Citation Impact
Citing Papers
Treatment Response Assessment in IDH-Mutant Glioma Patients by Noninvasive 3D Functional Spectroscopic Mapping of 2-Hydroxyglutarate
2015 StandoutNobel
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
2009 Standout
( R )-2-Hydroxyglutarate Is Sufficient to Promote Leukemogenesis and Its Effects Are Reversible
2013 StandoutScienceNobel
Clinical applications of urinary organic acids. Part 2. Dysbiosis markers.
2008
Hypoxia-Inducible Factors and the Response to Hypoxic Stress
2010 Standout
Direct Nonisotopic Assay of 3-Methylglutaconyl-CoA Hydratase in Cultured Human Skin Fibroblasts to Specifically Identify Patients with 3-Methylglutaconic Aciduria Type I
2004
Therapeutic Effects of l‐Carnitine and Propionyl‐l‐carnitine on Cardiovascular Diseases: A Review
2004
The Common Feature of Leukemia-Associated IDH1 and IDH2 Mutations Is a Neomorphic Enzyme Activity Converting α-Ketoglutarate to 2-Hydroxyglutarate
2010 Standout
Bioavailability and bioefficacy of polyphenols in humans. I. Review of 97 bioavailability studies
2005 Standout
Identification of natural inhibitors of Entamoeba histolytica cysteine synthase from microbial secondary metabolites
2015 StandoutNobel
Metabolic Reprogramming: A Cancer Hallmark Even Warburg Did Not Anticipate
2012 Standout
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
Microbial tryptophan catabolites in health and disease
2018 Standout
The Failing Heart — An Engine Out of Fuel
2007 Standout
ATP synthase from bovine mitochondria: complementary DNA sequence of the import precursor of a heart isoform of the .alpha. subunit
1989 StandoutNobel
Premature ageing in mice expressing defective mitochondrial DNA polymerase
2004 StandoutNature
Carnitine biosynthesis in mammals
2002
Metabolic Regulation of Hematopoietic Stem Cells in the Hypoxic Niche
2011 StandoutNobel
Sulfur-Containing Amino Acid Metabolism in Parasitic Protozoa
2005
The small intestine shields the liver from fructose-induced steatosis
2020
Oxygen sensing by HIF hydroxylases
2004 StandoutNobel
Two bovine genes for mitochondrial ADP/ATP translocase expressed differently in various tissues
1989 StandoutNobel
Fumarate and Succinate Regulate Expression of Hypoxia-inducible Genes via TET Enzymes
2015 StandoutNobel
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
DNA sequences of two expressed nuclear genes for human mitochondrial ADP/ATP translocase
1989 StandoutNobel
From Krebs to clinic: glutamine metabolism to cancer therapy
2016 Standout
Monovalent, reduced-size quantum dots for imaging receptors on living cells
2008 StandoutNobel
The Subsystems Approach to Genome Annotation and its Use in the Project to Annotate 1000 Genomes
2005 Standout
Cardiomyopathy in Multiple Acyl-CoA Dehydrogenase Deficiency
2007
Regulation of cancer cell metabolism
2011 Standout
Dynamics and functions of lipid droplets
2018 Standout
Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics
1995 Standout
The control and consequences of bacterial fermentation in the human colon
1991
Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy
1988
Understanding the Odd Science of Aging
2005 Standout
From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites
2016 Standout
Mitochondrial Membrane Permeabilization in Cell Death
2007 Standout
The Emerging Hallmarks of Cancer Metabolism
2016 Standout
Familial deficiency of dihydropyrimidine dehydrogenase. Biochemical basis for familial pyrimidinemia and severe 5-fluorouracil-induced toxicity.
1988
Isolated 3-Methylcrotonyl-CoA Carboxylase Deficiency: Evidence for an Allele-Specific Dominant Negative Effect and Responsiveness to Biotin Therapy
2004
PPARγ Is Required for Placental, Cardiac, and Adipose Tissue Development
1999 Standout
A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
1990 StandoutNature
Screening for defects of branched-chain amino acid metabolism
1994
New cancer targets emerging from studies of the Von Hippel‐Lindau tumor suppressor protein
2010 StandoutNobel
The Warburg Effect: How Does it Benefit Cancer Cells?
2016 Standout
Mitochondrial TCA cycle metabolites control physiology and disease
2020 Standout
Identification of additional IDH mutations associated with oncometabolite R(−)-2-hydroxyglutarate production
2011
The Enzymatic Basis for the Dehydrogenation of 3-Phenylpropionic Acid: In Vitro Reaction of 3- Phenylpropionyl-CoA with Various Acyl-CoA Dehydrogenases
1990
Mitochondria and cancer
2012 Standout
Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies
1995 StandoutNobel
Lacticacidemia
1993
Inflammation in obesity, diabetes, and related disorders
2022 Standout
Metabolic cardiomyopathies
2000
The oncometabolite 2‐hydroxyglutarate inhibits histone lysine demethylases
2011 StandoutNobel
Mitochondrial myopathies
1984
Mitochondrial diseases
1986
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
1984
Comparison of Five In Vitro Digestion Models To Study the Bioaccessibility of Soil Contaminants
2002 Standout
Short-Chain Fatty Acids and Human Colonic Function: Roles of Resistant Starch and Nonstarch Polysaccharides
2001 Standout
Mitochondrial Inheritance in a Mitochondrially Mediated Disease
1983
Teratogen-Mediated Inhibition of Target Tissue Response to Shh Signaling
1998 StandoutScience
Human Phosphoglycerate Dehydrogenase Produces the Oncometabolite d -2-Hydroxyglutarate
2014
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Cytochrome-c-oxidase deficient cardiomyocytes in the human heart--an age-related phenomenon. A histochemical ultracytochemical study.
1989
Gut Microbial Activity, Implications for Health and Disease: The Potential Role of Metabolite Analysis
2012
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
Mitochondrial dysfunction in fatty acid oxidation disorders: insights from human and animal studies
2015
Mitochondrial myopathies
1985
Complementation analysis of fatty acid oxidation disorders.
1987
Isolation and properties of cytochrome c oxidase from rat liver and quantification of immunological differences between isozymes from various rat tissues with subunit-specific antisera
1985
Adipocytes promote ovarian cancer metastasis and provide energy for rapid tumor growth
2011 Standout
The Effects of Plant Flavonoids on Mammalian Cells:Implications for Inflammation, Heart Disease, and Cancer
2000 Standout
Cancer Genome Landscapes
2013 StandoutScience
Lactate Dehydrogenase C Produces S-2-Hydroxyglutarate in Mouse Testis
2016
Clinical Approach to Genetic Cardiomyopathy in Children
1996
Studies on Drug Metabolism by Use of Isotopes XXVII: Urinary Metabolites of Rutin in Rats and the Role of Intestinal Microflora in the Metabolism of Rutin
1983
Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy
1988 StandoutScience
Host-Gut Microbiota Metabolic Interactions
2012 StandoutScience
Two genes encoding the bovine mitochondrial ATP synthase proteolipid specify precursors with different import sequences and are expressed in a tissue-specific manner.
1985 StandoutNobel
2006
3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured fibroblasts from patients with mevalonate kinase deficiency: differential response to lipid supplied by fetal bovine serum in tissue culture medium.
1990
Pharmacogenomics: Translating Functional Genomics into Rational Therapeutics
1999 StandoutScience
Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.
1985
Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain
1984
Studies on drug metabolism by use of isotopes XXVI: Determination of urinary metabolites of rutin in humans
1981
Works of D. Ketting being referenced
Diagnosis of Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Lymphocytes and Liver by a Gas Chromatographic Method: The Effect of Oral Riboflavin Supplementation
1992
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment
1991
D-Glyceric Acidemia: An Inborn Error Associated with Fructose Metabolism
1987
Gas chromatographic analysis of urinary volatile phenols in patients with gastro-intestinal disorders and normals
1973
Urinary and faecal excretion of metabolizes of tyrosine and phenylalanine in a patient with cystic fibrosis and severely impaired amino acid absorption
1971
Hereditary Mitochondrial Myopathy with Lactic Acidemia, A DeToni-Fanconi-Debr?? Syndrome, and a Defective Respiratory Chain in Voluntary Striated Muscles
1977
Determination of the absolute configuration of some biologically important urinary 2-hydroxydicarboxylic acids by capillary gas—liquid chromatography
1981
D-Glyceric acidemia in a patient with chronic metabolic acedosis
1976
Glutaric aciduria type II: Report on a previously undescribed metabolic disorder
1976
Gas chromatographic analysis of urinary tyrosine and phenylalanine metabolites in patients with gastrointestinal disorders
1971
Report of a Patient with Severe, Chronic Lactic Acidaemia and Pyruvate Carboxylase Deficiency
1977
New Defects of Pyrimidine Metabolism
1984
Inherited 3-methylglutaconic aciduria in two brothers—Another defect of leucine metabolism
1982
β-p-Hydroxyphenylhydracrylic acid as a urinary constituent in a patient with gastrointestinal disease
1973
Direct identification of propionylcarnitine in propionic acidaemia: Biochemical and clinical results of oral carnitine supplementation
1985
A patient with mevalonic aciduria presenting with hepatosplenomegaly, congenital anaemia, thrombocytopenia and leukocytosis
1988
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs
1982
Secondary carnitine deficiency.
1990