L. M. E. Smit

1.8k total citations
36 papers, 1.1k citations indexed

About

L. M. E. Smit is a scholar working on Molecular Biology, Neurology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, L. M. E. Smit has authored 36 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Neurology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in L. M. E. Smit's work include Myasthenia Gravis and Thymoma (5 papers), Metabolism and Genetic Disorders (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). L. M. E. Smit is often cited by papers focused on Myasthenia Gravis and Thymoma (5 papers), Metabolism and Genetic Disorders (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). L. M. E. Smit collaborates with scholars based in Netherlands, United States and United Kingdom. L. M. E. Smit's co-authors include F.G.I. Jennekens, H. Veldman, Iris E. Sommer, Jaap Valk, C. Jakobs, Marjo S. van der Knaap, Frederik Barkhof, Cornelis Jakobs, John H. J. Wokke and C.J.M. van den Oord and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Annals of Neurology.

In The Last Decade

L. M. E. Smit

36 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
L. M. E. Smit Netherlands 21 533 222 199 139 131 36 1.1k
Antonella Pini Italy 16 800 1.5× 292 1.3× 94 0.5× 92 0.7× 71 0.5× 55 1.2k
Toru Kurokawa Japan 20 589 1.1× 267 1.2× 178 0.9× 164 1.2× 36 0.3× 62 1.4k
A. Laquérrière France 23 590 1.1× 336 1.5× 271 1.4× 132 0.9× 57 0.4× 77 1.5k
Fumio Kanda Japan 21 545 1.0× 401 1.8× 335 1.7× 38 0.3× 100 0.8× 95 1.4k
Abe M. Chutorian United States 21 411 0.8× 338 1.5× 595 3.0× 171 1.2× 259 2.0× 57 1.6k
Francesco Nicita Italy 23 412 0.8× 244 1.1× 239 1.2× 188 1.4× 89 0.7× 94 1.3k
Vincenzo Salpietro Italy 22 481 0.9× 199 0.9× 245 1.2× 132 0.9× 56 0.4× 89 1.2k
Robert T. Leshner United States 20 604 1.1× 164 0.7× 354 1.8× 45 0.3× 125 1.0× 49 1.6k
Andrea Klein Switzerland 22 837 1.6× 211 1.0× 257 1.3× 94 0.7× 42 0.3× 70 1.5k
Philip Jardine United Kingdom 18 747 1.4× 343 1.5× 371 1.9× 78 0.6× 43 0.3× 33 1.6k

Countries citing papers authored by L. M. E. Smit

Since Specialization
Citations

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

Fields of papers citing papers by L. M. E. Smit

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. M. E. Smit. 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 L. M. E. Smit. The network helps show where L. M. E. Smit may publish in the future.

Co-authorship network of co-authors of L. M. E. Smit

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

All Works

20 of 20 papers shown
1.
Smit, L. M. E., Anouk Pijpe, Cornelis H. van der Vlies, et al.. (2024). Characteristics, treatments and outcomes in patients with severe burn wounds; a 10 year cohort study on acute and reconstructive treatment. PLoS ONE. 19(11). e0313287–e0313287. 2 indexed citations
2.
Coebergh, Jan, et al.. (2013). A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 gene. European Journal of Paediatric Neurology. 18(3). 413–415. 40 indexed citations
3.
Roeyers, Herbert, Ruth Raymaekers, Albert J. Allen, et al.. (2009). Differential Effects of Atomoxetine on Executive Functioning and Lexical Decision in Attention-Deficit/Hyperactivity Disorder and Reading Disorder. Journal of Child and Adolescent Psychopharmacology. 19(6). 699–707. 36 indexed citations
4.
Smit, L. M. E., et al.. (2005). [Three infants with constipation and muscular weakness: infantile botulism].. PubMed. 149(15). 826–31. 5 indexed citations
5.
Knaap, Marjo S. van der, L. M. E. Smit, Frederik Barkhof, et al.. (2005). Neonatal porencephaly and adult stroke related to mutations in collagen IV A1. Annals of Neurology. 59(3). 504–511. 96 indexed citations
6.
Knaap, Marjo S. van der, Gajja S. Salomons, Rong Li, et al.. (2005). Unusual variants of Alexander's disease. Annals of Neurology. 57(3). 327–338. 91 indexed citations
7.
Ouwerkerk, W. J. R. van, René van den Berg, J. A. E. van Wijk, et al.. (2004). Craniopagus: the Suriname–Amsterdam conjunction. Child s Nervous System. 20(8-9). 625–634. 7 indexed citations
8.
Gibson, K. Michael, Maneesh Gupta, Phillip L. Pearl, et al.. (2003). Significant behavioral disturbances in succinic semialdehyde dehydrogenase (SSADH) deficiency (Gamma-Hydroxybutyric aciduria). Biological Psychiatry. 54(7). 763–768. 94 indexed citations
9.
Smit, L. M. E. & Feico J. J. Halbertsma. (1997). Cerebral cavernous hemangiomas in childhood. Child s Nervous System. 13(10). 522–525. 10 indexed citations
10.
Huizing, Marjan, W. Ruitenbeek, Friedrich P. Thinnes, et al.. (1996). Deficiency of the Voltage-Dependent Anion Channel: A Novel Cause of Mitochondriopathy. Pediatric Research. 39(5). 760–765. 52 indexed citations
11.
12.
Benders, Ad A.G.M., J.H. Veerkamp, Arie Oosterhof, et al.. (1994). Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil.. Journal of Clinical Investigation. 94(2). 741–748. 58 indexed citations
13.
Smit, L. M. E., et al.. (1993). A Case of Macrocephaly, Hydrocephalus, Megacerebellum, White Matter Abnormalities and Rosenthal Fibres. Developmental Medicine & Child Neurology. 35(8). 732–736. 14 indexed citations
14.
Moorsel, J. M. van der Klei‐van, et al.. (1991). Infantile isolated sulphite oxidase deficiency: Report of a case with negative sulphite test and normal sulphate excretion. European Journal of Pediatrics. 150(3). 196–197. 24 indexed citations
15.
Jansen, J., A. J. M. Donker, W. J. Luth, & L. M. E. Smit. (1990). Moyamoya Disease Associated with Renovascular Hypertension. Neuropediatrics. 21(1). 44–47. 30 indexed citations
16.
Wokke, John H. J., et al.. (1990). Morphological changes in the human end plate with age. Journal of the Neurological Sciences. 95(3). 291–310. 99 indexed citations
17.
Leschot, N. J., et al.. (1988). Karyotyping urine sediment cells confirms trisomy 12 mosaicism detected at amniocentesis. Clinical Genetics. 34(2). 135–139. 21 indexed citations
18.
Kaiser, M. C., et al.. (1988). Computed tomographic diagnosis of septic sinus thrombosis and their complications. Neuroradiology. 30(2). 160–165. 23 indexed citations
19.
Smit, L. M. E., et al.. (1988). A myasthenic syndrome with congenital paucity of secondary synaptic clefts: CPSC Syndrome. Muscle & Nerve. 11(4). 337–348. 22 indexed citations
20.
Smit, L. M. E., et al.. (1987). A Congenital Myasthenic Disorder with Paucity of Secondary Synaptic Clefts: Deficiency and Altered Distribution of Acetylcholine Receptorsa. Annals of the New York Academy of Sciences. 505(1). 346–356. 10 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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