Mark D. Fleming

ScholarGPS® ID: 60438175592571

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

Field
Medicine
Discipline
Pathology
Top Specialties
Anemia | Mutation | Birth Defect | Cancer | Erythropoiesis | Metabolism | Iron Overload | Leukemia | Thalassemia | Lymphoma | Neoplasm | Iron Deficiency | Homeostasis | Molecular Genetics | Nutrition
Metrics Summary
Publication Count
194
Predicted Citations
28,384
Predicted h-index
80
Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

  • Publications
  • Books
  • Patents
  • NIH/NSF
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T-Lymphoblastic Lymphoma Cells Express High Levels of BCL2, S1P1, and ICAM1, Leading to a Blockade of Tumor Cell Intravasation (journal article)
Feng, Hui | Stachura, David L. | White, Richard M. | Gutierrez, Alejandro | Zhang, Lu | Sanda, Takaomi | Jette, Cicely A. | Testa, Joseph R. | Neuberg, Donna S. | Langenau, David M. | ... | Look, A. Thomas
Cancer Cell, volume 42, issue 6, pages 1130-1131 (2024).
10.1016/j.ccell.2024.05.019
Cite | Source
Comprehensive Genomic Analysis Identifies a Diverse Landscape of Sideroblastic and Nonsideroblastic Iron-Related Anemias with Novel and Pathogenic Variants in an Iron-Deficient Endemic Setting (journal article)
Sharma, Pankaj | Bhatia, Prateek | Singh, Minu | Jamwal, Manu | Pallavelangini, Swetha | Das, Reena | Malhotra, Pankaj | Attri, Savita V. | Ducamp, Sarah | Fleming, Mark D. | Trehan, Amita
The Journal of Molecular Diagnostics, volume 26, issue 5, pages 430-444 (2024).
10.1016/j.jmoldx.2024.01.011
Cited by (2) | Cite | Source
Folate depletion induces erythroid differentiation through perturbation of de novo purine synthesis (journal article)
Maynard, Adam G. | Pohl, Nancy K. | Mueller, Annabel P. | Petrova, Boryana | Wong, Alan Y. L. | Wang, Peng | Culhane, Andrew J. | Brook, Jeannette R. | Hirsch, Leah M. | Hoang, Ngoc | ... | Kanarek, Naama
Science Advances, volume 10, issue 5 (2024).
10.1126/sciadv.adj9479
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Successful cord blood transplantation for del7q myelodysplastic syndrome in Pearson marrow pancreas syndrome (journal article)
Belgacem, Zacharia H. | Dubois, Sonia M. | Jacoby, Elad | Martin, Paul L. | Parikh, Sumit B. | Fleming, Mark D. | Agarwal, Suneet
American Journal of Hematology, volume 98, issue 12 (2023).
10.1002/ajh.27107
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The Relationship between Protoporphyrin IX and Platelet Count in the Protoporphyrias (journal article)
Leaf, Rebecca Karp | Jiang, Paul Yanning | Goddu, R. Jay | Tran, Benny | Rebeiz, Lina | Elmariah, Sarina | Hodges, Pamela G | Mead, Jennifer | Trinidad, John | Saberi, Behnam | ... | Dickey, Amy
Blood, volume 142, issue Supplement 1, pages 5230-5230 (2023).
10.1182/blood-2023-180928
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Prospective observational pilot study of quantitative light dosimetry in erythropoietic protoporphyria (journal article)
Dickey, Amy K. | Rebeiz, Lina | Raef, Haya | Leaf, Rebecca K. | Elmariah, Sarina | Naik, Hetanshi | Anderson, Karl | Conley, Jared | Iyasere, Christiana | Zhao, Sophia | ... | Kochevar, Irene
Journal of the American Academy of Dermatology, volume 88, issue 5, pages 1148-1151 (2023).
10.1016/j.jaad.2022.11.036
Cited by (4) | Cite | Source
Loss of the placental iron exporter ferroportin 1 causes embryonic demise in late-gestation mouse pregnancy (journal article)
Cao, Chang | Fleming, Mark D.
Development, volume 149, issue 23 (2022).
10.1242/dev.201160
Cited by (4) | Cite | Source
Bitopertin, a Selective Glycine Transporter 1 Inhibitor, Reduced Protoporphyrin IX (PPIX) Level and Improved Liver Fibrosis in a Mouse Model of Erythropoietic Protoporphyria (EPP) (journal article)
Wu, Min | Ducamp, Sarah | Xiang, Yi | Putra, Juan | Fleming, Mark D. | MacDonald, Brian | Schmidt, Paul J
Blood, volume 140, issue Supplement 1, pages 8192-8193 (2022).
10.1182/blood-2022-168924
Cited by (4) | Cite | Source
Conditional Synthetic Lethality between the Initial Steps of Heme Biosynthesis and Pyridoxine Metabolism during Erythropoiesis (journal article)
Ducamp, Sarah | Sendamarai, Anoop | Fleming, Mark D.
Blood, volume 140, issue Supplement 1, pages 5346-5347 (2022).
10.1182/blood-2022-169421
Cite | Source
Outcomes of Hematologic Complications in Shwachman Diamond Syndrome: High Risk Features and Implications for Surveillance (journal article)
Galvin, Ashley | Reilly, Chris R. | Malsch, Maggie | Loveless, Sara | Antin, Joseph H. | Davies, Stella M | DiNardo, Courtney D. | Lane, Adam | Lindsley, Coleman | Nakano, Taizo A. | ... | Shimamura, Akiko
Blood, volume 140, issue Supplement 1, pages 2949-2950 (2022).
10.1182/blood-2022-164969
Cite | Source
Hereditary myopathies associated with hematological abnormalities (journal article)
Beecher, Grayson | Fleming, Mark D. | Liewluck, Teerin
Muscle & Nerve, volume 65, issue 4, pages 374-390 (2022).
10.1002/mus.27474
Cited by (8) | Cite | Source
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
Prevalence and Predictors of Iron Deficiency in Adolescent and Young Adult Outpatients: Implications for Screening (journal article)
Eiduson, Rose | Heeney, Matthew M. | Kao, Pei-Chi | London, Wendy B. | Fleming, Mark D. | Shrier, Lydia A.
Clinical Pediatrics, volume 61, issue 1, pages 66-75 (2022).
10.1177/00099228211059647
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
Maternal Iron Deficiency Modulates Placental Transcriptome and Proteome in Mid-Gestation of Mouse Pregnancy (journal article)
Cao, Chang | Prado, Miguel A | Sun, Liang | Rockowitz, Shira | Sliz, Piotr | Paulo, Joao A | Finley, Daniel | Fleming, Mark D
The Journal of Nutrition, volume 151, issue 5, pages 1073-1083 (2021).
10.1093/jn/nxab005
Cited by (13) | Cite | Source
Localization and Kinetics of the Transferrin-Dependent Iron Transport Machinery in the Mouse Placenta (journal article)
Cao, Chang | Fleming, Mark D
Current Developments in Nutrition, volume 5, issue 4, pages nzab025- (2021).
10.1093/cdn/nzab025
Cited by (7) | Cite | Source
ITK deficiency presenting as autoimmune lymphoproliferative syndrome (journal article)
Wallace, Jacqueline G. | Alosaimi, Mohammed F. | Khayat, Claudia Djambas | Jaber, Faris | Almutairi, Abduarahman | Beaussant-Cohen, Sarah | Pinkus, Geraldine | Fleming, Mark | Mehawej, Cybel | Chou, Janet | Geha, Raif S.
Journal of Allergy and Clinical Immunology, volume 147, issue 2, pages 743-745.e1 (2021).
10.1016/j.jaci.2020.06.019
Cited by (6) | Cite | Source
Global loss of Tfr2 with concomitant induced iron deficiency greatly ameliorates the phenotype of a murine thalassemia intermedia model (journal article)
Schmidt, Paul J. | Fitzgerald, Kevin | Butler, James S. | Fleming, Mark D.
American Journal of Hematology, volume 96, issue 2, pages 251-257 (2021).
10.1002/ajh.26048
Cited by (4) | Cite | Source