Reno S. Bladergroen - Concepedia

Author

Reno S. Bladergroen

Also Known As

Bladergroen, Reno, R S Bladergroen, R. Bladergroen, R.S Bladergroen, R.S. Bladergroen, Reno Bladergroen, Reno S Bladergroen, Reno S. Bladergroen

Publications

712

Citations

H-Index

Concepts

All Affiliations

Maastricht University Maastricht University Medical Centre Radboud University Medical Center Leiden University Medical Center Radboud University Nijmegen

About

Reno S. Bladergroen is an author at Maastricht University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	435
2	Engineering	1	1	153
3	Natural Sciences	1	1	19
4	Biochemistry	1	1	27
5	Immunology	1	1	43

Reno S. Bladergroen

Publications

585

Citations

H-Index

Page 1

	Year	Citations
Computing with DNA by operating on plasmids Tom Head, Grzegorz Rozenberg, Reno S. Bladergroen, Biosystems Dna SequencingEngineeringGeneticsComputational BiologyDna Analysis	2000	153
Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients Maurice A. M. Van Steensel, Valerie L. R. M. Verstraeten, Jorge Frank, Journal of Investigative Dermatology Genetic DisorderMedicineGeneticsInherited Metabolic DiseaseNovel Mutations	2006	85
A 2‐bp deletion in the <i>GJA1</i> gene is associated with oculo‐dento‐digital dysplasia with palmoplantar keratoderma Maurice A. M. Van Steensel, Liesbeth Spruijt, I. van der Bürgt, American Journal of Medical Genetics Part A Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesis	2004	79
Combined occurrence of filaggrin mutations and IL-10 or IL-13 polymorphisms predisposes to atopic dermatitis Aleksandra Lesiak, Piotr Kuna, Marcin Zakrzewski, Experimental Dermatology	2011	56
A Phenotype Resembling the Clouston Syndrome with Deafness Is Associated with a Novel Missense GJB2 Mutation Maurice A. M. Van Steensel, Peter M. Steijlen, Reno S. Bladergroen, Journal of Investigative Dermatology Deafness Is AssociatedGenetic DisorderGeneticsPathogenesisClouston Syndrome	2004	48
Prognostic relevance of CD163 and CD8 combined with EZH2 and gain of chromosome 18 in follicular lymphoma: a study by the Lunenburg Lymphoma Biomarker Consortium Wendy B.C. Stevens, Matías Mendeville, Robert Redd, Haematologica	2017	48
Novel missense mutations in the<i>FOXC2</i>gene alter transcriptional activity Maurice A. M. Van Steensel, Robert J. Damstra, Martijn V. Heitink, Human Mutation GeneticsImmunologyPathologyMolecular GeneticsDisease Gene Identification	2009	43
Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias Xiaoye Schneider‐Yin, Anne-Moon van Tuyll van Serooskerken, Marko Siegesmund, Journal of Hepatology Biallelic InactivationBiochemistryPathologyProtoporphyrinogen OxidaseAcute Porphyrias	2014	27
Protein output for DNA computing Christiaan V. Henkel, Reno S. Bladergroen, Crina I.A. Balog, Natural Computing Protein OutputNatural SciencesMolecular BiologyDna ReplicationProtein Engineering	2005	19
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry A.-M. van Tuyll van Serooskerken, Britt I. Drögemöller, Kornelis te Velde, British Journal of Dermatology	2011	14

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