Citation Impact
Citing Papers
The Systemic Amyloidoses
1997 Standout
Male development of chromosomally female mice transgenic for Sry
1991 StandoutNature
mRNA vaccines — a new era in vaccinology
2018 StandoutNobel
mRNA-based therapeutics — developing a new class of drugs
2014 StandoutNobel
The β-Thalassemias
1999 Standout
Primary Structure and Oxygen-Binding Properties of the Hemoglobin from Guanaco (Lama guanacoë,Tylopoda)
1990
Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations
2016 StandoutNobel
High hemoglobin mixed disulfide content in hemolysates from stressed shark
1990
Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group
2008
Complementation of reduced survival, hypotension, and renal abnormalities in angiotensinogen-deficient mice by the human renin and human angiotensinogen genes.
1997 StandoutNobel
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques
1989 StandoutNobel
Characterisation of functional domains within the mouse erythropoietin 3′ enhancer conveying oxygen-regulated responses in different cell lines
1994 StandoutNobel
Regulation of autoimmune diabetes by non‐islet‐specific T cells — a role for the glucocorticoid‐induced TNF receptor
2004 StandoutNobel
Sickle-cell disease
2010 Standout
Molecular biology of erythropoietin
1993 StandoutNobel
Regulation of β-globin gene expression: straightening out the locus
1996
mRNA transcript therapy
2014 StandoutNobel
Molecular analysis of deletions in the human β-globin gene cluster: Deletion junctions and locations of breakpoints
1990 StandoutNobel
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
Transcriptional regulation of gene expression: Mechanisms and pathophysiology
1994 StandoutNobel
Allelic inactivation regulates olfactory receptor gene expression
1994 StandoutNobel
Germanium and silver resistance, accumulation, and toxicity in microorganisms
1992 Standout
Hox genes in vertebrate development
1994 Standout
Position-independent, high-level expression of the human β-globin gene in transgenic mice
1987 Standout
Irresistible force meets immovable object: Transcription and the nucleosome
1991 StandoutNobel
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
2013 Standout
Gene conversions and their relation to homologous chromosome pairing
1986 StandoutNobel
DNA sequence variation associated with elevated fetal G gamma globin production
1985
Mouse model for the lysosomal disorder galactosialidosis and correction of the phenotype with overexpressing erythroid precursor cells.
1995 StandoutNobel
Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes
1985
THE EVOLUTION OF MULTIGENE FAMILIES: Human Haptoglobin Genes
1986 StandoutNobel
Extinction of the tumor necrosis factor locus, and of genes encoding the lipopolysaccharide signaling pathway.
1993 StandoutNobel
Deletion of the A gamma-globin gene in G gamma-delta beta-thalassemia.
1979
Intravenous immune globulin prevents venular vaso-occlusion in sickle cell mice by inhibiting leukocyte adhesion and the interactions between sickle erythrocytes and adherent leukocytes
2003
Long-Circulating and Target-Specific Nanoparticles: Theory to Practice
2001 Standout
Sickle cell anemia as a syndrome: A review of diagnostic features
1979
A gene deletion ending within a complex array of repeated sequences 3' to the human beta-globin gene cluster.
1986 StandoutNobel
Cerebrovascular accidents in sickle cell disease: rates and risk factors.
1998 Standout
The control of globin and other eukaryotic genes
1982 StandoutNobel
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia
1984
Interaction of Allosteric Effectors with α-Globin Chains and High Altitude Respiration of Mammals. The Primary Structure of Two Tylopoda Hemoglobins with High Oxygen Affinity: Vicuna(Lama vicugna)and Alpaca(Lama pacos)
1986
Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients
1984
Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers
1976
‘Silent’β‐thalassaemia caused by a ‘silent’β‐chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia
1982
A ChineseGγ+(Aγδβ)0thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
1985 StandoutNobel
SHORT GENE CONVERSIONS IN THE HUMAN FETAL GLOBIN GENE REGION: A BY-PRODUCT OF CHROMOSOME PAIRING DURING MEIOSIS?
1986 StandoutNobel
Gamma thalassemia resulting from the deletion of a gamma-globin gene.
1983
Half-lives of beta and gamma globin messenger RNAs and of protein synthetic capacity in cultured human reticulocytes
1985
Separation by hybrid isoelectric focusing of normal human plasma transthyretin (prealbumin) and a variant with a methionine for valine substitution associated with familial amyloidotic polyneuropathy
1986
The occurrence of different levels of Gγ chain and of the AγT variant of fetal hemoglobin in newborn babies from several countries
1983
Two novel arrangements of the human fetal globin genes: Gγ-Gγand Aγ-Aγ
1984 StandoutNobel
The role of membrane skeletal-associated alpha-globin in the pathophysiology of beta-thalassemia
1990
Organization of ?-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, ?-thalassemia, and ?-thalassemia-2
1982
Construction of a functional human suppressor tRNA gene: an approach to gene therapy for β-thalassaemia
1982 Nature
Establishment of mammalian cell lines containing multiple nonsense mutations and functional suppressor tRNA genes
1982 StandoutNobel
Ectopic expression of the H19 gene in mice causes prenatal lethality.
1991 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Regulated expression of genes inserted at the human chromosomal beta-globin locus by homologous recombination.
1988 StandoutNobel
Prevention of Type I Diabetes in Nonobese Diabetic Mice by Virus Infection
1988 Science
The Association of Hemoglobin Knossos and Hemoglobin Lepore in an Algerian Patient
1984
The Ratio of the Gγ and Aγ Chains: Variations due to Anomalies at the Molecular Level
1985
(Aγδβ)°‐Thalassaemia in Blacks is due to a deletion of 34 kbp of DNA
1985 StandoutNobel
Metal resistance in bacteria
1985
Evolution and present situation of the South American Camelidae
1995 Standout
The chemical heterogeneity of the fetal hemoglobin of black newborn babies and adults: a reevaluation
1981
The Caenorhabditis elegans gene lin-10 is broadly expressed while required specifically for the determination of vulval cell fates.
1990 StandoutNobel
Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.
1986 StandoutNobel
Developmental genetics of the human haemoglobins
1983
Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.
1980
Antioxidant Defenses in Fish: Biotic and Abiotic Factors
2005 Standout
Clinical diversity of sickle cell anemia: Genetic and cellular modulation of disease severity
1983
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
1998 Standout
Pluronic F-68 reduces the endothelial adherence and improves the rheology of liganded sickle erythrocytes.
1987
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
Functional analysis of an oxygen-regulated transcriptional enhancer lying 3' to the mouse erythropoietin gene.
1991 StandoutNobel
α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia
1979 Nature
Abnormal Adherence of Sickle Erythrocytes to Cultured Vascular Endothelium
1980
Silent β-Thalassemia Associated with Hb Knossos β27 (B9) Ala→Ser in Algeria
1983
The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease
1982
Alpha chain and gamma chain abnormal hemoglobins in newborn babies: Structural and genetic aspects
1983
Conservation of sequence and structure flanking the mouse and human β-globin loci: The β-globin genes are embedded within an array of odorant receptor genes
1999 StandoutNobel
Works of M. E. Gravely being referenced
Variability in the interaction of beta-thalassemia with the alpha-chain variants Hb G-Philadelphia and Hb Rampa.
1978
Radioimmunochemical characterization of hemoglobins Lepore and Kenya: unique antigenic determinants located on hybrid hemoglobins.
1978
Post-translational control of human hemoglobin synthesis; the number of alpha chain genes and the synthesis of HB S.
1978
The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults
1977
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
Minor hemoglobins in sickle cell anemia, β-thalassemia, and related conditions: A study of red cell fractions isolated by density gradient centrifugation
1975
Specific radioimmunochemical identification and quantitation of hemoglobins a2 and f
1976
Further studies of the frequency and significance of the Tgamma-chain of human fetal hemoglobin.
1979
Hb S, Hb G-PHILADELPHIA AND α-THALASSEMIA-2 IN A BLACK FAMILY
1980
Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at Birth
1977
Heterozygosity and Homozygosity for the High Oxygen Affinity Hemoglobin Tarrant or α126 (H9) ASP→ASN in two Mexican Families
1981
Radiochemical Characterization of Hemoglobins Lepore and Kenya: Unique Antigenic Determinants Located on Hybrid Hemoglobins
1978
The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis
1979
The Synthesis of Fetal Hemoglobin Types in red Blood Cells and in BFU-E Derived Colonies from Peripheral Blood of Patients with Sickle Cell Anemia, β+- and δβ-Thalassemia, Various forms of Hereditary Persistence of Fetal Hemoglobin, Normal Adults and Newborn
1979
Radioimmunoassay for Abnormal Hemoglobins
1977 Science
δβ-Thalassemia in a Mexican Family: Clinical Differences Among Homozygotes
1978
Alpha-Thalassemia-2 and the Variability of Hematological Values in Children with Sickle Cell Anemia
1981
Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin Synthesis
1980
THE RATIO OF Gγ AND Aγ CHAINS OF THE HEMOGLOBIN F SYNTHESIZED BY BFU‐E‐DERIVED COLONIES FROM BLOOD OF SUBJECTS WITH β+ THALASSEMIA AND RELATED HEMOGLOBINOPATHIES *
1980