Roel Smeets

2.8k total citations
33 papers, 2.1k citations indexed

About

Roel Smeets is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Roel Smeets has authored 33 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 20 papers in Clinical Biochemistry and 3 papers in Surgery. Recurrent topics in Roel Smeets's work include Mitochondrial Function and Pathology (27 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (15 papers). Roel Smeets is often cited by papers focused on Mitochondrial Function and Pathology (27 papers), Metabolism and Genetic Disorders (20 papers) and ATP Synthase and ATPases Research (15 papers). Roel Smeets collaborates with scholars based in Netherlands, Germany and Spain. Roel Smeets's co-authors include Jan Smeıtınk, Jan Loeffen, Lambert van den Heuvel, Frans J.M. Trijbels, Ralf Triepels, R. C. A. Sengers, Carin A. F. Buskens, Orly Elpeleg, Edwin C.M. Mariman and J. M. F. Trijbels and has published in prestigious journals such as New England Journal of Medicine, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Roel Smeets

33 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Roel Smeets Netherlands	22	1.9k	1.0k	160	129	110	33	2.1k
Canny Sugiana Australia	8	2.0k 1.1×	827 0.8×	133 0.8×	109 0.8×	108 1.0×	9	2.2k
Audrey Boutron France	21	1.2k 0.6×	627 0.6×	256 1.6×	77 0.6×	76 0.7×	47	1.6k
Jan Smeitink Netherlands	13	1.1k 0.6×	587 0.6×	60 0.4×	116 0.9×	68 0.6×	13	1.3k
Alexis A. Jourdain Switzerland	20	1.7k 0.9×	286 0.3×	204 1.3×	90 0.7×	83 0.8×	31	2.0k
Paula J. Waters Canada	24	1.2k 0.7×	1.1k 1.1×	47 0.3×	340 2.6×	74 0.7×	75	2.0k
Mark S. Sharpley United States	12	1.3k 0.7×	226 0.2×	178 1.1×	81 0.6×	93 0.8×	12	1.6k
Suzanne Hoppins United States	14	2.0k 1.1×	607 0.6×	68 0.4×	49 0.4×	140 1.3×	17	2.2k
Fredoen Valianpour Netherlands	15	1.4k 0.7×	413 0.4×	29 0.2×	96 0.7×	132 1.2×	16	1.6k
Nina A. Bonekamp Germany	21	1.6k 0.9×	301 0.3×	139 0.9×	68 0.5×	92 0.8×	27	1.9k
Masato Yano Japan	23	1.2k 0.6×	177 0.2×	152 0.9×	73 0.6×	55 0.5×	34	1.6k

Countries citing papers authored by Roel Smeets

Since Specialization

Citations

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

Fields of papers citing papers by Roel Smeets

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roel Smeets

This figure shows the co-authorship network connecting the top 25 collaborators of Roel Smeets. A scholar is included among the top collaborators of Roel Smeets 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 Roel Smeets. Roel Smeets 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

Renkema, G. Herma, Saskia B. Wortmann, Roel Smeets, et al.. (2014). SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors. European Journal of Human Genetics. 23(2). 202–209. 65 indexed citations

Jakobs, Bernadette S., Lambert P. van den Heuvel, Roel Smeets, et al.. (2013). A novel mutation in COQ2 leading to fatal infantile multisystem disease. Journal of the Neurological Sciences. 326(1-2). 24–28. 40 indexed citations

Janssen, Rolf J. R. J., Felix Distelmaier, Roel Smeets, et al.. (2009). Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder. Human Molecular Genetics. 18(18). 3365–3374. 28 indexed citations

Noordam, C., Vivek Dhir, Joanne McNelis, et al.. (2009). Inactivating PAPSS2 Mutations in a Patient with Premature Pubarche. New England Journal of Medicine. 360(22). 2310–2318. 110 indexed citations

Fernández-Moreira, Daniel, Cristina Ugalde, Roel Smeets, et al.. (2007). X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy. Annals of Neurology. 61(1). 73–83. 105 indexed citations

Gasparre, Giuseppe, Éric Hervouet, Marc Colombel, et al.. (2007). Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma. Human Molecular Genetics. 17(7). 986–995. 109 indexed citations

Ugalde, Cristina, Reetta Hinttala, Sharita Timal, et al.. (2006). Mutated ND2 impairs mitochondrial complex I assembly and leads to Leigh Syndrome. Molecular Genetics and Metabolism. 90(1). 10–14. 68 indexed citations

Grafakou, Olga, Konrad Oexle, Lambert van den Heuvel, et al.. (2003). Leigh syndrome due to compound heterozygosity of dihydrolipoamide dehydrogenase gene mutations. Description of the first E3 splice site mutation. European Journal of Pediatrics. 162(10). 714–718. 44 indexed citations

Ugalde, Cristina, Ralf Triepels, Marieke J. H. Coenen, et al.. (2003). Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene. Annals of Neurology. 54(5). 665–669. 88 indexed citations

10.

Janssen, Rolf J. R. J., Jan Smeıtınk, Roel Smeets, & Lambert van den Heuvel. (2002). CIA30 complex I assembly factor: a candidate for human complex I deficiency?. Human Genetics. 110(3). 264–270. 57 indexed citations

11.

Loeffen, Jan, Orly Elpeleg, Jan Smeitink, et al.. (2001). Mutations in the complex INDUFS2 gene of patients with cardiomyopathy and encephalomyopathy. Annals of Neurology. 49(2). 195–201. 162 indexed citations

12.

Heuvel, Lambert P.W.J. van den, A.J.M. Janssen, Roel Smeets, et al.. (2000). Combined Enzymatic Complex I and III Deficiency Associated with Mutations in the Nuclear Encoded NDUFS4 Gene. Biochemical and Biophysical Research Communications. 275(1). 63–68. 165 indexed citations

13.

Triepels, Ralf, Lambertus P. van den Heuvel, Jan Loeffen, et al.. (1999). Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I. Annals of Neurology. 45(6). 787–790. 164 indexed citations

14.

Loeffen, Jan, Ralf Triepels, Lambertus P. van den Heuvel, et al.. (1998). cDNA of Eight Nuclear Encoded Subunits of NADH:Ubiquinone Oxidoreductase: Human Complex I cDNA Characterization Completed. Biochemical and Biophysical Research Communications. 253(2). 415–422. 61 indexed citations

15.

Heuvel, Lambert van den, W. Ruitenbeek, Roel Smeets, et al.. (1998). Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit. The American Journal of Human Genetics. 62(2). 262–268. 224 indexed citations

16.

Loeffen, Jan, Roel Smeets, Jan Smeıtınk, et al.. (1998). The X‐chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: Tissue expression and mutation detection. Journal of Inherited Metabolic Disease. 21(3). 210–215. 16 indexed citations

17.

Loeffen, Jan, Lambert van den Heuvel, Roel Smeets, et al.. (1998). cDNA Sequence and Chromosomal Localization of the Remaining Three Human Nuclear Encoded Iron Sulphur Protein (IP) Subunits of Complex I: The Human IP Fraction Is Completed. Biochemical and Biophysical Research Communications. 247(3). 751–758. 19 indexed citations

18.

Triepels, Ralf, Lambert van den Heuvel, Jan Loeffen, et al.. (1998). The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients. Human Genetics. 103(5). 557–563. 18 indexed citations

19.

Smeitink, Jan, Jan Loeffen, Roel Smeets, et al.. (1998). Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I. Human Genetics. 103(2). 245–250. 17 indexed citations

20.

Loeffen, Jan, Jan Smeıtınk, Ralf Triepels, et al.. (1998). The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome. The American Journal of Human Genetics. 63(6). 1598–1608. 219 indexed citations

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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