Mirjam W.J. Luijendijk

Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II

Michael D. Weston, Mirjam W.J. Luijendijk, Kurt Humphrey et al. · The American Journal of Human Genetics · 2004 · 338 citations · Full text

Signal Transduction, Molecular Physiology, Signaling Pathway +6

A Novel Mutation Identified in the <i>DFNA5</i> Gene in a Dutch Family: A Clinical and Genetic Evaluation

Anne M.L.C. Bischoff, Mirjam W.J. Luijendijk, P.L.M. Huygen et al. · Audiology and Neurotology · 2003 · 84 citations

Aurora kinases in childhood acute leukemia: the promise of aurora B as therapeutic target

Stefanie A. Hartsink-Segers, C. Michel Zwaan, Carla Exalto et al. · Leukemia · 2012 · 83 citations · Full text

Disturbed<scp>CXCR</scp>4/<scp>CXCL</scp>12 axis in paediatric precursor B‐cell acute lymphoblastic leukaemia

Lieke C. J. van den Berk, Arian van der Veer, Marieke E. Willemse et al. · British Journal of Haematology · 2014 · 69 citations

Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)

Mirjam W.J. Luijendijk, Erwin van Wijk, Anne M.L.C. Bischoff et al. · Human Genetics · 2004 · 56 citations

Mendelian Disorder, Genetic Disorder, Genetics +6