J.A.M. Smeitink

482 total citations
17 papers, 348 citations indexed

About

J.A.M. Smeitink is a scholar working on Molecular Biology, Clinical Biochemistry and Epidemiology. According to data from OpenAlex, J.A.M. Smeitink has authored 17 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 3 papers in Epidemiology. Recurrent topics in J.A.M. Smeitink's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (11 papers) and ATP Synthase and ATPases Research (5 papers). J.A.M. Smeitink is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (11 papers) and ATP Synthase and ATPases Research (5 papers). J.A.M. Smeitink collaborates with scholars based in Netherlands, United States and United Kingdom. J.A.M. Smeitink's co-authors include R. C. A. Sengers, A. M. Stadhouders, J. M. F. Trijbels, Marjo S. van der Knaap, W. Ruitenbeek, Lambertus P. van den Heuvel, Saskia Koene, Richard J. Rodenburg, Victoria Nesbitt and Vincent Laugel and has published in prestigious journals such as Annals of Neurology, American Journal of Medical Genetics and Journal of Inherited Metabolic Disease.

In The Last Decade

J.A.M. Smeitink

17 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
J.A.M. Smeitink Netherlands	10	276	218	48	31	31	17	348
Lucy J. Otero United Kingdom	8	308 1.1×	180 0.8×	111 2.3×	27 0.9×	49 1.6×	8	415
Magalie Barth France	12	274 1.0×	171 0.8×	36 0.8×	27 0.9×	92 3.0×	32	378
Marina A. Schwab Germany	6	339 1.2×	323 1.5×	62 1.3×	30 1.0×	72 2.3×	6	453
Bert Dorland Netherlands	8	220 0.8×	93 0.4×	31 0.6×	32 1.0×	67 2.2×	11	347
L Vergani Italy	7	202 0.7×	204 0.9×	34 0.7×	26 0.8×	75 2.4×	8	300
J.M.F. Trijbels Netherlands	6	298 1.1×	239 1.1×	39 0.8×	15 0.5×	49 1.6×	7	413
Magdalena Pajdowska Poland	11	316 1.1×	209 1.0×	16 0.3×	34 1.1×	27 0.9×	22	422
W. Ruitenbeek Netherlands	16	598 2.2×	431 2.0×	31 0.6×	24 0.8×	51 1.6×	31	703
Geralyn Creadon‐Swindell United States	6	203 0.7×	205 0.9×	107 2.2×	37 1.2×	40 1.3×	7	297
Koujyu Katayama Japan	7	296 1.1×	191 0.9×	30 0.6×	15 0.5×	59 1.9×	9	385

Countries citing papers authored by J.A.M. Smeitink

Since Specialization

Citations

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

Fields of papers citing papers by J.A.M. Smeitink

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J.A.M. Smeitink

This figure shows the co-authorship network connecting the top 25 collaborators of J.A.M. Smeitink. A scholar is included among the top collaborators of J.A.M. 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 J.A.M. Smeitink. J.A.M. 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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17 of 17 papers shown

Hoischen, Alexander, et al.. (2013). PP6.8 – 1911 A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy. European Journal of Paediatric Neurology. 17. S47–S47. 3 indexed citations

Koene, Saskia, Richard J. Rodenburg, Marjo S. van der Knaap, et al.. (2012). Natural disease course and genotype‐phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases. Journal of Inherited Metabolic Disease. 35(5). 737–747. 100 indexed citations

Koene, Saskia, Tamás Kozicz, Richard J. Rodenburg, et al.. (2009). 63. Major depression in adolescent children consecutively diagnosed with mitochondrial disorder. Mitochondrion. 9(1). 77–77. 3 indexed citations

Smeitink, J.A.M., et al.. (2008). [Mitochondrial diseases; thinking beyond organ specialism necessary]. Data Archiving and Networked Services (DANS). 1 indexed citations

Braun, Kees P. J., et al.. (2004). Mitochondrial respiratory chain disease presenting as progressive bulbar paralysis of childhood. Journal of Inherited Metabolic Disease. 27(2). 281–283. 3 indexed citations

Heuvel, Lambertus P. van den, Murtada H. Farhoud, Ron A. Wevers, Baziel G.M. van Engelen, & J.A.M. Smeitink. (2003). Proteomics and neuromuscular diseases: theoretical concept and first results. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 40(1). 9–15. 11 indexed citations

Heuvel, Lambert P.W.J. van den & J.A.M. Smeitink. (2002). Identification of non-structural complex I genes which are responsible for isolated mitochondrial complex I deficiency. 1 indexed citations

Trijbels, J. M. F., R. C. A. Sengers, Edwin C.M. Mariman, et al.. (2001). Infantile Presentation of the mtDNA A3243G tRNALeu (UUR) Mutation. Neuropediatrics. 32(4). 183–190. 20 indexed citations

Knaap, Marjo S. van der, C. Jakobs, Georg F. Hoffmann, et al.. (1999). D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity?. Annals of Neurology. 45(1). 111–119. 59 indexed citations

10.

Jira, Petr, et al.. (1998). [Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease].. PubMed. 142(24). 1388–92. 10 indexed citations

11.

Huizing, Marjan, Udo Wendel, W. Ruitenbeek, et al.. (1998). Carnitine–acylcarnitine carrier deficiency: Identification of the molecular defect in a patient. Journal of Inherited Metabolic Disease. 21(3). 262–267. 30 indexed citations

12.

Rubio‐Gozalbo, M. Estela, W. Ruitenbeek, Herman Bentlage, et al.. (1997). Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV. European Journal of Pediatrics. 156(12). 931–934. 3 indexed citations

13.

Ausems, M.G.E.M., Egbert Bakker, Montserrat Durán-Bouza, et al.. (1997). Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation: Clinical, biochemical and DNA analyses in a four-generation family. American Journal of Medical Genetics. 68(2). 236–239. 19 indexed citations

14.

Roels, Frank, Marc Espeel, Hannah Mandel, et al.. (1995). Cell and tissue heterogeneity in peroxisomal patients. Ghent University Academic Bibliography (Ghent University). 11 indexed citations

15.

Stadhouders, A. M., et al.. (1993). A retrospective study of patients with the hereditary syndrome of congenital cataract, mitochondrial myopathy of heart and skeletal muscle and lactic acidosis. European Journal of Pediatrics. 152(3). 255–259. 35 indexed citations

16.

Smeitink, J.A.M., et al.. (1989). Fatal neonatal cardiomyopathy associated with cataract and mitochondrial myopathy. European Journal of Pediatrics. 148(7). 656–659. 37 indexed citations

17.

Smeitink, J.A.M., et al.. (1989). [The De Barsy syndrome].. PubMed. 57(2). 53–7. 2 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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