L.N. Went

3.1k citations
84 papers · 2.3k · h-index 28

Impact in

  • Genetics top 2%
    • Hemoglobinopathies and Related Disorders
  • Hematology top 5%
    • Iron Metabolism and Disorders

Papers in

    • Mitochondrial Function and Pathology 10
    • Porphyrin Metabolism and Disorders 8
    • Heme Oxygenase-1 and Carbon Monoxide 7
    • Hemoglobinopathies and Related Disorders 20

L.N. Went

83 papers receiving 2.0k citations

Peers

L.N. Went
Comparison fields: 5 of 111
  • Genetics 467
  • Hematology 305
  • Clinical Biochemistry 183
  • Neurology 275
  • Ophthalmology 153
Replace David W. Stockton with:
David W. Stockton United States
Lawrence Charnas United States
Michael B. Petersen Greece
Dalil Hamroun France
Cynthia J. Tifft United States
Fernando Kok Brazil
J. E. Wraith United Kingdom
Eiichiro Uyama Japan
Anne Slavotinek United States
Michele D’Urso Italy
L.N. Went relative to David W. Stockton United States David W. Stockton's profile →
Citations per field
00.5×2.6×
David W. Stockton · 1×
Citations per year

Countries citing papers authored by L.N. Went

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with L.N. Went Line = papers co-authored together L.N. Went links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 84 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.
1996153
2 1982124
3 1990115
4 1984103
5 198897
6 197094
7 198185
8 197280
9 197072
10
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.
199270
11 195961
12 196458
13 198657
14 196149
15 198249
16 196647
17 197544
18 196041
19 197139
20 196838

About L.N. Went

L.N. Went is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Hematology and Neurology, having authored 84 papers that have together received 2.3k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (20 papers), Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (10 papers), Iron Metabolism and Disorders (9 papers), Porphyrin Metabolism and Disorders (8 papers), Heme Oxygenase-1 and Carbon Monoxide (7 papers), melanin and skin pigmentation (6 papers) and Neonatal Health and Biochemistry (6 papers). The work is most often cited by research in Genetics (467 citations), Hematology (305 citations), Clinical Biochemistry (183 citations), Neurology (275 citations) and Ophthalmology (153 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, E.C. Klasen, M Vegter-van der Vlis, J.A. Oosterhuis and A.R. Wattendorff. Their work appears in journals such as Journal of the Neurological Sciences, Annals of Human Genetics, Journal of Medical Genetics, Human Genetics and Blood.

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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