Published in Arch Biochem Biophys on November 01, 1953
Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies. Br Med J (1968) 2.87
Observations on some fast haemoglobins: K, J, N, and Bart's. Br Med J (1958) 2.68
A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anaemia. J Clin Pathol (1970) 2.57
Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia. J Clin Invest (1968) 2.06
A haemoglobinopathy involving haemoglobin H and a new (Q) haemoglobin. Br Med J (1958) 2.05
Hemoglobinopathies: a longitudinal study over four decades. Dtsch Arztebl Int (2010) 2.00
Haemoglobin K in an East Indian and his family. Br Med J (1957) 1.45
Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease. J Clin Invest (1967) 1.41
Hemoglobin Porto Alegre, a possible polymer of normal hemoglobin in a Caucasian Brazilian family. Am J Hum Genet (1963) 1.20
Date on the occurrence of hemoglobin C and other abnormal hemoglobins in some African populations. Am J Hum Genet (1956) 1.17
Haemoglobin L; a new haemoglobin found in a Punjabi Hindu. Br Med J (1957) 1.10
The frequency of elevations in the A and fetal hemoglobin fractions in the natives of Liberia and adjacent regions, with data on haptoglobin and transferrin types. Am J Hum Genet (1961) 1.06
Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem. J Med Genet (1968) 1.03
LINKAGE OF THE BETA-CHAIN AND DELTA-CHAIN STRUCTURAL GENES OF HUMAN HEMOGLOBINS. Am J Hum Genet (1963) 1.02
A second and a third abnormal haemoglobin in Norfolk. Haemoglobin G Norfolk and haemoglobin D Norfolk. Br Med J (1963) 0.99
A study of the survival rate of cases of sickle-cell anaemia. Br Med J (1957) 0.99
Effect of cetiedil on erythrocyte sickling: new type of antisickling agent that may affect erythrocyte membranes. Proc Natl Acad Sci U S A (1980) 0.96
Hemoglobin Philly (beta 35 tyrosine phenylalanine): studies in the molecular pathology of hemoglobin. J Clin Invest (1969) 0.95
Intermolecular interactions, nucleation, and thermodynamics of crystallization of hemoglobin C. Biophys J (2002) 0.95
Stanleyville I and II: two new variants of adult haemoglobin. Br Med J (1959) 0.94
Chemical modifications that inhibit gelation of sickle hemoglobin. Proc Natl Acad Sci U S A (1974) 0.94
A survey for haemoglobins C and D in Uganda. Br Med J (1955) 0.94
Abnormal hemoglobins in a Brazilian Negro population. Am J Hum Genet (1962) 0.91
Aggregation of normal and sickle hemoglobin in high concentration phosphate buffer. Biophys J (2004) 0.87
Solubility test for Hb S. Br Med J (1971) 0.87
Prevalence of abnormal haemoglobins in pulmonary tuberculosis in three different ethnic groups. J Med Genet (1970) 0.86
A rapid paper-based test for quantifying sickle hemoglobin in blood samples from patients with sickle cell disease. Am J Hematol (2015) 0.84
In vitro effects of anthocyanin extracts from Justicia secunda Vahl on the solubility of haemoglobin S and membrane stability of sickle erythrocytes. Blood Transfus (2010) 0.84
Intra-erythrocytic haemoglobin crystals. J Clin Pathol (1957) 0.84
Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S. J Med Genet (1971) 0.83
Validation of a Low-Cost Paper-Based Screening Test for Sickle Cell Anemia. PLoS One (2016) 0.82
Haemoglobin D Punjab (D Los Angeles). J Med Genet (1974) 0.81
Automated mass screening for hemoglobin S: a rational method. Health Serv Rep (1973) 0.81
A NEW HAEMOGLOBIN IN A THAI FAMILY. A CASE OF HAEMOGLOBIN SIRIRAJ-BETA THALASSAEMIA. Br Med J (1965) 0.80
Age trends in the prevalence of the sickle cell trait. Health Serv Rep (1973) 0.78
Complete suppression of haemoglobin A synthesis in haemoglobin D Los Angeles--beta thalassaemia. J Clin Pathol (1968) 0.78
Detecting sickle haemoglobin. Br Med J (1972) 0.77
Haemoglobin D Ouled Rabah (beta 19[Bl] asn leads to lys) in a Tuareg tribe of the Southern Sahara. J Med Genet (1977) 0.77
High incidence of haemoglobin G Accra in a rural district in Jamaica. J Med Genet (1967) 0.76
Haemoglobin J in the French Canadian. J Med Genet (1970) 0.75
HOMOZYGOUS SICKLE-CELL ANAEMIA ARISING FROM TWO DIFFERENT HAEMOGLOBINS S. INTERACTION OF HAEMOGLOBINS S AND STANLEYVILLE-II. Br Med J (1964) 0.75
An improved solubility test for haemoglobin S. J Clin Pathol (1972) 0.75
The solubilization of deoxyhemoglobin S. Proc Natl Acad Sci U S A (1967) 0.75
Haemoglobin K Woolwich: a study of the family of a homozygote. J Med Genet (1980) 0.75
Genetic variants of hemoglobin and other blood proteins in the San Francisco Bay area. Calif Med (1970) 0.75
Hemoglobin C trait in Saskatchewan. Can Med Assoc J (1966) 0.75
Hemoglobin Okaloosa (beta 48 (CD7) leucine leads to arginine). An unstable variant with low oxygen affinity. J Clin Invest (1973) 0.75
Detecting sickle haemoglobin. Br Med J (1972) 0.75
Inherited anaemias in the Greek community of Cape Town. J Med Genet (1979) 0.75
The significance of the variable solvent and specific property solubility tests in protein chemistry. J Gen Physiol (1962) 0.75
Sickle cell anemia a molecular disease. Science (1949) 21.90
A new inherited abnormality of human hemoglobin. Proc Natl Acad Sci U S A (1950) 3.90
Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis. Am J Hum Genet (1953) 3.42
Human hemoglobin. Science (1953) 1.92
Ratio of sickle-cell anemia hemoglobin to normal hemoglobin in sicklemics. J Biol Chem (1951) 1.90
Hemoglobin J. Science (1956) 1.69
Hyposthenuria in sickle cell anemia: a reversible renal defect. J Clin Invest (1956) 1.53
Properties and inheritance of haemoglobin by asymmetric recombination. Nature (1959) 1.27
Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait. J Clin Invest (1951) 1.24
Chronic hemolytic anemia associated with thalassemia and sickling traits. Blood (1952) 1.23
Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin. Blood (1953) 1.20
Formation of normal and doubly abnormal haemoglobins by recombination of haemoglobin I with S and C. Nature (1959) 1.15
The abnormal human hemoglobins. Medicine (Baltimore) (1956) 1.14
Clinical states associated with alterations of the hemoglobin molecule; the Minot lecture. AMA Arch Intern Med (1955) 1.11
Sickle cell anemia, a molecular disease. Science (1949) 1.03
Electrophoretic separation of intermediate compounds in two reactions of ferrihemoglobin. Biochim Biophys Acta (1958) 1.02
The hemoglobins. Annu Rev Biochem (1956) 1.02
Genetic and biochemical studies of intermediate types of Cooley's anaemia. Br J Haematol (1955) 0.87
Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D. Blood (1955) 0.86
Hemolytic anemia presumably due to coexistence of the genes for thalassemia and sickling. Trans Assoc Am Physicians (1952) 0.84
Identification of the recombinant products of canine and human haemoglobins. Nature (1960) 0.83
Zone electrophoresis of abnormal hemoglobins; separation on paper of hemoglobins associated with sickle cell disease. Acta Haematol (1954) 0.82
A rapid diagnostic test for sickle cell anemia. Blood (1949) 0.81
CHEMICAL MODIFICATION OF ARGININE WITH 1,2-CYCLOHEXANEDIONE. J Biol Chem (1965) 0.80
DISSOCIATION AND ASSOCIATION OF HEMOGLOBIN SUBUNITS. Brookhaven Symp Biol (1964) 0.76
Thalassaemia and the abnormal human haemoglobins. Nature (1961) 0.75
Asymmetrical recombination of alkali-dissociated haemoglobin mixtures. Nature (1960) 0.75
BLOCKING OF TRYPTIC CLEAVAGE OF ARGINYL BONDS BY THE CHEMICAL MODIFICATION OF THE GUANIDO GROUP WITH BENZIL. Biochem Biophys Res Commun (1963) 0.75
A system of nomenclature for the varieties of human hemoglobin. Science (1953) 0.75
Interpretation of electrophoretic, solubility and denaturation data in the study of hemoglobin differences. Fed Proc (1957) 0.75
Human hemoglobin. Science (1952) 0.75
Specific recombination of the subunits of hemoglobin. Ann N Y Acad Sci (1960) 0.75