Leo Nijtmans

11.3k citations

108 papers · 8.5k indexed · h-index 57

Co-authors: Jan Smeıtınk Peter H.G.M. Willems Rutger O. Vogel Richard J. Rodenburg Werner J.H. Koopman Lambert P. van den Heuvel Les Grivell Marta Artal‐Sanz
Topics: Mitochondrial Function and Pathology (95 papers)ATP Synthase and ATPases Research (69 papers)Metabolism and Genetic Disorders (46 papers)
Cited by: Clinical Biochemistry Aging Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nucleic Acids Research Journal of Biological Chemistry
Partner nations: Netherlands Germany United Kingdom

In The Last Decade

Leo Nijtmans

107 papers receiving 8.5k citations

Peers

Countries citing papers authored by Leo Nijtmans

Since Specialization

Citations

This map shows the geographic impact of Leo Nijtmans's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Leo Nijtmans with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Leo Nijtmans more than expected).

Fields of papers citing papers by Leo Nijtmans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leo Nijtmans. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Leo Nijtmans. The network helps show where Leo Nijtmans may publish in the future.

Co-authorship network of co-authors of Leo Nijtmans

This figure shows the co-authorship network connecting the top 25 collaborators of Leo Nijtmans. A scholar is included among the top collaborators of Leo Nijtmans based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Leo Nijtmans. Leo Nijtmans is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Analysis of 953 Human Proteins from a Mitochondrial HEK293 Fraction by Complexome Profiling 2013 ·PLoS ONE ·Hans J. C. T. Wessels,Rutger O. Vogel,Robert N. Lightowlers,Johannes N. Spelbrink,Richard J. Rodenburg,Lambert P. van den Heuvel,Alain J. van Gool,Jolein Gloerich,Jan Smeıtınk,Leo Nijtmans	47
2	A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia 2012 ·Human Molecular Genetics ·Radek Szklarczyk,Bas F.J. Wanschers,Leo Nijtmans,Richard J. Rodenburg,Johannes Zschocke,Nicola Dikow,Mariël A.M. van den Brand,(unknown),Christian Gilissen,Joris A. Veltman,Marco Nooteboom,Werner J.H. Koopman,Peter H.G.M. Willems,Jan Smeıtınk,Martijn A. Huynen,Lambertus P. van den Heuvel	69
3	BOLA1 Is an Aerobic Protein That Prevents Mitochondrial Morphology Changes Induced by Glutathione Depletion 2012 ·Antioxidants and Redox Signaling ·Peter H.G.M. Willems,Bas F.J. Wanschers,J.J. Esseling,Radek Szklarczyk,Urszula Kudla,Isabel Duarte,Marleen Forkink,Marco Nooteboom,Herman G.P. Swarts,Jolein Gloerich,Leo Nijtmans,Werner J.H. Koopman,Martijn A. Huynen	45
4	Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts 2012 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Federica Valsecchi,Claire Monge,Marleen Forkink,Ad J.C. de Groof,Giovanni Bénard,Rodrigue Rossignol,Herman G.P. Swarts,Sjenet E. van Emst‐de Vries,Richard J. Rodenburg,Maria Antonietta Calvaruso,Leo Nijtmans,Bavo Heeman,Peggy Roestenberg,Bé Wieringa,Jan Smeıtınk,Werner J.H. Koopman,Peter H.G.M. Willems	57
5	A catalytic defect in mitochondrial respiratory chain complex I due to a mutation in NDUFS2 in a patient with Leigh syndrome 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Lock Hock Ngu,Leo Nijtmans,Felix Distelmaier,Hanka Venselaar,Sjenet E. van Emst‐de Vries,Mariël A.M. van den Brand,(unknown),Liesbeth T. Wintjes,Peter H.G.M. Willems,Lambertus P. van den Heuvel,Jan Smeıtınk,Richard J. Rodenburg	27
6	A Mutation in C2orf64 Causes Impaired Cytochrome c Oxidase Assembly and Mitochondrial Cardiomyopathy 2011 ·The American Journal of Human Genetics ·Merei Huigsloot,Leo Nijtmans,Radek Szklarczyk,Marieke J.H. Baars,Mariël A.M. van den Brand,(unknown),Lambertus P. van den Heuvel,Jan Smeıtınk,Martijn A. Huynen,Richard J. Rodenburg	65
7	NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease 2010 ·European Journal of Human Genetics ·Saskia J.G. Hoefs,Francjan J. van Spronsen,(unknown),Leo Nijtmans,Richard J. Rodenburg,Jan Smeıtınk,Lambert P. van den Heuvel	70
8	Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder 2009 ·Human Molecular Genetics ·Rolf J. R. J. Janssen,Felix Distelmaier,Roel Smeets,Tessa J.M. Wijnhoven,Elsebet Østergaard,N.G.J. Jaspers,Anja Raams,Stephan Kemp,Richard J. Rodenburg,Peter H.G.M. Willems,Lambert P.W.J. van den Heuvel,Jan Smeıtınk,Leo Nijtmans	28
9	Baculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency 2009 ·Human Mutation ·Saskia J.G. Hoefs,Cindy E. Dieteren,Richard J. Rodenburg,K Naess,Helene Bruhn,Rolf Wibom,Esther Wagena,Peter H.G.M. Willems,Jan Smeıtınk,Leo Nijtmans,Lambert P. van den Heuvel	41
10	Functional consequences of mitochondrial tRNATrp and tRNAArg mutations causing combined OXPHOS defects 2009 ·European Journal of Human Genetics ·P. Smits,Sandy Mattijssen,Éva Morava,Mariël van den Brand,(unknown),Frits A. Wijburg,Ger J.M. Pruijn,Jan Smeıtınk,Leo Nijtmans,Richard J. Rodenburg,Lambert van den Heuvel	29
11	Mitigation of NADH: Ubiquinone oxidoreductase deficiency by chronic Trolox treatment 2008 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Werner J.H. Koopman,Sjoerd Verkaart,Sjenet E. van Emst‐de Vries,Sander Grefte,Jan Smeıtınk,Leo Nijtmans,Peter H.G.M. Willems	45
12	Superoxide production is inversely related to complex I activity in inherited complex I deficiency 2007 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sjoerd Verkaart,Werner J.H. Koopman,Sjenet E. van Emst‐de Vries,Leo Nijtmans,(unknown),Jan Smeıtınk,Peter H.G.M. Willems	124
13	Human mitochondrial complex I assembly: A dynamic and versatile process 2007 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Rutger O. Vogel,Jan Smeıtınk,Leo Nijtmans	111
14	Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patients 2007 ·Molecular Genetics and Metabolism ·Rutger O. Vogel,Mariël A.M. van den Brand,Richard J. Rodenburg,Lambert P.W.J. van den Heuvel,Makoto Tsuneoka,Jan Smeıtınk,Leo Nijtmans	60
15	Cell Biological Consequences of Mitochondrial NADH: Ubiquinone Oxidoreductase Deficiency 2004 ·Current Neurovascular Research ·Jan Smeıtınk,Lambert van den Heuvel,Werner J.H. Koopman,Leo Nijtmans,Cristina Ugalde,Peter H.G.M. Willems	48
16	A structure for the yeast prohibitin complex: Structure prediction and evidence from chemical crosslinking and mass spectrometry 2002 ·Protein Science ·Jaap Willem Back,Marta Artal‐Sanz,Luitzen de Jong,Leo J. de Koning,Leo Nijtmans,Chris G. de Koster,Les Grivell,Hans van der Spek,Anton O. Muijsers	144
17	Prohibitins act as a membrane-bound chaperone for the stabilization of mitochondrial proteins 2000 ·The EMBO Journal ·Leo Nijtmans	459
18	Separation of intact pyruvate dehydrogenase complex using blue native agarose gel electrophoresis 2000 ·Electrophoresis ·Nadine S. Henderson,Leo Nijtmans,J. Gordon Lindsay,Eleonora Lamantea,Massimo Zeviani,Ian Holt	30
19	Riboflavin therapy 1999 ·Brain ·Lodovica Vergani,Maria Barile,C. Angelini,Alberto Burlina,Leo Nijtmans,M.P. Freda,Carmen Brizio,(unknown),Federica Dabbeni‐Sala	69
20	Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathy 1995 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Leo Nijtmans,P. G. Barth,Carsten R. Lincke,(unknown),Rob Zwart,Petr Klement,(unknown),W. Ruitenbeek,Ronald J. A. Wanders,Coby Van den Bogert	16

About Leo Nijtmans

Leo Nijtmans is a scholar working on Clinical Biochemistry, Aging and Molecular Biology, having authored 108 papers that have together received 8.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (95 papers), ATP Synthase and ATPases Research (69 papers) and Metabolism and Genetic Disorders (46 papers). The work is most often cited by research in Clinical Biochemistry (2.7k citations), Aging (211 citations) and Molecular Biology (7.4k citations). Leo Nijtmans has collaborated with scholars based in Netherlands, Germany and United Kingdom. Frequent co-authors include Jan Smeıtınk, Peter H.G.M. Willems, Rutger O. Vogel, Richard J. Rodenburg, Werner J.H. Koopman, Lambert P. van den Heuvel, Les Grivell, Marta Artal‐Sanz, Cindy E. Dieteren and Rolf J. R. J. Janssen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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