Cliff Shults

3.0k total citations · 1 hit paper
12 papers, 1.4k citations indexed

About

Cliff Shults is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Cliff Shults has authored 12 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Cliff Shults's work include Parkinson's Disease Mechanisms and Treatments (8 papers), Nuclear Receptors and Signaling (4 papers) and Neurological disorders and treatments (3 papers). Cliff Shults is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (8 papers), Nuclear Receptors and Signaling (4 papers) and Neurological disorders and treatments (3 papers). Cliff Shults collaborates with scholars based in United States and Australia. Cliff Shults's co-authors include Irene Litvan, Gregor K. Wenning, Kapil D. Sethi, Christopher G. Goetz, Ian G. McKeith, Niall Quinn, Kailash P. Bhatia, Anthony E. Lang, David J. Burn and Alice Rudolph and has published in prestigious journals such as Neurology, Annals of Neurology and Brain Research.

In The Last Decade

Cliff Shults

12 papers receiving 1.3k citations

Hit Papers

SIC Task Force appraisal of clinical diagnostic criteria ... 2003 2026 2010 2018 2003 250 500 750

Peers

Cliff Shults
Inga Liepelt Germany
M. H. Mark United States
Ilona Csóti Germany
E.M.J. Foncke Netherlands
Michail E. Kalaitzakis United Kingdom
E. Tolosa Spain
Cliff Shults
Citations per year, relative to Cliff Shults Cliff Shults (= 1×) peers Antony J. Harding

Countries citing papers authored by Cliff Shults

Since Specialization
Citations

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

Fields of papers citing papers by Cliff Shults

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cliff Shults. 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 Cliff Shults. The network helps show where Cliff Shults may publish in the future.

Co-authorship network of co-authors of Cliff Shults

This figure shows the co-authorship network connecting the top 25 collaborators of Cliff Shults. A scholar is included among the top collaborators of Cliff Shults 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 Cliff Shults. Cliff Shults is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Pankratz, Nathan, Karen Marder, Cheryl Halter, et al.. (2008). Clinical correlates of depressive symptoms in familial Parkinson's disease. Movement Disorders. 23(15). 2216–2223. 26 indexed citations
2.
Nichols, William C., et al.. (2007). LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. Neurology. 69(18). 1737–1744. 46 indexed citations
3.
Howell, Neil, Corinna Herrnstadt, Cliff Shults, & David A. Mackey. (2003). Low penetrance of the 14484 LHON mutation when it arises in a non‐haplogroup J mtDNA background. American Journal of Medical Genetics Part A. 119A(2). 147–151. 48 indexed citations
4.
Pankratz, Nathan, William C. Nichols, Cheryl Halter, et al.. (2003). Significant Linkage of Parkinson Disease to Chromosome 2q36-37. The American Journal of Human Genetics. 72(4). 1053–1057. 102 indexed citations
5.
Litvan, Irene, Kailash P. Bhatia, David J. Burn, et al.. (2003). SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders. Movement Disorders. 18(5). 467–486. 785 indexed citations breakdown →
6.
Pankratz, Nathan, William C. Nichols, Cheryl Halter, et al.. (2002). Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations. The American Journal of Human Genetics. 71(1). 124–135. 131 indexed citations
7.
Saitoh, T, Yu Xia, Eliezer Masliah, et al.. (1995). The CYP2D6B mutant allele is overrepresented in the Lewy body variant of Alzheimer's disease. Annals of Neurology. 37(1). 110–112. 69 indexed citations
8.
Shults, Cliff, et al.. (1993). Effect of selegiline (deprenyl) on the progression of disability in early Parkinson's disease. Acta Neurologica Scandinavica. 87(S146). 36–42. 13 indexed citations
9.
Shults, Cliff. (1993). Effect of selegiline (deprenyl) on the progression of disability in early Parkinson's disease. Parkinson Study Group.. PubMed. 146. 36–42. 10 indexed citations
10.
Shults, Cliff, Philip C Johnston, & Fred H. Gage. (1987). Comparison of substance K-like and substance P-like fibers and cells in the rat hippocampus. Brain Research. 426(2). 290–296. 25 indexed citations
11.
Bracha, H. Stefan, Cliff Shults, S.D. Glick, & Joel E. Kleinman. (1987). Spontaneous asymmetric circling behavior in hemi-parkinsonism; a human equivalent of the lesioned-circling rodent behavior. Life Sciences. 40(11). 1127–1130. 87 indexed citations
12.
Handelmann, Gail E., Cliff Shults, & Thomas L. O’Donohue. (1987). A developmental influence of substance P on its receptors. International Journal of Developmental Neuroscience. 5(1). 11–15. 12 indexed citations

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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