Lawrence J. Schut

4.7k citations
50 papers · 3.6k indexed · 1 hit paper · h-index 25
Topics
Genetic Neurodegenerative Diseases (38 papers)Mitochondrial Function and Pathology (31 papers)DNA Repair Mechanisms (8 papers)
Partner nations
United StatesCanadaJapan

In The Last Decade

Lawrence J. Schut

48 papers receiving 3.5k citations

Hit Papers

International Cooperative Ataxia Rating Scale for pharmac...199720262006201619972505007501000

Peers

Lawrence J. Schut
Comparison fields: 5 of 94
  • Cellular and Molecular Neuroscience 2.6k
  • Molecular Biology 2.3k
  • Neurology 1.1k
  • Neurology 564
  • Genetics 315
Replace M. Ben Hamida with:
M. Ben Hamida Tunisia
S. H. Subramony United States
Jean‐Paul Vonsattel United States
Katrin Bürk Germany
Luis Velázquez‐Pérez Cuba
Klas Wictorin Sweden
Carsten Saft Germany
Andrew Churchyard Australia
Mark S. LeDoux United States
Doris D. Wang United States
Lawrence J. Schut relative to M. Ben Hamida Tunisia M. Ben Hamida's profile →
Citations per field
00.5×1.5×2.0×
M. Ben Hamida · 1×
Citations per year

Countries citing papers authored by Lawrence J. Schut

Since Specialization
Citations

This map shows the geographic impact of Lawrence J. Schut'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 Lawrence J. Schut with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lawrence J. Schut more than expected).

Fields of papers citing papers by Lawrence J. Schut

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lawrence J. Schut. 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 Lawrence J. Schut. The network helps show where Lawrence J. Schut may publish in the future.

Co-authorship network of co-authors of Lawrence J. Schut

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence J. Schut. A scholar is included among the top collaborators of Lawrence J. Schut based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lawrence J. Schut. Lawrence J. Schut is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 16
2 0
3 110
4 469
5 45
6 1
7
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndromebreakdown →
1010
8 51
9 97
10
A dominant spinocerebellar ataxia gene (SCA5) in a family descendent from the paternal grandparents of President Lincoln maps to chromosome 11
4
11 253
12
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.
137
13 12
14 26
15 13
16 25
17 62
18 29
19 106
20 20

About Lawrence J. Schut

Lawrence J. Schut is a scholar working on Cellular and Molecular Neuroscience, Clinical Biochemistry and Molecular Biology, having authored 50 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (38 papers), Mitochondrial Function and Pathology (31 papers) and DNA Repair Mechanisms (8 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.6k citations), Neurology (1.1k citations) and Neurology (564 citations). Lawrence J. Schut has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Laura P.W. Ranum, John Day, Melinda L. Moseley, Stephen J. Kish, Thomas D. Bird, Harry T. Orr, Kellie Benzow, Christopher M. Gómez, Robert D. Currier and Michael D. Koob. Their work appears in journals such as Nature Genetics, Brain and 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.

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