Zhang, Kejian
Cincinnati Children's Hospital Medical Center · University of Cincinnati
6 papers on CoChatORCID 0000-0001-6334-9697
Most cited papers
- Verified
Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH
Zhang, K., Jordan, M. B., Marsh, R. A., Johnson, J. A., Kissell, D., Meller, J., Villanueva, J., Risma, K. A., Wei, Q., Klein, P. S., et al. (2011) · Blood
Autoimmune and Inflammatory Disorders ResearchImmunodeficiency and Autoimmune Disorders
Cited by 428
- Verified
Whole‐Exome Sequencing Reveals Overlap Between Macrophage Activation Syndrome in Systemic Juvenile Idiopathic Arthritis and Familial Hemophagocytic Lymphohistiocytosis
Kaufman, K. M., Linghu, B., Szustakowski, J. D., Husami, A., Yang, F., Zhang, K., Filipovich, A. H., Fall, N., Harley, J. B., Nirmala, N. R., et al. (2014) · Arthritis & Rheumatology
Autoimmune and Inflammatory Disorders ResearchImmunodeficiency and Autoimmune Disorders
Cited by 207
- Verified
Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza
Schulert, G. S., Zhang, M., Fall, N., Husami, A., Kissell, D., Hanosh, A., Zhang, K., Davis, K., Jentzen, J. M., Napolitano, L., et al. (2016) · Journal of Infectious Diseases
Autoimmune and Inflammatory Disorders ResearchInfluenza Virus Research Studies
Cited by 170
- Verified
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency
Boutboul, D., Kuehn, H. S., Van de Wyngaert, Z., Niemela, J. E., Callebaut, I., Stoddard, J., Lenoir, C., Barlogis, V., Farnarier, C., Vely, F., et al. (2018) · Journal of Clinical Investigation
Immunodeficiency and Autoimmune DisordersT-cell and B-cell Immunology
Cited by 169
- Verified
Mouse models of neutropenia reveal progenitor-stage-specific defects
Muench, D. E., Olsson, A., Ferchen, K., Pham, G., Serafin, R. A., Chutipongtanate, S., Dwivedi, P., Song, B., Hay, S., Chetal, K., et al. (2020) · Nature
Blood disorders and treatmentsImmunodeficiency and Autoimmune Disorders
Cited by 115
- Verified
A Heterozygous RAB27A Mutation Associated with Delayed Cytolytic Granule Polarization and Hemophagocytic Lymphohistiocytosis
Zhang, M., Bracaglia, C., Prencipe, G., Bemrich-Stolz, C. J., Beukelman, T., Dimmitt, R. A., Chatham, W. W., Zhang, K., Li, H., Walter, M. R., et al. (2016) · The Journal of Immunology
Autoimmune and Inflammatory Disorders ResearchImmune Cell Function and Interaction
Cited by 99
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