Citation Impact
Citing Papers
Gene expression profiling in a renal cell carcinoma cell line: dissecting VHL and hypoxia-dependent pathways.
2003 StandoutNobel
HIF prolyl and asparaginyl hydroxylases in the biological response to intracellular O2 levels
2003 StandoutNobel
Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans
2008
HIF Hydroxylase Pathways in Cardiovascular Physiology and Medicine
2015 StandoutNobel
Emerging roles of PKM2 in cell metabolism and cancer progression
2012 StandoutNobel
The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis
2009 Standout
Co‐ordinated programme of gene expression during asexual intraerythrocytic development of the human malaria parasite Plasmodium falciparum revealed by microarray analysis
2001
Structural basis for oxygen degradation domain selectivity of the HIF prolyl hydroxylases
2016 StandoutNobel
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
2007 Standout
TIGAR, a p53-Inducible Regulator of Glycolysis and Apoptosis
2006 Standout
Exercise-Induced Oxidative Stress: Cellular Mechanisms and Impact on Muscle Force Production
2008 Standout
Oxidative stress and gene regulation
2000
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose‐6‐phosphate dehydrogenase (G‐6‐PD) deficiency
2004
Guillain-Barré syndrome
2016 Standout
Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations
2016 StandoutNobel
Hematologically Important Mutations: Glucose-6-phosphate Dehydrogenase
1996
The Organization of the γ-Glutamyl Transferase Genes and Other Low Copy Repeats in Human Chromosome 22q11
1997
Glucose‐6‐phosphate metabolism in Plasmodium falciparum
2012
Eculizumab prevents anti-ganglioside antibody-mediated neuropathy in a murine model
2008
Glucose-6-phosphate isomerase deficiency
2000
Guillain–Barré Syndrome
2012 Standout
The immunobiology of Guillain‐Barré syndromes
2005
Triosephosphate isomerase deficiency: historical perspectives and molecular aspects
2000
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
Glucose-6-Phosphate Dehydrogenase Deficiency
1991
The Transcriptome of the Intraerythrocytic Developmental Cycle of Plasmodium falciparum
2003 Standout
Treatment of IgM antibody associated polyneuropathies using rituximab
2003
Structural Basis for Recognizing Phosphoarginine and Evolving Residue-Specific Protein Phosphatases in Gram-Positive Bacteria
2013 StandoutNobel
The prolyl hydroxylase enzymes that act as oxygen sensors regulating destruction of hypoxia-inducible factor α
2004 StandoutNobel
Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia
2002 StandoutNobel
Pathogenetic mechanisms of polycythemia vera and congenital polycythemic disorders
2001
Synthesis and evaluation of a new inhibitor of phosphoglucose isomerases: the enediolate analogue 5-phospho-D-arabinohydroxamate
1998
Mechanistic implications for Escherichia coli cofactor-dependent phosphoglycerate mutase based on the high-resolution crystal structure of a vanadate complex
2002
Idiopathic erythrocytosis: a disappearing entity
2009
Red cell pyruvate kinase deficiency: from genetics to clinical manifestations
2000
Methemoglobinemia: Etiology, Pharmacology, and Clinical Management
1999 Standout
Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2010
2011 Standout
Oxidants, oxidative stress and the biology of ageing
2000 StandoutNature
GlcNAc 2-Epimerase Can Serve a Catabolic Role in Sialic Acid Metabolism
2003 StandoutNobel
The Emerging Hallmarks of Cancer Metabolism
2016 Standout
Neurophysiological and immunohistochemical studies on Guillain-Barré syndrome with IgG anti-GalNAc-GD1a antibodies—effects on neuromuscular transmission
2004
Pathophysiological actions of neuropathy‐related anti‐ganglioside antibodies at the neuromuscular junction
2009
Reactive oxygen species, antioxidants, and the mammalian thioredoxin system1 1This review is based on the licentiate thesis “Thioredoxin reductase—interactions with the redox active compounds 1-chloro-2,4-dinitrobenzene and lipoic acid” by Jonas Nordberg, 2001, Karolinska Institute, Stockholm, ISBN 91-631-1064-4.
2001 Standout
Selection of Mutant CHO Cells with Constitutive Activation of the HIF System and Inactivation of the von Hippel-Lindau Tumor Suppressor
2001 StandoutNobel
GQ1b-seronegative Fisher syndrome: clinical features and new serological markers
2012
Molecular characterisation of the enolase gene from the human malaria parasite Plasmodium falciparum Evidence for ancestry within a photosynthetic lineage
1994
Molecular basis for polycythemia
1999
Regulation of the Erythropoietin Gene
1989
Abnormal hemoglobins with high oxygen affinity and erythrocytosis
1996
Effects of Thyroid Hormone on mRNAs of Phosphoglycerate Mutase Subunits in Rat Muscle during Development
2002
8-hydroxy-2′ -deoxyguanosine (8-OHdG): A Critical Biomarker of Oxidative Stress and Carcinogenesis
2009 Standout
Guillain-Barré syndrome
2005 Standout
The classification and diagnosis of erythrocytosis
2008
Cryptobiosis — a peculiar state of biological organization
2001 Standout
Carcinogenicity categorization of chemicals—new aspects to be considered in a European perspective
2004 Standout
Guidelines for the Early Management of Patients With Acute Ischemic Stroke
2013 Standout
Synergy Between Trehalose and Hsp104 for Thermotolerance in Saccharomyces cerevisiae
1996
Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis.
2005
Aerobic Glycolysis: Meeting the Metabolic Requirements of Cell Proliferation
2011 Standout
Regulation of hypoxia-inducible factor is preserved in the absence of a functioning mitochondrial respiratory chain
2001 StandoutNobel
A Plastid of Probable Green Algal Origin in Apicomplexan Parasites
1997 StandoutScience
Phosphocreatine-dependent protein phosphorylation in rat skeletal muscle
1992
Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1.
1992
The HIF Pathway and Erythrocytosis
2011
The histidine phosphatase superfamily: structure and function
2007
Oxidative Stress and Stress-Activated Signaling Pathways: A Unifying Hypothesis of Type 2 Diabetes
2002 Standout
Global Epidemiology of Campylobacter Infection
2015 Standout
The Chemistry and Biochemistry of Vanadium and the Biological Activities Exerted by Vanadium Compounds
2004 Standout
Mild hemolytic anemia, progressive neuromotor retardation and fatal outcome: a disorder of glycolysis, triose- phosphate isomerase deficiency.
2013
Evolution of a bifunctional enzyme: 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase.
1989
Pyruvate kinase M2 promotes de novo serine synthesis to sustain mTORC1 activity and cell proliferation
2012
Erythrocyte Enzymopathies in the Newborn
1981
Alterations in the activity and isozymic profile of human phosphofructokinase during malignant transformation in vivo and in vitro: transformation- and progression-linked discriminants of malignancy.
1985
Regulation of the Erythropoietin Gene
1999
Glucose-6-phosphate dehydrogenase deficiency
2008 Standout
Hematologically Important Mutations: Glucose-6-Phosphate Dehydrogenase
1997
Invited Review: Oxidation of Biological Systems: Oxidative Stress Phenomena, Antioxidants, Redox Reactions, and Methods for Their Quantification
2002 Standout
The VHL Tumor Suppressor Gene: Insights into Oxygen Sensing and Cancer.
2017 StandoutNobel
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
2014 Standout
Free Radicals in the Physiological Control of Cell Function
2002 Standout
Treatment of erythropoietin deficiency in mice with systemically administered siRNA
2012 StandoutNobel
Molecular analysis of a series of alleles in humans with reduced activity at the triosephosphate isomerase locus.
1996
Creatine and Creatinine Metabolism
2000 Standout
Works of R Rosa being referenced
Rabbit M type phosphoglycermutase: comparative effects of two thiol reagents, antibody reaction and hybridization studies
1988
Isolation and characterization of the gene encoding the muscle-specific isozyme of human phosphoglycerate mutase
1990
Structural modeling of the human erythrocyte bisphosphoglycerate mutase
1992
Chromosomal assignment of the human 2,3-bisphosphoglycerate mutase gene (BPGM) to region 7q34→7q22
1987
The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families
1996
[Diphosphoglyceromutase deficiency: new cases associated with erythrocytosis].
1984
Comportement immunologique de la glucose-6-phosphate-deshydrogenase érythrocytaire chez des mutants déficients
1970
Hereditary triose phosphate isomerase deficiency: seven new homozygous cases
1985
A New Glucose-6-phosphate Dehydrogenase Variant(G6PD Port-Royal)
1971
The enzymes of the glycolytic pathway in erythrocytes infected with Plasmodium falciparum malaria parasites
1988
Nuerological finding in triosephosphate isomerase deficiency
1985
Pattern of pyruvate kinase isozymes in erythroleukemia cell lines and in normal human erythroblasts
1984
Compound heterozygosity in a complete erythrocyte bisphosphoglycerate mutase deficiency
1992
IgM monoclonal antibody against terminal moiety of GM2, GalNAc-GD1a and GalNAc-GM1b from a pure motor chronic demyelinating polyneuropathy patient: effects on neurotransmitter release
2001
Possibility of prenatal diagnosis of hereditary triose phosphate isomerase deficiency
1986
Sequence of the human erythrocyte phosphoglycerate mutase by microsequencer and mass spectrometry.
1988
[Triosephosphate isomerase deficiency. Familial survey and prenatal detection].
1987
The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.
1978
Hybridation de la glucose-6-phosphate déshydrogénase des globules rouges et des globules blancs humains avec l'enzyme de différents tissus de rat
1969
Isolation and characterization of the human 2,3-bisphosphoglycerate mutase gene.
1988
Isolation, characterization, and structure of a mutant 89 Arg → Cys bisphosphoglycerate mutase
1989
Molecular cloning and sequencing of the human erythrocyte 2,3-bisphosphoglycerate mutase cDNA: revised amino acid sequence.
1986