Ruud K. B. Schuurman

Author

Also Known As

R K B SCHUURMAN, R K B Schuurman, R K Schuurman, R Schuurman, R. K. B. SCHUURMAN, R. K. B. Schuurman, R. Schuurman, R.K. Schuurman, R.K.B. Schuurman, Ruud K B Schuurman

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Leiden University Medical Center Leiden University Erasmus University Rotterdam Columbia University Hospital for Sick Children

About

Ruud K. B. Schuurman is an author at Leiden University Medical Center specializing in medicine, autoimmunity, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	19	750
2	Allergy	6	6	164
3	Health Sciences	3	3	63
4	Public Health	1	1	25
5	Biology	1	1	30

Ruud K. B. Schuurman

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stages Michel de Weers, Martie C. M. Verschuren, Margriet E. M. Kraakman, European Journal of Immunology	1993	204
B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemia. Michel de Weers, Gaby Brouns, Steve Hinshelwood, Journal of Biological Chemistry	1994	183
Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice Michel de Weers, Rob G.J. Mensink, Margriet E. M. Kraakman, Human Molecular Genetics X-linked AgammaglobulinemiaGeneticsTyrosine KinaseImmunologyPathology	1994	126
Polyclonal activation of human lymphocytes <i>in vitro</i>. I. Characterization of the lymphocyte response to a T cell-independent B cell mitogen. Ruud K. B. Schuurman, Erwin W. Gelfand, Hans‐Michael Dosch The Journal of Immunology	1980	124
Restricted utilization of germ‐line V<sub>H</sub>3 genes and short diverse third complementarity‐determining regions (CDR3) in human fetal B lymphocyte immunoglobulin heavy chain rearrangements Frank M. Raaphorst, Erik Timmers, Marcel Kenter, European Journal of Immunology	1992	87
Failure of lymphocyte-membrane HLA-A and -B expression in two siblings with combined immunodeficiency Ruud K. B. Schuurman, J. J. van Rood, Jaak M. Vossen, Clinical Immunology and Immunopathology Primary ImmunodeficiencyHistocompatibilityAutoimmune DiseaseHuman Leukocyte Antigen-B Expression	1979	66
Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity E. J. B. M. Mensink, A. Thompson, J. D. L. Schot, Human Genetics Genetic AnalysisAllelic VariantX-linked AgammaglobulinemiaGenetic DisorderMedicine	1986	63
V<sub>H</sub> gene usage in humans: biased usage of the V<sub>H</sub>6 gene in immature B lymphoid cells Jeffrey E. Berman, Katherine G. Nickerson, Roberta R. Pollock, European Journal of Immunology HistocompatibilityImmunogeneticsDevelopmental BiologyPreferential UsageVh Gene Usage	1991	60
X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus E. J. B. M. Mensink, A. Thompson, L. A. Sandkuyl, Human Genetics Primary ImmunodeficiencyImmunogeneticsAutoimmune DiseaseX-linked ImmunodeficiencyImmunodeficiencies	1987	54
Immunoglobulin heavy chain gene rearrangements in X‐linked agammaglobulinemia E. J. B. M. Mensink, Ruud K. B. Schuurman, J. D. L. Schot, European Journal of Immunology HistocompatibilityX-linked AgammaglobulinemiaImmunodeficienciesGeneticsImmunology	1986	53

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