Author

Rob van Zwieten

Observed names: R Van Zwieten, R van Zwieten, R. van Zwieten, Rob Van Zwieten, Van Zwieten, R, Zwieten, Rob Van, van Zwieten, Rob, van Zwieten, Robert

Institution: Sanquin

Observed institutions: Leiden University Medical Center, Universitair Ziekenhuis Leuven, Hospital de Sant Pau, Amsterdam UMC Location University of Amsterdam, Karolinska Institutet, Sanquin, Emma Kinderziekenhuis, St. Antonius Ziekenhuis, Prince of Wales Hospital, Koga Hospital, Amsterdam University Medical Centers, University of Amsterdam, Wageningen University & Research, KU Leuven

ORCID: 0000-0002-9673-2083

Observed ORCID: 0000-0002-9673-2083

OpenAlex ID: A5001766624

Neutrophil Fc gamma RIIIb deficiency, nature, and clinical consequences: a study of 21 individuals from 14 families

1995 · M de Haas, M Kleijer, et al. · Blood · 217

Inborn defects in the antioxidant systems of human red blood cells

2013 · Rob van Zwieten, Arthur J. Verhoeven, et al. · Free Radical Biology and Medicine · 180

Characterization of two monoclonal antibodies against cytochrome b558 of human neutrophils

1989 · AJ Verhoeven, BG Bolscher, et al. · Blood · 158

A family with complement factor D deficiency

2001 · Douwe H. Biesma, André J. Hannema, et al. · Journal of Clinical Investigation · 122

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Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization

2005 · Sigrid H.W. Beiboer, Tinka Wieringa‐Jelsma, et al. · Transfusion · 112

Purification and partial characterization of the b-type cytochrome from human polymorphonuclear leukocytes.

1985 · R Lutter, M L van Schaik, et al. · Journal of Biological Chemistry · 94

A phosphoprotein of Mr 47,000, defective in autosomal chronic granulomatous disease, copurifies with one of two soluble components required for NADPH:O2 oxidoreductase activity in human neutrophils.

1989 · B G Bolscher, R van Zwieten, et al. · Journal of Clinical Investigation · 86

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Cytochrome b deficiency in an autosomal form of chronic granulomatous disease. A third form of chronic granulomatous disease recognized by monocyte hybridization.

1985 · R S Weening, L Corbeel, et al. · Journal of Clinical Investigation · 85

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X-CGDbase: a database of X-CGD-causing mutations

1996 · Dirk Roosl, John T. Curnutte, et al. · Immunology Today · 84

Limitations on the use of dihydrorhodamine 123 for flow cytometric analysis of the neutrophil respiratory burst

1996 · L.J. van Pelt, R. van Zwieten, et al. · Journal of Immunological Methods · 82

Extracellular proton release by stimulated neutrophils.

1981 · R van Zwieten, R Wever, et al. · Journal of Clinical Investigation · 82

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Hemolysis in the spleen drives erythrocyte turnover

2020 · Thomas robert leon Klei, Jill Jasmine Dalimot, et al. · Blood · 80

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Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.

1999 · D Roos, R van Zwieten, et al. · PubMed · 78

Molecular basis of glutathione reductase deficiency in human blood cells

2006 · Nanne M. Kamerbeek, Rob van Zwieten, et al. · Blood · 77

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Cytochrome b, flavins, and ubiquinone-50 in enucleated human neutrophils (polymorphonuclear leukocyte cytoplasts).

1984 · R Lutter, R van Zwieten, et al. · Journal of Biological Chemistry · 60

Mannan-binding lectin (MBL)-mediated opsonization is enhanced by the alternative pathway amplification loop

2006 · Nannette Brouwer, Koert M. Dolman, et al. · Molecular Immunology · 55

Seven new mutations in the nicotinamide adenine dinucleotide reduced–cytochrome b5 reductase gene leading to methemoglobinemia type I

2001 · Jan Dekker, Michel H. M. Eppink, et al. · Blood · 55

A missense mutation in the heavy subunit of gamma-glutamylcysteine synthetase gene causes hemolytic anemia.

2000 · E Ristoff, C Augustson, et al. · PubMed · 49

The Rh complex exports ammonium from human red blood cells

2003 · Mirte B. Hemker, Goedele Cheroutre, et al. · British Journal of Haematology · 48

Immunocytochemical discovery of the 22- to 23-Kd subunit of cytochrome b558 at the surface of human peripheral phagocytes

1988 · M Nakamura, S Sendo, et al. · Blood · 44

The Gardos effect drives erythrocyte senescence and leads to Lu/BCAM and CD44 adhesion molecule activation

2020 · Thomas R. L. Klei, Jill J. Dalimot, et al. · Blood Advances · 39

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The cholesterol content of the erythrocyte membrane is an important determinant of phosphatidylserine exposure

2012 · Rob van Zwieten, Andrea E. Bochem, et al. · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · 35

Inherited Glutathione Reductase Deficiency and Plasmodium falciparum Malaria—A Case Study

2009 · Valentina Gallo, Evelin Schwarzer, et al. · PLoS ONE · 35

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Hereditary Spectrin Deficiency in Golden Retriever Dogs

2005 · Robbert J Slappendel, Rob van Zwieten, et al. · Journal of Veterinary Internal Medicine · 33

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Glycophorin-C sialylation regulates Lu/BCAM adhesive capacity during erythrocyte aging

2018 · T. R. L. Klei, D. Z. de Back, et al. · Blood Advances · 31

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Works count: 75

Citation count: 2,391

H-index: 28

I10-index: 37