Lambert P. van den Heuvel

Author

Also Known As

LAMBERT P. VAN DEN HEUVEL, Lambert P van den Heuvel, Lambert P. Van Den Heuvel, Lambert P. van Heuvel, Lambert P. van den Heuvel, Lambert P. van den Heuvel, Van Den Heuvel, Lambert P.

Publications

6.8K

Citations

H-Index

111

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center KU Leuven Radboud Institute for Molecular Life Sciences University Medical Center Utrecht

About

Lambert P. van den Heuvel is an author at Radboud University Nijmegen specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	36	4K
2	Natural Sciences	11	11	891
3	Engineering	3	3	333
4	Health Sciences	2	2	83
5	Public Health	2	2	111

Lambert P. van den Heuvel

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? N.M.J. van der Put, F. Gabreëls, E M Stevens, The American Journal of Human Genetics Developmental BiologySecond Common MutationNeural-tube DefectsGenetic DisorderMendelian Disorder	1998	1.6K
Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts A.J.M. Janssen, Frans J.M. Trijbels, R. C. A. Sengers, Clinical Chemistry	2007	361
Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency Marieke J. H. Coenen, Hana Antonická, Cristina Ugalde, New England Journal of Medicine MitophagyMitochondrial BiogenesisMitochondrial FunctionBiochemistryMitochondrial Translation	2004	192
Secondary mitochondrial dysfunction in propionic aciduria: a pathogenic role for endogenous mitochondrial toxins Marina A. Schwab, Sven W. Sauer, Jürgen G. Okun, Biochemical Journal	2006	189
Reconstructing the evolution of the mitochondrial ribosomal proteome P. Smits, Jan A. M. Smeitink, Lambert P. van den Heuvel, Nucleic Acids Research GeneticsMolecular BiologyGenomicsProtein SynthesisPhylogenetic Analysis	2007	183
Agrin Is a Major Heparan Sulfate Proteoglycan in the Human Glomerular Basement Membrane Alexander J. Groffen, Markus A. Rüegg, Henri B.P.M. Dijkman, Journal of Histochemistry & Cytochemistry	1998	179
Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease Ann Saada, Rutger O. Vogel, Saskia J.G. Hoefs, The American Journal of Human Genetics Mitochondrial BiogenesisMitochondrial FunctionGeneticsMolecular BiologyMitochondrial Medicine	2009	169
ATAD3 gene cluster deletions cause cerebellar dysfunction associated with altered mitochondrial DNA and cholesterol metabolism Radha Desai, Ann E. Frazier, Romina Durigon, Brain EngineeringMitochondrial DysfunctionGeneticsGenetic EpidemiologyMolecular Genetics	2017	157
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 Salvatore Scacco, Vittoria Petruzzella, Sandy Budde, Journal of Biological Chemistry	2003	143
Human mitochondrial complex I assembly is mediated by NDUFAF1 Rutger O. Vogel, Rolf J. R. J. Janssen, Cristina Ugalde, FEBS Journal Mitochondrial BiogenesisBiochemistryMitochondrial FunctionMedicineConditional Complex	2005	132

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