Stefan Heinen - Concepedia

Author

Stefan Heinen

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI)ORCID

Also Known As

Heinen, S, S Heinen, S. Heinen, S.h. Heinen, Stefan Heinen

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI)Friedrich Schiller University Jena University of Toronto Sunnybrook Health Science Centre Sunnybrook Research Institute

About

Stefan Heinen is an author at Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) specializing in medicine, immunology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	1.6K
2	Cell Biology	5	5	771
3	Health Sciences	4	4	612
4	Natural Sciences	1	1	201
5	Biochemistry	1	1	117

Stefan Heinen

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency Mihály Józsi, Christoph Licht, Svante Zipfel, Blood	2007	352
Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome Tamara Manuelian, Jens Hellwage, Seppo Meri, Journal of Clinical Investigation	2003	341
Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome Peter F. Zipfel, Matthew Edey, Stefan Heinen, PLoS Genetics Cfhr3 Is AssociatedImmunohematologyGeneticsImmunologyDefective Complement Regulation	2007	318
Factor H–related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation Stefan Heinen, Andrea Hartmann, Nadine Lauer, Blood	2009	266
A lymphatic defect causes ocular hypertension and glaucoma in mice Benjamin R. Thomson, Stefan Heinen, Marie Jeansson, Journal of Clinical Investigation Ocular DiseaseImmunologyOcular HypertensionGenetic DisruptionTranscriptional Regulation	2014	225
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II) Christoph Licht, Stefan Heinen, Mihály Józsi, Kidney International Dense Deposit DiseaseSignal TransductionMolecular PhysiologyDisease MechanismFactor H	2006	201
Defective complement control of Factor H (Y402H) and FHL-1 in age-related macular degeneration Christine Skerka, Nadine Lauer, Andreas A W A Weinberger, Molecular Immunology Complement SystemOcular DiseaseOphthalmologyExperimental OphthalmologyFactor H	2007	193
The C-terminus of complement regulator Factor H mediates target recognition: evidence for a compact conformation of the native protein Martin Oppermann, Tamara Manuelian, Mihály Józsi, Clinical & Experimental Immunology	2006	147
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome Stefan Heinen, Pilar Sánchez‐Corral, Michael S. Jackson, Human Mutation ImmunohematologyAllelic VariantRca ClusterGenetic DisorderGenetics	2006	147
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation Anne-lie Ståhl, Fariba Vaziri‐Sani, Stefan Heinen, Blood	2008	138

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