L.N. Went
Impact in
- Genetics top 2%
- Hemoglobinopathies and Related Disorders
- Hematology top 5%
- Iron Metabolism and Disorders
Papers in
-
- Mitochondrial Function and Pathology 11
- Porphyrin Metabolism and Disorders 9
- Heme Oxygenase-1 and Carbon Monoxide 8
- Retinal Development and Disorders 8
- Genetics 21
- Hemoglobinopathies and Related Disorders 20
- Co-authors
- J. E. MacIver (9 shared papers)G.W. Bruyn (6 shared papers)J. Van Steveninck (7 shared papers)G. Th. A. M. Bots (6 shared papers)D. Suurmond (5 shared papers)A.A. Schothorst (4 shared papers)M Vegter-van der Vlis (7 shared papers)E.C. Klasen (1 shared paper)
- Journals
- Journal of the Neurological Sciences (8 papers)Journal of Medical Genetics (6 papers)Annals of Human Genetics (6 papers)Blood (4 papers)Human Genetics (4 papers)
- Partner nations
- NetherlandsJamaicaUnited Kingdom
In The Last Decade
L.N. Went
87 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 111
- Genetics 494
- Hematology 322
- Clinical Biochemistry 196
- Ophthalmology 181
- Neurology 311
Countries citing papers authored by L.N. Went
This map shows the geographic impact of L.N. Went'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.N. Went with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L.N. Went more than expected).
Fields of papers citing papers by L.N. Went
This network shows the impact of papers produced by L.N. Went. 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.N. Went. The network helps show where L.N. Went may publish in the future.
Co-authors
The 25 scholars most cited alongside L.N. Went, 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 89 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia. | 1996 | 159 |
| 2 | 1982 | 140 | |
| 3 | 1990 | 119 | |
| 4 | 1984 | 109 | |
| 5 | 1988 | 106 | |
| 6 | 1970 | 105 | |
| 7 | 1981 | 91 | |
| 8 | 1972 | 87 | |
| 9 | Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin. | 1992 | 84 |
| 10 | 1970 | 76 | |
| 11 | 1959 | 65 | |
| 12 | 1986 | 64 | |
| 13 | 1964 | 61 | |
| 14 | 1982 | 55 | |
| 15 | 1961 | 53 | |
| 16 | 1960 | 52 | |
| 17 | 1966 | 51 | |
| 18 | 1975 | 44 | |
| 19 | 1971 | 43 | |
| 20 | 1968 | 42 |
About L.N. Went
L.N. Went is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Hematology and Neurology, having authored 89 papers that have together received 2.5k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (20 papers), Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (11 papers), Iron Metabolism and Disorders (9 papers), Porphyrin Metabolism and Disorders (9 papers), Heme Oxygenase-1 and Carbon Monoxide (8 papers), Retinal Development and Disorders (8 papers) and melanin and skin pigmentation (7 papers). The work is most often cited by research in Genetics (494 citations), Hematology (322 citations), Clinical Biochemistry (196 citations), Ophthalmology (181 citations) and Neurology (311 citations). L.N. Went has collaborated with scholars based in Netherlands, Jamaica and United Kingdom. Frequent co-authors include J. E. MacIver, G.W. Bruyn, J. Van Steveninck, G. Th. A. M. Bots, D. Suurmond, A.A. Schothorst, M Vegter-van der Vlis, E.C. Klasen, J.A. Oosterhuis and A.R. Wattendorff. Their work appears in journals such as Journal of the Neurological Sciences, Journal of Medical Genetics, Annals of Human Genetics, Blood and Human Genetics.
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.