ER
Eliezer A. Rachmilewitz

Elite Scholar

452
Works
17,727
Citations
70
H-Index
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Author Statistics
  • OpenAlex ID A5113576353
  • i10-Index 238
  • 2-Yr Mean Citedness 0.00
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Eliezer A. Rachmilewitz

Also known as: E A RACHMILEWITZ, E A Rachmilewitz, E L Rachmilewitz, E RACHMILEWITZ, E Rachmilewitz

452

Total Works

17,727

Citations

70

H-Index

238

i10-Index

Citation & Works Trend by Year
56 years active
Top Research Topics
Hemoglobinopathies and Related Disorders (293) Iron Metabolism and Disorders (139) Hemoglobin structure and function (88) Blood groups and transfusion (59) Acute Myeloid Leukemia Research (53)
Recent Publications
15 shown
Year Publication Title Citations Action
2019 The Red Blood Cell In Thalassemia * CRC Press eBooks 2
2017 Pathophysiology and treatment of patients with beta-thalassemia – an update F1000Research 91
2017 Faculty Opinions recommendation of New film-coated tablet formulation of deferasirox is well tolerated in patients with thalassemia or lower-risk MDS: Results of the randomized, phase II ECLIPSE study. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 2
2017 Faculty Opinions recommendation of FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Identification of embryo-fetal cells in celomic fluid using morphological and short-tandem repeats analysis. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Forced chromatin looping raises fetal hemoglobin in adult sickle cells to higher levels than pharmacologic inducers. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of HSP70 sequestration by free α-globin promotes ineffective erythropoiesis in β-thalassaemia. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of miRNA-embedded shRNAs for Lineage-specific BCL11A Knockdown and Hemoglobin F Induction. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Induction of fetal hemoglobin through enhanced translation efficiency of γ-globin mRNA. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 2
2017 Faculty Opinions recommendation of 53. From GWAS To the Clinic: Genome-Editing the Human BCL11A Erythroid Enhancer for Fetal Globin Elevation in the Hemoglobinopathies. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of Functional footprinting of regulatory DNA. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0
2017 Faculty Opinions recommendation of MicroRNA-486-3p regulates γ-globin expression in human erythroid cells by directly modulating BCL11A. Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature 0

Data source: OpenAlex API