Citation Impact
Citing Papers
The Molecular Genetics of Human Hemoglobin
1984
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
2008 StandoutNature
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions.
1986 Standout
Homozygous Inactivation of theNF1Gene in Bone Marrow Cells from Children with Neurofibromatosis Type 1 and Malignant Myeloid Disorders
1997
Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
1997
The Clinical Sequelae of Intravascular Hemolysis and Extracellular Plasma Hemoglobin
2005 Standout
CASK and Protein 4.1 Support F-actin Nucleation on Neurexins
2001 StandoutNobel
The β-Thalassemias
1999 Standout
The Agent of Bacillary Angiomatosis
1990 Standout
Flexibility and constraint in the nucleosome core landscape of Caenorhabditis elegans chromatin
2006 StandoutNobel
Molecular basis of human hypertension: Role of angiotensinogen
1992 Standout
1 The population genetics of the haemoglobinopathies
1998
6 β-Thalassaemia
1993
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease
2005
Sickle cell disease in India
2014
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1991 StandoutNature
Association between an oncogene and an anti-oncogene: the adenovirus E1A proteins bind to the retinoblastoma gene product
1988 StandoutNature
Osteoporosis: now and the future
2011 Standout
Hemolytic anemias: Diagnosis and Management
1992
WNT signaling in bone homeostasis and disease: from human mutations to treatments
2013 Standout
LACK OF EVIDENCE OF PERMANENT ENGRAFTMENT AFTER IN UTERO FETAL STEM CELL TRANSPLANTATION IN CONGENITAL HEMOGLOBINOPATHIES1
1996
8 The population genetics of the haemoglobinopathies
1993
Presence of fetal DNA in maternal plasma and serum
1997 Standout
The PDZ Domain of Human Erythrocyte p55 Mediates Its Binding to the Cytoplasmic Carboxyl Terminus of Glycophorin C
1997
The sequence of the gorilla fetal globin genes: evidence for multiple gene conversions in human evolution.
1984
Nonradioactive HLA class II typing using polymerase chain reaction and digoxigenin-11-2′-3′-dideoxyuridinetriphosphate-labeled oligonucleotide probes
1991
Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes
1988
Gene Defects in β‐Thalassemia and Their Prenatal Diagnosis
1990
Sickle-cell disease
2010 Standout
Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis
2003
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
1993 Standout
Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7
1992
The Polymerase Chain Reaction
1990
Homology requirements for unequal crossing over in humans.
1991 StandoutNobel
Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death
1994 Standout
7 Increased HbF in adult life
1993
World distribution of factor V Leiden
1995 Standout
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
1996
Why are some genetic diseases common?
1993
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Advances in thalassemia research
1984
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system
1995
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
1980
The nucleotide sequence of the rabbit embryonic globin gene beta 4.
1983
Efficient transfer of large DNA fragments from agarose gels to diazobenzyloxymethyl-paper and rapid hybridization by using dextran sulfate.
1979 Standout
Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.
1978
Human Retinoblastoma Susceptibility Gene: Cloning, Identification, and Sequence
1987 StandoutScience
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
Nucleotide sequence of 16-kilobase pairs of DNA 5' to the human epsilon-globin gene.
1985 StandoutNobel
Cerebrovascular accidents in sickle cell disease: rates and risk factors.
1998 Standout
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes
2009 Standout
The rate of telomere sequence loss in human leukocytes varies with age
1998 StandoutNobel
Marrow Transplantation for Thalassemiaa
1985 StandoutNobel
Detection of a novel DNA polymorphism in the beta-globin gene cluster.
1984 StandoutNobel
Developmentally regulated use of alternative promoters creates a novel platelet-derived growth factor receptor transcript in mouse teratocarcinoma and embryonic stem cells.
1989
Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA
1993 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
Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
1985 StandoutScienceNobel
PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES *
1980
Ionizable lipid nanoparticles for in utero mRNA delivery
2021 StandoutNobel
Prenatal Diagnosis of Homozygous α-Thalassemia
1979
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Immunodominant CD4+ T-cell epitope within nonstructural protein 3 in acute hepatitis C virus infection
1997 StandoutNobel
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
1986
An analysis of vertebrate mRNA sequences: intimations of translational control.
1991 Standout
Strategy linking several analytical methods of neonatal screening for sickle cell disease
2001
?-Thalassemia haplotypes in the Algerian population
1987
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Multiple DNA fragment polymorphisms associated with immunoglobulin mu chain switch-like regions in man.
1983 StandoutNobel
Regulated expression of genes inserted at the human chromosomal beta-globin locus by homologous recombination.
1988 StandoutNobel
Partial deletion of the α-globin structural gene in human α-thalassaemia
1980 Nature
The 3′ untranslated regions of the duplicated human α-globin genes are unexpectedly divergent
1980
Nucleosomes are phased along the mouse β-major globin gene in erythroid and nonerythroid cells
1986 StandoutNobel
The Molecular Genetics of Cancer
1987 StandoutScienceNobel
Prenatal Diagnosis Using DNA Polymorphisms
1983
Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.
1986
Heterogeneity in the molecular basis of hereditary persistence of fetal haemoglobin
1980 Nature
Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
1980
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG-MDS)
1997
Triplicated alpha-globin loci in humans.
1980
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
Molecular basis and prenatal diagnosis of beta-thalassemia
1988
Investigation of Genetic Linkage in Human Families
1987
The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia
2016 Standout
Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem
1998
Unexpected relationships between four large deletions in the human β-globin gene cluster
1983 StandoutNobel
Nucleotide sequence of the coding portion of human alpha globin messenger RNA.
1980
Dating of the human-ape splitting by a molecular clock of mitochondrial DNA
1985 Standout
Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs
1984 Standout
DPC4 , A Candidate Tumor Suppressor Gene at Human Chromosome 18q21.1
1996 StandoutScience
Differences in human α- and β-globin gene expression in mouse erythroleukemia cells: The role of intragenic sequences
1984 StandoutNobel
Works of YW Kan being referenced
Characterization of a spontaneous mutation in beta-thalassemia associated with advanced paternal age
1989
Rapid prenatal diagnosis of beta thalassemia using DNA amplification and nonradioactive probes
1989
Prenatal diagnosis of hemoglobin disorders.
1977
Molecular basis of hemoglobin-H disease in the Mediterranean population
1979
Delta +-thalassemia in Sardinia
1983
Inhibition of fetal globin gene switching in vivo in human and ovine fetuses.
1987
Isolation of hybrid cell clones that contain deletion and non-deletion defects of alpha-thalassemia in man
1980
A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA
1988
Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis
1992
Alpha globin gene number: population and restriction endonuclease studies
1980
The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosis
1987
Rapid prenatal diagnosis of beta thalassemia using DNA amplification and nonradioactive probes
1989
Molecular basis of hemoglobin-H disease in the Mediterranean population
1979
Alpha-thalassemia in two Mediterranean populations
1982
Molecular characterization of erythrocyte glycophorin C variants
1991
Delta +-thalassemia in Sardinia
1983
The inactive beta globin gene on a gamma delta beta thalassemia chromosome has a normal structure and functions normally in vitro
1988
Molecular characterization of erythrocyte glycophorin C variants
1991
The William Allan Memorial Award address: Thalassemia: molecular mechanism and detection.
1986
Sequence of the 3'-noncoding and adjacent coding regions of human gamma-globin mRNA.
1978
Alpha-thalassemia in blacks is due to gene deletion.
1979
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily
1993
The inactive beta globin gene on a gamma delta beta thalassemia chromosome has a normal structure and functions normally in vitro
1988
Hb Bart's level in cord blood and deletions of alpha-globin genes
1982