Published in Br J Haematol on June 01, 1991
Frequency and clinical significance of erythrocyte genetic abnormalities in Omanis. J Med Genet (1993) 1.05
Past, present & future scenario of thalassaemic care & control in India. Indian J Med Res (2011) 1.01
Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes. Hugo J (2010) 0.99
Prevalence and hematological profile of β-thalassemia and sickle cell anemia in four communities of Surat city. Indian J Hum Genet (2012) 0.96
Phenotypic heterogeneity of asian Indian inversion deletions gγ(aγδβ)0 breakpoint a and breakpoint B. Indian J Clin Biochem (2012) 0.93
Mutational spectrum of thalassemias in India. Indian J Hum Genet (2007) 0.90
The spectrum of beta thalassaemia mutations in the UAE national population. J Med Genet (1994) 0.88
Genetic Heterogeneity of Beta Globin Mutations among Asian-Indians and Importance in Genetic Counselling and Diagnosis. Mediterr J Hematol Infect Dis (2013) 0.87
A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka. J Community Genet (2010) 0.87
Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction. Malays J Med Sci (2013) 0.84
Host microsatellite alleles in malaria predisposition? Malar J (2005) 0.83
Thalassaemia among Asians in Britain. Thalassaemia Society is working to improve awareness. BMJ (1999) 0.81
Unique pattern of mutations in β-thalassemia patients in Western Uttar Pradesh. Indian J Hum Genet (2013) 0.80
Current Genetic Epidemiology of β-Thalassemias and Structural Hemoglobin Variants in the Lazio Region (Central Italy) Following Recent Migration Movements. Adv Hematol (2010) 0.78
Status of HbE variant among Rabha tribe of West Bengal, India. Indian J Med Res (2015) 0.78
Combination of two rare mutations causes β-thalassaemia in a Bangladeshi patient. Genet Mol Biol (2011) 0.78
Single-cell polymerase chain reaction-based pre-implantation genetic diagnosis using fragment analysis for β-thalassemia in an Indian couple with β-globin gene mutations. J Hum Reprod Sci (2012) 0.78
Screening of Five Common Beta Thalassemia Mutations in the Pakistani Population: A basis for prenatal diagnosis. Sultan Qaboos Univ Med J (2009) 0.78
Genotype-phenotype correlation of β-thalassemia spectrum of mutations in an Indian population. Hematol Rep (2012) 0.77
Medical genetics and genomic medicine in India: current status and opportunities ahead. Mol Genet Genomic Med (2015) 0.75
Efficiency and cost effectiveness: PAGE-SSCP versus MDE and Phast gels for the identification of unknown beta thalassaemia mutations. Mol Pathol (2003) 0.75
Antenatal screening for identification of couples for prenatal diagnosis of severe hemoglobinopathies in surat, South gujarat. J Obstet Gynaecol India (2012) 0.75
Interaction of - α 3.7, ß Thalassemia Mutation IVS 1-5 and HbD Punjab in a Family: A Case Report. Indian J Clin Biochem (2012) 0.75
The Prevalence Of β-Thalassemia Mutations in South Western Maharashtra. Indian J Clin Biochem (2012) 0.75
Subclinical haemorrhagic tendency exists in patients with β-thalassaemia major in early childhood. Australas Med J (2012) 0.75
Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia. Indian J Hematol Blood Transfus (2016) 0.75
The inhumanity of medicine. BMJ (1995) 13.98
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature (1985) 7.34
Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms. Nature (1986) 4.84
Alpha-thalassaemia caused by a polyadenylation signal mutation. Nature (1984) 4.41
Small vessels in the human brain: MR venography with deoxyhemoglobin as an intrinsic contrast agent. Radiology (1997) 4.13
K562 human leukaemic cells synthesise embryonic haemoglobin in response to haemin. Nature (1979) 3.75
Molecular basis of length polymorphism in the human zeta-globin gene complex. Proc Natl Acad Sci U S A (1983) 3.27
High incidence of malaria in alpha-thalassaemic children. Nature (1996) 3.12
Absence of malaria-specific mortality in children in an area of hyperendemic malaria. Trans R Soc Trop Med Hyg (1998) 3.09
Recent developments in the molecular genetics of human hemoglobin. Cell (1979) 3.09
The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion. Nature (1974) 3.04
A review of the molecular genetics of the human alpha-globin gene cluster. Blood (1989) 2.84
Highly variable regions of DNA flank the human alpha globin genes. Nucleic Acids Res (1981) 2.83
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene cluster. EMBO J (1986) 2.77
Globin synthesis in thalassaemia: an in vitro study. Nature (1965) 2.74
A highly conserved amino-acid sequence in thrombospondin, properdin and in proteins from sporozoites and blood stages of a human malaria parasite. Nature (1988) 2.70
First-trimester fetal diagnosis for haemoglobinopathies: three cases. Lancet (1982) 2.55
Extent of microstructural white matter injury in postconcussive syndrome correlates with impaired cognitive reaction time: a 3T diffusion tensor imaging study of mild traumatic brain injury. AJNR Am J Neuroradiol (2008) 2.55
DNA "fingerprints" and segregation analysis of multiple markers in human pedigrees. Am J Hum Genet (1986) 2.55
The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med (1982) 2.52
Embryonic erythroid differentiation in the human leukemic cell line K562. Proc Natl Acad Sci U S A (1981) 2.42
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease. Cell (1979) 2.41
Academia and industry: lessons from the unfortunate events in Toronto. Lancet (1999) 2.39
Survival and desferrioxamine in thalassaemia major. Br Med J (Clin Res Ed) (1982) 2.35
Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence? N Engl J Med (1981) 2.35
Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet (1990) 2.33
Cellular mechanism for the protective effect of haemoglobin S against P. falciparum malaria. Nature (1978) 2.28
Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease. Lancet (1989) 2.28
Haemoglobin Constant Spring--a chain termination mutant? Nature (1971) 2.25
alpha+-Thalassemia protects children against disease caused by other infections as well as malaria. Proc Natl Acad Sci U S A (1997) 2.19
The interaction between Plasmodium falciparum and P. vivax in children on Espiritu Santo island, Vanuatu. Trans R Soc Trop Med Hyg (1997) 2.12
Delta-beta-thalassemia is due to a gene deletion. Cell (1976) 2.12
Erythrocytes deficiency in glycophorin resist invasion by the malarial parasite Plasmodium falciparum. Nature (1982) 2.10
Surgical approach to cecal diverticulitis. J Am Coll Surg (1999) 2.07
Aplastic crisis due to parvovirus infection in pyruvate kinase deficiency. Lancet (1983) 2.05
Polycythemia associated with a hemoglobinopathy. J Clin Invest (1966) 1.98
Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia. Br J Haematol (1978) 1.98
A novel alpha-globin gene arrangement in man. Nature (1980) 1.98
The anaemia of P. falciparum malaria. Br J Haematol (1980) 1.97
Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol (2000) 1.95
Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemia. Proc Natl Acad Sci U S A (1979) 1.94
Cytosine arabinoside in the treatment of acute myeloblastic leukaemia. Lancet (1971) 1.94
Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16. Br Med J (Clin Res Ed) (1986) 1.93
The importance of anaemia in cerebral and uncomplicated falciparum malaria: role of complications, dyserythropoiesis and iron sequestration. Q J Med (1986) 1.90
Reliable routine estimation of small amounts of foetal haemoglobin by alkali denaturation. J Clin Pathol (1972) 1.88
Thalassaemia in the British. Br Med J (1973) 1.82
Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional. Proc Natl Acad Sci U S A (1980) 1.80
Benign sickle-cell anaemia. Lancet (1972) 1.79
Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex. Am J Hum Genet (1990) 1.76
Detection of somatic changes in human cancer DNA by DNA fingerprint analysis. Br J Cancer (1987) 1.74
Glycophorin as a possible receptor for Plasmodium falciparum. Lancet (1982) 1.69
An improved method for the characterization of human haemoglobin mutants: identification of alpha-2-beta-2-95GLU, haemoglobin N (Baltimore). Nature (1965) 1.68
Effects of foetal haemoglobin on susceptibility of red cells to Plasmodium falciparum. Nature (1977) 1.66
Iron absorption and loading in beta-thalassaemia intermedia. Lancet (1979) 1.66
Antenatal diagnosis of thalassaemia major. Br Med J (1978) 1.64
A newly defined X linked mental retardation syndrome associated with alpha thalassaemia. J Med Genet (1991) 1.61
Alpha-thalassemia. Curr Top Hematol (1983) 1.60
The anaemia of Plasmodium falciparum malaria. Br Med Bull (1982) 1.59
Thalassemia revisited. Cell (1982) 1.58
Melanesians and Polynesians share a unique alpha-thalassemia mutation. Am J Hum Genet (1985) 1.58
Further characterization of factor VIII-deficient mice created by gene targeting: RNA and protein studies. Blood (1996) 1.57
Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach. Nat Genet (1996) 1.57
Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain. Lancet (1971) 1.55
The pattern of disordered haemoglobin synthesis in homozygous and heterozygous beta-thalassaemia. Br J Haematol (1969) 1.54
Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution. Nucleic Acids Res (1984) 1.54
Haemoglobin Icaria, a new chain-termination mutant with causes alpha thalassaemia. Nature (1974) 1.53
Haemoglobin synthesis in beta-thalassaemia. Nature (1968) 1.52
Closing the diarrhoea diagnostic gap in Indian children by the application of molecular techniques. J Med Microbiol (2008) 1.49
Lectin-like polypeptides of P. falciparum bind to red cell sialoglycoproteins. Nature (1983) 1.48
Presence of gene for beta globin in homozygous beta0 thalassaemia. Nature (1976) 1.48
Prevention of iron loading in transfusion-dependent thalassaemia. Lancet (1978) 1.47
The alpha thalassaemias. Cell Mol Life Sci (2009) 1.47
Rearrangement of the T-cell-receptor beta-chain gene in the diagnosis of lymphoproliferative disorders. Lancet (1985) 1.46
Multiple arrangements of the human embryonic zeta globin genes. Nucleic Acids Res (1982) 1.45
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency. Blood (1996) 1.44
Haplotype analysis of the Mexican frameshift Cd 11 (-T) and -28 A->C beta-thalassemia alleles. Am J Hematol (1996) 1.43
Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group. Lancet (2000) 1.42
First-trimester fetal diagnosis for haemoglobinopathies: report on 200 cases. Lancet (1986) 1.42
Molecular basis for dominantly inherited inclusion body beta-thalassemia. Proc Natl Acad Sci U S A (1990) 1.42
Enhanced venous thrombus resolution in plasminogen activator inhibitor type-2 deficient mice. J Thromb Haemost (2014) 1.41
Theory and application of static field inhomogeneity effects in gradient-echo imaging. J Magn Reson Imaging (1997) 1.40
Superiority of acridine orange-stained buffy coat smears for diagnosis of partially treated neonatal septicemia. Acta Paediatr (1993) 1.39
PAMELA measurements of cosmic-ray proton and helium spectra. Science (2011) 1.39
Is the beta thalassaemia trait of clinical importance? Br J Haematol (2008) 1.39
Defective synthesis of HbE is due to reduced levels of beta E mRNA. Nature (1980) 1.38
Long-lived states to sustain hyperpolarized magnetization. Proc Natl Acad Sci U S A (2009) 1.38
Separation of the alpha and beta-chains of human hemoglobin. Nature (1968) 1.37
Fetal haemoglobin and malaria. Lancet (1976) 1.37
Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3. Am J Trop Med Hyg (1999) 1.36
Reduced erythrocyte survival following clearance of malarial parasitaemia in Thai patients. Br J Haematol (1987) 1.34
Pattern of maternal F-cell production during pregnancy. Lancet (1977) 1.32