Allelic Imbalance Analysis Using a Single-Nucleotide Polymorphism Microarray for the Detection of Bladder Cancer Recurrence by Coenen, Marieke J H, Ploeg, Martine, Schijvenaars, Mascha M V A P, Cornel, Erik B, Karthaus, Herbert F M, Scheffer, Hans, Witjes, J Alfred, Franke, Barbara, Kiemeney, Lambertus A L M

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The -2518A>G promoter polymorphism in the CCL2 gene is not associated with systemic sclerosis susceptibility or phenotype: Results from a multicenter study of European Caucasian pa... by Radstake, Timothy R.D.J, Vonk, Madelon C, Dekkers, Marieke, Schijvenaars, Mascha M.V.A.P, Treppichio, William L, Lafyatis, Robert, Riemekasten, Gabriela, van den Hoogen, Frank, Coenen, Marieke J.H

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Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia by Vermeer, Sascha, Hoischen, Alexander, Meijer, Rowdy P.P., Gilissen, Christian, Neveling, Kornelia, Wieskamp, Nienke, de Brouwer, Arjan, Koenig, Michel, Anheim, Mathieu, Assoum, Mirna, Drouot, Nathalie, Todorovic, Slobodanka, Milic-Rasic, Vedrana, Lochmüller, Hanns, Stevanin, Giovanni, Goizet, Cyril, David, Albert, Durr, Alexandra, Brice, Alexis, Kremer, Berry, van de Warrenburg, Bart P.C., Schijvenaars, Mascha M.V.A.P., Heister, Angelien, Kwint, Michael, Arts, Peer, van der Wijst, Jenny, Veltman, Joris, Kamsteeg, Erik-Jan, Scheffer, Hans, Knoers, Nine

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Further characterization of the genetic defect of the Bent tail mouse, a mouse model for human neural tube defects by Klootwijk, Riko, Schijvenaars, Mascha M.V.A.P., Mariman, Edwin C.M., Franke, Barbara

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TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy by Hofstra, Julia M, Coenen, Marieke J H, Schijvenaars, Mascha M V A P, Berden, Jo H M, van der Vlag, Johan, Hoefsloot, Lies H, Knoers, Nine V A M, Wetzels, Jack F M, Nijenhuis, Tom

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An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1) by Franke, Barbara, Vermeulen, Sita H.H.M., Steegers-Theunissen, Regine P.M., Coenen, Marieke J., Schijvenaars, Mascha M.V.A.P., Scheffer, Hans, den Heijer, Martin, Blom, Henk J.

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Genetic variants in toll-like receptors are not associated with rheumatoid arthritis susceptibility or anti-tumour necrosis factor treatment outcome by Coenen, Marieke J H, Enevold, Christian, Barrera, Pilar, Schijvenaars, Mascha M V A P, Toonen, Erik J M, Scheffer, Hans, Padyukov, Leonid, Kastbom, Alf, Klareskog, Lars, Barton, Anne, Kievit, Wietske, Rood, Maarten J, Jansen, Tim L, Swinkels, Dorine, van Riel, Piet L C M, Franke, Barbara, Bendtzen, Klaus, Radstake, Timothy R D J

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Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype by Coenen, Marieke J H, Tieleman, Alide A, Schijvenaars, Mascha M V A P, Leferink, Maike, Ranum, Laura P W, Scheffer, Hans, van Engelen, Baziel G M

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