Citation Impact
Citing Papers
Fetal Hemoglobin, Sickling, and Sickle Cell Disease
1990
The Molecular Genetics of Human Hemoglobin
1984
Senegal haplotype is associated with higher HbF than benin and cameroon haplotypes in African children with sickle cell anemia
1993
Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea
1989 Standout
Hypervariability of simple sequences as a general source for polymorphic DNA markers
1989 Standout
Volume-stimulated, Cl−-dependent K+ efflux is highly expressed in young human red cells containing normal hemoglobin or HbS
1987
Foreign body reaction to biomaterials
2008 Standout
Time‐dependent insulin oligomer reaction pathway prior to fibril formation: Cooling and seeding
2009 StandoutNobel
Cancer Stem Cells: Impact, Heterogeneity, and Uncertainty
2012 Standout
Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia
1995 Standout
Genetic Analysis of Innate Immunity
2006 StandoutNobel
Predicting clinical severity in sickle cell anaemia
2005
The Molecular Genetics of Philadelphia Chromosome–Positive Leukemias
1988
Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr–Abl positive cells
1996 Standout
Evaluation of a Density-Based Rapid Diagnostic Test for Sickle Cell Disease in a Clinical Setting in Zambia
2014
Gradients in surface nanotopography used to study platelet adhesion and activation
2013 StandoutNobel
Alpha thalassemia and stroke risk in sickle cell anemia
1994
Effects of herbimycin A and its derivatives on growth and differentiation of Ph1-positive acute lymphoid leukemia cell lines
1994 StandoutNobel
Internal initiation of translation of eukaryotic mRNA directed by a sequence derived from poliovirus RNA
1988 StandoutNature
Charybdotoxin blocks with high affinity the Ca-activated K+ channel of Hb A and Hb S red cells: Individual differences in the number of channels
1988
Sickle Cell Hemoglobin Polymerization
1990
Na+/H+ exchange is increased in sickle cell anemia and young normal red cells
1990
Sickle-cell disease
2010 Standout
Biosynthesis of the reverse transcriptase of hepatitis B viruses involves de novo translational initiation not ribosomal frameshifting
1989 StandoutNatureNobel
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
Cerebrovascular accidents in children with sickle-cell disease and alpha-thalassemia
1988
Therapeutic Strategies for Prevention of Sickle Cell Dehydration
2001
The paradox of hemoglobin SC disease
2003
Unique fusion of bcr and c-abl genes in Philadelphia chromosome positive acute lymphoblastic leukemia
1987
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Seeding “one-dimensional crystallization” of amyloid: A pathogenic mechanism in Alzheimer's disease and scrapie?
1993 Standout
Microsatellites: simple sequences with complex evolution
2004 Standout
Arginine metabolism and nutrition in growth, health and disease
2008 Standout
Cation transport and volume regulation in sickle red blood cells
1993
Arginine supplementation of sickle transgenic mice reduces red cell density and Gardos channel activity
2002
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
Localization of the site of recombination in formation of the Lepore Boston globin gene.
1981
Supramolecular Polymerization
2009 Standout
Expression of a Distinctive BCR-ABL Oncogene in Ph 1 -Positive Acute Lymphocytic Leukemia (ALL)
1988 Science
Mutant Potassium Channels with Altered Binding of Charybdotoxin, a Pore-Blocking Peptide Inhibitor
1989 StandoutScienceNobel
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
Maintenance of elevated fetal hemoglobin levels by decitabine during dose interval treatment of sickle cell anemia
2002
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
Induction of Chronic Myelogenous Leukemia in Mice by the P210 bcr/abl Gene of the Philadelphia Chromosome
1990 StandoutScienceNobel
Variable Philadelphia breakpoints and potential lineage restriction of bcr rearrangement in acute lymphoblastic leukemia
1988
Is there left-handed DNA at the ends of yeast chromosomes?
1983 StandoutNatureNobel
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia
1984
The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes
2009 Standout
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
Human globin ψB2is not a globin-related sequence
1982 StandoutNobel
An analysis of vertebrate mRNA sequences: intimations of translational control.
1991 Standout
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes
1987
Hemoglobin S gelation and sickle cell disease
1987
Membrane Transport in Sickle Cell Disease
2002
Deoxygenation inhibits the volume-stimulated, Cl(-)-dependent K+ efflux in SS and young AA cells: a cytosolic Mg2+ modulation
1987
Kinetics of sickle hemoglobin polymerization
1985
Hematologically and Genetically Distinct Forms of Sickle Cell Anemia in Africa
1985
A member of a new repeated sequence family which is conserved throughout eucaryotic evolution is found between the human δ and β globin genes
1981
Kinetics of sickle hemoglobin polymerization
1985
The Aquaporin Family of Water Channel Proteins in Clinical Medicine
1997 StandoutNobel
Molecular Genetics of Acute Lymphoblastic Leukemia
2005
Molecular basis of biomaterial-mediated foreign body reactions
2001
Abnormal methylation of the calcitonin gene marks progression of chronic myelogenous leukemia
1991
Density-based separation in multiphase systems provides a simple method to identify sickle cell disease
2014
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
1998 Standout
Effects of DNA methylation on topoisomerase I and II cleavage activities.
1994 StandoutNobel
Acute priapism associated with the use of sildenafil in a patient with sickle cell trait
2000
Pathophysiology of the Aquaporin Water Channels
1996 StandoutNobel
Functional Significance of Cell Volume Regulatory Mechanisms
1998 Standout
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.
1989 Standout
Two closely linked but separable promoters for human neuronal nitric oxide synthase gene transcription.
1995 StandoutNobel
The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions
1984 StandoutNobel
The first intron in the human c-abl gene is at least 200 kilobases long and is a target for translocations in chronic myelogenous leukemia.
1987 Nobel
Self-Assembly of β-Amyloid 42 Is Retarded by Small Molecular Ligands at the Stage of Structural Intermediates
2000 StandoutNobel
Delay Time of Hemoglobin S Polymerization Prevents Most Cells from Sickling in Vivo
1987 Science
HbS-Oman Heterozygote: A New Dominant Sickle Syndrome
1998
Works of JG Mears being referenced
CML patients in blast crisis have breakpoints localized to a specific region of the BCR
1987
Alpha-thalassemia is related to prolonged survival in sickle cell anemia
1983
Dense cells in sickle cell anemia: the effects of gene interaction
1984
Alpha-thalassemia is related to prolonged survival in sickle cell anemia
1983
Isolation and characterization of cloned DNA: the delta and beta globin genes in homozygous beta + thalassemia
1981
Frequent and extensive deletion during the 9,22 translocation in CML
1986
Variable breakpoints on the Philadelphia chromosome in chronic myelogenous leukemia
1985