupe, Andrew;
    • Rowland, Charles;
    • Nowotny, Petra;
    • Kauwe, John S.K.;
    • Smemo, Scott;
    • Hinrichs, Anthony;
    • Tacey, Kristina;
    • Toombs, Timothy A.;
    • Kwok, Shirley;
    • Catanese, Joseph;
    • White, Thomas J.;
    • Maxwell, Taylor J.;
    • Hollingworth, Paul;
    • Abraham, Richard;
    • Rubinsztein, David C.;
    • Brayne, Carol;
    • Wavrant-De Vrièze, Fabienne;
    • Hardy, John;
    • O'Donovan, Michael
    Publication type:
    Article

  • The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.

    Published in:
    Human Molecular Genetics, 2000, v. 9, n. 15, p. 2275, doi. 10.1093/oxfordjournals.hmg.a018918
    By:
    • Lambert, Jean-Charles;
    • Goumidi, Louisa;
    • Vrièze, Fabienne Wavrant-De;
    • Frigard, Bernard;
    • Harris, Judith M.;
    • Cummings, Alistair;
    • Coates, John;
    • Pasquier, Florence;
    • Cottel, Dominique;
    • Gaillac, Marianne;
    • Clair, David;
    • Mann, David M.A.;
    • Hardy, John;
    • Lendon, Corinne L.;
    • Amouyel, Philippe;
    • Chartier-Harlin, Marie-Christine
    Publication type:
    Article

  • Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series.

    Published in:
    Movement Disorders, 2010, v. 25, n. 6, p. 771, doi. 10.1002/mds.22970
    By:
    • van de Leemput, Joyce;
    • Wavrant-De Vrièze, Fabienne;
    • Rafferty, Ian;
    • Bras, Jose M.;
    • Giunti, Paola;
    • Fisher, Elizabeth MC;
    • Hardy, John A.;
    • Singleton, Andrew B.;
    • Houlden, Henry
    Publication type:
    Article

  • Linkage exclusion in French families with probable Parkinson's disease.

    Published in:
    Movement Disorders, 2000, v. 15, n. 6, p. 1075, doi. 10.1002/1531-8257(200011)15:6<1075::AID-MDS1004>3.0.CO;2-2
    By:
    • Farrer, Matt;
    • Destée, Alain;
    • Becquet, Estelle;
    • Wavrant-De Vrièze, Fabienne;
    • Mouroux, Vincent;
    • Richard, Florence;
    • Defebvre, Luc;
    • Lincoln, Sarah;
    • Hardy, John;
    • Amouyel, Philippe;
    • Chartier-Harlin, Marie-Christine
    Publication type:
    Article