Jan Smeitink

2.3k citations

13 papers · 1.3k indexed · 1 hit paper · h-index 13

Co-authors: Lambert van den Heuvel S. DiMauro Frans J.M. Trijbels P. Smits R. C. A. Sengers Roel Smeets Jan Loeffen Orly Elpeleg
Topics: Metabolism and Genetic Disorders (9 papers)Mitochondrial Function and Pathology (8 papers)ATP Synthase and ATPases Research (5 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: SHILAP Revista de lepidopterologíaNature Reviews Genetics Annals of Neurology
Partner nations: Netherlands United States Italy

In The Last Decade

Jan Smeitink

13 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The genetics and pathology of oxidative phosphorylation

2001 545 citations Jan Smeitink, Lambert van den Heuvel et al. Nature Reviews Genetics profile →

Peers

Countries citing papers authored by Jan Smeitink

Since Specialization

Citations

This map shows the geographic impact of Jan Smeitink'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 Jan Smeitink with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jan Smeitink more than expected).

Fields of papers citing papers by Jan Smeitink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan Smeitink. 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 Jan Smeitink. The network helps show where Jan Smeitink may publish in the future.

Co-authorship network of co-authors of Jan Smeitink

This figure shows the co-authorship network connecting the top 25 collaborators of Jan Smeitink. A scholar is included among the top collaborators of Jan Smeitink 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 Jan Smeitink. Jan Smeitink is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Mitochondrial Translation and Beyond: Processes Implicated in Combined Oxidative Phosphorylation Deficiencies 2010 ·SHILAP Revista de lepidopterología ·P. Smits,Jan Smeitink,Lambert van den Heuvel	155
2	Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene 2007 ·Annals of Neurology ·Marcel M. Verbeek,Gerry C. H. Steenbergen‐Spanjers,Michèl A.A.P. Willemsen,Frans A. Hol,Jan Smeitink,Jürgen Seeger,Padraic J. Grattan‐Smith,Monique M. Ryan,Georg F. Hoffmann,Maria Alice Donati,Nenad Blau,Ron A. Wevers	19
3	Defective protein glycosylation in patients with cutis laxa syndrome 2005 ·European Journal of Human Genetics ·Éva Morava,Suzan Wopereis,Paul Coucke,(unknown),Thomas Voit,Jan Smeitink,Ron A. Wevers,Stephanie Grünewald	58
4	Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation 2003 ·European Journal of Pediatrics ·Olga Grafakou,Konrad Oexle,Lambert van den Heuvel,Roel Smeets,Frans J.M. Trijbels,Hans H. Goebel,N. U. Bosshard,Andrea Superti‐Furga,Beat Steinmann,Jan Smeitink	44
5	Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. 2003 ·Olga Grafakou,Konrad Oexle,Lambert van den Heuvel,Roel Smeets,Frans J.M. Trijbels,Hans H. Goebel,N. U. Bosshard,Andrea Superti‐Furga,Beat Steinmann,Jan Smeitink	13
6	Variable clinical presentation of lysosomal β-mannosidosis in patients with null mutations 2002 ·Molecular Genetics and Metabolism ·(unknown),Katherine A. Nummy,Alan Cooper,Ron A. Wevers,Jan Smeitink,Wim J. Kleijer,Karen H. Friderici	35
7	The genetics and pathology of oxidative phosphorylationbreakdown → 2001 ·Nature Reviews Genetics ·Jan Smeitink,Lambert van den Heuvel,S. DiMauro	545
8	Human NADH:Ubiquinone Oxidoreductase 2001 ·Journal of Bioenergetics and Biomembranes ·Jan Smeitink,R. C. A. Sengers,Frans J.M. Trijbels,Lambert van den Heuvel	100
9	Mutations in the complex INDUFS2 gene of patients with cardiomyopathy and encephalomyopathy 2001 ·Annals of Neurology ·Jan Loeffen,Orly Elpeleg,Jan Smeitink,Roel Smeets,(unknown),Hanna Mandel,R. C. A. Sengers,Frans J.M. Trijbels,Lambert van den Heuvel	162
10	Characterization of the Human Porin Isoform 1 (HVDAC1) Gene by Amplification on the Whole Human Genome: A Tool for Porin Deficiency Analysis 2000 ·Biochemical and Biophysical Research Communications ·Angela Messina,Francesca Guarino,Marta Oliva,Lambert P. van den Heuvel,Jan Smeitink,Vito De Pinto	15
11	The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients 1998 ·Human Genetics ·Ralf Triepels,Lambert van den Heuvel,Jan Loeffen,Roel Smeets,Frans J.M. Trijbels,Jan Smeitink	18
12	Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I 1998 ·Human Genetics ·Jan Smeitink,Jan Loeffen,Roel Smeets,Ralf Triepels,W. Ruitenbeek,Frans J.M. Trijbels,Lambert van den Heuvel	17
13	Cloning of the Human Carnitine-Acylcarnitine Carrier cDNA and Identification of the Molecular Defect in a Patient 1997 ·The American Journal of Human Genetics ·Marjan Huizing,Vito Iacobazzi,Lodewijk IJlst,Paul J.M. Savelkoul,W. Ruitenbeek,Lambert van den Heuvel,Cesare Indiveri,Jan Smeitink,Frans J.M. Trijbels,Ronald J. A. Wanders,Ferdinando Palmieri	117

About Jan Smeitink

Jan Smeitink is a scholar working on Clinical Biochemistry, Biochemistry and Molecular Biology, having authored 13 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (8 papers) and ATP Synthase and ATPases Research (5 papers). The work is most often cited by research in Clinical Biochemistry (587 citations), Molecular Biology (1.1k citations) and Biochemistry (73 citations). Jan Smeitink has collaborated with scholars based in Netherlands, United States and Italy. Frequent co-authors include Lambert van den Heuvel, S. DiMauro, Frans J.M. Trijbels, P. Smits, R. C. A. Sengers, Roel Smeets, Jan Loeffen, Orly Elpeleg, Hanna Mandel and Ron A. Wevers. Their work appears in journals such as SHILAP Revista de lepidopterología, Nature Reviews Genetics and Annals of Neurology.

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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