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Gordon W. Stewart

Observed names: G STEWART, G Stewart, G W Stewart, G. STEWART, G. Stewart, G. W. STEWART, G. W. Stewart, G.W Stewart, G.W. STEWART, G.W. Stewart, GW Stewart, Gordon Stewart, Gordon W Stewart, Gordon W. STEWART, STEWART G, STEWART G. M, STEWART GW, STEWART, G, STEWART, GW, Stewart, G, Stewart, GW, Stewart, Gordon, Stewart, Gw
Observed institutions: St Bartholomew's Hospital, Inserm, University of Cambridge, Royal Cornwall Hospital, Western General Hospital, The Royal Free Hospital, Western Isles Hospital, Northwick Park Hospital, St Helier Hospital, Yale University, Assistance Publique – Hôpitaux de Paris, St Mary's Hospital, Pediatrics and Genetics, Bicêtre Hospital, University College London, University of Bari Aldo Moro, University of Naples Federico II, Ruhr University Bochum
ORCID: 0000-0002-6110-3949
Observed ORCID: 0000-0002-6110-3949
OpenAlex ID: A5024649853
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1
2013 · Immacolata Andolfo, Seth L. Alper, et al. · Blood · 319
Neutral-lipid storage disease: a new disorder of lipid metabolism.
1975 · I Chanarin, A Patel, et al. · BMJ · 280
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Chloride-activated passive potassium transport in human erythrocytes.
1980 · P B Dunham, G W Stewart, et al. · Proceedings of the National Academy of Sciences · 248
Thrombo‐embolic Disease After Splenectomy for Hereditary Stomatocytosis
1996 · Gordon W. Stewart, John A. L. Amess, et al. · British Journal of Haematology · 206
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders
2015 · M.‐J. King, L. Garçon, et al. · International Journal of Laboratory Hematology · 173
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Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1
2005 · Lesley J Bruce, Hannah C Robinson, et al. · Nature Genetics · 165
Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia
2005 · David C. Rees, Achille Iolascon, et al. · British Journal of Haematology · 162
Increased human red cell cation passive permeability below 12 °C
1980 · G. W. Stewart, J. C. Ellory, et al. · Nature · 132
Anion-dependent cation transport in erythrocytes
1982 · J. C. Ellory, P. B. Dunham, et al. · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 123
The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein
2008 · Lesley J. Bruce, Hélène Guizouarn, et al. · Blood · 122
Isolation of cDNA coding for an ubiquitous membrane protein deficient in high Na+, low K+ stomatocytic erythrocytes
1992 · GW Stewart, BE Hepworth-Jones, et al. · Blood · 116
Epithelial Na + channels and stomatin are expressed in rat trigeminal mechanosensory neurons
2000 · B. Fricke, R. Lints, et al. · Cell and Tissue Research · 105
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome
2011 · Joanna F. Flatt, Hélène Guizouarn, et al. · Blood · 94
THE HUMAN ERYTHROCYTE Cl‐DEPENDENT Na‐K COTRANSPORT SYSTEM AS A POSSIBLE MODEL FOR STUDYING THE ACTION OF LOOP DIURETICS
1982 · J.C. ELLORY, G.W. STEWART · British Journal of Pharmacology · 92
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Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy)*
1974 · P. K. THOMAS, D. B. CALNE, et al. · Annals of Human Genetics · 89
Red blood cell membrane defects.
2003 · Achille Iolascon, Silverio Perrotta, et al. · PubMed · 88
FAMILIAL PSEUDOHYPERKALqMIA A New Syndrome
1979 · G STEWART · The Lancet · 84
Stomatin: a putative cation transport regulator in the red cell membrane
1993 · G.W. Stewart, A.C. Argent, et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 81
Familial Pseudohyperkalemia Maps to the Same Locus as Dehydrated Hereditary Stomatocytosis (Hereditary Xerocytosis)
1999 · A. Iolascon, G.W. Stewart, et al. · Blood · 72
Genomewide Search for Dehydrated Hereditary Stomatocytosis (Hereditary Xerocytosis): Mapping of Locus to Chromosome 16 (16q23-qter)
1998 · M. Carella, G. Stewart, et al. · The American Journal of Human Genetics · 71
Hemolytic disease due to membrane ion channel disorders
2004 · Gordon W Stewart · Current Opinion in Hematology · 65
Methyl-beta-cyclodextrin stimulates glucose uptake in Clone 9 cells: a possible role for lipid rafts
2004 · Kay BARNES, Jean C. INGRAM, et al. · Biochemical Journal · 64
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Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24.
2000 · S Grootenboer, P O Schischmanoff, et al. · PubMed · 64
The “stomatin” gene and protein in overhydrated hereditary stomatocytosis
2003 · Britta Fricke, Annette C. Argent, et al. · Blood · 62
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Hereditary dehydrated and overhydrated stomatocytosis: recent advances
1999 · Jean Delaunay, Gordon Stewart, et al. · Current Opinion in Hematology · 57
Works count: 150
Citation count: 4,533
H-index: 36
I10-index: 74
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