Graham Roger Serjeant

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Philosophy

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Graham Roger Serjeant's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Sickle-cell disease (1984) (662)
OUTBREAK OF APLASTIC CRISES IN SICKLE CELL ANAEMIA ASSOCIATED WITH PARVOVIRUS-LIKE AGENT (1981) (375)
Stroke in a cohort of patients with homozygous sickle cell disease. (1992) (373)
The interaction of alpha-thalassemia and homozygous sickle-cell disease. (1982) (282)
Causes of death in sickle-cell disease in Jamaica. (1982) (272)
The natural history of sickle cell disease. (1982) (243)
Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. (1986) (235)
Acute splenic sequestration in homozygous sickle cell disease: natural history and management. (1985) (228)
Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both. (1984) (216)
Priapism and impotence in homozygous sickle cell disease. (1980) (215)
Improved survival in homozygous sickle cell disease: lessons from a cohort study (1995) (188)
Outcome of Pregnancy in Homozygous Sickle Cell Disease (2004) (179)
The Irreversibly Sickled Cell; a Determinant of Haemolysis in Sickle Cell Anaemia (1969) (176)
SICKLE CELL DISEASE IN ORISSA STATE, INDIA (1986) (175)
The painful crisis of homozygous sickle cell disease. A study of the risk factors. (1987) (172)
Incidence and natural history of proliferative sickle cell retinopathy: observations from a cohort study. (2005) (164)
The emerging understanding of sickle cell disease (2001) (160)
The painful crisis of homozygous sickle cell disease: clinical features (1994) (160)
Prevention of pneumococcal infection in children with homozygous sickle cell disease. (1984) (150)
Early deaths in Jamaican children with sickle cell disease. (1978) (149)
Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. (1981) (144)
Two different forms of homozygous sickle cell disease occur in Saudi Arabia (1991) (138)
Human parvovirus infection in homozygous sickle cell disease (1993) (136)
Screening cord bloods for detection of sickle cell disease in Jamaica. (1974) (131)
Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease. (1987) (122)
Oral zinc sulphate in sickle-cell ulcers. (1970) (120)
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2 (1992) (120)
An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age. (1995) (118)
Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns (1986) (117)
Behaviour of untreated proliferative sickle retinopathy. (1980) (114)
MEDROXYPROGESTERONE ACETATE AND HOMOZYGOUS SICKLE-CELL DISEASE (1982) (114)
Ocular findings in homozygous sickle cell anemia in Jamaica. (1972) (112)
Gallstones in sickle cell disease: observations from The Jamaican Cohort study. (2000) (111)
Central retinal artery occlusion without retrobulbar hemorrhage after retrobulbar anesthesia. (1982) (111)
STILBOESTROL AND STUTTERING PRIAPISM IN HOMOZYGOUS SICKLE-CELL DISEASE (1985) (110)
Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. (2002) (106)
Clinical presentation of homozygous sickle cell disease. (1985) (102)
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. (1992) (99)
Albuminuria and renal function in homozygous sickle cell disease: observations from a cohort study. (2007) (96)
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene. (1984) (95)
Prepubertal growth and skeletal maturation in children with sickle cell disease. (1986) (95)
Ocular findings in hemoglobin SC disease in Jamaica. (1972) (94)
Risk factors for proliferative sickle retinopathy. (1990) (91)
Fetal hemoglobin and clinical severity of homozygous sickle cell disease in early childhood. (1981) (90)
Climate and painful crisis of sickle-cell disease in Jamaica. (1976) (89)
Leg ulceration in sickle cell anemia. (1974) (89)
Relatively Benign Sickle-cell Anaemia in 60 Patients Aged Over 30 in the West Indies (1968) (86)
The Development of Haematological Changes in Homozygous Sickle Cell Disease: a Cohort Study from Birth to 6 Years (1981) (85)
Fetal haemoglobin and early manifestations of homozygous sickle cell disease. (1992) (84)
Cerebrovascular complications and parvovirus infection in homozygous sickle cell disease. (2001) (82)
Mortality from sickle cell disease in Africa (2005) (81)
Resting metabolic rate in homozygous sickle cell disease. (1993) (81)
Delayed adolescent growth in homozygous sickle cell disease. (1994) (81)
alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. (1983) (79)
Glomerulonephritis after human parvovirus infection in homozygous sickle-cell disease (1995) (79)
Management of sickle cell disease; lessons from the Jamaican Cohort Study. (1993) (79)
Haematological factors associated with proliferative retinopathy in homozygous sickle cell disease. (1981) (78)
Is there an acute-phase response in steady-state sickle cell disease? (1993) (77)
Bacteraemia in homozygous sickle cell disease in Africa: is pneumococcal prophylaxis justified? (2006) (76)
Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease (1982) (75)
Height and weight reference curves for homozygous sickle cell disease (2000) (73)
The Clinical Features of Sickle‐Cell/β Thalassaemia in Jamaica (1973) (73)
Natural history and determinants of clinical severity of sickle cell disease (1995) (72)
The development and use of an antibody capture radioimmunoassay for specific IgM to a human parvovirus-like agent (1982) (71)
Coagulation Changes during the Steady State in Homozygous Sickle‐Cell Disease in Jamaica (1975) (71)
Septicemia caused by Salmonella infection: an overlooked complication of sickle cell disease. (1997) (71)
Leg ulceration in sickle cell disease: medieval medicine in a modern world. (2005) (69)
Recurrent infections in homozygous sickle cell disease (1999) (69)
Haematological response to parvovirus B19 infection in homozygous sickle-cell disease (2001) (69)
Heights, Weights, and Skeletal Age of Jamaican Adolescents with Sickle Cell Anaemia (1972) (69)
Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (1980) (66)
The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene (1988) (66)
Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem (2011) (65)
One hundred years of sickle cell disease (2010) (65)
The clinical features of sickle cell disease. (1993) (65)
Irreversibly Sickled Cells and Splenomegaly in Sickle‐Cell Anaemia (1970) (65)
Pulse oximetry in a cohort study of sickle cell disease. (1997) (64)
Parvovirus associated aplastic crisis in homozygous sickle cell disease. (1987) (63)
Protein C and protein S in homozygous sickle cell disease: does hepatic dysfunction contribute to low levels? (1997) (63)
Sickle cell disease and age at menarche in Jamaican girls: observations from a cohort study (2001) (63)
Comparison of Sickle Cell‐β° Thalassaemia with Homozygous Sickle Cell Disease (1979) (61)
Patterns of visual loss in untreated sickle cell retinopathy (1988) (60)
New classification of peripheral retinal vascular changes in sickle cell disease. (1994) (60)
A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease? (1985) (60)
Sickle cell retinopathy in Jamaican children: further observations from a cohort study. (1988) (58)
A trial of folate supplementation in children with homozygous sickle cell disease (1983) (58)
Benign clinical course in homozygous sickle cell disease: a search for predictors. (1997) (57)
Geography and the Clinical Picture of Sickle Cell Disease (1989) (57)
A randomized clinical trial of scatter photocoagulation of proliferative sickle cell retinopathy. (1991) (57)
Factors associated with lowered intelligence in homozygous sickle cell disease. (1995) (57)
Observations on the Natural History of Dactylitis in Homozygous Sickle Cell Disease (1981) (56)
Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease. (1985) (55)
Energy intake and resting metabolic rate in preschool Jamaican children with homozygous sickle cell disease. (2002) (55)
Ocular findings of elderly cases of homozygous sickle-cell disease in Jamaica. (1976) (54)
An assessment of lung volumes and gas transfer in sickle-cell anaemia (1971) (53)
Postsplenectomy course in homozygous sickle cell disease. (1999) (52)
Post‐natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental Hb F levels (1982) (52)
ROLE OF SPLENECTOMY IN HOMOZYGOUS SICKLE CELL DISEASE IN CHILDHOOD (1984) (51)
Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease (1983) (50)
Gall stones in Jamaican children with homozygous sickle cell disease. (1989) (50)
The conjunctival sign in sickle cell anemia. A relationship with irreversibly sickled cells. (1972) (49)
Sensori-neural hearing loss in Jamaicans with SS disease. (1973) (49)
Pregnancy in Jamaican women with homozygous sickle cell disease. Fetal and maternal outcome (1986) (48)
Is there an energy deficiency in homozygous sickle cell disease? (1995) (48)
Renal function in patients over 40 with homozygous sickle-cell disease. (1981) (47)
Dopamine D4 receptor variant in Africans, D4valine194glycine, is insensitive to dopamine and clozapine: report of a homozygous individual. (1996) (47)
Chronic leg ulceration in homozygous sickle cell disease: the role of venous incompetence (2002) (46)
Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster. (1984) (46)
The Clinical Features of Haemoglobin SC Disease in Jamaica (1973) (46)
Elderly survivors with homozygous sickle cell disease. (2007) (46)
The New Genetics and Clinical Practice 3rd edn. (1992) (46)
Phenotype/genotype relationships in sickle cell disease: a pilot twin study. (2005) (45)
The Mechanisms of Low Birth Weight in Infants of Mothers With Homozygous Sickle Cell Disease (2007) (45)
Comparison of homozygous sickle cell disease in Northern Greece and Jamaica (1990) (44)
Comparison of Haematological Features of the β0 and β+ Thalassaemia Traits in Jamaican Negroes (1977) (43)
Ocular findings in sickle cell thalassemia in Jamaica. (1972) (43)
Significance of fever in Jamaican patients with homozygous sickle cell disease (2001) (42)
A randomized clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. I. Preliminary results. (1983) (42)
A Comparison of Erythrocyte Characteristics in Sickle Cell Syndromes in Jamaica (1972) (42)
Current concerns in haematology. 1. Is the painful crisis of sickle cell disease a "steal" syndrome? (1990) (42)
NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE (1979) (42)
EARLY SPLENOMEGALY IN HOMOZYGOUS SICKLE-CELL DISEASE: AN INDICATOR OF SUSCEPTIBILITY TO INFECTION (1978) (41)
Fetal haemoglobin in homozygous sickle cell disease. (1975) (41)
Early rise in the "pitted" red cell count as a guide to susceptibility to infection in childhood sickle cell anaemia. (1982) (41)
The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. (1988) (41)
Sickle cell disease in Uganda: a time for action. (2004) (41)
Determinants of nocturnal enuresis in homozygous sickle cell disease. (1990) (40)
Calcification of Bruch's membrane in angioid streaks with homozygous sickle cell disease. (1987) (40)
Nocturnal enuresis in normal Jamaican children. Implications for therapy. (1991) (40)
Sickle cell retinopathy in young children in Jamaica. (1982) (39)
Newborn screening for sickle cell disease in Brazil: the Campinas experience. (2004) (39)
The Sickle-cell and Altitude (1971) (39)
BLOOD PRESSURE IN ADULTS WITH HOMOZYGOUS SICKLE CELL DISEASE (1981) (39)
The haematology of homozygous sickle cell disease after the age of 40 years (1991) (38)
Haematological indices in normal negro children: a Jamaican cohort from birth to five years. (1980) (37)
The geography of sickle cell disease: Opportunities for understanding its diversity. (1994) (37)
Postural vasoconstriction and leg ulceration in homozygous sickle cell disease. (1997) (36)
Psychosocial aspects of sickle cell disease. (1976) (36)
Penile prostheses in the management of impotence in sickle cell disease. (1987) (35)
Factors affecting prepubertal growth in homozygous sickle cell disease. (1996) (35)
Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis. (1998) (35)
The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes (1981) (35)
Invasive pneumococcal disease in homozygous sickle cell disease: Jamaican experience 1973-1997. (2001) (34)
Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth (2018) (34)
Homozygous sickle cell disease in Jamaica. (1973) (32)
Screening for sickle-cell disease in Brazil (2000) (32)
Inhaled nitric oxide for acute chest syndrome in people with sickle cell disease. (2008) (32)
Endoscopic and gastric acid studies in homozygous sickle cell disease and upper abdominal pain. (1989) (32)
Sickle cell disease in India: A perspective (2016) (31)
Bacteriology of sickle cell leg ulcers. (1986) (31)
Sickle cell‐hereditary persistence of fetal haemoglobin and its differentiation from other sickle cell syndromes (1988) (30)
Biliary sludge in sickle cell disease. (1996) (30)
Platelet activation and endothelial cell dysfunction in sickle cell disease is unrelated to reduced antioxidant capacity (2003) (30)
Predictors of renal function progression in adults with homozygous sickle cell disease (2016) (29)
Sexual development and fertility of Jamaican female patients with homozygous sickle cell disease. (1981) (29)
Angioid streaks in Jamaican patients with homozygous sickle cell disease. (1981) (29)
Portal vein thrombosis in a child with homozygous sickle-cell disease. (1993) (29)
Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors. (2017) (29)
Influence of genotype on the natural history of untreated proliferative sickle retinopathy--an angiographic study. (1991) (29)
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes. (1987) (29)
Clinical presentation of sickle cell-hemoglobin C disease. (1986) (29)
Detection of Alpha Thalassaemia in Negro Infants (1980) (29)
Unusual chorioretinal degeneration in sickle cell disease. Possible sequelae of posterior ciliary vessel occlusion. (1973) (29)
Neonatal screening for sickle cell disease in the Eastern Province of Saudi Arabia. (1984) (28)
Topical antibiotics in chronic sickle cell leg ulcers. (1986) (28)
Photocoagulation and diathermy in the treatment of proliferative sickle retinopathy. (1974) (28)
Increased renal reflectivity in sickle cell disease: prevalence and characteristics. (1995) (28)
Nocturnal enuresis in sickle cell haemoglobinopathies. (1990) (28)
The mechanism of low testosterone levels in homozygous sickle-cell disease. (1994) (28)
Sickle cell retinopathy in Jamaican children: a search for prognostic factors. (1983) (28)
Body shape in young children with homozygous sickle cell disease. (1983) (28)
Hb S-β-Thalassemia: Molecular, Hematological and Clinical Comparisons (2011) (27)
The Determinants of Irreversibly Sickled Cells in Homozygous Sickle Cell Disease (1978) (26)
Non-gouty arthritis in sickle cell disease: report of 37 consecutive cases. (1984) (26)
Comparison of sickle cell-beta0 thalassaemia with homozygous sickle cell disease. (1979) (26)
Sickle Cell and Altitude (1972) (26)
A Randomized Clinical Trial of Feeder Vessel Photocoagulation of Proliferative Sickle Cell Retinonathy: II. Update and Analysis of Risk Factors (1984) (26)
HURRICANE GILBERT ANAEMIA (1989) (26)
Recommendations for neonatal screening for haemoglobinopathies (1988) (25)
Choroidal neovascularisation induced by photocoagulation in sickle cell disease. (1981) (25)
An update on techniques of photocoagulation treatment of proliferative sickle cell retinopathy (1991) (25)
Clinical features of pulmonary lesions in sickle-cell anaemia. (1970) (25)
A comparison of sickle cell syndromes in Northern Greece (1991) (25)
Cholelithiasis in Jamaican patients with homozygous sickle cell disease (1977) (25)
Peak expiratory flow rate and the acute chest syndrome in homozygous sickle cell disease. (1991) (25)
The radiological features of avascular necrosis of the femoral head in homozygous sickle cell disease. (1981) (25)
Social Effects of Leg Ulceration in Sickle Cell Anemia (1977) (24)
Macular vasculature, visual acuity, and irreversibly sickled cells in homozygous sickle cell disease. (1982) (24)
Haematological factors associated with proliferative retinopathy in sickle cell-haemoglobin C disease. (1981) (24)
INADEQUACY OF Hb BART'S AS AN INDICATOR OF α THALASSAEMIA (1982) (24)
Urea kinetics in adults with homozygous sickle cell disease. (1988) (23)
The internal auditory canel and sensori-neural hearing loss in homozygous sickle cell disease (1975) (23)
Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work? (2017) (23)
Testosterone deficiency and extreme retardation of puberty in homozygous sickle-cell disease. (1995) (23)
Measurement of glomerular filtration rate in homozygous sickle cell disease: a comparison of 51Cr-EDTA clearance, creatinine clearance, serum creatinine and beta 2 microglobulin. (1990) (23)
Systemic lupus erythematosus and sickle-cell anaemia. (1976) (23)
HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HÆMOGLOBIN AND HOMOZYGOUS SICKLE-CELL DISEASE (1977) (22)
Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease. (1995) (22)
Normal pregnancy in a patient with multiple myeloma and sickle cell anaemia. (1971) (22)
Neural tube defects in hurricane aftermath (1991) (22)
Treatment and prevention of sickle-cell crisis. (1971) (22)
Renal length in sickle cell disease: observations from a cohort study. (1996) (22)
Is the painful crisis of sickle-cell disease due to sickling? (1991) (22)
Pneumococcal and other infections in children with sickle-cell hemoglobin C (SC) disease. (1982) (22)
Adolescent blood pressure in a cohort study of sickle cell disease. (1993) (22)
Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers. (2000) (22)
Heights and weights of Jamaican children with homozygous sickle cell disease. (1977) (22)
The effect of splenectomy for hypersplenism on whole body protein turnover, resting metabolic rate and growth in sickle cell disease. (1996) (21)
Focal echogenic lesions in the spleen in sickle cell disease. (1993) (21)
Salmon-patch hemorrhages after central retinal artery occlusion in sickle cell disease. (1981) (21)
Blood rheology and proliferative retinopathy in homozygous sickle cell disease. (1986) (21)
The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem (2015) (20)
The in vivo sickle phenomenon: a reappraisal. (1973) (20)
Photocoagulation in proliferative sickle retinopathy: results of a 5-year study. (1980) (20)
Prevalence of antibodies to hepatitis C virus and other markers in Jamaica. (1995) (20)
Foetal haemoglobin in homozygous sickle cell disease: a study of patients with low HBF levels. (2001) (20)
The case for dedicated sickle cell centres (2006) (20)
Iris atrophy in sickle cell disease. (1986) (20)
CHRONIC TRANSFUSION PROGRAMMES IN SICKLE CELL DISEASE: PROBLEM OR PANACEA? (1997) (20)
The Development of Haemoglobin A2 in Normal Negro Infants and in Sickle Cell Disease (1978) (20)
Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions. (1991) (19)
MAPPING OF ANTIGENIC SITES ON HUMAN HAEMOGLOBIN BY MEANS OF MONOCLONAL ANTIBODIES AND HAEMOGLOBIN VARIANTS (1981) (19)
Blood transfusion in sickle cell disease: a cautionary tale (2003) (19)
Observations on the epidemiology of sickle cell disease. (1981) (19)
Cardio-pulmonary responses and gas exchange during exercise in adults with homozygous sickle-cell disease (sickle-cell anaemia). (1973) (19)
Propionyl-L-carnitine in chronic leg ulcers of homozygous sickle cell disease: a pilot study. (1997) (19)
Sickle Cell Disease in Central India: A Potentially Severe Syndrome (2016) (19)
Haematological risk factors for pregnancy outcome in Jamaican women with homozygous sickle cell disease (1994) (19)
Plasma haemoglobin and complement activation in sickle cell disease. (1981) (19)
Pneumonia in young children with homozygous sickle cell disease: risk and clinical features (1985) (18)
Airline travel in sickle-cell disease (1998) (18)
Urographic findings in homozygous sickle cell disease. (1978) (18)
Isoxsuprine hydrochloride in the therapy of sickle cell leg ulceration. (1977) (18)
Glomerular function and hyperuricaemia in sickle cell disease. (1984) (17)
Retinal and choroidal neovascularization in sickle cell disease. (1980) (17)
Delayed menarche in homozygous sickle cell disease. (1986) (17)
Antiphospholipid antibodies in homozygous sickle cell disease. (1992) (17)
Serum urate concentrations in homozygous sickle cell disease (1981) (17)
Outcome of iatrogenic choroidal neovascularisation in sickle cell disease. (1990) (16)
A simple micromethod for the measurement of fetal haemoglobin. (1975) (16)
Screening for the sickle cell gene in Gujarat, India: a village-based model (2012) (16)
Radiological changes associated with leg ulcers in the tropics. (1972) (16)
RBC transfusion in sickle cell anemia (HbSS):experience from the Jamaican Cohort Study (2001) (16)
Delayed skeletal maturation in sickle cell anemia in Jamaica. (1973) (16)
Blood rheology and proliferative retinopathy in sickle cell-haemoglobin C disease. (1984) (15)
Body Habitus of Jamaican Adults with Sickle Cell Anemia (1972) (15)
Genetical, Functional, and Physical Studies of Hemoglobins (1972) (15)
The epidemiology of Sickle Cell Disorder: A challenge for Africa (2005) (15)
Dominant influence of gamma-globin promoter polymorphisms on fetal haemoglobin expression in sickle cell disease. (2004) (15)
alpha thalassemia in black populations. (1980) (15)
Treatment of sickle cell disease in early childhood in Jamaica. (1985) (15)
Ocular findings in children with sickle cell haemoglobin C disease in Jamaica. (1974) (14)
Leg ulcers in sickle-cell anaemia. (1970) (14)
Interpretation of lung function tests in the sickle-cell haemoglobinopathies. (1978) (14)
Cardiac performance in children with homozygous sickle cell disease. (1987) (14)
Resolution of chronic hepatic sequestration in a patient with homozygous sickle cell disease receiving hydroxyurea. (2003) (14)
Epiretinal membranes in sickle cell disease. (1987) (14)
A survey of parasites in primary school children in Dominica, West Indies. (1981) (14)
Influence of alpha thalassaemia on the retinopathy of homozygous sickle cell disease. (1993) (14)
Haemoglobin spanish town α27 GLU – VAL (B8) (1976) (14)
A randomized controlled trial of solcoseryl and duoderm in chronic sickle-cell ulcers. (1993) (14)
ACUTE SPLENIC SEQUESTRATION IN JAMAICAN ADULTS WITH HOMOZYGOUS SICKLE CELL DISEASE: A ROLE OF ALPHA THALASSAEMIA (1991) (14)
Laser photocoagulation for proliferative retinopathy in sickle haemoglobin C disease (1993) (14)
Interaction of the ααα globin gene haplotype and sickle haemoglobin (1984) (14)
Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia. (1976) (13)
Erythropoietin and renal function in sickle-cell disease. (1982) (13)
The Effect of Splenectomy on Whole Body Protein Turnover in Homozygous Sickle Cell Disease (1991) (13)
Systemic Salmonella infections in sickle cell anaemia. (1989) (13)
Ulcerative colitis in sickle cell disease. (1987) (13)
General anesthesia in sickle cell disease. (1980) (13)
Patterns of low‐affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease (2002) (13)
Mass Spectral Analysis of Asymmetric Hemoglobin Hybrids: Demonstration of Hb FS (α2γβS) in Sickle Cell Disease (2001) (13)
Red Cell Size and the Clinical and Haematological Features of Homozygous Sickle Cell Disease (1981) (12)
The Politics of Sickle Cell and Thalassaemia (2001) (12)
Fetal growth in women with homozygous sickle cell disease: an observational study. (2013) (12)
Recurrent visual loss in homozygous sickle cell disease. (1985) (12)
Elevated IL-1α and CXCL10 Serum Levels Occur in Patients with Homozygous Sickle Cell Disease and a History of Acute Splenic Sequestration (2012) (12)
Recurrent infections in sickle cell disease: haematological and immune studies. (1985) (12)
Alpha thalassaemia and the haematology of normal Jamaican children. (1985) (12)
Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History. (2015) (12)
A whole blood solubility and centrifugation test for sickle cell hemoglobin: a clinical trial. (1972) (12)
Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes. (2012) (12)
Ocular findings in Saudi Arabian patients with sickle cell disease. (1995) (11)
Recent advances in the treatment of proliferative sickle cell retinopathy (1992) (11)
Haemoglobin SC disease in Jamaica. (1973) (11)
Duodenal ulceration in sickle cell anaemia. (1973) (11)
Sickle haemoglobin and pregnancy. (1983) (10)
Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects (1998) (10)
Abnormal thyroid hormone and thyrotropin levels in homozygous sickle cell disease. (1989) (10)
Corynebacterium diphtheriae in sickle cell leg ulcers in Jamaica. (1985) (10)
Haemoglobin Variant Screening in Jamaica: Meeting Student's Request (2016) (10)
The clinical features in adults sickle cell anaemia in Jamaica. (1970) (10)
Neodymium-YAG laser vitreolysis in sickle cell retinopathy. (1987) (10)
Sickle-cell and altitude. (1972) (10)
Pregnancy in sickle cell-haemoglobin C (SC) disease. A retrospective study of birth size and maternal weight gain. (2016) (10)
Sickle cell-hemoglobin D Iran: benign sickle cell syndrome. (1982) (10)
Abnormal venous function in patients with homozygous sickle cell (SS) disease and chronic leg ulcers (2000) (9)
The progression of sickle cell eye disease in Jamaica (1975) (9)
The Role of Preventive Medicine in Sickle Cell Disease (1996) (9)
Treatment of subretinal neovascularization associated with angioid streaks in sickle cell retinopathy. Case report. (1987) (9)
Sickle cell trait and leg ulceration. (1970) (9)
Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene cluster. (1987) (9)
A randomized clinical trial of feeder vessel photocoagulation of proliferative sickle cell retinopathy. II. Update and analysis of risk factors. (1984) (9)
PAINFUL CRISES IN SICKLE CELL DISEASE AFTER FLUORESCEIN ANGIOGRAPHY (1985) (9)
Splenic opacification in homozygous sickle cell disease. (1981) (9)
Determinants of Haemoglobin Level in Sickle Cell‐Haemoglobin C Disease (1979) (9)
Evolving locally appropriate models of care for Indian sickle cell disease (2016) (9)
Retinal changes in sickle cell/hereditary persistence of fetal haemoglobin syndrome. (1983) (8)
Body habirus of Jamaican adults with sickle cell anemia. (1972) (8)
General anaesthesia in sickle-cell disease. (1979) (8)
Painful crises in sickle-cell disease (1996) (8)
Alpha thalassaemia and the macular vasculature in homozygous sickle cell disease. (1983) (8)
Daily variability in resting levels of cardiovascular variables in normal subjects and those with homozygous sickle cell disease (1995) (8)
Pulmonary artery pressure and the acute chest syndrome in homozygous sickle cell disease. (1993) (7)
Management of sickle cell disease: challenges and risks of transfusion (2016) (7)
Comparison of haematological features of the beta0 and beta+ thalassaemia traits in Jamaican Negroes. (1977) (7)
Growth curves for normal Jamaican neonates. (2006) (7)
Sickle cell anaemia in Nigeria: a comparison between Benin and Lagos. (1994) (7)
Screening for the beta-thalassaemia trait: hazards among populations of West African Ancestry (2011) (7)
Heights and weights of West Indian children with the sickle cell trait. (1978) (7)
Alpha thalassemia and homozygous sickle cell disease. (1981) (7)
Blood transfusion in sickle cell disease (1985) (7)
The dilemma of defining clinical severity in homozygous sickle cell disease. (2004) (7)
Mononuclear cells in sickle cell disease: subpopulations and in vitro response to mitogens. (1984) (7)
Acceptability of antenatal diagnosis for sickle-cell disease among Jamaican mothers and female patients. (1988) (7)
The Spleen in Sickle Cell Disease (2002) (7)
Retained Placenta in Homozygous Sickle Cell Disease (2009) (6)
The red cell distribution width in sickle cell disease--is it of clinical value? (2008) (6)
World Sickle Cell Day: Lessons for India (2017) (6)
Biliary surgery in patients with sickle-cell anaemia. (1992) (6)
The metacarpal index in homozygous sickle-cell disease. (1988) (6)
Pattern of pregnancy weight gain in homozygous sickle cell disease and effect on birth size. (2011) (6)
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica (2016) (6)
Five-year follow-up of Jamaican adults with sickle cell anaemia. (1975) (6)
Transfusion in Sickle Cell Disease: Experience from a Gujarat Centre (2014) (6)
Awareness of sickle cell disease among high school students in Kingston, Jamaica. (1976) (6)
Sickle cell beta thalassaemia in Jamaica. (1973) (6)
Gall stones in homozygous sickle cell disease. (1989) (6)
Homozygous sickle cell disease in Central India & Jamaica: A comparison of newborn cohorts (2020) (6)
HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome. (1998) (5)
Complement and immunoglobulin levels in early childhood in homozygous sickle cell disease. (1986) (5)
Sickle Cell Disease in Saudi Arabia: The Asian Haplotype (2004) (5)
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene. (1979) (5)
Serum immunoglobulin levels in children with homozygous sickle cell disease. (1982) (5)
Sickle haemoglobin and haemoglobin Stanleyville II: possible confusion with sickle cell-haemoglobin C disease. (2005) (5)
Haemophilus influenzae osteomyelitis complicating dactylitis in homozygous sickle cell disease (1990) (5)
Clinical judgment and sickle cell disease. (1993) (5)
Newborn Screening for Sickle Cell Disease in India: The Need for Defining Optimal Clinical Care (2014) (5)
Ocular findings in sickle cell-haemoglobin O Arab disease. (1979) (5)
Microchromatographic quantitation of hemoglobin A levels in phenotypes of sickle cell-beta(+) thalassemia. (1997) (5)
Comparison of sickle cell beta o-thalassemia and sickle cell beta +-thalassemia in black populations. (1982) (5)
Avascular necrosis of the femoral head in Saudi Arabians with homozygous sickle cell disease - risk factors. (1995) (5)
Pregnancy outcome in homozygous sickle cell disease: observations from the Jamaican Birth Cohort (2021) (5)
The Bone Pain Crisis of Sickle Cell Disease and Malaria: Observations from Gujarat, India (2017) (5)
Testing for the random occurrence of sickle cell disease in a study of 100,000 Jamaican newborns. (1990) (5)
Jamaica, the Caribbean and sickle cell disease. (2012) (5)
The interaction of alpha thalassaemia with SS disease. (1978) (4)
Cord blood screening for sickle hemoglobin: evidence against a female preponderance of hemoglobin S. (1981) (4)
Use of blood specimens collected on filter paper in screening for abnormal hemoglobins. (1976) (4)
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin (2017) (4)
Skeletal development of Jamaican children with homozygous sickle cell disease. (1978) (4)
Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease. (1982) (4)
Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples (2016) (4)
Oral zinc sulphate treatment of chronic non-sickle cell ulcers in Jamaica. (1975) (4)
Shortening of the digits in sickle cell anaemia: a sequela of the hand-foot syndrome. (1971) (3)
Newborn Screening for Sickle Cell Disease: Jamaican Experience. (2015) (3)
Peripheral retinal vasculature in normal Jamaican children. (1994) (3)
Comparison of clinical, hematological and molecular findings of Jamaican and Sicilian patients with sickle cell disease. (1990) (3)
Negro alpha-thalassaemia: genetic studies in homozygous sickle cell disease. (1980) (3)
Sickle haemoglobin comes of age. (2014) (3)
Sickle cell-hemoglobin Caribbean--a benign syndrome. (1982) (3)
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell disease. (2001) (3)
The Challenge of Sickle Cell Disease in Saudi Arabia (1990) (3)
Psychological distress among younger siblings of patients with homozygous sickle cell disease in the Jamaican cohort study. (2000) (3)
The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia. (1988) (3)
Treatment of iatrogenic choriovitreal neovascularisation in sickle cell disease. (1991) (3)
Delayed diagnosis of homozygous sickle cell disease in Jamaica. (1992) (3)
Haemoglobin Spanish Town alpha27 Glu replaced by Val (B8). (1976) (3)
Iron Deficiency among Jamaican Adolescents. (2015) (3)
Penicillin-resistant Streptococcus pneumoniae in a Jamaican patient with homozygous sickle-cell disease. (1996) (3)
Intravenous oxpentifylline and the painful crisis of sickle cell disease (2016) (2)
The red cell distribution width - is it of clinical value? (1991) (2)
Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobin. (1984) (2)
Diabetic retinopathy and visual loss in a Jamaican population. (1987) (2)
Fetal hemoglobin and the irreversibly sickled cell in sickle cell disease (1974) (2)
Gamma chain variants in Jamaican newborns. (1976) (2)
What's new in sickle cell disease? (1988) (2)
Sickle Cell Disease: Thoughts for India From the Jamaican Cohort Study (2021) (2)
Skinfold thickness and nutritional status in young Jamaican children. (1983) (2)
4 The clinical features of sickle cell disease (1993) (2)
Sickle Cell Disease in Central India: High Prevalence of Sickle/Beta Thalassemia and Severe Dsiease Phenotype (2015) (2)
Empyema of gallbladder in a child with homozygous sickle-cell disease. (1990) (2)
β-Thalassemia Mutations in Jamaica: Geographic Variation in Small Communities (2018) (1)
A Note on the Prevalence of Impaternity in Jamaica (2017) (1)
Beta-chain variants in Jamaican newborns. (1978) (1)
Counselling mothers of babies with the sickle cell trait: to be or not to be. (2011) (1)
Letter: Fetal hemoglobin and the irreversibly sickled cell in sickle cell disease. (1974) (1)
Odisha Revisited: A Personal Account (2021) (1)
The sickle cell trait and leg ulceration. (1972) (1)
Patterns of attendance at Jamaican sickle cell clinics 1952 to 1981. (1984) (1)
The development of cardiomegaly in homozygous sickle cell disease. (1985) (1)
Haemoglobin F Victoria Jubilee (alpha 2 A gamma 2 80 Asp-Try). (1975) (1)
A second example of haemoglobin F Texas I (α2Aγ25Glu→Lys) in a Jamaican infant (1977) (1)
Perinatal factors in students admitted to the University of the West Indies data from the Jamaican Perinatal Study. (2010) (1)
Risk Factors for Proliferative Sickle Retinopathy (1990) (1)
Pregnancy in Jamaican women with homozygous sickle cell disease. Fetal and maternal outcome (1986) (1)
Sickle-cell anaemia before Herrick. (1972) (1)
Prevention of sickle cell disease: observations on females with the sickle cell trait from the Manchester project, Jamaica (2015) (1)
Determinants ofnocturnal enuresis inhomozygous sickle cell disease (1990) (0)
disease . retinopathy of homozygous sickle cell Influence of alpha thalassaemia on the (2003) (0)
British support for Caribbean research (1991) (0)
21.10.6 Sickle-cell disease and the kidney (2010) (0)
Screening for the sickle cell gene in Gujarat, India: a village-based model (2012) (0)
Renal function in patients over 40 with homozygous sickle-cell disease (1981) (0)
Voluntary premarital screening to prevent sickle cell disease in Jamaica: does it work? (2017) (0)
Sickle cell screening and its value in Jamaica (1989) (0)
Gall-bladder sludge in sickle cell disease: A precursor of gall-stones? (1993) (0)
homozygous sickle cell disease . with proliferative retinopathy in Haematological factors associated (0)
Adolescent growth in homozygous sickle-cell disease is delayed but follows a normal pattern - abstract (1993) (0)
Haemoglobin caribbean beta91 (F7) Leu replaced by Arg: a mildly haemoglobin with a low oxygen affinity. (1976) (0)
Jamaican children . Peripheral retinal vasculature in normal (0)
Early splenomegaly and septicaemia in homozygous sickle cell disease: A birth cohort study (2022) (0)
Retinal changes insickle cell/hereditary persistence offetal haemoglobin syndrome (1983) (0)
Iris atrophy in sickle cell disease Table 1 Crude prevalence rates of ' spontaneous ' iris atrophy Patients Eyes (0)
Book Review: The Hemoglobinopathies (1950) (0)
Author Index for Volume 69 (1998) (0)
Uncommon Differential Diagnosis to Homozygous Sickle Cell Disease (2016) (0)
Heart size and chest shape in homozygous sickle cell disease. (1983) (0)
Leg ulcerationinsicklecell anemia (1974) (0)
The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report (2019) (0)
Neonatal screening for sickle hemoglobin. (1979) (0)
with homozygous sickle cell disease . Angioid streaks in Jamaican patients (2004) (0)
Megaloblastic change in sickle cell disease obscured by genetically determined microcytosis. (1986) (0)
Sickle cell disease continued. (1985) (0)
Jamaica and Research in Sickle Cell Disease (2017) (0)
Ventilatory response to carbon dioxide in sickle-cell disease. (1977) (0)
Alphathalassaemia andthemacular vasculature inhomozygous sickle cell disease (1983) (0)
in Screening for Abnormal Hemoglobins (1976) (0)
Effect of thermal stimuli on peripheral blood flow in homozygous sickle cell disease: A preliminary study (1996) (0)
B19 Virus Infection and the Aplastic Crisis (2018) (0)
’ s response to reviews Title : The additional genetic diagnosis of homozygous Sickle Cell Disease in a patient with Waardenburg-Shah Syndrome : A Case Report (2018) (0)
children in Jamaica . Sickle cell retinopathy in young (0)
Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programme (2022) (0)
Erectile dysfunction with chemotherapy (2000) (0)
Epiretinal membranes in sickle cell disease Fig (0)
Ocular findings inelderly casesofhomozygous sickle-cell disease inJamaica (1976) (0)
Reply to R Apatu (1993) (0)
Gamma Chain Variants in Jamaican Newborns (1976) (0)
homozygous sickle cell disease . and irreversibly sickled cells in Macular vasculature , visual acuity , (0)
disease . syndrome in homozygous sickle cell Peak expiratory flow rate and the acute chest (2007) (0)
disease in Jamaica . sickle cell haemoglobin C Ocular findings in children with (2005) (0)
Is hemoglobin C relevant to the genesis of proliferans retinopathy? (1976) (0)
TheSickle-cell andAltitude (1971) (0)
Immunoglobulin receptor polymorphisms in stroke and sickle cell disease (2000) (0)
Epiretinal membranes insickle cell disease (1987) (0)
Iris atrophy insickle cell disease (1986) (0)
Sickle cell diseasecontinued. (1985) (0)
Anassessment oflungvolumes andgastransfer in sickle-cell anaemia (1971) (0)
GallstonesinJamaican children withhomozygous sickle cell disease (1989) (0)
The Chhattisgarh state screening programme for the sickle cell gene: a cost-effective approach to a public health problem (2015) (0)
Peakexpiratory flowrateandtheacutechest syndrome inhomozygous sickle cell disease (2011) (0)
Hb F Kingston (G gamma 55 [D6] Met leads to Arg). (1982) (0)
Nocturnal enuresis insickle cell haemoglobinopathies (1990) (0)
Newborn screening for sickle cell disease in Jamaica: logistics and experience with umbilical cord samples (2016) (0)
Heights, Weights, andSkeletal AgeofJamaican Adolescents withSickle Cell Anaemia (1972) (0)
Energy intake and resting metabolic rate in preschool Jamaican children with homozygous sickle cell disease 1 , 2 (0)
Chapter 116 – Infections in sickle cell disease (2010) (0)
Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS (2022) (0)
RESTING METABOLIC RATE IN SICKLE CELL DISEASE. AUTHOR'S REPLY (1993) (0)
and Clozapine: Report of a Homozygous Individual D4Valinel94Glycine, Is Insensitive to Dopamine (1996) (0)
A second example of haemoglobin F Texas 1 (alpha2Agamma25Glu replaced by Lys) in a Jamaican infant. (1977) (0)
Anthropometric measurements of school children in Dominica, West Indies. (1981) (0)
Body habitus of Jamaican adults with sickle cell--haemoglobin C (SC) disease. (1979) (0)
The haematology of Jamaicans: red cell indices in HbAA, HbAS, HbAC, and HbA-HPFH genotypes (2022) (0)
Antiphospholipid antibodies inhomozygous sickle cell disease (1992) (0)

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