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R. Schwaab · SciRah

Researcher profile · Semantic Scholar

R. Schwaab

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R. Schwaab — researcher profile on SciRah

h-index: 36
Works: 108
Citations: 4,994

Most-cited papers

Haemophilia A: Mutation Type Determines Risk of Inhibitor Formation
R. Schwaab, H. Brackmann, C. Meyer, J. Seehafer +5 more
1995Thrombosis and Haemostasis372 citations
Semantic Scholar
Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males
O. El-Maarri, T. Becker, J. Junen, S. Manzoor +4 more
2007Human Genetics285 citations
Semantic Scholar
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition.
E. Tuddenham, R. Schwaab, J. Seehafer, D. Millar +13 more
1994Nucleic Acids Research255 citations Open access
Semantic Scholar
Immune Tolerance for the Treatment of Factor VIII Inhibitors ‐ Twenty Years' ‘Bonn Protocol’
H. Brackmann, J. Oldenburg, R. Schwaab
1996Vox Sanguinis241 citations
Semantic Scholar
HLA Genotype of Patients with Severe Haemophilia A due to Intron 22 Inversion with and without Inhibitors of Factor VIII
J. Oldenburg, J. Picard, R. Schwaab, H. Brackmann +2 more
1997Thrombosis and Haemostasis215 citations
Semantic Scholar
Haemophilia A: from mutation analysis to new therapies
J. Graw, H. Brackmann, J. Oldenburg, R. Schneppenheim +2 more
2005Nature reviews genetics202 citations
Semantic Scholar
Impact of polymorphisms of the major histocompatibility complex class II, interleukin‐10, tumor necrosis factor‐α and cytotoxic T‐lymphocyte antigen‐4 genes on inhibitor development in severe hemophilia A
A. Pavlova, D. Delev, S. Lacroix-Desmazes, R. Schwaab +4 more
2009Journal of Thrombosis and Haemostasis196 citations Open access
Semantic Scholar
Inhibitor development in correlation to factor VIII genotypes
J. Oldenburg, O. El-Maarri, R. Schwaab
2002Haemophilia183 citations Open access
Semantic Scholar
Environmental and genetic factors influencing inhibitor development.
J. Oldenburg, J. Schröder, H. Brackmann, C. Müller-Reible +2 more
2004Seminars in hematology (Print)178 citations
Semantic Scholar
Haemophilia B: database of point mutations and short additions and deletions--eighth edition
F. Giannelli, P. Green, S. S. Sommer, M.-C. Poon +7 more
1998Nucleic Acids Res.161 citations
Semantic Scholar
Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.
J. Becker, R. Schwaab, A. Möller-Taube, U. Schwaab +5 more
1996American Journal of Human Genetics159 citations
Semantic Scholar
A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor.
M. Jacquemin, A. Benhida, K. Peerlinck, Benoît Desqueper +9 more
2000Blood128 citations
Semantic Scholar
Induction of Immune Tolerance in Haemophilia A Inhibitor Patients by the ‘Bonn Protocol’: Predictive Parameter for Therapy Duration and Outcome
J. Oldenburg, R. Schwaab, H. Brackmann
1999Vox Sanguinis116 citations Open access
Semantic Scholar
Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex
J. Oldenburg, B. von Brederlow, A. Fregin, S. Rost +11 more
2000Thrombosis and Haemostasis111 citations
Semantic Scholar
Risk factors for inhibitor development in hemophilia A.
J. Oldenburg, H. Brackmann, R. Schwaab
2000Haematologica97 citations
Semantic Scholar
Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy
J. Oldenburg, E. Quenzel, U. Harbrecht, A. Fregin +6 more
1997British Journal of Haematology96 citations Open access
Semantic Scholar
Results of a Screening for von Willebrand Disease Type 2N in Patients with Suspected Haemophilia A or von Willebrand Disease Type 1
R. Schneppenheim, U. Budde, S. Krey, E. Drewke +4 more
1996Thrombosis and Haemostasis92 citations
Semantic Scholar
Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease.
R. Schneppenheim, U. Budde, T. Obser, J. Brassard +5 more
2001Blood90 citations
Semantic Scholar
Methylation at Global LINE-1 Repeats in Human Blood Are Affected by Gender but Not by Age or Natural Hormone Cycles
O. El-Maarri, M. Walier, F. Behne, J. V. van Uum +11 more
2011PLoS ONE88 citations Open access
Semantic Scholar
Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII gene
O. El-Maarri, U. Herbiniaux, J. Graw, J. Schröder +8 more
2005Journal of Thrombosis and Haemostasis83 citations Open access
Semantic Scholar
Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene
R. Michel, A. Lalloz, R. Schwaab, J. McVey +2 more
1994British Journal of Haematology83 citations
Semantic Scholar
Inhibitor development and mortality in non‐severe hemophilia A
C. Eckhardt, J. Loomans, A. van Velzen, M. Peters +8 more
2015Journal of Thrombosis and Haemostasis73 citations Open access
Semantic Scholar
Stabilization of transgene expression by incorporation of E3 region genes into an adenoviral factor IX vector and by transient anti-CD4 treatment of the host.
W. Poller, S. Schneider-Rasp, U. Liebert, F. Merklein +5 more
1996Gene Therapy73 citations
Semantic Scholar
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M allele.
J. Faber, W. Poller, S. Weidinger, M. Kirchgesser +3 more
1994American Journal of Human Genetics70 citations
Semantic Scholar
Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs
R. Schwaab, J. Oldenburg, U. Schwaab, D. Johnson +4 more
1995British Journal of Haematology68 citations
Semantic Scholar
Haemophilia B (sixth edition): a database of point mutations and short additions and deletions
F. Giannelli, Peter M. Green, S. S. Sommer, M.-C. Poon +6 more
1996Nucleic Acids Res.66 citations Open access
Semantic Scholar
De novo factor VIII gene intron 22 inversion in a female carrier presents as a somatic mosaicism.
J. Oldenburg, Simone Rost, O. El-Maarri, Marco Leuer +3 more
2000Blood63 citations
Semantic Scholar
Assay discrepancy in mild haemophilia A due to a factor VIII missense mutation (Asn694Ile) in a large Danish family
R. Schwaab, J. Oldenburg, G. Kemball-Cook, T. Albert +3 more
2000British Journal of Haematology48 citations Open access
Semantic Scholar
Expression of CYP19 (aromatase) mRNA in the human temporal lobe.
B. Stoffel-Wagner, M. Watzka, Stephan Steckelbroeck, R. Schwaab +3 more
1998Biochemical and Biophysical Research Communications - BBRC47 citations
Semantic Scholar
A novel tetracycline-controlled transactivator–transrepressor system enables external control of oncolytic adenovirus replication
H. Fechner, X. Wang, M. Srour, U. Siemetzki +8 more
2003Gene Therapy45 citations
Semantic Scholar
NovoSeven® in immune tolerance therapy
H. Brackmann, E. Effenberger, L. Hess, R. Schwaab +1 more
2000Blood Coagulation and Fibrinolysis45 citations
Semantic Scholar
Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein
R. Schwaab, J. Oldenburg, M. Lalloz, U. Schwaab +5 more
1997Human Genetics43 citations
Semantic Scholar
Allelic Discrimination of Factor V Leiden Using a 5’ Nuclease Assay
D. Happich, R. Schwaab, Peter Hanfland, D. Hoernschemeyer
1999Thrombosis and Haemostasis38 citations
Semantic Scholar
Analysis of the essential sequences of the factor VIII gene in twelve haemophilia A patients by single‐stranded conformation polymorphism
D. David, I. Moreira, M. Lalloz, H. Rosa +8 more
1994Blood Coagulation and Fibrinolysis37 citations
Semantic Scholar
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data
V. Ivaškevičius, R. Jurgutis, S. Rost, A. Müller +6 more
2001British Journal of Haematology36 citations Open access
Semantic Scholar
Factor VIII intron‐1 inversion: frequency and inhibitor prevalence
O. El-Maarri, J. Schröder, R. Schwaab, C. Müller +1 more
2006Journal of Thrombosis and Haemostasis35 citations Open access
Semantic Scholar
Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci
H. Singer, M. Walier, N. Nüsgen, C. Meesters +9 more
2011Human Molecular Genetics32 citations Open access
Semantic Scholar
Lack of F8 mRNA: a novel mechanism leading to hemophilia A.
O. El-Maarri, H. Singer, C. Klein, M. Watzka +10 more
2006Blood32 citations
Semantic Scholar
Molecular Biology of Blood Coagulation
J. Oldenburg, R. Schwaab
2001Seminars in Thrombosis and Hemostasis32 citations
Semantic Scholar
The haemophilia A mutation search test and resource site, home page of the factor VIII mutation database: HAMSTeRS
A. Wacey, G. Kemball-Cook, H. Kazazian, S. Antonarakis +3 more
1996Nucleic Acids Res.31 citations Open access
Semantic Scholar
Significance of F8 missense mutations with respect to inhibitor formation
R. Schwaab, A. Pavlova, T. Albert, Michael J. Caspers +1 more
2013Thrombosis and Haemostasis30 citations
Semantic Scholar
Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene
E. Tuddenham, D. Cooper, J. Gitschier, M. Higuchi +9 more
199130 citations Open access
Semantic Scholar
Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization
R. Schneppenheim, H. Lenk, T. Obser, J. Oldenburg +5 more
2004Thrombosis and Haemostasis29 citations
Semantic Scholar
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.
J. Oldenburg, R. Schwaab, T. Grimm, K. Zerres +3 more
1993American Journal of Human Genetics24 citations
Semantic Scholar
Application of the TaqMan-PCR for Genotyping of the Prothrombi G20210A Mutation and of the Thermolabile Methylenetetrahydrofolate Reductase Mutation
Dirk Happich, Katharina Madlener, R. Schwaab, Peter Hanfland +1 more
2000Thrombosis and Haemostasis20 citations
Semantic Scholar
A G+3-to-T donor splice site mutation leads to skipping of exon 50 in von Willebrand factor mRNA.
G. Mertes, Michael Ludwig, B. Finkelnburg, Michael Krawczak +3 more
1994Genomics19 citations
Semantic Scholar
Measurements of DNA Methylation at Seven Loci in Various Tissues of CD1 Mice
Laurynas Daugela, N. Nüsgen, M. Walier, J. Oldenburg +2 more
2012PLoS ONE16 citations Open access
Semantic Scholar
The B-cell epitope of the monoclonal anti-factor VIII antibody ESH8 characterized by peptide array analysis
T. Albert, C. Egler, Stanislav Jakuschev, Ulrike Schuldenzucker +6 more
2008Thrombosis and Haemostasis16 citations
Semantic Scholar
Analysis of expression kinetics and activity of a new B-domain truncated and full-length FVIII protein in three different cell lines
A. Haack, C. Schmitt, W. Poller, J. Oldenburg +3 more
1999Annals of Hematology16 citations
Semantic Scholar
Immune tolerance induction: a role for recombinant activated factor VII (rFVIIa)?
H. Brackmann, W. Effenberger, L. Hess, R. Schwaab +1 more
1998European journal of haematology. Supplementum16 citations
Semantic Scholar

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