Marshall S. Horwitz

University of Washington — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

67h-index19.9kcitations307works1.82yr avg
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Research Topics

Virus-based gene therapy research(78), Blood disorders and treatments(65), Immunodeficiency and Autoimmune Disorders(36), Viral Infectious Diseases and Gene Expression in Insects(33), Acute Myeloid Leukemia Research(31)

Publications307 total

3242 – INFLAMMATORY STRESS AS A DRIVER AND INTERVENTION STRATEGY IN RUNX1-FAMILIAL PLATELET DISORDER
Experimental Hematology·2025
Genetics of interstitial lung diseases: a state-of-the-art review
European Respiratory Journal·2025· 2 cited
Germline copy number variants in RUNX1: An updated case report and a decade-old red herring
BJC Reports·2025Open Access
Targeting the CD74 signaling axis suppresses inflammation and rescues defective hematopoiesis in <i>RUNX1</i> -familial platelet disorder
Science Translational Medicine·2025· 10 citedOpen Access
Genetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies
Genetics in Medicine Open·2025· 2 citedOpen Access
Bayesian Phylogenetic Lineage Reconstruction with Loss of Heterozygosity Mutations Derived from Single-Cell RNA Sequencing
Methods in molecular biology·2025
Detection of human brain cancers using genomic and immune cell characterization of cerebrospinal fluid through CSF-BAM
2024· 1 citedOpen Access
G-CSF resistance of ELANE-mutant neutropenia depends on SERF1-containing truncated–neutrophil elastase aggregates
Journal of Clinical Investigation·2024· 1 citedOpen Access
CD74 Signaling Regulates Inflammatory Stress to Drive Defective Hematopoiesis and Fitness Advantage of Progenitors in RUNX1-Familial Platelet Disorder
Blood·2024Open Access
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial <scp>DNA</scp> Depletion/Deletions Disease
Annals of Neurology·2024· 4 citedOpen Access
Genetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies
2024· 1 citedOpen Access
Clinical Outcomes of Lung Transplant Recipients with Idiopathic, Familial and Progressive Pulmonary Fibrosis and Shortened Telomeres - A Retrospective Observation in a Case Series at the University of Washington Medical Center, Seattle, USA
2024
Interplay between Inflammatory Microenvironment and RUNX1-Mediated Transcriptomic Changes Drives Defective Hematopoiesis in Familial Platelet Disorder
Blood·2023
Neutrophil Elastase Catalytic Activity Regulates Granulopoiesis
Blood·2023Open Access
27. Five-year experience of evaluating individuals at-risk for underlying genetic predisposition to hematologic malignancy
Cancer Genetics·2023
PB0725 Tissue Factor on Human Immunodeficiency Virus and Dengue Virus as the Molecular Basis for Hemostatic Pathology
Research and Practice in Thrombosis and Haemostasis·2023Open Access
Derivation of Naïve Human Embryonic Stem Cells Using a CHK1 Inhibitor
Stem Cell Reviews and Reports·2023· 2 citedOpen Access
Supplementary Table 4 from HIF Induces Human Embryonic Stem Cell Markers in Cancer Cells
2023Open Access
Supplementary Figures 1-12 from HIF Induces Human Embryonic Stem Cell Markers in Cancer Cells
2023Open Access
Data from HIF Induces Human Embryonic Stem Cell Markers in Cancer Cells
2023Open Access
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Frequent Co-authors

Gustavo Droguett(5), Hamish S. Scott(5), Zhijun Duan(5), Yaron Ilan(5), Christopher N Hahn(4), Richard Person(4), Kathleen F. Benson(4), Jeremy Wechsler(4), Tom Walsh(4), Anne Davidson(4), Jayanta Roy Chowdhury(4), Chan‐Eng Chong(3), Catherine Carmichael(3), Milena Babic(3), Andrew E. Timms(3), H. Leighton Grimes(3), Mary‐Claire King(3), Jeffrey M. Bergelson(2), Anita Krithivas(2), Richard L. Crowell(2)