David Weatherall

Q: What Schools Are Affiliated With David Weatherall

David Weatherall is affiliated with the following schools: University of Liverpool, University of Oxford

Why Is David Weatherall Influential?

According to Wikipedia, Sir David John Weatherall, was a British physician and researcher in molecular genetics, haematology, pathology and clinical medicine. Early life and education David Weatherall was born in Liverpool. He was educated at Calday Grange Grammar School and then attended Medical School at the University of Liverpool where he served as Treasurer of the Liverpool Medical Students Society in 1954.

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David Weatherall'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

Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010 (2012) (8152)
Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: a systematic analysis for the Global Burden of Disease Study 2010 (2012) (7185)
A systematic analysis of global anemia burden from 1990 to 2010. (2014) (1464)
Abnormal human haemoglobins (1966) (1339)
Inherited haemoglobin disorders: an increasing global health problem. (2001) (1184)
Common values in assessing health outcomes from disease and injury: disability weights measurement study for the Global Burden of Disease Study 2010 (2012) (1159)
Oxford textbook of medicine (1996) (1121)
Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates (2013) (817)
The thalassaemia syndromes (1965) (808)
Global Burden of Sickle Cell Anaemia in Children under Five, 2010–2050: Modelling Based on Demographics, Excess Mortality, and Interventions (2013) (719)
The inherited diseases of hemoglobin are an emerging global health burden. (2010) (710)
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16 (1985) (702)
Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias (2001) (637)
Iron and infection. (1988) (601)
The thalassemia syndromes. (2016) (533)
A review of the molecular genetics of the human alpha-globin gene cluster. (1989) (525)
Sickle cell disease (2018) (475)
K562 human leukaemic cells synthesise embryonic haemoglobin in response to haemin (1979) (468)
Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis (2010) (461)
A highly conserved amino-acid sequence in thrombospondin, properdin and in proteins from sporozoites and blood stages of a human malaria parasite (1988) (379)
The α-thalassemias. (2014) (341)
High frequencies of α-thalassaemia are the result of natural selection by malaria (1986) (327)
Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK (1990) (316)
World distribution, population genetics, and health burden of the hemoglobinopathies. (2012) (316)
alpha+-Thalassemia protects children against disease caused by other infections as well as malaria. (1997) (307)
DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees. (1986) (298)
The Anaemia of P. falciparum Malaria (1980) (297)
The global distribution of the Duffy blood group (2011) (292)
The spectrum of β‐thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis (1991) (288)
Cellular mechanism for the protective effect of haemoglobin S against P. falciparum malaria (1978) (285)
The interaction of alpha-thalassemia and homozygous sickle-cell disease. (1982) (282)
Negative epistasis between the malaria-protective effects of α+-thalassemia and the sickle cell trait (2005) (259)
Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms (1986) (256)
α-Thalassaemia caused by a polyadenylation signal mutation (1983) (251)
FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: THREE CASES (1982) (250)
Thalassemia — a global public health problem (1996) (249)
Haemoglobin Constant Spring—A Chain Termination Mutant ? (1971) (243)
The importance of anaemia in cerebral and uncomplicated falciparum malaria: role of complications, dyserythropoiesis and iron sequestration. (1986) (239)
Disorders of hemoglobin: Genetics, pathophysiology, and clinical management, second edition (2009) (236)
Globin Synthesis in Thalassaemia: An in vitro Study (1965) (213)
An Immune Basis for Malaria Protection by the Sickle Cell Trait (2005) (212)
An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore) (1965) (207)
Hereditary persistence of fetal hemoglobin: a study of 79 affected persons in 15 Negro families in Baltimore. (1963) (207)
Survival and desferrioxamine in thalassaemia major. (1982) (200)
Benign sickle-cell anaemia. (1972) (193)
Molecular basis for dominantly inherited inclusion body beta-thalassemia. (1990) (191)
REARRANGEMENT OF THE T-CELL-RECEPTOR β-CHAIN GENE IN THE DIAGNOSIS OF LYMPHOPROLIFERATIVE DISORDERS (1985) (188)
Polycythemia associated with a hemoglobinopathy. (1966) (188)
Molecular characterisation of a hypervariable region downstream of the human alpha‐globin gene cluster. (1986) (187)
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation. (1972) (182)
Optimal management of β thalassaemia intermedia (2011) (180)
Thalassaemia (2018) (178)
Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach (1996) (177)
Malaria and the Red Cell (1982) (176)
Effects of foetal haemoglobin on susceptibility of red cells to Plasmodium falciparum (1977) (170)
Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3. (1999) (169)
The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion. (1974) (164)
High incidence of malaria in α-thalassaemic children (1996) (163)
The Effect of α +-Thalassaemia on the Incidence of Malaria and Other Diseases in Children Living on the Coast of Kenya (2006) (163)
IRON ABSORPTION AND LOADING IN β-THALASSÆMIA INTERMEDIA (1979) (162)
Erythrocytes deficient in glycophorin resist invasion by the malarial parasite Plasmodium falciparum (1982) (160)
Recent developments in the molecular genetics of human hemoglobin (1979) (158)
A functional element necessary for fetal hemoglobin silencing. (2011) (155)
Multicentric origin of hemochromatosis gene (HFE) mutations. (1999) (155)
Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution. (1984) (154)
Highly variable regions of DNA flank the human alpha globin genes. (1981) (153)
The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β‐Thalassaemia * (1969) (151)
The definition and epidemiology of non-transfusion-dependent thalassemia. (2012) (151)
A SECOND GENETIC LOCUS FOR AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE (1988) (148)
Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations (2000) (147)
Embryonic erythroid differentiation in the human leukemic cell line K562. (1981) (146)
The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease (1979) (141)
Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence? (1981) (141)
Thalassemia as a global health problem: recent progress toward its control in the developing countries (2010) (140)
The interaction between Plasmodium falciparum and P. vivax in children on Espiritu Santo island, Vanuatu. (1996) (140)
Inherited Disorders of Hemoglobin (2006) (139)
Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. (1987) (138)
The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications. (2003) (138)
The Principles of Human Biochemical Genetics (1975) (137)
The new genetics and clinical practice (1982) (136)
Association of thalassaemia intermedia with a beta‐globin gene haplotype (1987) (135)
The Alpha Thalassaemias (2009) (134)
GLYCOPHORIN AS A POSSIBLE RECEPTOR FOR PLASMODIUM FALCIPARUM (1982) (134)
Iron-chelating therapy. (1988) (134)
Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia. (1979) (131)
Molecular basis of length polymorphism in the human zeta-globin gene complex. (1983) (131)
The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis (1988) (131)
4 Pathophysiology of thalassaemia (1998) (129)
Academia and industry: increasingly uneasy bedfellows (2000) (127)
Genetic variation and susceptibility to infection: the red cell and malaria (2008) (127)
Fetal Haemoglobin Production and the Sickle Gene in the Oases of Eastern Saudi Arabia (1978) (126)
Hemoglobinopathies worldwide: present and future. (2008) (125)
Separation of the α and β-Chains of Human Haemoglobin (1968) (124)
The molecular basis of alpha‐thalassaemia in Thailand. (1984) (124)
Iron metabolism in haemodialysis patients. A study of the management of iron therapy and overload. (1979) (123)
Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000 (2014) (123)
Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease. (1987) (122)
PRENATAL DIAGNOSIS OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE WITH A DNA PROBE (1986) (118)
The Increased Susceptibility of Young Red Cells to Invasion by the Malarial Parasite Plasmodium falciparum (1980) (118)
Haemoglobin Synthesis during Human Foetal Development (1973) (117)
A novel α-globin gene arrangement in man (1980) (115)
Reduced erythrocyte survival following clearance of malarial parasitaemia in Thai patients (1987) (114)
The challenge of haemoglobinopathies in resource‐poor countries (2011) (113)
The thalassaemias. (2008) (111)
Surface antigen expression on Plasmodium falciparum-infected erythrocytes is modified in alpha- and beta-thalassemia (1991) (110)
The Haemoglobin Constitution of Infants with the Haemoglobin Bart's Hydrops Foetalis Syndrome (1970) (107)
Studies in haemoglobin E beta‐thalassaemia (2008) (106)
Maternal synthesis of haemoglobin F in pregnancy. (1973) (105)
Semi-quantitative estimation of the distribution of fetal hemoglobin in red cell populations. (1962) (105)
Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases (2000) (104)
Thalassemia and malaria: new insights into an old problem. (1999) (104)
Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific). (1995) (103)
Disorders of Hemoglobin (2009) (102)
Deficient heme synthesis as the cause of noninducibility of hemoglobin synthesis in a friend erythroleukemia cell line (1979) (102)
Haemoglobin and red cell enzyme changes in juvenile myeloid leukaemia. (1968) (102)
APLASTIC CRISIS DUE TO PARVOVIRUS INFECTION IN PYRUVATE KINASE DEFICIENCY (1983) (102)
Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional. (1980) (101)
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. (1986) (100)
Common genetic disorders of the red cell and the 'malaria hypothesis'. (1987) (97)
High incidence of malaria in alpha-thalassaemic children. (1996) (95)
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex. (1990) (95)
The therapeutic reactivation of fetal haemoglobin. (1998) (95)
Iron absorption and loading in beta-thalassaemia intermedia. (1979) (94)
UGT1A1 variation and gallstone formation in sickle cell disease. (2005) (93)
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers. (1994) (93)
Genetic control of F cells in human adults. (1979) (92)
HÆMOGLOBIN-H DISEASE DUE TO A UNIQUE HÆMOGLOBIN VARIANT WITH AN ELONGATED α-CHAIN (1971) (91)
Abnormal Haemoglobins in the Neonatal Period and their Relationship to Thalassaemia * (1963) (91)
DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE (1989) (91)
A new genetic basis for hemoglobin-H disease. (1980) (90)
Academic freedom in clinical research. (2002) (89)
Melanesians and Polynesians share a unique alpha-thalassemia mutation. (1985) (89)
Iron overload in the Asian community. (2009) (89)
History of genetic disease: Thalassaemia: the long road from bedside to genome (2004) (88)
The distribution of haemoglobin C and its prevalence in newborns in Africa (2013) (88)
Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia (1983) (87)
A Genetically Determined Disorder with Features both of Thalassaemia and Congenital Dyserythropoietic Anaemia (1973) (85)
A case for developing North-South partnerships for research in sickle cell disease. (2005) (85)
The anaemia of Plasmodium falciparum malaria. (1982) (85)
The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis. (1990) (84)
Alpha-thalassaemia caused by a polyadenylation signal mutation. (1983) (83)
The Troubled Helix: Social and Psychological Implications of the New Human Genetics (1996) (83)
The doctor's dilemma (1993) (81)
PREVENTION OF IRON LOADING IN TRANSFUSION-DEPENDENT THALASSÆMIA (1978) (80)
Emergence of Western diseases in the tropical world: the experience with chronic cardiovascular diseases. (1998) (80)
The ten commandments (1989) (80)
Genetic variability in response to infection: malaria and after (2002) (79)
Fortnightly review: The thalassaemias (1997) (79)
alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease. (1983) (79)
δβ-Thalassemia is due to a gene deletion (1976) (78)
A Form of Hereditary Persistence of Fetal Haemoglobin Characterized by Uneven Cellular Distribution of Haemoglobin F and the Production of Haemoglobins A and A2 in Homozygotes (1975) (78)
The inhumanity of medicine (1994) (78)
Pathophysiology of thalassaemia. (1998) (76)
Plasmodium vivax: a cause of malnutrition in young children. (1997) (76)
Lectin-like polypeptides of P. falciparum bind to red cell sialoglycoproteins (1983) (76)
The Patterns of Fetal Haemoglobin Production in Leukaemia (1976) (76)
A MODEL FOR THE PERSISTENCE OR REACTIVATION OF FETAL HÆMOGLOBIN PRODUCTION (1976) (76)
A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α‐Thalassaemia (1969) (75)
Increased Microerythrocyte Count in Homozygous α+-Thalassaemia Contributes to Protection against Severe Malarial Anaemia (2008) (74)
Red cells I: inherited anaemias (2000) (74)
Interaction of heterocellular hereditary persistence of foetal haemoglobin with β thalassaemia and sickle cell anaemia (1976) (74)
Keynote Address: The Challenge of Thalassemia for the Developing Countries (2005) (73)
Haemoglobin Icaria, a new chain-termination mutant which causes α thalassaemia (1974) (73)
Major rearrangement in the human β-globin gene cluster (1981) (73)
IRON OVERLOAD IN MILD SIDEROBLASTIC ANAEMIAS (1983) (72)
Defective synthesis of HbE is due to reduced levels of βE mRNA (1980) (72)
The inherited disorders of haemoglobin: an increasingly neglected global health burden (2011) (72)
The interaction of α thalassaemia with heterozygous β thalassaemia (1982) (72)
Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease) (1967) (70)
The Hemoglobin E Syndromes (1998) (70)
Globin genes in Micronesia: origins and affinities of Pacific Island peoples. (1990) (68)
The British form of hereditary persistence of fetal hemoglobin results from a single base mutation adjacent to an S1 hypersensitive site 5' to the A gamma globin gene. (1986) (68)
Thalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia. (1983) (68)
Recent advances in understanding haemochromatosis: a transition state (2004) (66)
2003 William Allan Award address. The Thalassemias: the role of molecular genetics in an evolving global health problem. (2004) (66)
Hepatic sequestration in sickle cell anaemia. (1985) (66)
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)
The population genetics and dynamics of the thalassemias. (2010) (65)
Developmental and Acquired Variations in Erythrocyte Carbonic Anhydrase Isozymes (1967) (64)
Multiple arrangements of the human embryonic zeta globin genes. (1982) (64)
Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms. (1983) (64)
Treatment of thalassaemia major with phenylbutyrate and hydroxyurea (1997) (64)
Haemoglobin Synthesis in β-Thalassaemia (1968) (64)
The molecular basis for the thalassaemias in Sri Lanka (2003) (64)
Thalassaemia in the British (1973) (63)
Isolation and immunocytochemical characterization of human bone marrow stromal macrophages in hemopoietic clusters (1988) (63)
MOLECULAR BASIS FOR MILD FORMS OF HOMOZYGOUS BETA-THALASSAEMIA (1981) (63)
Haemoglobin synthesis during erythroid maturation in -thalassaemia. (1972) (63)
Blood and its disorders (1974) (62)
A newly defined X linked mental retardation syndrome associated with alpha thalassaemia. (1991) (62)
Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations (1984) (62)
Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin. (1977) (62)
Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean (2009) (62)
Haemoglobin Bart's in Saudi Arabia (1975) (61)
THE MOLECULAR BASIS FOR THE CLINICAL DIVERSITY OF β THALASSAEMIA IN CYPRIOTS (1983) (61)
Biochemical Phenotypes of Thalassemia in the American Negro Population * (1964) (60)
Intensive iron-chelation therapy with desferrioxamine in iron-loading anaemias. (1978) (60)
A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease? (1985) (60)
Haemoglobin E β thalassaemia in Sri Lanka (2005) (60)
PATTERN OF MATERNAL F-CELL PRODUCTION DURING PREGNANCY (1977) (60)
The polyadenylation site mutation in the alpha-globin gene cluster. (1988) (60)
Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin. (1982) (59)
Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow. (1975) (59)
FETAL HÆMOGLOBIN AND MALARIA (1976) (58)
STUDIES ON HEMOGLOBIN BIOSYNTHESIS: ASYNCHRONOUS SYNTHESIS OF HEMOGLOBIN A AND HEMOGLOBIN A2 BY ERYTHROCYTE PRECURSORS. (1965) (57)
The synthesis of human haemoglobin A 2 during erythroid maturation. (1972) (57)
Antenatal diagnosis of thalassaemia major. (1978) (57)
Regular Review: Iron and infection (1988) (57)
Science and Technology for Disease Control: Past, Present, and Future (2006) (57)
Invasion and growth of Plasmodium falciparum in different types of human erythrocyte. (1977) (56)
High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined (1986) (56)
Science in the undergraduate curriculum during the 20th century (2006) (56)
Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait. (2015) (56)
Rare β‐thalassaemia mutations in Asian Indians (1991) (55)
Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease. (1985) (55)
Molecular characterization of a high A2 beta thalassemia by direct sequencing of single strand enriched amplified genomic DNA. (1989) (54)
The Evolving Spectrum of the Epidemiology of Thalassemia. (2018) (54)
Fetal haemoglobin augmentation in E/β0 thalassaemia: clinical and haematological outcome (2005) (54)
A lectin-like receptor is involved in invasion of erythrocytes by Plasmodium falciparum. (1983) (54)
Thalassemia in the Next Millennium: Keynote Address a (1998) (54)
HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) AND δβ THALASSAEMIA (1979) (54)
ABNORMAL HUMAN HEMOGLOBINS. IX. CHEMISTRY OF HEMOGLOBIN J-BALTIMORE. (1963) (53)
Haemoglobin synthesis during human foetal development. (1976) (53)
α THALASSAEMIA IN PAPUA NEW GUINEA (1984) (53)
Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia (1977) (53)
Interaction of malaria with a common form of severe thalassemia in an Asian population (2009) (53)
Human globin gene analysis for a patient with beta-o/delta beta-thalassemia. (1975) (53)
The thalassemias. (1967) (53)
Host genetics and infectious disease (1996) (53)
Haemoglobin Constant Spring has an unstable α chain messenger RNA (1982) (53)
Beta thalassemia in Melanesia: association with malaria and characterization of a common variant (IVS-1 nt 5 G----C). (1988) (52)
Analysis of an inversion within the human beta globin gene cluster. (1985) (52)
Age-related changes in adaptation to severe anemia in childhood in developing countries (2007) (52)
Presence of gene for β globin in homozygous β0 thalassaemia (1976) (51)
Why are hemoglobin F levels increased in HbE/beta thalassemia? (1999) (50)
Effect of alpha thalassaemia on the rheology of homozygous sickle cell disease (1983) (50)
ENZYME DEFICIENCY IN HÆMOLYTIC DISEASE OF THE NEWBORN (1960) (50)
Foetal erythropoiesis in human leukaemia (1975) (50)
Genetic determinants of jaundice and gallstones in haemoglobin E β thalassaemia (2001) (50)
The role of genomics in studying genetic susceptibility to infectious disease. (1997) (49)
Genomics and Global Health: Time for a Reappraisal (2003) (49)
Acanthocytosis, normolipoproteinaemia and multiple tics (1970) (49)
Absence of malaria-specific mortality in children in an area of hyperendemic malaria. (1997) (48)
Haemoglobin F(Malta): a New Foetal Haemoglobin Variant with a High Incidence in Maltese Infants (1969) (48)
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat. (1985) (48)
Thalassaemia and malaria, revisited. (1997) (48)
A NEW TRIPLICATED α‐GLOBIN GENE ARRANGEMENT IN MAN (1981) (48)
The membrane characteristics of Plasmodium falciparum‐infected and ‐uninfected heterozygous α0thalassaemic erythrocytes (2002) (48)
Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemia a (1998) (48)
Clinical features and molecular analysis of acquired hemoglobin H disease. (1983) (47)
Science and medical education: is it time to revisit Flexner? (2011) (47)
Academia and industry: lessons from the unfortunate events in Toronto (1999) (47)
Haemoglobin E beta thalassaemia in Sri Lanka. (2005) (47)
Alpha thalassemia and the hematology of homozygous sickle cell disease in childhood. (1986) (47)
Molecular genetics of human hemoglobin. (1976) (46)
The Heterogeneity of Normal Hb A2‐β Thalassaemia in Greece (1979) (45)
Genetic disorders of hemoglobin. (1999) (45)
Preliminary surveys for the prevalence of the thalassemia genes in some African populations. (1971) (45)
Phenotype/genotype relationships in sickle cell disease: a pilot twin study. (2005) (45)
The clinical and pathophysiological features of malarial anaemia. (2005) (44)
A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the beta-globin gene complex. (1989) (44)
Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion (1974) (44)
High fetal hemoglobin production in sickle cell anemia in the eastern province of Saudi Arabia is genetically determined. (1986) (44)
Molecular basis of thalassaemia. (1976) (43)
Progress Toward the Control and Management of the Thalassemias. (2016) (43)
Two New Haemoglobin Variants involving Proline Substitutions (1969) (43)
Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain. (1971) (43)
Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management (2010) (43)
Red blood cell phenotypes in the α+ thalassaemias from early childhood to maturity (1996) (43)
Population and genetic studies suggest a single origin for the Indian deletion β° thalassaemia (1984) (42)
NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE (1979) (42)
Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion. (1977) (42)
FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: REPORT ON 200 CASES (1986) (42)
Management and Prognosis (2008) (42)
A direct estimate of the number of human γ-globin genes (1976) (41)
Reduced soluble transferrin receptor concentrations in acute malaria in Vanuatu. (1999) (41)
RELATIVE ROLES OF GENETIC FACTORS, DIETARY DEFICIENCY, AND INFECTION IN ANAEMIA IN VANUATU, SOUTH-WEST PACIFIC (1985) (41)
Gene therapy in perspective (1991) (41)
The molecular basis of alpha thalassemia in India. Its interaction with the sickle cell gene. (1988) (41)
Polynesian origins and affinities: globin gene variants in eastern Polynesia. (1987) (40)
The alpha-chain-termination mutants and their relation to the alpha-thalassaemias. (1975) (40)
Red cells II: acquired anaemias and polycythaemia (2000) (40)
Cystic Fibrosis of the Pancreas: Involvement of MUC6 Mucin in Obstruction of Pancreatic Ducts (1997) (39)
The molecular basis for phenotypic variability of the common thalassaemias. (1995) (39)
A novel molecular basis for beta thalassemia intermedia poses new questions about its pathophysiology. (2005) (39)
Deferiprone versus desferrioxamine in thalassaemia, and T2* validation and utility (2003) (39)
Is hemoglobin instability important in the interaction between hemoglobin E and beta thalassemia? (1998) (39)
Coma Associated with Vincristine Therapy (1973) (38)
Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis (1978) (38)
FURTHER EVIDENCE OF LINKAGE BETWEEN THE BETA AND DELTA LOCI GOVERNING HUMAN HEMOGLOBIN AND THE POPULATION DYNAMICS OF LINKED GENES. (1963) (38)
Antibody‐dependent red cell removal during P. falciparum malaria: the clearance of red cells sensitized with an IgG anti‐D (1989) (38)
The Clinical and Biosynthetic Characterization of αβ‐Thalassaemia (1972) (37)
The global problem of genetic disease (2005) (37)
HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (1975) (37)
From genotype to phenotype: genetics and medical practice in the new millennium. (1999) (37)
Scope and limitations of gene therapy. (1995) (36)
Genetic and molecular diversity in nondeletion Hb H disease. (1981) (36)
ABC of clinical haematology: The hereditary anaemias (1997) (36)
Familial sideroblastic anaemia: problem of Xg and X chromosome inactivation. (1970) (36)
Concomitant inheritance of α‐thalassemia in β°‐thalassemia/hb e disease (1985) (36)
Genomics and global health (2002) (36)
Human globin gene expression: Control of β, δ and δβ chain production (1978) (35)
Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions. (1987) (35)
The role of the inherited disorders of hemoglobin, the first "molecular diseases," in the future of human genetics. (2013) (35)
The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes (1981) (35)
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency. (1996) (35)
Alpha thalassaemia in British people. (1985) (35)
Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia. (2001) (35)
Developmental genetics of the human haemoglobins. (1983) (35)
Genetic disorders of haemoglobin (2000) (35)
Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring. (1984) (35)
Haemoglobin Radcliffe (α2β299(G1)Ala): A High Oxygen‐Affinity Variant Causing Familial Polycythaemia (1977) (35)
High resolution gene mapping of the human alpha globin locus. (1987) (34)
Disorders of Hemoglobin: Hemoglobin E Disorders (2009) (34)
Restriction mapping of a new deletion responsible for G gamma (delta beta)o thalassemia. (1981) (34)
A novel rearrangement of the human beta-like globin gene cluster. (1981) (34)
Cell cycle distribution of erythroblasts in P. falciparum malaria. (2009) (34)
FEASIBILITY OF PRENATAL DIAGNOSIS OF β-THALASSAEMIA WITH SYNTHETIC DNA PROBES IN TWO MEDITERRANEAN POPULATIONS (1985) (34)
Analysis of the human a-globin gene cluster reveals a highly informative genetic locus ( haplotype / genetic linkage / recombinatlon / polymorphism ) (34)
Adaptation to anemia in hemoglobin E-ß thalassemia. (2010) (33)
Editorial retrospective. Iron loading in thalassemia--five years with the pump. (1983) (33)
Evidence against immune haemolysis in falciparum malaria in Thailand (1986) (33)
Prenatal diagnosis of the common haemoglobin disorders. (1985) (33)
The Negro Variety of Hereditary Persistence of Fetal Haemoglobin is a Mild Form of Thalassaemia (1976) (33)
δβ‐Thalassaemia in a Chinese Family (1972) (33)
HEMOGLOBIN CONSTANT SPRING, AN UNUSUAL α‐CHAIN VARIANT INVOLVED IN THE ETIOLOGY OF HEMOGLOBIN H DISEASE (1974) (33)
Homozygous state for Hb Constant Spring (slow-moving Hb X components). (1974) (32)
Switch from foetal to adult haemoglobin synthesis in normal and hypophysectomised sheep (1976) (32)
The acute phase response in children with mild and severe malaria in Papua New Guinea. (2009) (32)
Erythrocytes deficiency in glycophorin resist invasion by the malarial parasite Plasmodium falciparum. (1982) (32)
The coombs direct antiglobulin test in Kenyans. (1983) (32)
A NEW DNA POLYMORPHISM FOR PRENATAL DIAGNOSIS OF β-THALASSAEMIA IN MEDITERRANEAN POPULATIONS (1984) (32)
Characterization of β-globin mRNA in the β0 thalassemias (1978) (32)
Localisation of human alpha globin to 16p13.3----pter. (1988) (32)
The Lost Art of Healing (1997) (32)
The Thalassemias: The Role of Molecular Genetics in an Evolving Global Health Problem * * Previously (2004) (32)
The direct antiglobulin test in P. falciparum malaria (1982) (32)
Pitfalls of genetic testing. (1996) (31)
Synthesis in vitro of anti-Lepore haemoglobin. (1973) (31)
The importance of micromapping the gene frequencies for the common inherited disorders of haemoglobin (2010) (31)
Haemoglobin J Tongariki is associated with α thalassaemia (1978) (31)
Thalassaemia in Vanuatu, South‐West Pacific: frequency and haematological phenotypes of young children (1995) (30)
Maturity onset diabetes of the young is not linked to the insulin gene. (1983) (30)
Detection of Alpha Thalassaemia in Negro Infants (1980) (29)
Determination of Alpha Thalassaemia Phenotypes by Messenger RNA Analysis (1980) (29)
The physician scientist: an endangered but far from extinct species. (1991) (29)
(Aγδβ)° thalassaemia: similarity of phenotype in four different molecular defects, including one newly described (1984) (29)
Sickle beta 0 thalassemia in Eastern Saudi Arabia. (1980) (29)
The direct antiglobulin test in P. falciparum malaria. (1982) (29)
On dinosaurs and medical textbooks (1995) (29)
Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosis. (1994) (29)
THE MOLECULAR BASIS FOR THE HAEMOGLOBIN BART'S HYDROPS FETALIS SYNDROME IN CYPRUS (1981) (29)
Hereditary Persistence of Foetal Haemoglobin associated with a γβ Fusion Variant, Haemoglobin Kenya (1973) (28)
Thalassemia Revisited (1982) (28)
Relationship of Hemoglobin Bart's and H To Alpha Thalassemia * (1964) (28)
Thalassemia in Sri Lanka: a progress report. (2004) (28)
The impact of genetics on medical education and training. (1999) (28)
Introduction to the problem of hemoglobin E-beta thalassemia. (2000) (28)
Plasmodium yoelii: blood oxygen and brain function in the infected mouse. (1983) (28)
IRON CHELATION WITH ORAL DESFERRIOXAMINE (1980) (28)
Meiotic recombination between two polymorphic restriction sites within the beta globin gene cluster. (1986) (27)
Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis. (1983) (27)
A Novel Deletion in the β‐Globin Gene Complex (1985) (27)
The deoxyuridine suppression test in severe anaemia following Plasmodium falciparum malaria. (1984) (26)
The anaemia of Plasmodium falciparum malaria. (1983) (26)
Spreading Germs: Disease Theories and Medical Practice in Britain, 1865– 1900 (2002) (26)
The British type of non‐deletion HPFH: characterization of developmental changes in vivo and erythroid growth in vitro (1982) (26)
Science and the Quiet Art The role of medical research in health care (1995) (26)
Mechanism of anaemia in resistant visceral leishmaniasis. (1986) (26)
Vascular occlusion and infarction in sickle cell crisis and the sickle chest syndrome. (1985) (26)
Restriction endonuclease maps of the β‐like globin gene cluster in the British and Greek forms of HPFH, and for one example of Gγβ+ HPFH (1982) (26)
Biochemical and Clinical Aspects of Hemoglobin Abnormalities (1980) (25)
Polycythemia resulting from abnormal hemoglobins. (1969) (25)
A novel alpha-globin gene arrangement in man. (1980) (25)
Towards molecular medicine; reminiscences of the haemoglobin field, 1960–2000 (2001) (25)
The Genetic Basis of Hb Q‐H Disease (1980) (25)
Haemoglobin Constant Spring has an unstable alpha chain messenger RNA. (1982) (25)
The evolutionary and clinical implications of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances (2017) (25)
Distribution and Population Genetics of the Thalassaemias (2008) (25)
Hemoglobin E beta-thalassemia: an increasingly common disease with some diagnostic pitfalls. (1998) (25)
Muscle cell injury, haemolysis and dark urine in children with falciparum malaria in Papua New Guinea. (2006) (25)
BONE-MARROW TRANSPLANTATION FOR SICKLE-CELL ANAEMIA (1988) (25)
Occurrence of Gγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia (1979) (24)
Fetal haemoglobin and malaria. (1976) (24)
INADEQUACY OF Hb BART'S AS AN INDICATOR OF α THALASSAEMIA (1982) (24)
The treatment of thalassemia--slow progress and new dilemmas. (1993) (24)
IRON ABSORPTION IN IRON-LOADING ANÆMIAS: EFFECT OF SUBCUTANEOUS DESFERRIOXAMINE INFUSIONS (1977) (24)
Globin Synthesis in Normal Human Bone Marrow (1976) (23)
Mapping the Code. The Human Genome Project and the Choices of Modern Science (1991) (23)
Characterization of the breakpoint of a 3.5-kb deletion of the β-globin gene (1991) (23)
Iron overload and iron-chelating therapy in hemoglobin E-beta thalassemia. (2000) (23)
Enzyme deficiency in haemolytic disease of the newborn. (1960) (23)
The Molecular Pathology of the Thalassaemias (2008) (22)
Defective synthesis of HbE is due to reduced levels of beta E mRNA. (1980) (22)
Antenatal Diagnosis How to Deliver a Comprehensive Service in the United Kingdom (1990) (22)
THE THALASSAEMIAS (1976) (22)
Alpha thalassaemia in Papua New Guinea. (1984) (22)
Iron induced increase in red cell size in haemodialysis patients. (1979) (22)
Changes in the Chromosome and Haemoglobin Patterns in a Patient with Erythro-leukaemia (1965) (22)
Oral iron chelation therapy for thalassaemia: an uncertain scene (2000) (22)
A SPONTANEOUS DELETION OF β33/34 Val IN EXON 2 OF THE β GLOBIN GENE (Hb KOREA) PRODUCES THE PHENOTYPE OF DOMINANT β THALASSAEMIA (1991) (21)
Science and the Quiet Art: Medical Research and Patient Care (1995) (21)
Thalassaemia intermedia. (1987) (21)
Methemoglobinemia and ascorbate deficiency in hemoglobin E β thalassemia: metabolic and clinical implications. (2012) (21)
Iron balance and the management of iron overload in beta-thalassemia intermedia. (1988) (21)
DIRECT DETECTION OF β°39 THALASSAEMIC MUTATION WITH Mae 1 (1985) (21)
Surface Antigen Expression on Plasmodium falciparum-infected Erythrocytes Is Modified in cx-and f Thalassemia By (20)
Prenatal diagnosis of thalassaemia. (1984) (20)
An improved method for the characterization of human haemoglobin mutants: identification of alpha-2-beta-2-95GLU, haemoglobin N (Baltimore). (1965) (20)
G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C. (1979) (20)
Systems biology and red cells. (2011) (20)
Genetic factors as determinants of infectious disease transmission in human communities. (1988) (19)
α‐Globin gene deletions associated with Hb J Tongariki (1982) (19)
Hepcidin detects iron deficiency in Sri Lankan adolescents with a high burden of hemoglobinopathy: A diagnostic test accuracy study (2017) (19)
Separation of the alpha and beta-chains of human hemoglobin. (1968) (19)
Chromosomes with one, two, three, and four fetal globin genes: molecular and hematologic analysis. (1986) (19)
Problems for biomedical research at the academia-industrial interface (2003) (19)
Busulphan and bone marrow depression. (1969) (19)
Evidence for the genetic identity of alpha chain determinants in hemoglobins A, A2 and F. (1962) (19)
Restriction endonuclease maps of the beta-like globin gene cluster in the British and Greek forms of HPFH, and for one example of G gamma beta + HPFH. (1982) (19)
Haemoglobin Synthesis in Human Erythroid Bursts during Ontogeny: Reproducibility and Sensitivity to Culture Conditions (1981) (19)
Control mechanisms in human haemolgobin synthesis. (1968) (19)
Developmental biology of human hemoglobins. (2016) (19)
A nationwide survey of hospital-based thalassemia patients and standards of care and a preliminary assessment of the national prevention program in Sri Lanka (2019) (19)
Iron status and anaemia in Sri Lankan secondary school children: A cross-sectional survey (2017) (18)
Haemoglobin Bart's hydrops syndrome in Greece. (1980) (18)
Heroic gene surgery (1994) (18)
Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S. (1972) (18)
Oral iron chelation therapy for thalassaemia: an uncertain scene. Annotation (2000) (17)
Studies of Red‐Cell Membrane Function in Heterozygous β Thalassaemia and Other Hypochromic Anaemias (1974) (17)
Haemoglobin and the Inherited Disorders of Globin Synthesis (2007) (17)
Direct detection of haemoglobin E with MnlI. (1987) (17)
Molecular basis for acquired haemoglobin H disease (1977) (17)
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease. (1979) (17)
Deferiprone for thalassaemia (2000) (17)
Human Haemoglobin Variants and their Characteristics (1976) (17)
Identification of slow-moving haemoglobins in haemoglobin H disease from different racial groups. (1972) (17)
Iron metabolism in murine erythroleukaemic cells (1983) (17)
Teaching ethics to medical students. (1995) (17)
DISORDERED GLOBIN SYNTHESIS IN THALASSEMIA (1969) (17)
Characterization of an Indian (δβ)° thalassaemia (1984) (17)
5-AZACYTIDINE FOR BETA-THALASSAEMIA? (1983) (16)
Feasibility of prenatal diagnosis of β thalassaemia by DNA polymorphisms in an Italian population (1986) (16)
ANTI-ERYTHROCYTE AUTOIMMUNISATION DURING CHRONIC FALCIPARUM MALARIA (1981) (16)
β0 THALASSÆMIA—TIME FOR A REAPPRAISAL ? (1974) (16)
Genetic control of diabetes mellitus (1992) (16)
Bone marrow transplantation for thalassemia. (1987) (16)
The Molecular Basis for Phenotypic Diversity of Genetic Disease (1995) (16)
Genetic and Molecular Analysis of Mild Forms of Homozygous β‐Thalassemia (1985) (16)
Molecular pathology of single gene disorders. (1987) (16)
Iron absorption in non-transfused iron loading anaemias: prediction of risk for iron loading, and response to iron chelation treatment, in beta thalassaemia intermedia and congenital sideroblastic anaemias. (1984) (15)
Examining undergraduate examinations (1991) (15)
ALPHA GLOBIN GENOTYPES IN TWO NORTH EUROPEAN POPULATIONS (1986) (15)
A Variation in the Electrophoretic Pattern of Human Erythrocyte Carbonic Anhydrase (1964) (15)
Allelic variation and linkage properties of a highly polymorphic restriction fragment in humans. (1984) (15)
Haemoglobin synthesis in human bone marrow culture. (1972) (15)
alpha thalassemia in black populations. (1980) (15)
Thalassaemia in a Gurkha Family (1960) (15)
A Chronic Granulomatous Syndrome of Unknown Origin (1990) (15)
HEMOGLOBIN J (BALTIMORE) COEXISTING IN A FAMILY WITH HEMOGLOBIN S. (1964) (15)
A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemia. (1979) (15)
Homozygous beta thalassaemia in Liberia. (1975) (15)
Hydralazine-induced necrotising vasculitis. (1981) (15)
Is the β thalassaemia trait of clinical importance? (2008) (14)
Assessing the Quality of Health Care (1992) (14)
Molecules and man (1987) (14)
Assay of Thalassaemic Messenger RNA in the Wheat Germ System (1976) (14)
THE RED CELL AND THE MALARIAL PARASITE (1980) (14)
Different Hematologic Phenotypes Are Associated with the Leftward (-a 42 ) and Rightward (-a 37 ) a +-Thalassemia Deletions (14)
Haemoglobin Synthesis by Fetal Erythroid Cells in an Adult Environment (1981) (14)
Juvenile chronic myeloid leukaemia. (1970) (14)
The genetics of common diseases: the implications of population variability. (1996) (14)
Sickle-cell disease: a call to action (2015) (14)
The spectrum of β thalassaemia in Burma (1992) (14)
Alpha thalassaemia and extended alpha globin genes in Sri Lanka. (2013) (14)
Interaction of the ααα globin gene haplotype and sickle haemoglobin (1984) (14)
Haemoglobin variants, iron status and anaemia in Sri Lankan adolescents with low red cell indices: A cross sectional survey. (2018) (13)
Globin gene mapping in normal Hb A2 types of β‐thalassaemia (1982) (13)
A study of genetic linkage heterogeneity in adult polycystic kidney disease (1987) (13)
Haemoglobin synthesis in beta-thalassaemia. (1968) (13)
CELLULAR ORIGINS OF THE FETAL-HÆMOGLOBIN-CONTAINING CELLS OF NORMAL ADULTS (1979) (13)
Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia. (1976) (13)
The distribution of nascent globin chains on human reticulocyte polysomes. (1971) (13)
Anaemia: pathophysiology, classification, and clinical features (2010) (13)
Hemoglobin E‐β‐Thalassemia: Progress Report from the International Study Group (2005) (13)
The thalassaemia syndromes. 2nd Edition. (1972) (13)
Emerging insights in the management of hemoglobin E beta thalassemia (2010) (13)
Single and Combination Drug Therapy for Fetal Hemoglobin Augmentation in Hemoglobin E‐β0‐Thalassemia: Considerations for Treatment (2005) (13)
Surface Antigen Expression on Plasmodium falciparum-infected Erythrocytes Is Modified in cx-and fThalassemia By G.A.Luzzi,*A.H.Merry,$C.1.Newbold,*K.Marsh,* (1991) (13)
Analysis ofthehumana-globin genecluster reveals ahighly informative genetic locus (1986) (12)
DIRECT DETECTION OF HAEMOGLOBIN E WITH SYNTHETIC OLIGONUCLEOTIDES (1986) (12)
Deferiprone and hepatic fibrosis. (2003) (12)
G gamma delta beta thalassaemia and g gamma HPFH (Hb Kenya type): comparison of 2 new cases. (1977) (12)
Cytosine arabinoside in the treatment of acute myeloblastic leukaemia. (1971) (12)
Avoidance and Population Control (2008) (12)
Continuous long-term culture of human bone marrow. (1981) (12)
Bone marrow transplantation for thalassemia and other inherited disorders of hemoglobin [editorial] (1992) (12)
Alpha-thalassaemia and the malaria hypothesis. (1987) (12)
Thalassemia: the long road from the bedside through the laboratory to the community (2010) (12)
CHAPTER 2 – The Thalassemias (1967) (12)
Screening procedures for quantitative abnormalities in hemoglobin synthesis. (1981) (11)
The slow road to gene therapy (1988) (11)
Fast hemoglobin in lead poisoning. (1966) (11)
IMPLICATIONS FOR MEDICAL PRACTICE AND HUMAN BIOLOGY (1984) (11)
The anaemia of malaria. (1988) (11)
Concomitant inheritance of alpha-thalassemia in beta 0- thalassemia/Hb E disease. (1985) (11)
Localisation of human a globin to 16 p 13 . 3-- pter (11)
Property law as a barrier to energy upgrades in multi-owned properties: insights from a study of England and Scotland (2018) (11)
Haemoglobin synthesis in alpha-thalassaemia (haemoglobin H disease). (1967) (11)
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka (2019) (11)
Hematologic disorders of children in developing countries. (2002) (11)
Haemoglobin Synthesis in Human Fetal Liver Maintained in Short‐Term Tissue Culture (1975) (11)
Heterogeneity and origins of the alpha-thalassemias. (1987) (11)
Framing and Mapping the Governance Barriers to Energy Upgrades in Flats (2017) (11)
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyes. (1981) (11)
Genomics and Clinical Medicine (2008) (10)
The genetic control of protein synthesis: The haemoglobin model (1974) (10)
THE SIGNIFICANCE OF HAEMOGLOBIN H IN PATIENTS WITH MENTAL RETARDATION OR MYELOPROLIFERATIVE DISEASE (1982) (10)
Control of Haemoglobin Synthesis (1967) (10)
Examining undergraduate examinations. (1991) (10)
Clinical Features and Molecular Analysis of the a Thalassemia / Mental Retardation Syndromes . II . Cases without Detectable Abnormality of the a Globin Complex A . (2006) (10)
REGIONAL LOCALISATION OF THE HUMAN α-GLOBIN GENES (1981) (10)
Gene transfection: A step nearer gene therapy? (1984) (10)
Characterisation of a new alpha thalassemia 1 defect due to a partial deletion of the alpha globin gene complex. (1980) (10)
THE CLINICAL AND CHEMICAL HETEROGENEITY OF THE β‐THALASSEMIAS (1974) (10)
Letters to the EditorJUVENILE CHRONIC MYELOID LEUKÆMIA (1970) (10)
Current trends in the diagnosis and management of haemoglobinopathies (2007) (10)
The Role of Nature and Nurture in Common Diseases: Garrod's Legacy (1995) (10)
Genetic markers in human blood (1969) (10)
A fetal hemoglobin variant of unusual genetic interest. (1962) (10)
Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindreds. (1988) (10)
Molecular Rearrangements of the Human α‐Globin Gene Cluster (1985) (9)
Historical Perspectives: The Many and Diverse Routes to Our Current Understanding of the Thalassaemias (2008) (9)
UGT 1 A 1 variation and gallstone formation in sickle cell disease (2005) (9)
Hemoglobin E-beta-thalassemia: Progress report from the International Study Group. (2005) (9)
Pharmaceutical quality: an urgent and unresolved issue (2012) (9)
A New Year's resolution after a lost decade (2003) (9)
The heterogeneity of normal Hb A2-beta thalassaemia in Greece. (1979) (9)
Rapid detection of a 13.4-kb deletion causing delta beta thalassemia in an Egyptian family by polymerase chain reaction. (1993) (9)
Ahaptoglobinaemia in Melanesia: DNA and malarial antibody studies. (1987) (9)
Genomics and world health: a decade on (2012) (9)
Haemoglobin J Tongariki is associated with alpha thalassaemia. (1978) (9)
The Conflict between the Science and the Art of Clinical Practice in the Next Millennium (1999) (9)
α+‐Thalassaemia and pregnancy in a malaria endemic region of Papua New Guinea (2006) (9)
Raised Hb F levels in sickle cell disease are caused by a determinant linked to the beta globin gene cluster. (1987) (9)
Major rearrangement in the human beta-globin gene cluster. (1981) (8)
Haemoglobin Radcliffe (alpha2beta299(Gi)Ala): a high oxygen-affinity variant causing familial polycythaemia. (1977) (8)
Gene therapy: Repairing haemoglobin disorders with ribozymes (1998) (8)
The β and δβ Thalassaemias in Association with Structural Haemoglobin Variants (2008) (8)
Thalassaemia: The Biography (2010) (8)
Molecular Basis for Some Disorders of Haemoglobin Synthesis—I* (1974) (8)
The control of human hemoglobin synthesis and function in health and disease. (2016) (8)
Alpha thalassaemia and the macular vasculature in homozygous sickle cell disease. (1983) (8)
THE CLINICAL AND MOLECULAR HETEROGENEITY OF THE THALASSEMIA SYNDROMES * (1980) (8)
Patterns of Globin Chain Synthesis in Erythroid Colonies Grown from Sheep Marrow of Different Developmental Stages (1979) (8)
Pharmacogenomics of Deferiprone Metabolism. (2005) (8)
Benign sickle-cell anaemia. (1972) (8)
Thalassaemia intermedia: interaction of the triple alpha-globin gene arrangement and heterozygous beta-thalassaemia. (1987) (8)
The frequency and origin of the sickle cell mutation in the district of Coruche/Portugal (1989) (8)
The Regulation of the Differential Expression of the Human Globin Genes During Development (1986) (8)
Rapid detection of a 13.4-kb deletion causing delta beta thalassemia in an Egyptian family by polymerase chain reaction (1993) (8)
Folic-acid Deficiency and Megaloblastic Erythropoiesis in Myelofibrosis (1964) (8)
Iron loading and thalassemia--experimental successes and practical realities. (1977) (8)
THE MOLECULAR BASIS FOR β° THALASSAEMIA INTERMEDIA IN AN IRANIAN INDIVIDUAL (1982) (8)
Disorders of Hemoglobin: Clinical Aspects of β Thalassemia and Related Disorders (2009) (8)
Molecular biology at the bedside. (1986) (8)
THE BIOCHEMICAL LESION IN THALASSAEMIA (1968) (8)
High resolution gene mapping of the human oa globin locus (2004) (8)
Epistasis and the sensitivity of phenotypic screens for beta thalassaemia (2014) (8)
A new triplicated alpha-globin gene arrangement in man. (1981) (7)
-Thalassaemia: clinical and biosynthetic characteristics. (1972) (7)
Molecular and cell biology in clinical medicine: introduction. (1987) (7)
Alpha thalassemia and homozygous sickle cell disease. (1981) (7)
Disorders of the synthesis or function of haemoglobin (2010) (7)
The Pathophysiology of the Thalassaemias (2008) (7)
Rare Hemoglobin Variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB: c.206T>C) in Sri Lankan Families (2015) (7)
Adaptation to anemia in hemoglobin E-β thalassemia (Blood (2010) 116, 24 (5368-5370)) (2011) (7)
Human haemoglobin genetics. (1979) (7)
The spectrum of beta thalassaemia in Burma. (1992) (7)
Haemoglobin Icaria, a new chain-termination mutant with causes alpha thalassaemia. (1974) (7)
Pharmacological treatment of monogenic disease (2003) (7)
Prenatal diagnosis of the major haemoglobin disorders. (1989) (7)
Southeast Asian ovalocytosis and pregnancy in a malaria-endemic region of Papua New Guinea. (2007) (7)
Globin gene mapping studies in Sardinian patients homozygous for beta zero Thalassaemia. (1983) (7)
Is modern genetics a blind alley? No (2010) (7)
THE AVA II Ψβ POLYMORPHISM IS LINKED TO THE COMMON MEDITERRANEAN β+ THALASSAEMIA MUTATION (1985) (7)
The α Thalassaemias and their Interactions with Structural Haemoglobin Variants (2008) (6)
The developmental genetics of human hemoglobin. (1985) (6)
The molecular basis of thalassemia. (1976) (6)
High frequency of beta thalassaemia in a small island population in Melanesia. (1987) (6)
The genetics of the thalassaemias. (1969) (6)
Selective expression within the human alpha globin gene complex following chromosome-dependent transfer into diploid mouse erythroleukaemia cells. (1983) (6)
Negative epistasis between the malaria-protective effects of alpha (+) thalassaemia and the sickle cell trait [MIM-TW-395505] (2005) (6)
The centenary of Garrod's Croonian lectures. (2008) (6)
Molecular Basis of Thalassaemia (1975) (6)
Non-deletion haemoglobin H disease in Papua New Guinea. (1987) (6)
Characterization of the breakpoint of a 3.5-kb deletion of the beta-globin gene. (1991) (6)
Hematologic Changes and Hemoglobin Analysis in β Thalassemia Heterozygotes during the First Year of Life (1982) (6)
The interaction of alpha thalassaemia and sickle cell–beta° thalassaemia (1988) (6)
Abnormal haemoglobins (1978) (6)
London and Amsterdam (1976) (6)
Antenatal diagnosis of the haemoglobin disorders by analysis of foetal DNA. (1983) (6)
Proceedings: Hb Kenya: a clue to the genetic control of human foetal haemoglobin synthesis. (1974) (6)
Thalassaemia: the long road from the bedside through the laboratory to the community (2011) (6)
A Taq1 γ-globin DNA polymorphism: an African-specific marker (1986) (6)
A Comparison of the Homozygous States for Gγ and GγAγδβ Thalassaemia (1979) (6)
Commentary on "The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5' HS4" by M. Neishabury et al. (2012) (6)
First Trimester Diagnosis of the Hemoglobin Disorders (1985) (6)
THE POTENTIAL MOLECULAR MECHANISM OF THALASSEMIAS AND RELATED DISORDERS (1974) (6)
Globin gene expression in Hb Lepore‐BAC transgenic mice (2006) (5)
Cellular structure and function. (1969) (5)
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene. (1979) (5)
Cyril Clarke and the prevention of rhesus haemolytic disease of the newborn (2012) (5)
DNA in medicine. Implications for medical practice and human biology. (1984) (5)
Approach to the Diagnosis of -Thalassaemia by DNA Analysis (1987) (5)
Malarial anemia and STAT6 (2009) (5)
Iron chelation with oral deferiprone in patients with thalassemia. (1998) (5)
Thalassaemia: Classification, Genetics and Relationship to Other Inherited Disorders of Haemoglobin (2008) (5)
OBSTETRIC OUTCOME IN FIRST TRIMESTER FETAL DIAGNOSIS FOR THE HAEMOGLOBINOPATHIES (1983) (5)
Headache: an important symptom possibly linked to white matter lesions in thalassaemia (2019) (5)
Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia. (1979) (5)
Marriage patterns in Sri Lanka and the prevalence of parental consanguinity in patients with β-thalassaemia: a cross-sectional descriptive analysis (2019) (5)
Online Biomedical Resources for Malaria-Related Red Cell Disorders (2013) (5)
Genetic influences on bone disease in thalassemia. (1998) (5)
Health Policy and Technological Innovation (1994) (5)
The Laboratory Diagnosis of the Thalassaemias (2008) (5)
CHELATION REGIMENS WITH DESFERRIOXAMINE (1977) (5)
Book of the Month: Philosophy for Medicine (2004) (5)
Genetic haematological disorders (2009) (4)
Tropical medicine in and out of the tropics (1996) (4)
Advances in red blood cell biology (1982) (4)
David Ricardo: A Biography (1976) (4)
Bone marrow transplantation for thalassemia and other inherited disorders of hemoglobin. (1992) (4)
Interaction of five globin gene abnormalities in a Cambodian family (1986) (4)
Phenotypic Prediction in β‐Thalassemia (1998) (4)
Genetic disorders of human haemoglobin as models for analysing gene regulation. (1984) (4)
Sir David Weatherall reflects on genetics and personalized medicine. Interviewed by Ulrike Knies-Bamforth. (2006) (4)
Medicine in the new millennium (2000) (4)
THE MOLECULAR BASIS FOR SOME GENETIC DISORDERS OF HAEMOGLOBIN SYNTHESIS (1981) (4)
Molecular basis of beta-thalassemia in Thailand. (1987) (4)
Introduction (2001) (4)
sickle cell gene The molecular basis of alpha thalassemia in India. Its interaction with the (2011) (4)
Survival and complications in patients with haemoglobin E thalassaemia in Sri Lanka: a prospective, longitudinal cohort study (2021) (4)
Delta-beta-thalassemia is due to a gene deletion. (1976) (4)
Research conduct and the case of Nancy Olivieri Miriam Shuchman (2005) (4)
Thalassaemia in an Irish family (1968) (4)
Neonatal Haematology (1967) (4)
Homozygous β thalassaemia in Liberia. (1975) (4)
Genetic overlap (1994) (4)
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Globin chain synthesis and clinical and hematologic findings in double heterozygotes for the silent and classical ß-thalassemia genes, and their parents (1979) (0)
The Ava II psi beta polymorphism is linked to the common Mediterranean beta + thalassaemia mutation. (1985) (0)
Mutations in the hepcidin gene HAMP and the hemojuvelin gene (2004) (0)
The Molecular Basis of P-Thalamia in Thailand: Application to Prenatal Diagnosis (2006) (0)
Altered Fates - Gene-Therapy and the Re-Tooling of Human Life, by J. Lyon, P. Gorner (1995) (0)
Comprar Thalassaemia: The Biography | David Weatherall | 9780199565603 | Oxford University Press (2010) (0)
IRON-METABOLISM IN TRANSFORMED ERYTHROID-CELLS (1980) (0)

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