| Identification of a ferrireductase required for efficient transferrin-dependent iron uptake in erythroid cells RS Ohgami, DR Campagna, EL Greer, B Antiochos, A McDonald, J Chen, ... Nature genetics 37 (11), 1264-1269, 2005 | 831 | 2005 |
| Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA) KE Finberg, MM Heeney, DR Campagna, Y Aydınok, HA Pearson, ... Nature genetics 40 (5), 569-571, 2008 | 807 | 2008 |
| The Steap proteins are metalloreductases RS Ohgami, DR Campagna, A McDonald, MD Fleming Blood 108 (4), 1388-1394, 2006 | 729 | 2006 |
| Physiologic expression of Sf3b1K700E causes impaired erythropoiesis, aberrant splicing, and sensitivity to therapeutic spliceosome modulation EA Obeng, RJ Chappell, M Seiler, MC Chen, DR Campagna, PJ Schmidt, ... Cancer cell 30 (3), 404-417, 2016 | 375 | 2016 |
| Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors SB Lizarraga, SP Margossian, MH Harris, DR Campagna, AP Han, ... Development 137 (11), 1907-1917, 2010 | 294 | 2010 |
| Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia DL Guernsey, H Jiang, DR Campagna, SC Evans, M Ferguson, ... Nature genetics 41 (6), 651-653, 2009 | 257 | 2009 |
| HRG1 is essential for heme transport from the phagolysosome of macrophages during erythrophagocytosis C White, X Yuan, PJ Schmidt, E Bresciani, TK Samuel, D Campagna, ... Cell metabolism 17 (2), 261-270, 2013 | 255 | 2013 |
| The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron–sulfur cluster biogenesis C Pondarré, BB Antiochos, DR Campagna, SL Clarke, EL Greer, KM Deck, ... Human molecular genetics 15 (6), 953-964, 2006 | 246 | 2006 |
| The molecular defect in hypotransferrinemic mice CC Trenor III, DR Campagna, VM Sellers, NC Andrews, MD Fleming Blood, The Journal of the American Society of Hematology 96 (3), 1113-1118, 2000 | 216 | 2000 |
| Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD) PK Chakraborty, K Schmitz-Abe, EK Kennedy, H Mamady, T Naas, ... Blood, The Journal of the American Society of Hematology 124 (18), 2867-2871, 2014 | 194 | 2014 |
| Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis C Pondarre, DR Campagna, B Antiochos, L Sikorski, H Mulhern, ... Blood 109 (8), 3567-3569, 2007 | 158 | 2007 |
| Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations AK Bergmann, DR Campagna, EM McLoughlin, S Agarwal, MD Fleming, ... Pediatric blood & cancer 54 (2), 273-278, 2010 | 146 | 2010 |
| X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation VN Tubman, JE Levine, DR Campagna, R Monahan-Earley, AM Dvorak, ... Blood 109 (8), 3297-3299, 2007 | 139 | 2007 |
| UBE2O remodels the proteome during terminal erythroid differentiation AT Nguyen, MA Prado, PJ Schmidt, AK Sendamarai, JT Wilson-Grady, ... Science 357 (6350), eaan0218, 2017 | 128 | 2017 |
| A mutation in a mitochondrial transmembrane protein is responsible for the pleiotropic hematological and skeletal phenotype of flexed-tail (f/f) mice MD Fleming, DR Campagna, JN Haslett, CC Trenor, NC Andrews Genes & development 15 (6), 652-657, 2001 | 106 | 2001 |
| Primary ciliary dyskinesia in mice lacking the novel ciliary protein Pcdp1 L Lee, DR Campagna, JL Pinkus, H Mulhern, TA Wyatt, JH Sisson, ... Molecular and cellular biology 28 (3), 949-957, 2008 | 105 | 2008 |
| Identification of a Steap3 endosomal targeting motif essential for normal iron metabolism T Lambe, RJ Simpson, S Dawson, T Bouriez-Jones, TL Crockford, ... Blood, The Journal of the American Society of Hematology 113 (8), 1805-1808, 2009 | 99 | 2009 |
| Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts DI Shah, N Takahashi-Makise, JD Cooney, L Li, IJ Schultz, EL Pierce, ... Nature 491 (7425), 608-612, 2012 | 96 | 2012 |
| A murine model of chronic lymphocytic leukemia based on B cell-restricted expression of Sf3b1 mutation and Atm deletion S Yin, RG Gambe, J Sun, AZ Martinez, ZJ Cartun, FFD Regis, Y Wan, ... Cancer Cell 35 (2), 283-296. e5, 2019 | 93 | 2019 |
| nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse RS Ohgami, DR Campagna, B Antiochos, EB Wood, JJ Sharp, JE Barker, ... Blood 106 (10), 3625-3631, 2005 | 90 | 2005 |
