G. Dewald - Concepedia

Author

G. Dewald

University of Bonn

Also Known As

G DEWALD, G Dewald, G. DEWALD, G. Dewald, George Dewald

Publications

334

Citations

H-Index

Concepts

All Affiliations

University of Bonn

About

G. Dewald is an author at University of Bonn specializing in medicine, immunology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	99
2	Health Sciences	2	2	38
3	Natural Sciences	1	1	21
4	Biology	1	1	23
5	Diabetes	1	1	25

G. Dewald

Publications

299

Citations

H-Index

Page 1

	Year	Citations
Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and men Konrad Bork, D Gül, G. Dewald British Journal of Dermatology	2005	80
Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients. Dominique Stoppa-Lyonnet, Christiane Duponchel, T Meo, PubMed	1991	56
Family study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analyses. Katsushi Tokunaga, G. Dewald, K Omoto, PubMed	1986	29
HLA-A, B, C, DR, Bf, and C2 Alleles in Insulin-Dependent Diabetes Mellitus with Proliferative Retinopathy J. Bertrams, G. Dewald, Manfred Spitznas, Immunobiology Proliferative RetinopathyDiabetic RetinopathyOcular DiseaseAutoimmune DiseaseOphthalmology	1980	25
Exclusion of the HLA Locus from a Large Portion of the Long Arm of Chromosome 6 Friedrich Kueppers, G. Dewald, H Gordon, Human Heredity HistocompatibilityHlaHealthy ParentsCytogeneticsGenetics	1977	23
Polymorphism of the Second Component of Human Complement (C2) G. Dewald, Ch. Rittner Vox Sanguinis	1979	21
Fine Mapping of MEP1A, the Gene Encoding the α Subunit of the Metalloendopeptidase Meprin, to Human Chromosome 6p21 W. Jiang, G. Dewald, Ellen K. Brundage, Biochemical and Biophysical Research Communications Natural SciencesGeneticsMetalloproteinProtein GeneticsMolecular Biology	1995	21
HLA-linked complement polymorphisms (C2, BF) in psoriasis G. Dewald, C.‐E. Lange, E. Schmeel, Archives of Dermatological Research Autoimmune DiseaseMedicineImmunologyClinical DermatologyAutoimmunity	1983	15
Polymorphism of Human Complement Component C6: An Amino Acid Substitution (GLU/ALA) within the Second Thrombospondin Repeat Differentiates between the Two Common Allotypes C6A and C6B G. Dewald, Markus M. Nöthen, Sven Cichon Biochemical and Biophysical Research Communications HistocompatibilityImmunohematologyComplement SystemAllelic VariantSecond Thrombospondin Repeat	1993	15
The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3 G. Dewald, Sven Cichon, S. P. BRYANT, Annals of Human Genetics	1996	14

Page 1