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Author Details

Siob??n B Keel
University of Washington School of Medicine
2007
48
20
PMIDPaper TitleJournal TitlePublished Year
37505211Evidence-based consensus guidelines for the diagnosis and management of protoporphyria-related liver dysfunction in erythropoietic protoporphyria and X-linked protoporphyria.Hepatology2024
37862462Reply: Contrasting effect of iron supplementation in protoporphyria.Hepatology2024
36041558Evidence-based consensus guidelines for the diagnosis and management of erythropoietic protoporphyria and X-linked protoporphyria.J Am Acad Dermatol2023
37602041A Novel Presentation of Refractory Immune Thrombocytopenia in Anti-synthetase Syndrome: A Case Report.Cureus2023
37339483Phase 1/2 study of sorafenib added to cladribine, high-dose cytarabine, G-CSF, and mitoxantrone in untreated AML.Blood Adv2023
37027823RNA interference therapy in acute hepatic porphyrias.Blood2023
34758064Hematologic complications with age in Shwachman-Diamond syndrome.Blood Adv2022
35809951Inferior Vena Cava Obstruction Complicating Remote Venovenous Extracorporeal Membrane Oxygenation Bridge to Lung Transplantation.Chest2022
35740603Phase 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
35130502NCCN Guidelines® Insights: Myelodysplastic Syndromes, Version 3.2022.J Natl Compr Canc Netw2022
35278369Lamin B1 deletion in myeloid neoplasms causes nuclear anomaly and altered hematopoietic stem cell function.Cell Stem Cell2022
35173273Physician and patient perceptions on randomization of treatment intensity for unfit adults with acute myeloid leukemia and other high-grade myeloid neoplasm.Leukemia2022
34931301Cerebrospinal fluid flow cytometry and risk of central nervous system relapse after hyperCVAD in adults with acute lymphoblastic leukemia.Cancer2022
34298585SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.Hum Mutat2021
33510405Germline variants drive myelodysplastic syndrome in young adults.Leukemia2021
33560381Restoring RUNX1 deficiency in RUNX1 familial platelet disorder by inhibiting its degradation.Blood Adv2021
33637765Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome.Nat Commun2021
34889426The clinical and laboratory evaluation of patients with suspected hypocellular marrow failure.Hematology Am Soc Hematol Educ Program2021
34469508Association of unbalanced translocation der(1;7) with germline GATA2 mutations.Blood2021
34453453The transfusion management of beta thalassemia in the United States.Transfusion2021
31586148Early hospital discharge after intensive induction chemotherapy for adults with acute myeloid leukemia or other high-grade myeloid neoplasm.Leukemia2020
31690837Evaluating the Patient-Reported Outcomes Measurement Information System scales in acute intermittent porphyria.Genet Med2020
30530752Single-cell analyses demonstrate that a heme-GATA1 feedback loop regulates red cell differentiation.Blood2019
31648317ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.Blood Adv2019
31427279Normal peripheral blood neutrophil numbers accompanying <i>ELANE</i> whole gene deletion mutation.Blood Adv2019
31010849Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromes.Blood2019
30600763Bone Marrow Morphology Associated With Germline <i>RUNX1</i> Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy.Pediatr Dev Pathol2019
30030275A novel disease-causing synonymous exonic mutation in <i>GATA2</i> affecting RNA splicing.Blood2018
30260477Transfusion practices and complications in thalassemia.Transfusion2018
27824607Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.Eur Respir J2017
28716860Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.Blood2017
28653329Acquired RhD mosaicism identifies fibrotic transformation of thrombopoietin receptor-mutated essential thrombocythemia.Transfusion2017
26712909Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies.Blood2016
27169803Delayed globin synthesis leads to excess heme and the macrocytic anemia of Diamond Blackfan anemia and del(5q) myelodysplastic syndrome.Sci Transl Med2016
27418648Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.Haematologica2016
27497531Identifying Inherited and Acquired Genetic Factors Involved in Poor Stem Cell Mobilization and Donor-Derived Malignancy.Biol Blood Marrow Transplant2016
27259050Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.Am J Hum Genet2016
27258031Diamond Blackfan Anemia: A Nonclassical Patient With Diagnosis Assisted by Genomic Analysis.J Pediatr Hematol Oncol2016
25239263Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.Haematologica2015
26482161Pitfalls in Erythrocyte Protoporphyrin Measurement for Diagnosis and Monitoring of Protoporphyrias.Clin Chem2015
26551679Coordinate expression of heme and globin is essential for effective erythropoiesis.J Clin Invest2015
25782630Evidence that the expression of transferrin receptor 1 on erythroid marrow cells mediates hepcidin suppression in the liver.Exp Hematol2015
25581430Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy.Nat Genet2015
23376999Mice lacking the sodium-dependent phosphate import protein, PiT1 (SLC20A1), have a severe defect in terminal erythroid differentiation and early B cell development.Exp Hematol2013
22198155Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis.Exp Hematol2012
19890136The microcytic red cell and the anemia of inflammation.N Engl J Med2009
18258918A heme export protein is required for red blood cell differentiation and iron homeostasis.Science2008
17365847Alpha-delta platelet storage pool deficiency in three generations.Platelets2007
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Collaborators

University of Washington
Co-authored papers 8
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Co-authored papers 8
University of Washington
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
The University of Chicago
Co-authored papers 5
University of Washington, USA Brotman Baty Institute for Precision Medicine
Co-authored papers 4
Fred Hutchinson Cancer Center.
Co-authored papers 4
Oregon Health & Science University
Co-authored papers 2
Co-authored papers 2
UT MD Anderson Cancer Center
Co-authored papers 2
University Hospital Heidelberg
Co-authored papers 2
University of Washington
Co-authored papers 2
Adelaide Medical School, University of Adelaide
Co-authored papers 2
Houston Methodist Hospital
Co-authored papers 2
National Institutes of Health
Co-authored papers 1
Emory University School of Medicine
Co-authored papers 1
Hannover Medical School
Co-authored papers 1
National Heart Lung and Blood Institute Division of Intramural Research
Co-authored papers 1
Clinical Center, National Institutes of Health
Co-authored papers 1
MD Anderson Cancer Center
Co-authored papers 1
The Ohio State University
Co-authored papers 1
University of Washington School of Medicine
Co-authored papers 1
Knight Cancer Institute, Oregon Health & Science University
Co-authored papers 1
University of Washington
Co-authored papers 1
St. Anna Children's Cancer Research Institute (CCRI)
Co-authored papers 1
University of Colorado Division of Hematology
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University of Texas MD Anderson Cancer Center
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