Lawrence J. Schut

4.7k total citations · 1 hit paper
50 papers, 3.6k citations indexed

About

Lawrence J. Schut is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Lawrence J. Schut has authored 50 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Cellular and Molecular Neuroscience, 35 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Lawrence J. Schut's work include Genetic Neurodegenerative Diseases (38 papers), Mitochondrial Function and Pathology (31 papers) and DNA Repair Mechanisms (8 papers). Lawrence J. Schut is often cited by papers focused on Genetic Neurodegenerative Diseases (38 papers), Mitochondrial Function and Pathology (31 papers) and DNA Repair Mechanisms (8 papers). Lawrence J. Schut collaborates with scholars based in United States, Canada and Japan. Lawrence J. Schut's 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 and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Lawrence J. Schut

48 papers receiving 3.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

1997 1.0k citations P Trouillas, T Takayanagi et al. Journal of the Neurological Sciences profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	CCG•CGG interruptions in high‐penetrance SCA8 families increase RAN translation and protein toxicity 2021 ·EMBO Molecular Medicine ·B. Pérez, Hannah K. Shorrock, Mónica Báñez-Coronel, Tao Zu, Lisa E. L. Romano, Lauren A. Laboissonniere, Tammy Reid, Yoshio Ikeda, Kaalak Reddy, Christopher M. Gómez, Thomas D. Bird, Tetsuo Ashizawa, Lawrence J. Schut, Alfredo Brusco, J. Andrew Berglund, Lis Hasholt, Jørgen E. Nielsen, S. H. Subramony, Laura P.W. Ranum	16
2	Cerebral Gangliogliomas of Childhood 2015 ·Progress in tumor research ·Leslie N. Sutton, Roger J. Packer, R. A. Zimmerman, Derek A. Bruce, Lawrence J. Schut	0
3	Spinocerebellar ataxia type 8 2000 ·Neurology ·John Day, Lawrence J. Schut, Melinda L. Moseley, (unknown), Laura P.W. Ranum	110
4	An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) 1999 ·Nature Genetics ·Michael D. Koob, Melinda L. Moseley, Lawrence J. Schut, Kellie Benzow, Thomas D. Bird, John Day, Laura P.W. Ranum	469
5	Brain Glyceraldehyde-3-Phosphate Dehydrogenase Activity in Human Trinucleotide Repeat Disorders 1998 ·Archives of Neurology ·Stephen J. Kish, Íscia Lopes‐Cendes, Mark Guttman, Yoshiaki Furukawa, Massimo Pandolfo, Guy A. Rouleau, Brian M. Ross, Martha Nance, Lawrence J. Schut, Lee Fang Ang, L. DiStefano	45
6	Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients 1998 ·Human Mutation ·(unknown), Kellie Benzow, Lawrence J. Schut, (unknown), Dennis Livingston	1
7	International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome breakdown → 1997 ·Journal of the Neurological Sciences ·P Trouillas, T Takayanagi, Mark Hallett, Robert D. Currier, S. H. Subramony, K. Wessel, Alan Bryer, Hans‐Christoph Diener, S. Massaquoi, Christopher M. Gómez, Paula Coutinho, M. Ben Hamida, G Campanella, Alessandro Filla, Lawrence J. Schut, (unknown), (unknown), Norbert Nighoghossian, B. V. Manyam	1010
8	Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and machado‐joseph disease 1996 ·Annals of Neurology ·Íscia Lopes‐Cendes, Patrı́cia Maciel, Stephen J. Kish, Cláudia Gaspar, Isabel Silveira, Yves Robitaille, H. Brent Clark, Arnulf H. Koeppen, Martha Nance, Lawrence J. Schut, Paula Coutinho, Jorge Sequeiros, Guy A. Rouleau	51
9	Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype 1995 ·Acta Neuropathologica ·Yves Robitaille, Lawrence J. Schut, Stephen J. Kish	97
10	A dominant spinocerebellar ataxia gene (SCA5) in a family descendent from the paternal grandparents of President Lincoln maps to chromosome 11 1994 ·The American Journal of Human Genetics ·Laura P.W. Ranum, Julie K. Lundgren, Lawrence J. Schut	4
11	Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11 1994 ·Nature Genetics ·Laura P.W. Ranum, Lawrence J. Schut, Julie K. Lundgren, Harry T. Orr, Dennis Livingston	253
12	Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset. 1994 ·PubMed ·Laura P.W. Ranum, Ming‐Yi Chung, Sandro Banfi, Alan Bryer, Lawrence J. Schut, Raj Ramesar, Lisa Duvick, Alanna E. McCall, S. H. Subramony, Lev G. Goldfarb	137
13	Brain amino acid reductions in one family with chromosome 6p—linked dominantly inherited olivopontocerebellar atrophy 1991 ·Annals of Neurology ·Stephen J. Kish, Yves Robitaille, Munir El‐Awar, Joseph J. Gilbert, John H. N. Deck, Li‐Jan Chang, Lawrence J. Schut	12
14	Selective delayed alternation deficits in dominantly inherited olivopontocerebellar atrophy 1991 ·Brain and Cognition ·Munir El‐Awar, Stephen J. Kish, Marlene Oscar‐Berman, Yves Robitaille, Lawrence J. Schut, Morris Freedman	26
15	Quinolinic acid catabolism is increased in cerebellum of patients with dominantly inherited olivopontocerebellar atrophy 1991 ·Annals of Neurology ·Stephen J. Kish, Fu Du, (unknown), Yves Robitaille, Melvyn J. Ball, Lawrence J. Schut, Oleh Hornykiewicz, Robert Schwarcz	13
16	Cerebellar [3H]inositol 1,4,5-trisphosphate binding is markedly decreased in human olivopontocerebellar atrophy 1989 ·Brain Research ·Stephen J. Kish, Peter P. Li, Yves Robitaille, Robert D. Currier, Joseph J. Gilbert, Lawrence J. Schut, Jerry J. Warsh	25
17	The spectrum of imaging and neuropsychological findings in Pick's disease 1989 ·Neurology ·David S. Knopman, Kathy J. Christensen, Lawrence J. Schut, Robert E. Harbaugh, (unknown), Thanh Duc Ngo, William H. Frey	62
18	The Coexistence and Differentiation of Late Onset Huntington's Disease and Alzheimer's Disease: A Case Report and Review of the Literature 1988 ·Journal of the American Geriatrics Society ·(unknown), Angeline R. Mastri, Lawrence J. Schut	29
19	Cognitive deficits in olivopontocerebellar atrophy: Implications for the cholinergic hypothesis of Alzheimer's dementia 1988 ·Annals of Neurology ·Stephen J. Kish, Munir El‐Awar, Lawrence J. Schut, Larry Leach, Marlene Oscar‐Berman, (unknown)	106
20	Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy 1987 ·Annals of Neurology ·Stephen J. Kish, Robert D. Currier, Lawrence J. Schut, Thomas L. Perry, (unknown)	20

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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