Showing 1 - 6 results of 6 for search 'van Duijn Cornelia M', query time: 0.06s Refine Results
  1. 1
    A polymorphism in the regulatory region of <it>PRNP </it>is associated with increased risk of sporadic Creutzfeldt-Jakob disease

    A polymorphism in the regulatory region of <it>PRNP </it>is associated with increased risk of sporadic Creutzfeldt-Jakob disease by Will Robert G, Knight Richard SG, Croes Esther A, Bishop Matthew T, Sanchez-Juan Pascual, van Duijn Cornelia M, Manson Jean C

    Published 2011
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  2. 2
    No evidence for association between <it>tau </it>gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

    No evidence for association between <it>tau </it>gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease by Arias-Vasquez Alejandro, Giannattasio Claudia, Green Alison, Bishop Matthew T, Sánchez-Juan Pascual, Poleggi Anna, Knight Richard SG, van Duijn Cornelia M

    Published 2007
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  3. 3
    Type 2 diabetes gene <it>TCF7L2 </it>polymorphism is not associated with fetal and postnatal growth in two birth cohort studies

    Type 2 diabetes gene <it>TCF7L2 </it>polymorphism is not associated with fetal and postnatal growth in two birth cohort studies by Hofman Albert, Uitterlinden Andre G, van Duijn Cornelia M, de Kort Sandra WK, Mook-Kanamori Dennis O, Moll Henriëtte A, Steegers Eric AP, Hokken-Koelega Anita CS, Jaddoe Vincent WV

    Published 2009
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  4. 4
    Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes

    Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes by Rivera Natalia V, Carreras-Torres Robert, Roncarati Roberta, Viviani-Anselmi Chiara, De Micco Francesca, Mezzelani Alessandra, Koch Werner, Hoppmann Petra, Kastrati Adnan, Stewart Alexandre FR, Chen Li, Roberts Robert, Karssen Lennart C, Amin Najaf, Trimarco Valentina, Izzo Raffaele, Iaccarino Guido, Condorelli Gerolama, Puca Annibale A, Pagnotta Paolo, Airoldi Flavio, Trimarco Bruno, van Duijn Cornelia M, Condorelli Gianluigi, Briguori Carlo

    Published 2013
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  5. 5
    The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project

    The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project by Arias-Vásquez Alejandro, Oulhaj Abderrahim, Mateo Ignacio, Kölsch Heike, Heun Reinhard, Gwilliam Rhian, Deloukas Panos, Alvarez Victoria, Coto Eliecer, Barber Rachel, Kehoe Patrick G, Brown Kristelle, Wilcock Gordon K, Lehmann Michael G, Belbin Olivia, Cortina-Borja Mario, Hammond Naomi, Warden Donald R, Combarros Onofre, Schuur Maaike, Aulchenko Yurii S, Ikram M Arfan, Breteler Monique M, van Duijn Cornelia M, Morgan Kevin, Smith A David, Lehmann Donald J

    Published 2010
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  6. 6
    A meta-analysis of genome-wide data from five European isolates reveals an association of <it>COL22A1</it>, <it>SYT1</it>, and <it>GABRR2 </it>with serum creatinine level

    A meta-analysis of genome-wide data from five European isolates reveals an association of <it>COL22A1</it>, <it>SYT1</it>, and <it>GABRR2 </it>with serum creatinine level by Oostra Ben A, Meitinger Thomas, Boban Mladen, Hastie Nick, Campbell Susan, Schreiber Stefan, Gnewuch Carsten, Zemunik Tatijana, Zgaga Lina, Nöthlings Ute, Kolcic Ivana, Ellinghaus David, Polasek Ozren, Isaacs Aaron, Melville Scott A, Wild Sarah H, Johansson Asa, Aulchenko Yurii S, Franke Andre, Hayward Caroline, Vitart Veronique, De Grandi Alessandro, Pattaro Cristian, Riegler Peter, Minelli Cosetta, Wright Alan F, Campbell Harry, van Duijn Cornelia M, Gyllensten Ulf, Wilson James F, Krawczak Michael, Rudan Igor, Pramstaller Peter P

    Published 2010
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