L.N. Went
Impact in
- Genetics top 2%
- Hemoglobinopathies and Related Disorders
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
- Genetics 21
- Hemoglobinopathies and Related Disorders 20
-
- Hereditary Neurological Disorders 14
- Genetic Neurodegenerative Diseases 9
- Co-authors
- J. E. MacIver (9 shared papers)G.W. Bruyn (6 shared papers)Gerard Th. A. M. Bots (6 shared papers)John Van Steveninck (7 shared papers)Dick Suurmond (5 shared papers)Albert A. Schothorst (4 shared papers)M Vegter-van der Vlis (8 shared papers)Eduard 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)Nature (4 papers)Documenta Ophthalmologica (4 papers)
- Partner nations
- NetherlandsJamaicaUnited States
In The Last Decade
L.N. Went
87 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 91
- Genetics 486
- Cellular and Molecular Neuroscience 358
- Ophthalmology 219
- Neurology 197
- Molecular Biology 748
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 | 168 |
| 2 | 1982 | 143 | |
| 3 | 1990 | 119 | |
| 4 | 1984 | 108 | |
| 5 | 1988 | 105 | |
| 6 | 1970 | 103 | |
| 7 | 1981 | 98 | |
| 8 | 1972 | 87 | |
| 9 | Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin. | 1992 | 85 |
| 10 | 1970 | 76 | |
| 11 | 1986 | 71 | |
| 12 | 1959 | 62 | |
| 13 | 1964 | 62 | |
| 14 | 1982 | 57 | |
| 15 | 1960 | 53 | |
| 16 | 1961 | 52 | |
| 17 | 1966 | 52 | |
| 18 | 1975 | 45 | |
| 19 | 1968 | 43 | |
| 20 | 1971 | 42 |
About L.N. Went
L.N. Went is a scholar working on Genetics, Cellular and Molecular Neuroscience, Ophthalmology, Molecular Biology 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), Retinal Development and Disorders (16 papers), Hereditary Neurological Disorders (14 papers), Genetic Neurodegenerative Diseases (9 papers), Porphyrin Metabolism and Disorders (9 papers), Visual perception and processing mechanisms (7 papers), Glaucoma and retinal disorders (7 papers) and Cutaneous Melanoma Detection and Management (4 papers). The work is most often cited by research in Genetics (486 citations), Cellular and Molecular Neuroscience (358 citations), Ophthalmology (219 citations), Neurology (197 citations) and Molecular Biology (748 citations). L.N. Went has collaborated with scholars based in Netherlands, Jamaica and United States. Frequent co-authors include J. E. MacIver, G.W. Bruyn, Gerard Th. A. M. Bots, John Van Steveninck, Dick Suurmond, Albert A. Schothorst, M Vegter-van der Vlis, Eduard C. Klasen, Jendo A. Oosterhuis and A. Rolf Wattendorff. Their work appears in journals such as Journal of the Neurological Sciences, Journal of Medical Genetics, Annals of Human Genetics, Nature and Documenta Ophthalmologica.
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.