Gregory J. Kato

RED Consulting (Norway) — Norway

Medicine · Health Sciences

72h-index17.1kcitations414works1.52yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(331), Iron Metabolism and Disorders(168), Blood groups and transfusion(50), Myeloproliferative Neoplasms: Diagnosis and Treatment(49), Erythrocyte Function and Pathophysiology(47)

Publications414 total

CD39 polymorphism enables lung thrombosis in sickle cell disease
UNC Libraries·2026Open Access
CD39 polymorphism enables lung thrombosis in sickle cell disease
Nature Communications·2026Open Access
G-CSF receptor is a signaling node linking thrombo-inflammation to vaso-occlusion in sickle cell disease: Target for a new phase 2 trial
Blood·2025· 1 citedOpen Access
Current clinical concerns for patients with hereditary hemochromatosis – a Delphi consensus study
Blood·2025Open Access
Ten-Year Longitudinal Study Clarifies Impact of Hemolysis and Pulmonary Hypertension on Patients with Sickle Cell Anemia
American Journal of Respiratory and Critical Care Medicine·2025Open Access
Targeted Proteomic Analysis of Sickle Cell Disease Patients With Elevated Tricuspid Regurgitation Velocity
PROTEOMICS - CLINICAL APPLICATIONS·2025
Cerebrospinal fluid haptoglobin levels and outcome after aneurysmal subarachnoid haemorrhage: Evidence from Mendelian randomization
PLoS ONE·2025Open Access
Design of the RHEMEDY Study: A Phase 2/3 Safety, Efficacy and Pharmacokinetics Study of CSL889 in Adults and Adolescents With Sickle Cell Disease During Vaso-Occlusive Crisis
Journal of sickle cell disease.·2025Open Access
Advancing a Patient- and Carer-Centered Approach for the Clinical Development of New Therapeutics for Aneurysmal Subarachnoid Hemorrhage: Insights From a Qualitative Study
Journal of patient-centered research and reviews·2025Open Access
Small-molecule inhibitor screen to identify mechanisms of sickle hemoglobin clearance by liver endothelium
Blood Vessels Thrombosis & Hemostasis·2025Open Access
A Phase 2 Prospective Randomized Trial of Topical Sodium Nitrite in Patients with Sickle Cell Disease and Leg Ulcers
Blood·2024
Nontargeted Plasma Proteomic Analysis in Sickle Cell Disease Implicates Pathways Involving Cell Structure, Immunity and Heme and Oxygen Transport in the Occurrence of Leg Ulcers
Blood·2024
Transcriptomic Profiling Supports the Phenotypic Classification of Stable-State Sickle Cell Disease Patients
Blood·2024
Targeted proteomic analysis of sickle cell disease patients with elevated tricuspid regurgitation velocity
2024Open Access
Phase 1 Study of the Safety and Pharmacokinetics of CSL889 (Hemopexin) in Adults with SCD
Journal of sickle cell disease.·2024· 4 citedOpen Access
Hemoglobin scavenger receptor CD163 as a potential biomarker of hemolysis-induced hepatobiliary injury in sickle cell disease
American Journal of Physiology-Cell Physiology·2024· 7 citedOpen Access
Low global arginine bioavailability: a common phenomenon in pulmonary hypertension
American Journal of Physiology-Lung Cellular and Molecular Physiology·2024Open Access
Riociguat in patients with sickle cell disease and hypertension or proteinuria (STERIO-SCD): a randomised, double-blind, placebo controlled, phase 1–2 trial
The Lancet Haematology·2024· 7 citedOpen Access
Iron restriction in sickle cell disease: When less is more
American Journal of Hematology·2024· 10 citedOpen Access
Impaired hemoglobin clearance by sinusoidal endothelium promotes vaso-occlusion and liver injury in sickle cell disease
Haematologica·2023· 6 citedOpen Access
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Frequent Co-authors

Mark T. Gladwin(30), Roberto F. Machado(13), Oswaldo Castro(13), James G. Taylor(11), Vandana Sachdev(11), Victor R. Gordeuk(11), Martin H. Steinberg(7), Claudia R. Morris(7), Chi V. Dang(7), Lakshmanan Krishnamurti(6), Robyn J. Barst(6), Jane A. Little(5), Lori A. Hunter(5), Erika B. Rosenzweig(5), David B. Badesch(5), Kathryn L. Hassell(5), Onyinye Onyekwere(5), Mehdi Nouraie(5), Caterina P. Minniti(5), Wynona Coles(4)