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Author Details
Full Name
Siob??n B Keel
Affiliation
University of Washington School of Medicine
ORCID
Career Start Year
2007
Papers
48
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37505211
Evidence-based consensus guidelines for the diagnosis and management of protoporphyria-related liver dysfunction in erythropoietic protoporphyria and X-linked protoporphyria.
Hepatology
2024
37862462
Reply: Contrasting effect of iron supplementation in protoporphyria.
Hepatology
2024
36041558
Evidence-based consensus guidelines for the diagnosis and management of erythropoietic protoporphyria and X-linked protoporphyria.
J Am Acad Dermatol
2023
37602041
A Novel Presentation of Refractory Immune Thrombocytopenia in Anti-synthetase Syndrome: A Case Report.
Cureus
2023
37339483
Phase 1/2 study of sorafenib added to cladribine, high-dose cytarabine, G-CSF, and mitoxantrone in untreated AML.
Blood Adv
2023
37027823
RNA interference therapy in acute hepatic porphyrias.
Blood
2023
34758064
Hematologic complications with age in Shwachman-Diamond syndrome.
Blood Adv
2022
35809951
Inferior Vena Cava Obstruction Complicating Remote Venovenous Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation.
Chest
2022
35740603
Phase 1/2 Trial of CLAG-M with Dose-Escalated Mitoxantrone in Combination with Fractionated-Dose Gemtuzumab Ozogamicin for Newly Diagnosed Acute Myeloid Leukemia and Other High-Grade Myeloid Neoplasms.
Cancers (Basel)
2022
35130502
NCCN Guidelines® Insights: Myelodysplastic Syndromes, Version 3.2022.
J Natl Compr Canc Netw
2022
35278369
Lamin B1 deletion in myeloid neoplasms causes nuclear anomaly and altered hematopoietic stem cell function.
Cell Stem Cell
2022
35173273
Physician and patient perceptions on randomization of treatment intensity for unfit adults with acute myeloid leukemia and other high-grade myeloid neoplasm.
Leukemia
2022
34931301
Cerebrospinal fluid flow cytometry and risk of central nervous system relapse after hyperCVAD in adults with acute lymphoblastic leukemia.
Cancer
2022
34298585
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.
Hum Mutat
2021
33510405
Germline variants drive myelodysplastic syndrome in young adults.
Leukemia
2021
33560381
Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradation.
Blood Adv
2021
33637765
Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome.
Nat Commun
2021
34889426
The clinical and laboratory evaluation of patients with suspected hypocellular marrow failure.
Hematology Am Soc Hematol Educ Program
2021
34469508
Association of unbalanced translocation der(1;7) with germline GATA2 mutations.
Blood
2021
34453453
The transfusion management of beta thalassemia in the United States.
Transfusion
2021
31586148
Early hospital discharge after intensive induction chemotherapy for adults with acute myeloid leukemia or other high-grade myeloid neoplasm.
Leukemia
2020
31690837
Evaluating the Patient-Reported Outcomes Measurement Information System scales in acute intermittent porphyria.
Genet Med
2020
30530752
Single-cell analyses demonstrate that a heme-GATA1 feedback loop regulates red cell differentiation.
Blood
2019
31648317
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
Blood Adv
2019
31427279
Normal peripheral blood neutrophil numbers accompanying <i>ELANE</i> whole gene deletion mutation.
Blood Adv
2019
31010849
Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromes.
Blood
2019
30600763
Bone Marrow Morphology Associated With Germline <i>RUNX1</i> Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy.
Pediatr Dev Pathol
2019
30030275
A novel disease-causing synonymous exonic mutation in <i>GATA2</i> affecting RNA splicing.
Blood
2018
30260477
Transfusion practices and complications in thalassemia.
Transfusion
2018
27824607
Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.
Eur Respir J
2017
28716860
Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.
Blood
2017
28653329
Acquired RhD mosaicism identifies fibrotic transformation of thrombopoietin receptor-mutated essential thrombocythemia.
Transfusion
2017
26712909
Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.
Blood
2016
27169803
Delayed globin synthesis leads to excess heme and the macrocytic anemia of Diamond Blackfan anemia and del(5q) myelodysplastic syndrome.
Sci Transl Med
2016
27418648
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
Haematologica
2016
27497531
Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.
Biol Blood Marrow Transplant
2016
27259050
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.
Am J Hum Genet
2016
27258031
Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.
J Pediatr Hematol Oncol
2016
25239263
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.
Haematologica
2015
26482161
Pitfalls in Erythrocyte Protoporphyrin Measurement for Diagnosis and Monitoring of Protoporphyrias.
Clin Chem
2015
26551679
Coordinate expression of heme and globin is essential for effective erythropoiesis.
J Clin Invest
2015
25782630
Evidence that the expression of transferrin receptor 1 on erythroid marrow cells mediates hepcidin suppression in the liver.
Exp Hematol
2015
25581430
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.
Nat Genet
2015
23376999
Mice lacking the sodium-dependent phosphate import protein, PiT1 (SLC20A1), have a severe defect in terminal erythroid differentiation and early B cell development.
Exp Hematol
2013
22198155
Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis.
Exp Hematol
2012
19890136
The microcytic red cell and the anemia of inflammation.
N Engl J Med
2009
18258918
A heme export protein is required for red blood cell differentiation and iron homeostasis.
Science
2008
17365847
Alpha-delta platelet storage pool deficiency in three generations.
Platelets
2007
1 - 48 of 48
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Fred Hutchinson Cancer Center.
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Oregon Health & Science University
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Co-authored papers
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University of Washington
Co-authored papers
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Anna L Brown
Adelaide Medical School, University of Adelaide
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Houston Methodist Hospital
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National Institutes of Health
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Emory University School of Medicine
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Gudrun G??hring
Hannover Medical School
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Neal S Young
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