Citation Impact
Citing Papers
The Molecular Genetics of Human Hemoglobin
1984
The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeat
1982 Nature
Expression and characterization of truncated human heme oxygenase (hHO-1) and a fusion protein of hHO-1 with human cytochrome P450 reductase
1995
The Clinical Sequelae of Intravascular Hemolysis and Extracellular Plasma Hemoglobin
2005 Standout
Lungs in thalassaemia major patients receiving regular transfusion
1996
Multicenter Comparison of Magnetic Resonance Imaging and Transcranial Doppler Ultrasonography in the Evaluation of the Central Nervous System in Children With Sickle Cell Disease
2000
The β-Thalassemias
1999 Standout
HIV-1 entry into quiescent primary lymphocytes: Molecular analysis reveals a labile, latent viral structure
1990 Standout
Phototherapy for Neonatal Jaundice
2008 Standout
Stroke prevention in sickle cell disease
2000
Pulmonary function abnormalities in thalassemia major and the role of iron overload.
1994
Intraperitoneal Cisplatin plus Intravenous Cyclophosphamide versus Intravenous Cisplatin plus Intravenous Cyclophosphamide for Stage III Ovarian Cancer
1996 Standout
Insulin resistance and hyperinsulinemia in homozygous β-thalassemia
1995
System-based approach to management of neonatal jaundice and prevention of kernicterus
2002
Blood Transfusion and Lung Function in Children with Thalassemia Major
1992
Diabetes in Asia
2009 Standout
Iron Chelators for Thalassaemia
1998
Advances in clinical research in sickle cell disease
2008
Sickle-cell disease
2010 Standout
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Cardiopulmonary Assessment in Beta-Thalassemia Major
1990
7 Increased HbF in adult life
1993
Neonatal Hyperbilirubinemia
2001 Standout
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Hinf I polymorphism 3′ to the human β-globin gene detected by the polymerase chain reaction (PCR)
1989 StandoutNobel
Iron-Chelating Therapy
1988
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
1984 Standout
Advances in thalassemia research
1984
A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.
1975
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
Characterization of an Indian (δβ)° thalassaemia
1984
Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
1979
Imaging by nuclear magnetic resonance in patients with chronic ischemic heart disease.
1984
Restriction mapping of a new deletion responsible forGγ(δβ)° thalassaemia
1981
Sickle cell anemia as a syndrome: A review of diagnostic features
1979
Clinical Features of Bilirubin Encephalopathy
1990
How Bilirubin Gets into the Brain
1990
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
The complete nucleotide sequence of mouse immunoglobulin γ2a gene and evolution of heavy chain genes: further evidence for intervening sequence-mediated domain transfer
1981 StandoutNobel
Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
1988 StandoutScienceNobel
Nucleotide sequence of 16-kilobase pairs of DNA 5' to the human epsilon-globin gene.
1985 StandoutNobel
The control of globin and other eukaryotic genes
1982 StandoutNobel
MOLECULAR GENETICS OF HUMAN HEMOGLOBIN
1976
A history of the human fetal globin gene duplication
1981 StandoutNobel
An Individual with Hb‐Lepore‐Baltimore‐ δβ‐Thalassaemia in a Yugoslavian Family
1976
The linkage arrangement of four rabbit β-like globin genes
1979
Clinical pharmacology, physiology and pathophysiology of superficial veins‐2.
1994
Hemoglobins Lepore and Anti-Lepore
1978
The Liver in Thalassaemia Major: Ultra‐Structural Observations
1977
Detection of a novel DNA polymorphism in the beta-globin gene cluster.
1984 StandoutNobel
Does Hyperbilirubinemia Damage the Brain of Healthy Full-Term Infants?
1990
Major rearrangement in the human β-globin gene cluster
1981 Nature
The evolution and sequence comparison of two recently diverged mouse chromosomal β-globin genes
1979
A mouse α-globin-related pseudogene lacking intervening sequences
1980 StandoutNatureNobel
The synthesis of the Gγ and Aγ chains of human fetal hemoglobin in erythroid colonies cultured from peripheral blood BFUe's of normal adults and newborn and of subjects with an Aγ or a Gγ chain abnormal fetal hemoglobin
1980
Hb switching in chickens
1980
Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?
1982
Nuclear Magnetic Resonance Technology for Medical Studies
1984 StandoutScienceNobel
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
A gene deletion ending at the midpoint of a repetitive DNA sequence in one form of hereditary persistence of fetal haemoglobin
1982 Nature
THE MUTATION AND POLYMORPHISM OF THE HUMAN β-GLOBIN GENE AND ITS SURROUNDING DNA
1984
Two novel arrangements of the human fetal globin genes: Gγ-Gγand Aγ-Aγ
1984 StandoutNobel
Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
1985 StandoutScienceNobel
Expression of a Bacterial Gene in Mammalian Cells
1980 StandoutScienceNobel
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Human globin ψB2is not a globin-related sequence
1982 StandoutNobel
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Ordering of mouse immunoglobulin heavy chain genes by molecular cloning
1981 StandoutNatureNobel
Molecular cloning and characterization of the human β-like globin gene cluster
1980
Characterisation of deletions which affect the expression of fetal globin genes in man
1979 Nature
Nucleotide sequences of immunoglobulin epsilon genes of chimpanzee and orangutan: DNA molecular clock and hominoid evolution.
1987 StandoutNobel
The Gγ‐δβ‐thalassemia and Gγ‐β°‐HPFH conditions in combination with β‐thalassemia and Hb S
1977
Genetic Dissection of Complex Traits
1994 StandoutScience
Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in Africa
1985
Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G? and A? types of ? chain
1984
Investigation of Chronic Venous Insufficiency
2000 Standout
(Aγδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA
1985 StandoutNobel
Intraperitoneal Cisplatin with Systemic Thiosulfate Protection
1982
Anomaly in the γ chain heterogeneity of the newborn
1977 Nature
Base substitutions, length differences and DNA strand asymmetries in the human Gγ and Aγ fetal globin gene region
1981 StandoutNobel
A catalogue of splice junction sequences
1982 Standout
(Aγδβ)° thalassaemia: similarity of phenotype in four different molecular defects, including one newly described
1984
Mutation in LDL Receptor: Alu-Alu Recombination Deletes Exons Encoding Transmembrane and Cytoplasmic Domains
1985 StandoutScienceNobel
Isolation of Duplicated Human c-src Genes Located on Chromosomes 1 and 20
1985 StandoutNobel
Developmental genetics of the human haemoglobins
1983
Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease
1979 Nature
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Neonatal Bilirubinemia in Production of Long-Term Neurological Deficits
1968
Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin
1980 Nature
Rapid and efficient cosmid cloning
1981 Standout
Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.
1977
Heme-Containing Oxygenases
1996 Standout
Iron-Chelating Therapy and the Treatment of Thalassemia
1997
HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) AND δβ THALASSAEMIA
1979
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Recent advances in the quantitation of human fetal hemoglobins with different gamma chains
1980
Abnormal Glucose Tolerance in Transfusion-Dependent β-Thalassemic Patients
2001
Identification of human immunodeficiency virus sequences by using in vitro enzymatic amplification and oligomer cleavage detection
1987 StandoutNobel
Different 3' end points of deletions causing delta beta-thalassemia and hereditary persistence of fetal hemoglobin: implications for the control of gamma-globin gene expression in man.
1983
Physical mapping of the globin gene deletion in hereditary persistence of foetal haemoglobin (HPFH)
1980
Adrenal Function in Thalassemia Major Following Long-term Treatment With Multiple Transfusions and Chelation Therapy
1987
Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes
1986 StandoutNatureNobel
The regulated expression of β-globin genes introduced into mouse erythroleukemia cells
1983 StandoutNobel
Insertion of DNA sequences into the human chromosomal β-globin locus by homologous recombination
1985 StandoutNatureNobel
Unexpected relationships between four large deletions in the human β-globin gene cluster
1983 StandoutNobel
Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin Synthesis
1980
Recombination and balanced chromosome polymorphism suggested by DNA sequences 5' to the human delta-globin gene.
1983 StandoutNobel
The nucleotide sequence of the human β-globin gene
1980
Works of C Hyman being referenced
Further Studies of the Postnatal Change in Chemical Heterogeneity of Human Fetal Hemoglobin in Several Abnormal Conditions
1975
CNS Abnormalities After Neonatal Hemolytic Disease or Hyperbilirubinemia
1969
An individual with ?Miyada?-like hemoglobin indistinguishable from hemoglobin A2
1973
Cerebral vasculopathy in sickle cell anemia: diagnostic contribution of positron emission tomography.
1999
Venous Distensibility in Essential Hypertension
1969
LONGITUDINAL STUDY OF THE INCIDENCE OF CENTRAL NERVOUS SYSTEM DAMAGE FOLLOWING ERYTHROBLASTOSIS FETALIS
1954
THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS*
1974
Central Nervous System Involvement by Leukemia in Children. II. Therapy with Intrathecal Methotrexate
1965
Carbohydrate Metabolism and Pancreatic Islet-cell Function in Thalassemia Major
1977
ENDOCRINE FUNCTION IN THALASSEMIA
1977
Combined Subcutaneous and High‐Dose Intravenous Deferoxamine Therapy of Thalassemiaa
1985
dl‐α‐TOCOPHEROL, IRON, AND LIPOFUSCIN IN THALASSEMIA*
1974
History of plethysmography.
1961
Hearing Loss in Children with Neonatal Hyperbilirubinemia
1963
Pulmonary Function Abnormalities in Thalassemia Patients on a Hypertransfusion Program
1980