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Benjamin L. Ebert

Benjamin L. Ebert

D-Index & Metrics

Biology and Biochemistry

D-Index
120
Citations
163818
World Ranking
616
National Ranking
393

Medicine

D-Index
120
Citations
163919
World Ranking
3648
National Ranking
2015

Overview

Benjamin L. Ebert is affiliated with Harvard University in the United States. Their research contributes extensively to the fields of medicine and biochemistry, genetics, and molecular biology, with a particular focus on hematology, molecular biology, genetics, immunology, and oncology.

The main topics addressed in their work include acute myeloid leukemia research, myeloproliferative neoplasms diagnosis and treatment, protein degradation and inhibitors, cancer genomics and diagnostics, ubiquitin and proteasome pathways, multiple myeloma research and treatments, and lymphoma diagnosis and treatment.

Some of Benjamin L. Ebert's recent publications comprise:

  • Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN (2022, Blood)
  • International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data (2022, Blood)
  • Molecular International Prognostic Scoring System for Myelodysplastic Syndromes (2022, NEJM Evidence)
  • Cancer therapy shapes the fitness landscape of clonal hematopoiesis (2020, Nature Genetics)
  • Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes (2020, Nature Medicine)

Ebert's frequent collaborators include Pradeep Natarajan, Abhishek Niroula, Alexander G. Bick, Md Mesbah Uddin, and Christopher J. Gibson. These partnerships highlight an active engagement in cooperative research efforts.

Their publications are often found in notable scientific venues, such as:

  • Blood
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Circulation
  • Blood Advances
  • Journal of Clinical Oncology

Best Publications

  • Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles

    Aravind Subramanian;Pablo Tamayo;Vamsi K. Mootha;Sayan Mukherjee

  • Genome-Scale CRISPR-Cas9 Knockout Screening in Human Cells

    Ophir Shalem;Ophir Shalem;Neville E Sanjana;Neville E Sanjana;Ella Hartenian;Xi-Shun Shi

  • MicroRNA expression profiles classify human cancers

    Jun Lu;Gad Getz;Eric A. Miska;Eric A. Miska;Ezequiel Alvarez-Saavedra

  • Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel

    Hartmut Döhner;Elihu Estey;David Grimwade;Sergio Amadori

  • Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes

    Siddhartha Jaiswal;Pierre Fontanillas;Jason Flannick;Jason Flannick;Alisa Manning

  • The landscape of somatic copy-number alteration across human cancers

    Rameen Beroukhim;Craig H. Mermel;Craig H. Mermel;Dale Porter;Guo Wei

  • Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.

    Ross L. Levine;Ross L. Levine;Martha Wadleigh;Jan Cools;Benjamin L. Ebert;Benjamin L. Ebert

  • Clonal Hematopoiesis and risk of atherosclerotic cardiovascular disease

    Siddhartha Jaiswal;Pradeep Natarajan;Pradeep Natarajan;Alexander J. Silver;Christopher J. Gibson

  • Clinical effect of point mutations in myelodysplastic syndromes.

    Rafael Bejar;Kristen Stevenson;Omar Abdel-Wahab;Naomi Galili

  • Clonal hematopoiesis of indeterminate potential and its distinction from myelodysplastic syndromes

    David P. Steensma;Rafael Bejar;Siddhartha Jaiswal;R. Coleman Lindsley

  • MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia.

    Yana Pikman;Benjamin H Lee;Thomas Mercher;Elizabeth McDowell

  • Rational design of highly active sgRNAs for CRISPR-Cas9–mediated gene inactivation

    John G Doench;Ella Hartenian;Daniel B Graham;Zuzana Tothova

  • Lenalidomide Causes Selective Degradation of IKZF1 and IKZF3 in Multiple Myeloma Cells

    Jan Krönke;Namrata D. Udeshi;Anupama Narla;Peter Grauman

  • Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia

    Marc H. G. P. Raaijmakers;Siddhartha Mukherjee;Shangqin Guo;Siyi Zhang

  • Stem cell gene expression programs influence clinical outcome in human leukemia

    Kolja Eppert;Katsuto Takenaka;Eric R Lechman;Levi Waldron

  • Densely Interconnected Transcriptional Circuits Control Cell States in Human Hematopoiesis

    Noa Novershtern;Noa Novershtern;Noa Novershtern;Aravind Subramanian;Lee N. Lawton;Raymond H. Mak

  • Identification of RPS14 as a 5q - syndrome gene by RNA interference screen

    Benjamin L. Ebert;Jennifer Pretz;Jocelyn Bosco;Cindy Y. Chang

  • Ribosomopathies: human disorders of ribosome dysfunction.

    Anupama Narla;Benjamin L. Ebert;Benjamin L. Ebert

  • Acute myeloid leukemia ontogeny is defined by distinct somatic mutations

    R. Coleman Lindsley;Brenton G. Mar;Emanuele Mazzola;Peter V. Grauman

  • Perivascular Gli1+ progenitors are key contributors to injury-induced organ fibrosis

    Rafael Kramann;Rafael Kramann;Rebekka K. Schneider;Derek P. DiRocco;Flavia Machado

Frequent Co-Authors

Todd R. Golub
Todd R. Golub Harvard University
Donna Neuberg
Donna Neuberg Harvard University
Ross L. Levine
Ross L. Levine Memorial Sloan Kettering Cancer Center
Fatima Al-Shahrour
Fatima Al-Shahrour Spanish National Cancer Research Centre
David P. Steensma
David P. Steensma Harvard University
Björn Nilsson
Björn Nilsson Lund University
Richard Stone
Richard Stone Harvard University
D. Gary Gilliland
D. Gary Gilliland Fred Hutchinson Cancer Research Center
Steven A. Carr
Steven A. Carr Broad Institute
David E. Root
David E. Root Broad Institute

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