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Suthat Fucharoen

Suthat Fucharoen

D-Index & Metrics

Biology and Biochemistry

D-Index
60
Citations
14598
World Ranking
11855
National Ranking
8

Overview

Suthat Fucharoen is affiliated with Mahidol University in Thailand and has a significant body of research focused primarily within the field of Medicine. Their work spans multiple subfields including Genetics, Hematology, Molecular Biology, Physiology, and Pediatrics, Perinatology and Child Health.

The main research areas covered by this scientist include:

  • Hemoglobinopathies and Related Disorders
  • Iron Metabolism and Disorders
  • Blood groups and transfusion
  • Erythrocyte Function and Pathophysiology
  • Prenatal Screening and Diagnostics
  • Trace Elements in Health
  • Epigenetics and DNA Methylation

Frequent co-authors reflect collaborations with researchers such as Kittiphong Paiboonsukwong, Saovaros Svasti, Orapan Sripichai, Somdet Srichairatanakool, and Suradej Hongeng. These collaborations show sustained joint work on related topics and publications.

Major publication venues for this scientist's work include:

  • Hemoglobin
  • Scientific Reports
  • Molecules
  • British Journal of Haematology
  • Life Sciences

Some recent publications provide insight into the scope and focus of research themes:

  • Update in Laboratory Diagnosis of Thalassemia, 2020, Frontiers in Molecular Biosciences
  • Gut leakage enhances sepsis susceptibility in iron-overloaded β-thalassemia mice through macrophage hyperinflammatory responses, 2020, American Journal of Physiology-Gastrointestinal and Liver Physiology
  • Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice, 2020, Journal of Inflammation Research
  • Increased susceptibility to dextran sulfate-induced mucositis of iron-overload β-thalassemia mice, another endogenous cause of septicemia in thalassemia, 2021, Clinical Science
  • Thalassemia in Thailand, 2022, Hemoglobin

Best Publications

  • High levels of GDF15 in thalassemia suppress expression of the iron regulatory protein hepcidin.

    Toshihiko Tanno;Natarajan V Bhanu;Patricia A Oneal;Sung-Ho Goh

  • Hemoglobin H disease: not necessarily a benign disorder

    David H K Chui;Suthat Fucharoen;Vivian Chan

  • Sustained dystrophin expression induced by peptide-conjugated morpholino oligomers in the muscles of mdx mice.

    Natee Jearawiriyapaisarn;Hong M Moulton;Brian Buckley;Jennifer Roberts

  • Membrane Phospholipid Asymmetry in Human Thalassemia

    Frans A. Kuypers;Jie Yuan;Rachel A. Lewis;L. Michael Snyder

  • Hb H disease: clinical course and disease modifiers

    Suthat Fucharoen;Vip Viprakasit

  • Restoration of hemoglobin A synthesis in erythroid cells from peripheral blood of thalassemic patients.

    Giuseppina Lacerra;Halina Sierakowska;Clementina Carestia;Suthat Fucharoen

  • Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine

    Suthat Fucharoen;Pranee Winichagoon

  • A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E

    Manit Nuinoon;Wattanan Makarasara;Taisei Mushiroda;Iswari Setianingsih

  • Haemoglobinopathies in Southeast Asia

    Suthat Fucharoen;Pranee Winichagoon

  • International reproducibility of single breathhold T2* MR for cardiac and liver iron assessment among five thalassemia centers.

    Paul Kirk;Taigang He;Lisa J. Anderson;Michael Roughton

  • A scoring system for the classification of β-thalassemia/Hb E disease severity

    Orapan Sripichai;Wattanan Makarasara;Thongperm Munkongdee;Chutima Kumkhaek

  • Severity differences in β‐thalassaemia/haemoglobin E syndromes: implication of genetic factors

    Pranee Winichagoon;Varaporn Thonglairoam;Suthat Fucharoen;Prapon Wilairat

  • Improvement in oxidative stress and antioxidant parameters in β-thalassemia/Hb E patients treated with curcuminoids

    Ruchaneekorn W. Kalpravidh;Noppadol Siritanaratkul;Praphaipit Insain;Ratiya Charoensakdi

  • Clinical manifestation of beta-thalassemia/hemoglobin E disease.

    Suthat Fucharoen;Phairawh Ketvichit;Pensri Pootrakul;Noppadol Siritanaratkul

  • Platelet inhibition by nitrite is dependent on erythrocytes and deoxygenation.

    Sirada Srihirun;Thanaporn Sriwantana;Supeenun Unchern;Dusadee Kittikool

  • Genetic factors affecting clinical severity in beta-thalassemia syndromes.

    Pranee Winichagoon;Suthat Fucharoen;Ping Chen;Prawase Wasi

  • The Unusual Pathobiology of Hemoglobin Constant Spring Red Blood Cells

    S.L. Schrier;A. Bunyaratvej;A. Khuhapinant;S. Fucharoen

  • Restoration of Human β-Globin Gene Expression in Murine and Human IVS2–654 Thalassemic Erythroid Cells by Free Uptake of Antisense Oligonucleotides

    Thipparat Suwanmanee;Halina Sierakowska;Giuseppina Lacerra;Saovaros Svasti

  • Increased circulating activated endothelial cells, vascular endothelial growth factor, and tumor necrosis factor in thalassemia

    Punnee Butthep;Saknarong Rummavas;Raewadee Wisedpanichkij;Sumalee Jindadamrongwech

  • Flow cytometric quantitation of red blood cell vesicles in thalassemia.

    Kovit Pattanapanyasat;Egarit Noulsri;Suthat Fucharoen;Surada Lerdwana

Frequent Co-Authors

Siriporn C. Chattipakorn
Siriporn C. Chattipakorn Chiang Mai University
Duncan R. Smith
Duncan R. Smith Mahidol University
John B. Porter
John B. Porter University College London
Jisnuson Svasti
Jisnuson Svasti Mahidol University
Philippe Leboulch
Philippe Leboulch Brigham and Women's Hospital
Ryszard Kole
Ryszard Kole University of North Carolina at Chapel Hill
Dudley J. Pennell
Dudley J. Pennell National Institutes of Health
Robert C. Hider
Robert C. Hider King's College London
Russell E. Ware
Russell E. Ware Cincinnati Children's Hospital Medical Center
David J. Weatherall
David J. Weatherall University of Oxford

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