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Biology and Biochemistry

D-Index
54
Citations
20430
World Ranking
15353
National Ranking
6409

Overview

Stacie M. Anderson is a researcher affiliated with the National Institutes of Health in the United States. Their work spans the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions also in Medicine. Within these broad areas, the subfields most represented in their output include Molecular Biology, Immunology, Cancer Research, Genetics, and Hematology.

The main topics of Anderson's research focus on Genomics and Chromatin Dynamics, CRISPR and Genetic Engineering, RNA modifications and cancer, Immune Cell Function and Interaction, Epigenetics and DNA Methylation, Acute Myeloid Leukemia Research, and T-cell and B-cell Immunology.

Among their recent published papers are the following:

  • Perspectives on ENCODE, 2020, Nature
  • Single-Cell Analyses Reveal Megakaryocyte-Biased Hematopoiesis in Myelofibrosis and Identify Mutant Clone-Specific Targets, 2020, Molecular Cell
  • In vivo CRISPR screens reveal a HIF-1α-mTOR-network regulates T follicular helper versus Th1 cells, 2022, Nature Communications
  • Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes, 2022, Nature
  • Snapshot: a package for clustering and visualizing epigenetic history during cell differentiation, 2023, BMC Bioinformatics

Frequently collaborating with Anderson are Elisabeth F. Heuston, David M. Bodine, Belinda Giardine, Cheryl A. Keller, and Ross C. Hardison. These coauthors have appeared alongside Anderson in multiple publications, indicating ongoing research partnerships.

Anderson publishes regularly in notable scientific journals, with the most frequent venues being Nature, bioRxiv (Cold Spring Harbor Laboratory), Molecular Cell, Nature Communications, and BMC Bioinformatics.

Best Publications

  • Bone marrow cells regenerate infarcted myocardium

    Donald Orlic;Jan Kajstura;Stefano Chimenti;Igor Jakoniuk

  • Erythrocyte P antigen: cellular receptor for B19 parvovirus

    Kevin E. Brown;Stacie M. Anderson;Neal S. Young

  • The TCF1-Bcl6 axis counteracts type I interferon to repress exhaustion and maintain T cell stemness.

    Tuoqi Wu;Yun Ji;E. Ashley Moseman;Haifeng C. Xu

  • Postnatal NG2 proteoglycan-expressing progenitor cells are intrinsically multipotent and generate functional neurons.

    Shibeshih Belachew;Ramesh Chittajallu;Ramesh Chittajallu;Adan A. Aguirre;Xiaoqing Yuan

  • Single-cell RNA-seq reveals TOX as a key regulator of CD8+ T cell persistence in chronic infection.

    Chen Yao;Hong-Wei Sun;Neal E. Lacey;Yun Ji

  • Fas antigen expression on CD34+ human marrow cells is induced by interferon gamma and tumor necrosis factor alpha and potentiates cytokine-mediated hematopoietic suppression in vitro

    Jaroslaw Maciejewski;Carmine Selleri;Stacie Anderson;Neal S. Young

  • Resistance to Parvovirus B19 Infection Due to Lack of Virus Receptor (Erythrocyte P Antigen)

    Kevin E. Brown;Jonathan R. Hibbs;Giorgio Gallinella;Stacie M. Anderson

  • Wnt5a inhibits canonical Wnt signaling in hematopoietic stem cells and enhances repopulation

    Michael J. Nemeth;Lilia Topol;Stacie M. Anderson;Yingzi Yang

  • Increased expression of Fas antigen on bone marrow CD34+ cells of patients with aplastic anaemia

    Jaroslaw P. Maciejewski;Carmine Selleri;Tadatsugu Sato;Stacie Anderson

  • Self-assembled B19 parvovirus capsids, produced in a baculovirus system, are antigenically and immunogenically similar to native virions.

    Sachiko Kajigaya;Hiroyuki Fujii;Anne Field;Stacie Anderson

  • The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia.

    Lucio H. Castilla;Lisa Garrett;Neeraj Adya;Donald Orlic

  • Interferon-gamma and tumor necrosis factor-alpha suppress both early and late stages of hematopoiesis and induce programmed cell death.

    Carmine Selleri;Tadatsugu Sato;Stacie Anderson;Neal S. Young

  • Functional and Epigenetic Studies Reveal Multistep Differentiation and Plasticity of In Vitro-Generated and In Vivo-Derived Follicular T Helper Cells

    Kristina T. Lu;Yuka Kanno;Jennifer L. Cannons;Robin Handon

  • Differential Expression of Interleukin-17A and -17F Is Coupled to T Cell Receptor Signaling via Inducible T Cell Kinase

    Julio Gomez-Rodriguez;Nisebita Sahu;Robin Handon;Todd S. Davidson

  • The level of mRNA encoding the amphotropic retrovirus receptor in mouse and human hematopoietic stem cells is low and correlates with the efficiency of retrovirus transduction

    Donald Orlic;Laurie J. Girard;Craig T. Jordan;Stacie M. Anderson

  • Autoimmune Lymphoproliferative Syndrome with Defective Fas: Genotype Influences Penetrance

    Christine E. Jackson;Roxanne E. Fischer;Amy P. Hsu;Stacie M. Anderson

  • Pluripotent hematopoietic stem cells contain high levels of mRNA for c-kit, GATA-2, p45 NF-E2, and c-myb and low levels or no mRNA for c-fms and the receptors for granulocyte colony-stimulating factor and interleukins 5 and 7

    Donald Orlic;Stacie Anderson;Leslie G. Biesecker;Brian P. Sorrentino

  • SAP regulates T cell–mediated help for humoral immunity by a mechanism distinct from cytokine regulation

    Jennifer L. Cannons;Li J. Yu;Dragana Jankovic;Shane Crotty

  • Neutralizing linear epitopes of B19 parvovirus cluster in the VP1 unique and VP1-VP2 junction regions.

    T Saikawa;S Anderson;M Momoeda;S Kajigaya

  • A severe and consistent deficit in marrow and circulating primitive hematopoietic cells (long-term culture-initiating cells) in acquired aplastic anemia

    Jaroslaw P. Maciejewski;Carmine Selleri;Tadatsugu Sato;Stacie Anderson

Frequent Co-Authors

David M. Bodine
David M. Bodine National Institutes of Health
Martha Kirby
Martha Kirby National Institutes of Health
Neal S. Young
Neal S. Young National Institutes of Health
Pamela L. Schwartzberg
Pamela L. Schwartzberg National Institutes of Health
Fabio Candotti
Fabio Candotti National Institutes of Health
Ross C. Hardison
Ross C. Hardison Pennsylvania State University
Jaroslaw P. Maciejewski
Jaroslaw P. Maciejewski Cleveland Clinic
Vittorio Gallo
Vittorio Gallo National Institutes of Health
Jennifer M. Puck
Jennifer M. Puck University of California, San Francisco
Abdel G. Elkahloun
Abdel G. Elkahloun National Human Genome Research Institute

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