Dean R. Campagna

ScholarGPS® ID: 91974207391031

Affiliation
Boston Children's Hospital, Boston, United States
Affiliation History

Field
Medicine
Discipline
Pathology
Top Specialties
Anemia | Mutation | Birth Defect | Cancer | Metabolism | Cancer Cell
Metrics Summary
Publication Count
52
Predicted Citations
5,905
Predicted h-index
31
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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Congenital X‐linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6 (journal article)
Renella, Raffaele | Gagne, Katelyn | Beauchamp, Ellen | Fogel, Jonathan | Perlov, Aleksej | Sola, Mireia | Schlaeger, Thorsten | Hofmann, Inga | Shimamura, Akiko | Ebert, Benjamin L. | ... | Williams, David A.
American Journal of Hematology, volume 97, issue 1, pages 18-29 (2022).
10.1002/ajh.26382
Cited by (1) | Cite | Source
A synonymous coding variant that alters ALAS2 splicing and causes X‐linked sideroblastic anemia (journal article)
Oakley, Jamie Heather | Campagna, Dean R. | Sun, Liang | Rockowitz, Shira | Sliz, Piotr | Boudreaux, Jeanne | Woods, Gary | Fleming, Mark D.
Pediatric Blood & Cancer, volume 69, issue 1 (2022).
10.1002/pbc.29309
Cited by (1) | Cite | Source
Pyridoxine Response in Mouse Alas2 Knock-in Models of X-Linked Sideroblastic Anemia and X-Linked Protoporphyria (journal article)
Ducamp, Sarah | Schmidt, Paul J | Campagna, Dean R | Fleming, Mark D.
Blood, volume 138, issue Supplement 1, pages 925-925 (2021).
10.1182/blood-2021-150683
Cited by (1) | Cite | Source
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature (journal article)
Heeney, Matthew M. | Berhe, Simon | Campagna, Dean R. | Oved, Joseph H. | Kurre, Peter | Shaw, Peter J. | Teo, Juliana | Shanap, Mayada A. | Hassab, Hoda M. | Glader, Bertil E. | ... | Fleming, Mark D.
Human Mutation, volume 42, issue 11, pages 1367-1383 (2021).
10.1002/humu.24267
Cited by (12) | Cite | Source
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemia (journal article)
Crispin, Andrew | Guo, Chaoshe | Chen, Caiyong | Campagna, Dean R. | Schmidt, Paul J. | Lichtenstein, Daniel | Cao, Chang | Sendamarai, Anoop K. | Hildick-Smith, Gordon J. | Huston, Nicholas C. | ... | Ducamp, Sarah
Journal of Clinical Investigation, volume 130, issue 10, pages 5245-5256 (2020).
10.1172/JCI135479
Cited by (15) | Cite | Source
A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm Deletion (journal article)
Yin, Shanye | Gambe, Rutendo G. | Sun, Jing | Martinez, Aina Zurita | Cartun, Zachary J. | Regis, Fara Faye D. | Wan, Youzhong | Fan, Jean | Brooks, Angela N. | Herman, Sarah E.M. | ... | Wang, Lili
Cancer Cell, volume 35, issue 2, pages 283-296.e5 (2019).
10.1016/j.ccell.2018.12.013
Cited by (65) | Cite | Source
Recurrent heteroplasmy for the MT-ATP6 p.Ser148Asn (m.8969G>A) mutation in patients with syndromic congenital sideroblastic anemia of variable clinical severity (journal article)
Berhe, Simon | Heeney, Matthew M. | Campagna, Dean R. | Thompson, John F. | White, Eric J. | Ross, Tristen | Peake, Roy W. A. | Hanrahan, Jeffery D. | Rodriguez, Vilmarie | Renaud, Deborah L. | ... | Fleming, Mark D.
Haematologica, volume 103, issue 12, pages e561-e563 (2018).
10.3324/haematol.2018.199109
Cited by (9) | Cite | Source | Open Access
Integrated Genomic and Proteomic Analysis of Murine CLL-like Cells Reveals SF3B1 Mutation to Impact DNA Damage Response and BCR Signaling (journal article)
Wang, Lili | Yin, Shanye | Martinez, Aina zurita | Regis, Fara Faye | Brooks, Angela | Herman, Sarah E. M. | Ten Hacken, Elisa | Obeng, Esther | Campagna, Dean | Fleming, Mark D. | ... | Wu, Catherine J.
Blood, volume 132, issue Supplement 1, pages 947-947 (2018).
10.1182/blood-2018-99-117691
Cite | Source
Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice (journal article)
Hofmann, Inga | Geer, Mitchell J. | Vögtle, Timo | Crispin, Andrew | Campagna, Dean R. | Barr, Alastair | Calicchio, Monica L. | Heising, Silke | van Geffen, Johanna P. | Kuijpers, Marijke J. E. | ... | Senis, Yotis A.
Blood, volume 132, issue 13, pages 1399-1412 (2018).
10.1182/blood-2017-08-802769
Cited by (33) | Cite | Source
Pancreatic lipomatosis in Diamond–Blackfan anemia: The importance of genetic testing in bone marrow failure disorders (journal article)
Gansner, John M. | Furutani, Elissa | Campagna, Dean R. | Fleming, Mark D. | Shimamura, Akiko
American Journal of Hematology, volume 93, issue 9, pages 1194-1195 (2018).
10.1002/ajh.25155
Cited by (1) | Cite | Source
Normalizing hepcidin predicts TMPRSS6 mutation status in patients with chronic iron deficiency (journal article)
Heeney, Matthew M. | Guo, Dongjing | De Falco, Luigia | Campagna, Dean R. | Olbina, Gordana | Kao, Paige P.-C. | Schmitz-Abe, Klaus | Rahimov, Fedik | Gutschow, Patrick | Westerman, Keith | ... | Fleming, Mark D.
Blood, volume 132, issue 4, pages 448-452 (2018).
10.1182/blood-2017-03-773028
Cited by (16) | Cite | Source
, a Mitochondrial Iron-Sulfur Cluster Assembly Co-Chaperone, Is a Novel Candidate Gene for Congenital Sideroblastic Anemia (journal article)
Crispin, Andrew | Schmidt, Paul | Campagna, Dean | Cao, Chang | Lichtenstein, Daniel | Sendamarai, Anoop | Guo, Chaoshe | Chen, Caiyong | Hildick-Smith, Gordon J | Huston, Nicolas C | ... | Ducamp, Sarah
Blood, volume 130, issue Suppl_1, pages 79-79 (2017).
10.1182/blood.V130.Suppl_1.79.79
Cited by (5) | Cite | Source
Chasing a moving target: Detection of mitochondrial heteroplasmy for clinical diagnostics (journal article)
White, Eric J. | Ross, Tristen | Lopez, Edgardo | Nikiforov, Anastasia | Gault, Christopher | Batorsky, Rebecca | Darcy, Christopher | Campagna, Dean R. | Fleming, Mark D. | Thompson, John F.
bioRxiv (2017).
10.1101/222109
Cited by (4) | Cite | Source | Open Access
UBE2O remodels the proteome during terminal erythroid differentiation (journal article)
Nguyen, Anthony T. | Prado, Miguel A. | Schmidt, Paul J. | Sendamarai, Anoop K. | Wilson-Grady, Joshua T. | Min, Mingwei | Campagna, Dean R. | Tian, Geng | Shi, Yuan | Dederer, Verena | ... | Finley, Daniel
Science, volume 357, issue 6350 (2017).
10.1126/science.aan0218
Cited by (105) | Cite | Source | Open Access
Ringed sideroblasts in β‐thalassemia (journal article)
Cattivelli, Kim | Campagna, Dean R. | Schmitz‐Abe, Klaus | Heeney, Matthew M. | Yaish, Hassan M. | Caruso Brown, Amy E. | Kearney, Susan | Walkovich, Kelly | Markianos, Kyriacos | Fleming, Mark D. | Neufeld, Ellis J.
Pediatric Blood & Cancer, volume 64, issue 5 (2017).
10.1002/pbc.26324
Cited by (5) | Cite | Source | Open Access
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia (journal article)
Lichtenstein, Daniel A. | Crispin, Andrew W. | Sendamarai, Anoop K. | Campagna, Dean R. | Schmitz-Abe, Klaus | Sousa, Cristovao M. | Kafina, Martin D. | Schmidt, Paul J. | Niemeyer, Charlotte M. | Porter, John | ... | Fleming, Mark D.
Blood, volume 128, issue 15, pages 1913-1917 (2016).
10.1182/blood-2016-05-719062
Cited by (32) | Cite | Source | Open Access
Physiologic Expression of Sf3b1 K700E Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome Modulation (journal article)
Obeng, Esther A. | Chappell, Ryan J. | Seiler, Michael | Chen, Michelle C. | Campagna, Dean R. | Schmidt, Paul J. | Schneider, Rebekka K. | Lord, Allegra M. | Wang, Lili | Gambe, Rutendo G. | ... | Ebert, Benjamin L.
Cancer Cell, volume 30, issue 3, pages 404-417 (2016).
10.1016/j.ccell.2016.08.006
Cited by (283) | Cite | Source | Open Access
Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterations (journal article)
Mangum, Joshua E. | Hardee, Justin P. | Fix, Dennis K. | Puppa, Melissa J. | Elkes, Johnathon | Altomare, Diego | Bykhovskaya, Yelena | Campagna, Dean R. | Schmidt, Paul J. | Sendamarai, Anoop K. | ... | Patton, Jeffrey R.
Scientific Reports, volume 6, issue 1 (2016).
10.1038/srep26202
Cited by (26) | Cite | Source | Open Access
Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9 (journal article)
Schmitz-Abe, Klaus | Ciesielski, Szymon J. | Schmidt, Paul J. | Campagna, Dean R. | Rahimov, Fedik | Schilke, Brenda A. | Cuijpers, Marloes | Rieneck, Klaus | Lausen, Birgitte | Linenberger, Michael L. | ... | Fleming, Mark D.
Blood, volume 126, issue 25, pages 2734-2738 (2015).
10.1182/blood-2015-09-659854
Cited by (60) | Cite | Source | Open Access
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels (journal article)
Rathkolb, Birgit | Klempt, Martina | Sabrautzki, Sibylle | Michel, Dian | Klaften, Matthias | Laufs, Jürgen | Sedlmeier, Reinhard | Hans, Wolfgang | Fuchs, Helmut | Muckenthaler, Martina U. | ... | Aigner, Bernhard
BioMetals, volume 28, issue 2, pages 293-306 (2015).
10.1007/s10534-015-9824-1
Cited by (3) | Cite | Source