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Lambert P. van den Heuvel | doi.page

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Lambert P. van den Heuvel

Radboud University Nijmegen(NL)Radboud University Medical Center(NL)Radboud Institute for Molecular Life Sciences(NL)

Publications by Year

Research Areas

Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, RNA modifications and cancer, Complement system in diseases

Most-Cited Works

→ A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects?(1998)1,559 cited
→ Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts(2007)362 cited
→ Mitochondrial complex I: Structure, function and pathology(2006)274 cited
→ Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency(2004)193 cited
→ Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins(2006)189 cited
→ Reconstructing the evolution of the mitochondrial ribosomal proteome(2007)184 cited

→ Agrin Is a Major Heparan Sulfate Proteoglycan in the Human Glomerular Basement Membrane(1998)

179 cited

→ Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease(2009)169 cited

→ ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism(2017)158 cited

→ Pathological Mutations of the Human NDUFS4 Gene of the 18-kDa (AQDQ) Subunit of Complex I Affect the Expression of the Protein and the Assembly and Function of the Complex(2003)143 cited