Dorus A. Mans - Concepedia

Author

Dorus A. Mans

Radboud University Nijmegen ORCID

Also Known As

D A Mans, D Mans, D. A. Mans, Dorus A Mans, Dorus A. Mans, Dorus Mans, Dorus A. Mans, Mans, Dorus, Stef J F Letteboer

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Radboud Institute for Molecular Life Sciences University Medical Center Utrecht University of Tübingen

About

Dorus A. Mans is an author at Radboud University Nijmegen specializing in medicine, cell biology, and cell signaling.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	17	1.9K
2	Cell Biology	13	13	1.1K
3	Natural Sciences	3	3	265
4	Biology	2	2	278
5	Public Health	1	1	87

Dorus A. Mans

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome Christian Gilissen, Heleen H. Arts, Alexander Hoischen, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsSensenbrenner Syndrome	2010	274
An organelle-specific protein landscape identifies novel diseases and molecular mechanisms Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu, Nature Communications	2016	255
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Nature Cell Biology Ciliopathy GenesFunctional GenomicsGliomaGeneticsGene Regulation	2015	245
Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19 Cecilie Bredrup, Sophie Saunier, Machteld M. Oud, The American Journal of Human Genetics UrologyMendelian DisorderRenal InsufficiencyGenetic DisorderGenetics	2011	235
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290 Nicholas T. Gorden, Heleen H. Arts, Melissa A. Parisi, The American Journal of Human Genetics Molecular NeuroscienceJoubert SyndromeMedicineGeneticsGenetic Disorder	2008	227
CiliaCarta: An integrated and validated compendium of ciliary genes Teunis J. P. van Dam, Julie Kennedy, Robin van der Lee, PLoS ONE GeneticsGene CharacterizationMolecular GeneticsDisease Gene IdentificationGenomics	2019	169
CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation Rim Hjeij, Alexandros Onoufriadis, Christopher M. Watson, The American Journal of Human Genetics	2014	165
<i>C14ORF179</i> encoding IFT43 is mutated in Sensenbrenner syndrome Heleen H. Arts, Ernie M.H.F. Bongers, Dorus A. Mans, Journal of Medical Genetics	2011	144
Active Transport and Diffusion Barriers Restrict Joubert Syndrome-Associated ARL13B/ARL-13 to an Inv-like Ciliary Membrane Subdomain Sebiha Cevik, Anna A. W. M. Sanders, Erwin van Wijk, PLoS Genetics Membrane AnchoringPathologyCytoskeletonCellular PhysiologyCell Signaling	2013	110
Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice Karsten Boldt, Dorus A. Mans, Jungyeon Won, Journal of Clinical Investigation BiologyPhotoreceptor CellDevelopmental BiologySignal TransductionMedicine	2011	109

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