L. M. E. Smit
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
- Neurology top 5%
Papers in
-
- RNA regulation and disease 3
- Mitochondrial Function and Pathology 3
- RNA Research and Splicing 2
- Neurology 11
- Myasthenia Gravis and Thymoma 5
- Botulinum Toxin and Related Neurological Disorders 2
- Co-authors
- F.G.I. Jennekens (5 shared papers)H. Veldman (4 shared papers)Iris E. Sommer (1 shared paper)Jaap Valk (3 shared papers)C. Jakobs (5 shared papers)Marjo S. van der Knaap (2 shared papers)Frederik Barkhof (2 shared papers)John H. J. Wokke (1 shared paper)
- Journals
- Child s Nervous System (3 papers)Journal of Inherited Metabolic Disease (3 papers)Developmental Medicine & Child Neurology (2 papers)Human Genetics (2 papers)Neuropediatrics (2 papers)
- Partner nations
- NetherlandsUnited StatesUnited Kingdom
In The Last Decade
L. M. E. Smit
36 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 82
- Clinical Biochemistry 131
- Neurology 199
- Cellular and Molecular Neuroscience 222
- Immunology and Allergy 55
- Molecular Biology 533
Countries citing papers authored by L. M. E. Smit
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
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-authors
The 25 scholars most cited alongside L. M. E. Smit, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1990 | 99 | |
| 2 | 2005 | 96 | |
| 3 | 2003 | 94 | |
| 4 | 2005 | 91 | |
| 5 | MR of the caudal regression syndrome: embryologic implications. | 1994 | 62 |
| 6 | 1994 | 58 | |
| 7 | 1997 | 56 | |
| 8 | 1996 | 52 | |
| 9 | 1996 | 43 | |
| 10 | 2013 | 40 | |
| 11 | 2009 | 36 | |
| 12 | 1980 | 32 | |
| 13 | 1990 | 31 | |
| 14 | 1990 | 30 | |
| 15 | 1990 | 28 | |
| 16 | 1991 | 24 | |
| 17 | 1989 | 24 | |
| 18 | 1988 | 23 | |
| 19 | 1988 | 22 | |
| 20 | 1988 | 21 |
About L. M. E. Smit
L. M. E. Smit is a scholar working on Molecular Biology, Neurology, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Clinical Biochemistry, having authored 36 papers that have together received 1.1k indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Metabolism and Genetic Disorders (4 papers), RNA regulation and disease (3 papers), Mitochondrial Function and Pathology (3 papers), Cellular transport and secretion (3 papers), Botulinum Toxin and Related Neurological Disorders (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Clinical Biochemistry (131 citations), Neurology (199 citations), Cellular and Molecular Neuroscience (222 citations), Immunology and Allergy (55 citations) and Molecular Biology (533 citations). L. M. E. Smit has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include F.G.I. Jennekens, H. Veldman, Iris E. Sommer, Jaap Valk, C. Jakobs, Marjo S. van der Knaap, Frederik Barkhof, John H. J. Wokke, C.J.M. van den Oord and Cornelis Jakobs. Their work appears in journals such as Child s Nervous System, Journal of Inherited Metabolic Disease, Developmental Medicine & Child Neurology, Human Genetics and Neuropediatrics.
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.