Radboud University Nijmegen

Molecular markers for urothelial bladder cancer prognosis: toward implementation in clinical practice (2014) Van Rhijn BWG, Catto JW, Goebell P, Knuechel R, Shariat SF, Van Der Poel HG, Sanchez-Carbayo M, et al. Journal article Altered GPM6A/M6 Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human and Drosophila (2014) Gregor A, Kramer JM, Van Der Voet M, Schanze I, Uebe S, Donders R, Reis A, et al. Journal article An Open Alternative for SMT-based Verification of SCADE Models (2014) Basold H, Günther H, Huhn M, Milius S Conference contribution Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA (2014) Earp MA, Kelemen LE, Magliocco AM, Swenerton KD, Chenevix-Trench G, Lu Y, Hein A, et al. Journal article A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility (2014) Lopez-Isac E, Bossini-Castillo L, Simeon CP, Victoria Egurbide M, Jose Alegre-Sancho J, Luis Callejas J, Andres Roman-Ivorra J, et al. Journal article Defined morphological criteria allow reliable diagnosis of colorectal serrated polyps and predict polyp genetics (2014) Rau T, Agaimy A, Gehoff A, Geppert CI, Jung K, Knobloch K, Langner C, et al. Journal article Injectable self-gelling composites for bone tissue engineering based on gellan gum hydrogel enriched with different bioglasses (2014) Douglas TEL, Piwowarczyk W, Pamula E, Liskova J, Schaubroeck D, Leeuwenburgh SCG, Brackman G, et al. Journal article, Original article Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study (2014) Johnson N, Dudbridge F, Orr N, Gibson L, Jones ME, Schoemaker MJ, Folkerd EJ, et al. Journal article Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis (2014) Mayes MD, Bossini-Castillo L, Gorlova O, Martin JE, Zhou X, Chen WV, Assassi S, et al. Journal article A complex microcephaly syndrome in a Pakistani family associated with a novel missense mutation in RBBP8 and a heterozygous deletion in NRXN1 (2014) Agha Z, Iqbal Z, Azam M, Siddique M, Willemsen MH, Kleefstra T, Zweier C, et al. Journal article