Citation Impact

Citing Papers

H 2 S as a Physiologic Vasorelaxant: Hypertension in Mice with Deletion of Cystathionine γ-Lyase
2008 StandoutScience
Glutathione S-conjugates as prodrugs to target drug-resistant tumors
2014
Mitochondrial DNA Somatic Mutations (Point Mutations and Large Deletions) and Mitochondrial DNA Variants in Human Thyroid Pathology
2002
Cisplatin nephrotoxicity: Mechanisms and renoprotective strategies
2008 Standout
The scent of disease: volatile organic compounds of the human body related to disease and disorder
2011 Standout
Positionally Cloned Gene for a Novel Glomerular Protein—Nephrin—Is Mutated in Congenital Nephrotic Syndrome
1998 Standout
Prevalence of Lysosomal Storage Disorders
1999 Standout
Chemotherapy-Induced Ca2+ Release Stimulates Breast Cancer Stem Cell Enrichment
2017 StandoutNobel
How effective is antenatal care in preventing maternal mortality and serious morbidity? An overview of the evidence
2001 Standout
Etiology and pathogenesis of preeclampsia: Current concepts
1998
Pre-eclampsia
2005 Standout
Management of Oxidative Stress by Heme Oxygenase-1 in Cisplatin-induced Toxicity in Renal Tubular Cells
2002
The Study of the Effects of Diet on Metabolism and Nutrition (STEDMAN) weight loss project: Rationale and design
2005
Demographic history and linkage disequilibrium in human populations
1997 StandoutNobel
The genetical archaeology of the human genome
1996 StandoutNobel
Early clinical symptoms and incidence of aspartylglucosaminuria in Finland
1993
Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy
2018 StandoutNobel
Antioxidants in the treatment of severe pre‐eclampsis an explanatory randomised controlled trial
1997
Mitochondrial Overload and Incomplete Fatty Acid Oxidation Contribute to Skeletal Muscle Insulin Resistance
2008 Standout
Diagnostic terminology and morphologic criteria for cytologic diagnosis of thyroid lesions: A synopsis of the National Cancer Institute Thyroid Fine‐Needle Aspiration State of the Science Conference
2008 Standout
Molecular and Genetic Aspects of Preeclampsia: State of the Art
2000
β-Arrestin1 mediates nicotinic acid–induced flushing, but not its antilipolytic effect, in mice
2009 StandoutNobel
Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH)
2003
Pre-eclampsia: a disorder of placental mitochondria?
1998
mtDNA Analysis of Nile River Valley Populations: A Genetic Corridor or a Barrier to Migration?
1999 StandoutNobel
Defective Brain Energy Metabolism Shown by in vivo 31P MR Spectroscopy in 28 Patients with Mitochondrial Cytopathies
1993
Extensive Linkage Disequilibrium in Small Human Populations in Eurasia
2002 StandoutNobel
Minisatellite diversity supports a recent African origin for modern humans
1996 StandoutNobel
The oncometabolite 2‐hydroxyglutarate inhibits histone lysine demethylases
2011 StandoutNobel
Friedreich Ataxia: Molecular Mechanisms, Redox Considerations, and Therapeutic Opportunities
2010
mtDNA sequence diversity in Africa.
1996 StandoutNobel
A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
2005 Standout
Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease.
1991
Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population.
1996 StandoutNobel
Analysis of acidic metabolites by capillary column GC and GC/MS
1983
Genes and languages in Europe: an analysis of mitochondrial lineages.
1995 StandoutNobel
Amine Precursors and Depression
1975
Biogenic Amines and Depression
1975 Standout
?On-off? phenomenon in Parkinson's disease: Correlation to the concentration of dopa in plasma
1984 StandoutNobel
Screening for hyperglycaemia in pregnancy: a rapid update for the National Screening Committee
2010 StandoutNobel
Oxidative stress, mitochondrial damage and neurodegenerative diseases.
2013 Standout
A systematic review and evaluation of the use of tumour markers in paediatric oncology: Ewing's sarcoma and neuroblastoma
2003
DOPA and amino acid levels in plasma and cerebrospinal fluid of patients with parkinson's disease before and during treatment with L-dOPA
1973
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
D‐2‐Hydroxyglutaric aciduria: Unravelling the biochemical pathway and the genetic defect
2006
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
2003 Standout
Creatine and Creatinine Metabolism
2000 Standout
Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain
1984

Works of O. Borud being referenced

Pre‐Eclampsia‐A Mitochondrial Disease?
1989
Cystathioninuria in Down's syndrome
1989
Increased lactate in cerebrospinal fluid from 7 siblings in a family with mitochondrial myopathy and cerebellar ataxia
1987
Regulation of γ-glutamyltransferase in cisplatin-resistant and -sensitive colon carcinoma cells after acute cisplatin and oxidative stress exposures
2000
Aspartylglucosaminuria in northern Norway: a molecular and genealogical study.
1994
Mitochondrial Diseases and Myopathies: A Series of Muscle Biopsy Specimens with Ultrastructural Changes in the Mitochondria
1992
Fatal Lactic Acidosis in a Newborn Attributable to a Congenital Defect of Pyruvate Dehydrogenase
1976
The metabolism of L-3,4-dihydroxyphenylalanine in man
1970
Gas chromatographic and mass spectrometric studies on urinary organic acids in a patient with congenital lactic acidosis due to pyruvate decarboxylase deficiency
1977
ASPARTYLGLYCOSAMINURIA IN NORTHERN NORWAY
1976
N-acetylnormetanephrine and N-acetylmetanephrine in urine from patients with neuroblastoma
1970
Biochemical and clinical studies of Friedreich's ataxia
1981
Rankless by CCL
2026