Newburger, Peter E.
University of Massachusetts Chan Medical School
6 papers on CoChatORCID 0000-0002-8615-673X
Most cited papers
- Verified
Cloning the gene for an inherited human disorder—chronic granulomatous disease—On the basis of its chromosomal location
Royer-Pokora, B., Kunkel, L. M., Monaco, A. P., Goff, S. C., Newburger, P. E., Baehner, R. L., Cole, F. S., Curnutte, J. T., & Orkin, S. H. (1986) · Nature
Neutrophil, Myeloperoxidase and Oxidative MechanismsImmunodeficiency and Autoimmune Disorders
Cited by 833
- Verified
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease
Bustamante, J., Arias, A. A., Vogt, G., Picard, C., Galicia, L. B., Prando, C., Grant, A. V., Marchal, C. C., Hubeau, M., Chapgier, A., et al. (2011) · Nature Immunology
Immunodeficiency and Autoimmune DisordersTuberculosis Research and Epidemiology
Cited by 287
- Verified
The Genetic Landscape of Diamond-Blackfan Anemia
Ulirsch, J. C., Verboon, J. M., Kazerounian, S., Guo, M. H., Yuan, D., Ludwig, L. S., Handsaker, R. E., Abdulhay, N. J., Fiorini, C., Genovese, G., et al. (2018) · The American Journal of Human Genetics
Blood disorders and treatmentsGenomics and Rare Diseases
Cited by 272
- Verified
Induction of phagocyte cytochrome b heavy chain gene expression by interferon gamma.
Newburger, P. E., Ezekowitz, R. A., Whitney, C., Wright, J., & Orkin, S. H. (1988) · Proceedings of the National Academy of Sciences
Neutrophil, Myeloperoxidase and Oxidative MechanismsRedox biology and oxidative stress
Cited by 140
- Verified
Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9
Schmitz-Abe, K., Ciesielski, S. J., Schmidt, P. J., Campagna, D. R., Rahimov, F., Schilke, B. A., Cuijpers, M., Rieneck, K., Lausen, B., Linenberger, M. L., et al. (2015) · Blood
Iron Metabolism and DisordersHemoglobinopathies and Related Disorders
Cited by 75
- Verified
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart Disease
Morton, S. U., Shimamura, A., Newburger, P. E., Opotowsky, A. R., Quiat, D., Pereira, A. C., Jin, S. C., Gurvitz, M., Brueckner, M., Chung, W. K., et al. (2021) · JAMA Cardiology
Congenital Heart Disease StudiesGenomics and Rare Diseases
Cited by 62
Go further with a free account
Verify every reference, keep papers in a library, and ask questions across them.
Sign up - it is free