Mirjam W.J. Luijendijk

Author

Radboud University Nijmegen

Also Known As

M W J Luijendijk, M.W.J. Luijendijk, Mirjam W. J. Luijendijk, Mirjam W. Luijendijk, Mirjam W.J. Luijendijk

Publications

736

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Erasmus MC - Sophia Children’s Hospital

About

Mirjam W.J. Luijendijk is an author at Radboud University Nijmegen specializing in genetics, medicine, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	417
2	Cell Biology	2	2	361
3	Health Sciences	1	1	23
4	Molecular Genetics	1	1	23
5	Auditory Hair Cells	1	1	23

Mirjam W.J. Luijendijk

Publications

727

Citations

H-Index

Page 1

	Year	Citations
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, The American Journal of Human Genetics Signal TransductionMolecular PhysiologySignaling PathwayG Protein-coupled ReceptorGenetic Disorder	2004	338
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, Audiology and Neurotology	2003	84
Aurora kinases in childhood acute leukemia: the promise of aurora B as therapeutic target Stefanie A. Hartsink-Segers, C. Michel Zwaan, Carla Exalto, Leukemia	2012	83
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, British Journal of Haematology	2014	69
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, Human Genetics Mendelian DisorderGenetic DisorderGeneticsMotor Head DomainCytoskeleton	2004	56
Disturbed CXCR4/CXCL12 Axis In Pediatric Precursor B-Cell Acute Lymphoblastic Leukemia Lieke C. J. van den Berk, Arian van der Veer, Marieke E. Willemse, Blood	2013	29
Cross-Sectional Analysis of Hearing Threshold in Relation to Age in a Large Family with Cochleovestibular Impairment Thoroughly Genotyped for DFNA9/<i>COCH</i> Steven J. H. Bom, Martijn H. Kemperman, Mirjam W.J. Luijendijk, Annals of Otology Rhinology & Laryngology	2003	24
Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs☆ Mirjam W.J. Luijendijk, T.J.R. van de Pol, Gerard van Duijnhoven, Genomics GeneticsMolecular GeneticsAuditory ScienceHealth SciencesMrna Expression Analysis	2003	23
Cochleovestibular and Ocular Features in a Dutch DFNA11 Family Anne M.L.C. Bischoff, Ronald J. E. Pennings, P.L.M. Huygen, Otology & Neurotology	2006	21

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