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
- Congenital heart defects research 2
- RNA Research and Splicing 2
- Neurology 11
- Myasthenia Gravis and Thymoma 5
- Co-authors
- Iris E. Sommer (1 shared paper)F.G.I. Jennekens (5 shared papers)H. Veldman (4 shared papers)Jaap Valk (3 shared papers)C. Jakobs (5 shared papers)Marjo S. van der Knaap (2 shared papers)Frederik Barkhof (2 shared papers)Christl Vermeij‐Keers (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (3 papers)Child s Nervous System (3 papers)Annals of Neurology (2 papers)Human Genetics (2 papers)Developmental Medicine & Child Neurology (2 papers)
- Partner nations
- NetherlandsUnited StatesCanada
In The Last Decade
L. M. E. Smit
35 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 81
- Clinical Biochemistry 143
- Neurology 206
- Cellular and Molecular Neuroscience 239
- Immunology and Allergy 53
- Pediatrics, Perinatology and Child Health 148
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 35 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 114 | |
| 2 | 1990 | 109 | |
| 3 | 2005 | 101 | |
| 4 | 2003 | 98 | |
| 5 | MR of the caudal regression syndrome: embryologic implications. | 1994 | 75 |
| 6 | 1997 | 67 | |
| 7 | 1994 | 63 | |
| 8 | 1996 | 58 | |
| 9 | 1996 | 48 | |
| 10 | 2013 | 42 | |
| 11 | 1990 | 40 | |
| 12 | 2009 | 37 | |
| 13 | 1980 | 37 | |
| 14 | 1990 | 32 | |
| 15 | 1990 | 31 | |
| 16 | 1988 | 28 | |
| 17 | 1989 | 27 | |
| 18 | 1991 | 27 | |
| 19 | 1988 | 25 | |
| 20 | 1988 | 23 |
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 35 papers that have together received 1.2k indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (5 papers), Metabolism and Genetic Disorders (4 papers), Cellular transport and secretion (3 papers), RNA regulation and disease (3 papers), Mitochondrial Function and Pathology (3 papers), Congenital heart defects research (2 papers), RNA Research and Splicing (2 papers) and Fetal and Pediatric Neurological Disorders (2 papers). The work is most often cited by research in Clinical Biochemistry (143 citations), Neurology (206 citations), Cellular and Molecular Neuroscience (239 citations), Immunology and Allergy (53 citations) and Pediatrics, Perinatology and Child Health (148 citations). L. M. E. Smit has collaborated with scholars based in Netherlands, United States and Canada. Frequent co-authors include Iris E. Sommer, F.G.I. Jennekens, H. Veldman, Jaap Valk, C. Jakobs, Marjo S. van der Knaap, Frederik Barkhof, Christl Vermeij‐Keers, Rutger A. J. Nievelstein and Cornelis Jakobs. Their work appears in journals such as Journal of Inherited Metabolic Disease, Child s Nervous System, Annals of Neurology, Human Genetics and Developmental Medicine & Child 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.