Citation Impact
Citing Papers
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
2003
HIF-1-Mediated Suppression of Acyl-CoA Dehydrogenases and Fatty Acid Oxidation Is Critical for Cancer Progression
2014 StandoutNobel
Homocysteine and vascular disease
1999 Standout
Astrocytes: biology and pathology
2009 Standout
Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism.
1993
Hyperhomocysteinaemia
1999
Large-scale gene function analysis with the PANTHER classification system
2013 Standout
Autophagy and Viruses: Adversaries or Allies?
2013 Standout
Molybdenum cofactor biosynthesis in humans. Identification of two complementation groups of cofactor-deficient patients and preliminary characterization of a diffusible molybdopterin precursor.
1989
The Common Feature of Leukemia-Associated IDH1 and IDH2 Mutations Is a Neomorphic Enzyme Activity Converting α-Ketoglutarate to 2-Hydroxyglutarate
2010 Standout
The biochemical basis of mitochondrial diseases
1988
Microbial tryptophan catabolites in health and disease
2018 Standout
Role for ELOVL3 and Fatty Acid Chain Length in Development of Hair and Skin Function
2004 StandoutNobel
Identification and characterization of a spinal muscular atrophy-determining gene
1995 Standout
Plasma Homocysteine as a Risk Factor for Dementia and Alzheimer's Disease
2002 Standout
GPCR-Mediated Signaling of Metabolites
2017
Sphingolipids and their metabolism in physiology and disease
2017 Standout
Coronary risk factors measured in childhood and young adult life are associated with coronary artery calcification in young adults: The muscatine study
1996 Standout
Nonalcoholic Fatty Liver Disease
2002 Standout
HIF-1 mediates metabolic responses to intratumoral hypoxia and oncogenic mutations
2013 StandoutNobel
Disorders of purine and pyrimidine metabolism
2005
Hepatocyte-specific Pten deficiency results in steatohepatitis and hepatocellular carcinomas
2004 StandoutNobel
Nitisinone in the Treatment of Hereditary Tyrosinaemia Type 1
2006
Steatohepatitis, Spontaneous Peroxisome Proliferation and Liver Tumors in Mice Lacking Peroxisomal Fatty Acyl-CoA Oxidase
1998
Gout
2009 Standout
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
2009 StandoutNature
Peroxisomal bifunctional enzyme deficiency.
1989
A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease
1995 Standout
Locating proteins in the cell using TargetP, SignalP and related tools
2007 Standout
What a difference a hydroxyl makes: mutant IDH, (R)-2-hydroxyglutarate, and cancer
2013 StandoutNobel
A novel mouse model of hepatocarcinogenesis triggered by AID causing deleterious p53 mutations
2008 StandoutNobel
Determination of the structures of respiratory enzyme complexes from mammalian mitochondria
1995 StandoutNobel
Quality control: from molecules to organelles
1999
β-Oxidation of fatty acids in mitochondria, peroxisomes, and bacteria: A century of continued progress
1995
Platelet Activation and Atherothrombosis
2007 Standout
Homocysteine and Risk of Ischemic Heart Disease and Stroke
2002 Standout
Myocardial Substrate Metabolism in the Normal and Failing Heart
2005 Standout
Peroxisomal fatty acid β-oxidation in HepG2 cells
1991
Chapter 5 Spatiotemporal Dynamics of the ER‐derived Peroxisomal Endomembrane System
2008
Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy
1988
Metabolic aspects of peroxisomal β-oxidation
1991
Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.
1994
Peroxisomal protein targeting and identification of peroxisomal targeting signals in cholesterol biosynthetic enzymes
2000
D‐2‐hydroxyglutaric acid induces oxidative stress in cerebral cortex of young rats
2003
Homocysteinemia: Association of a metabolic disorder with vascular disease and thrombosis
1993
Sensors and regulators of intracellular pH
2009 Standout
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
2015 Standout
Cytochrome P450 ω-Hydroxylase Pathway of Tocopherol Catabolism
2002 Standout
Pyruvate carboxylase deficiency: Metabolic characteristics and new neurological aspects
2005
Molybdenum cofactor transfer from bacteria to nematode mediates sulfite detoxification
2019 StandoutNobel
Homocysteine and Atherothrombosis
1998 Standout
d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder
1997
Biogenesis of Molybdenum Cofactors
1990
Pmp27 promotes peroxisomal proliferation.
1995
Substrate specificities of rat liver peroxisomal acyl-CoA oxidases: palmitoyl-CoA oxidase (inducible acyl-CoA oxidase), pristanoyl-CoA oxidase (non-inducible acyl-CoA oxidase), and trihydroxycoprostanoyl-CoA oxidase.
1992
Cell biology and molecular basis of denitrification
1997 Standout
Physiological Implications of Hydrogen Sulfide: A Whiff Exploration That Blossomed
2012 Standout
Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)
2013 Standout
PEX11 promotes peroxisome division independently of peroxisome metabolism
2002
Controlled Clinical Trial of Dichloroacetate for Treatment of Congenital Lactic Acidosis in Children
2006
A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, β-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency
1985
Metabolism of Very Long-Chain Fatty Acids: Genes and Pathophysiology
2014
The Enzymes, Regulation, and Genetics of Bile Acid Synthesis
2003 Standout
Luminescent Chemodosimeters for Bioimaging
2012 Standout
Sulfites in Foods: Uses, Analytical Methods, Residues, Fate, Exposure Assessment, Metabolism, Toxicity, and Hypersensitivity
1986
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Peroxisomal d -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency
1998
A vesicle carrier that mediates peroxisome protein traffic from the endoplasmic reticulum
2010 StandoutNobel
Homocysteine and Thrombotic Disease
1997
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
Diabetic Cardiomyopathy
2018 Standout
Mitochondrial Disorders in the Nervous System
2008
Bone Dysplasia as a Key Feature in Three Patients with a Novel Congenital Disorder of Glycosylation (CDG) Type II Due to a Deep Intronic Splice Mutation in TMEM165
2012
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
Complementation analysis of fatty acid oxidation disorders.
1987
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
1988
Maintaining Ancient Organelles
2015
Biochemistry and physiology of aerobic carbon monoxide-utilizing bacteria
1986
The presence and distribution of reduced folates in Escherichia coli dihydrofolate reductase mutants.
1990 StandoutNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
The Mononuclear Molybdenum Enzymes
1996 Standout
Adipocytes promote ovarian cancer metastasis and provide energy for rapid tumor growth
2011 Standout
Identification of Pex13p a peroxisomal membrane receptor for the PTS1 recognition factor.
1996 StandoutNobel
Clinical Approach to Genetic Cardiomyopathy in Children
1996
The Mononuclear Molybdenum Enzymes
2014 Standout
mPPAR gamma 2: tissue-specific regulator of an adipocyte enhancer.
1994 Standout
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
1998 Standout
Investigating the functional link between TMEM165 and SPCA1
2019 StandoutNobel
Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders
1995
Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.
1985
Involvement of chlA, E, M, and N loci in Escherichia coli molybdopterin biosynthesis
1987
Very long chain fatty acids in higher animals—A review
1995
Hepatocyte-specific Pten deficiency results in steatohepatitis and hepatocellular carcinomas
2004 StandoutNobel
Effects of age, lipoproteins, and hemostatic parameters on the role of homocyst(e)inemia as a cardiovascular risk factor in men.
1994
Works of H. Ogier being referenced
Hepatic peroxisomes in adrenoleukodystrophy and related syndromes: Cytochemical and morphometric data
1988
Infantile Refsum disease: an inherited peroxisomal disorder
1987
Carbohydrate-deficient glycoprotein syndrome type I: a new cause of dysostosis multiplex
1998
Évolution favorable sous traitement par NTBC de l'insuffisance hépatique aiguë révélatrice de la tyrosinémie héréditaire de type I
1999
The fasting test in paediatrics: Application to the diagnosis of pathological hypo- and hyperketotic states
1990
Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.
1993
Diet-responsive proconvertin (factor VII) deficiency inhomocystinuria
1983
A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).
1988
Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disorders
1982
[Heterogeneity of carnitine palmitoyltransferase deficiencies. Deficiency of CPT I in the hepatic form and CPT II in the muscular form].
1986
Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase
1983
Vigabatrin therapy in six patients with succinic semialdehyde dehydrogenase deficiency
1995
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency
1993
Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction
1985
[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum].
1982
Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family
1983
Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder
1981