Kuijpers, Taco W.

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

Astle, W. J., Elding, H., Jiang, T., Allen, D., Ruklisa, D., Mann, A. L., Mead, D., Bouman, H., Riveros-Mckay, F., Kostadima, M. A., et al. (2016) · Cell

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 1,224

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

Chen, L., Ge, B., Casale, F. P., Vasquez, L., Kwan, T., Garrido-Martín, D., Watt, S., Yan, Y., Kundu, K., Ecker, S., et al. (2016) · Cell

Genetic Associations and EpidemiologyEpigenetics and DNA Methylation

Cited by 679

Whole-genome sequencing of patients with rare diseases in a national health system

Turro, E., Astle, W. J., Megy, K., Gräf, S., Greene, D., Shamardina, O., Allen, H. L., Sanchis-Juan, A., Frontini, M., Thys, C., et al. (2020) · Nature

Genomics and Rare DiseasesGenetic Associations and Epidemiology

Cited by 554

Mesenchymal inflammation drives genotoxic stress in hematopoietic stem cells and predicts disease evolution in human pre-leukemia

Zambetti, N. A., Ping, Z., Chen, S., Kenswil, K. J. G., Mylona, M. A., Sanders, M. A., Hoogenboezem, R. M., Bindels, E. M. J., Adisty, M. N., Van Strien, P. M. H., et al. (2016) · Cell stem cell

Blood disorders and treatmentsHematopoietic Stem Cell Transplantation

Cited by 342

Human nlrp3 inflammasome activation is nox1-4 independent

van Bruggen, R., Köker, M. Y., Jansen, M., van Houdt, M., Roos, D., Kuijpers, T. W., & van den Berg, T. K. (2010) · Blood

Inflammasome and immune disordersImmune Response and Inflammation

Cited by 202

Extrapulmonary Aspergillus infection in patients with CARD9 deficiency

Rieber, N., Gazendam, R. P., Freeman, A. F., Hsu, A. P., Collar, A. L., Sugui, J. A., Drummond, R. A., Rongkavilit, C., Hoffman, K., Henderson, C., et al. (2016) · JCI Insight

Immunodeficiency and Autoimmune DisordersAntifungal resistance and susceptibility

Cited by 171

When Actin is Not Actin’ Like It Should: A New Category of Distinct Primary Immunodeficiency Disorders

Sprenkeler, E. G. G., Webbers, S. D. S., & Kuijpers, T. W. (2021) · Journal of Innate Immunity

Immunodeficiency and Autoimmune DisordersBlood disorders and treatments

Cited by 54

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Ito, Y., Carss, K. J., Duarte, S. T., Hartley, T., Keren, B., Kurian, M. A., Marey, I., Charles, P., Mendonça, C., Nava, C., et al. (2018) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 41

Risk factor analysis of cerebral white matter hyperintensities in children with sickle cell disease

van der Land, V., Mutsaerts, H. J. M. M., Engelen, M., Heijboer, H., Roest, M., Hollestelle, M. J., Kuijpers, T. W., Nederkoorn, P. J., Cnossen, M. H., Majoie, C. B. L. M., et al. (2016) · British Journal of Haematology

Hemoglobinopathies and Related DisordersAdvanced MRI Techniques and Applications

Cited by 30

Elevation of proinflammatory cytokines in patients with Aicardi-Goutières syndrome

Takanohashi, A., Prust, M., Wang, J., Gordish-Dressman, H., Bloom, M., Rice, G. I., Schmidt, J. L., Crow, Y. J., Lebon, P., Kuijpers, T. W., et al. (2013) · Neurology

Inflammasome and immune disordersinterferon and immune responses

Cited by 25

Development of an Affinity-Based Probe to Profile Endogenous Human Adenosine A 3 Receptor Expression

Beerkens, B. L. H., Snijders, I. M., Snoeck, J., Liu, R., Tool, A. T. J., Le Dévédec, S. E., Jespers, W., Kuijpers, T. W., van Westen, G. J. P., Heitman, L. H., et al. (2023) · Journal of Medicinal Chemistry

Adenosine and Purinergic SignalingClick Chemistry and Applications

Cited by 6