Citation Impact
Citing Papers
Surveillance for Foodborne Disease Outbreaks—United States, 2006
2009 Standout
Allele-Specific Hybridization Using Oligonucleotide Probes of Very High Specific Activity: Discrimination of the Human β A - and β S -Globin Genes
1984
The Molecular Genetics of Human Hemoglobin
1984
Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19·2 million participants
2016 Standout
Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
2008 Standout
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
1991 Standout
An Improved Method for Prenatal Diagnosis of Genetic Diseases by Analysis of Amplified DNA Sequences
1987
Global Epidemiology of Hemoglobin Disorders
1998
Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
1997
Bone marrow transplantation in thalassemia
1997
SURVIVAL AND CAUSES OF DEATH IN THALASSAEMIA MAJOR
1989
Mutation Analysis of 3 Genes in Patients With Leber Congenital Amaurosis
2000
The β-Thalassemias
1999 Standout
Decline in Invasive Pneumococcal Disease after the Introduction of Protein–Polysaccharide Conjugate Vaccine
2003 Standout
6 β-Thalassaemia
1993
The molecular basis of blood coagulation
1988 Standout
Maternal and child undernutrition and overweight in low-income and middle-income countries
2013 Standout
Assessment of Quality-of-Life Outcomes
1996 Standout
Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect
2016 Standout
Bcl-2 functions in an antioxidant pathway to prevent apoptosis
1993 Standout
Principal components analysis corrects for stratification in genome-wide association studies
2006 Standout
A Comparison of Observational Studies and Randomized, Controlled Trials
2000 Standout
Restriction enzymes and their isoschizomers
1990 StandoutNobel
8 The population genetics of the haemoglobinopathies
1993
DNA Damage and Oxygen Radical Toxicity
1988 StandoutScience
A moderate transfusion regimen may reduce iron loading in beta‐ thalassemia major without producing excessive expansion of erythropoiesis
1997
A Risk-Benefit Assessment of Iron-Chelation Therapy
1997
The Effect of Folic Acid Fortification on Plasma Folate and Total Homocysteine Concentrations
1999 Standout
Effect of Age at the Start of Iron Chelation Therapy on Gonadal Function in β-Thalassemia Major
1990
7 Increased HbF in adult life
1993
Role of oxidative stress in neurodegeneration: recent developments in assay methods for oxidative stress and nutraceutical antioxidants
2004
Genetic Alterations during Colorectal-Tumor Development
1988 Standout
Comparison of chorionic villus sampling and amniocentesis for fetal karyotyping at 10-13 weeks' gestation
1994
Integrative transformation of Caenorhabditis elegans
1986 StandoutNobel
C. elegans cell survival gene ced-9 encodes a functional homolog of the mammalian proto-oncogene bcl-2
1994 StandoutNobel
Activation of C. elegans cell death protein CED-9 by an ammo-acid substitution in a domain conserved in Bcl-2
1994 StandoutNatureNobel
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
8 Prenatal diagnosis and screening of the haemoglobinopathies
1998
Iron-Chelating Therapy
1988
Prevention of congenital abnormalities by periconceptional multivitamin supplementation.
1993
Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
1983
Construction and characterization of genomic libraries from specific human chromosomes.
1982
Correlation of the physical and genetics maps in the lin-12 region of caenorahabditis elegans
1987 StandoutNobel
Molecular cloning of the gene for human anti-haemophilic factor IX
1982 Nature
Altering Genotype and Phenotype by DNA-Mediated Gene Transfer
1980 StandoutScienceNobel
Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
1982 Nature
Prenatal Diagnosis of β-Thalassemia
1983
Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites.
1980
Improved Detection of the Sickle Mutation by DNA Analysis
1982
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
A NEW DNA POLYMORPHISM IN THE β-GLOBIN GENE CLUSTER CAN BE USED FOR ANTENATAL DIAGNOSIS OF β-THALASSAEMIA
1983
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
FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES
1986
Mitochondrial DNA and human evolution
1987 StandoutNature
Gene amplification and gene correction in somatic cells
1982 StandoutNobel
Marrow Transplantation for Thalassemiaa
1985 StandoutNobel
Detection of a novel DNA polymorphism in the beta-globin gene cluster.
1984 StandoutNobel
Diversity of murine gamma genes and expression in fetal and adult T lymphocytes
1986 StandoutNatureNobel
Copper Homeostasis and Neurodegenerative Disorders (Alzheimer's, Prion, and Parkinson's Diseases and Amyotrophic Lateral Sclerosis)
2006 Standout
Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?
1998
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
Nonrandom association of polymorphic restriction sites in the β-globin gene cluster
1982
Prevention of Cardiac Disease by Subcutaneous Deferoxamine in Patients with Thalassemia Major
1985
Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
1985 StandoutScienceNobel
X chromosome-linked muscular dystrophy (mdx) in the mouse.
1984 Standout
Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.
1993 Standout
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Prenatal Diagnosis of Sickle-Cell Anemia in the First Trimester of Pregnancy
1983
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
1986 Standout
Evolution of the Hemoglobin S and C Genes in World Populations
1980 Science
Actin gene family of Caenorhabditis elegans
1983
Hypervariable ‘minisatellite’ regions in human DNA
1985 StandoutNature
Prenatal Diagnosis Using DNA Polymorphisms
1983
Polymorphism of the Hinf I restriction site located 1 Kb 5? to the human ?-globin gene
1982
DNA restriction fragment length polymorphisms and heterozygosity in the human genome
1984
Multiple arrangements of viral DNA and an activated host oncogene in bursal lymphomas
1982 StandoutNatureNobel
THE MOLECULAR GENETICS OF HUMAN HEMOGLOBINS
1980
Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.
1986 StandoutNobel
Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
1988 StandoutScience
Heme-Containing Oxygenases
1996 Standout
Rapid Prenatal Diagnosis of Sickle Cell Anemia by a New Method of DNA Analysis
1987
Iron-Chelating Therapy and the Treatment of Thalassemia
1997
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer.
1988 Standout
Chromosomes with one, two, three, and four fetal globin genes: molecular and hematologic analysis
1986
Strategies for multilocus linkage analysis in humans.
1984 Standout
Direct detection of the common Mediterranean beta-thalassemia gene with synthetic DNA probes. An alternative approach for prenatal diagnosis.
1983
Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem
1998
Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes
1986 StandoutNatureNobel
The DNA sequence of the 5′ flanking region of the human 0-gk bin gene: evolutionary conservation and polymorphic differences
1982
Incorporating utility-based quality-of-life assessment measures in clinical trials. Two examples.
1989
A polymorphic DNA marker genetically linked to Huntington's disease
1983 StandoutNature
Effects and safety of periconceptional oral folate supplementation for preventing birth defects
2015
Oxygen toxicity, oxygen radicals, transition metals and disease
1984 Standout
Differences in human α- and β-globin gene expression in mouse erythroleukemia cells: The role of intragenic sequences
1984 StandoutNobel
Mapping the Human Genome, Cloned Genes, DNA Polymorphisms, and Inherited Disease
1982
Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy
1982 Nature
Works of B. Modell being referenced
Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.
1980
Alpha thalassaemia hydrops fetalis in the UK: the importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha thalassaemia trait
1992
THE BAIGAS OF MADHYA PRADESH: A DEMOGRAPHIC STUDY
1997
Genetic screening for ethnic minorities.
1990
Folic acid to reduce neonatal mortality from neural tube disorders
2010
Transfusion requirements and effects in patients with thalassaemia major
1991
What proportion of congenital abnormalities can be prevented?
1993
EFFECT OF FETAL DIAGNOSTIC TESTING ON BIRTH-RATE OF THALASSAEMIA MAJOR IN BRITAIN
1984
Impact of public health on human genetics.
1989
Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations
1984
Advances in the use of iron-chelating agents for the treatment of iron overload.
1979
Factors affecting the uptake of prenatal diagnosis for sickle cell disease.
1992
Distribution and control of some genetic disorders.
1988
Thalassaemia in Azerbaijan.
1994
Prevention and control of haemoglobinopathies.
1995
DIRECT GENE ANALYSIS OF CHORIONIC VILLI: A POSSIBLE TECHNIQUE FOR FIRST-TRIMESTER ANTENATAL DIAGNOSIS OF HAEMOGLOBINOPATHIES
1981
Survival and desferrioxamine in thalassaemia major.
1982
Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms
1980 Nature
Association of thalassaemia intermedia with a beta‐globin gene haplotype
1987
Community control of genetic and congenital disorders
1997
Medical research council European trial of chorion villus sampling
1992
Population and genetic studies suggest a single origin for the Indian deletion β° thalassaemia
1984
Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations
1984