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Birth Defects Research. Part A, Clinical and Molecular Teratology|November 5, 2004
Further characterization of the genetic defect of the Bent tail mouse, a mouse model for human neural tube defectsRiko Klootwijk, Mascha M V A P Schijvenaars, Edwin C M Mariman, et al.
European Journal of Human Genetics : EJHG|January 13, 2011
Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotypeMarieke J H Coenen, Alide A Tieleman, Mascha M V A P Schijvenaars, et al.
Pharmacogenomics|February 19, 2014
Full-gene sequencing analysis of NAT2 and its relationship with isoniazid pharmacokinetics in Venezuelan children with tuberculosisLilly M Verhagen, Marieke Jh Coenen, Diana López, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 24, 2009
An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1)Barbara Franke, Sita H H M Vermeulen, Regine P M Steegers-Theunissen, et al.
Human Immunology|November 27, 2008
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 patientsTimothy R D J Radstake, Madelon C Vonk, Marieke Dekkers, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 18, 2008
Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrenceMarieke J H Coenen, Martine Ploeg, Mascha M V A P Schijvenaars, et al.
Plos One|July 15, 2014
TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathyJulia M Hofstra, Marieke J H Coenen, Mascha M V A P Schijvenaars, et al.
Plos One|December 24, 2010
Genetic variants in toll-like receptors are not associated with rheumatoid arthritis susceptibility or anti-tumour necrosis factor treatment outcomeMarieke J H Coenen, Christian Enevold, Pilar Barrera, et al.
Ophthalmology|July 28, 2020
Development of a Genotype Assay for Age-Related Macular Degeneration: The EYE-RISK ConsortiumAnita de Breuk, Ilhan E Acar, Eveline Kersten, et al.
American Journal of Human Genetics|November 25, 2010
Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxiaSascha Vermeer, Alexander Hoischen, Rowdy P P Meijer, et al.
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