Cheryl Halter

1.9k total citations
18 papers, 1.4k citations indexed

About

Cheryl Halter is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Cheryl Halter has authored 18 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Cheryl Halter's work include Parkinson's Disease Mechanisms and Treatments (13 papers), Nuclear Receptors and Signaling (8 papers) and Neurological diseases and metabolism (5 papers). Cheryl Halter is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (13 papers), Nuclear Receptors and Signaling (8 papers) and Neurological diseases and metabolism (5 papers). Cheryl Halter collaborates with scholars based in United States, Spain and Italy. Cheryl Halter's co-authors include Tatiana Foroud, William C. Nichols, Nathan Pankratz, Alice Rudolph, Clifford W. Shults, P. Michael Conneally, Richard H. Myers, Jeanne C. Latourelle, James F. Gusella and Jemma B. Wilk and has published in prestigious journals such as The Lancet, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Cheryl Halter

18 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Cheryl Halter United States 13 1.0k 544 422 394 268 18 1.4k
Jennifer S. Montimurro United States 14 983 1.0× 487 0.9× 396 0.9× 442 1.1× 231 0.9× 16 1.4k
Ana Djarmati Germany 19 845 0.8× 605 1.1× 499 1.2× 233 0.6× 162 0.6× 29 1.3k
Manu Sharma Germany 17 1.0k 1.0× 552 1.0× 680 1.6× 380 1.0× 311 1.2× 41 1.6k
Brian Fiske United States 11 859 0.8× 436 0.8× 482 1.1× 243 0.6× 347 1.3× 28 1.5k
Reema Paudel United Kingdom 16 785 0.8× 521 1.0× 401 1.0× 320 0.8× 445 1.7× 20 1.4k
Kari J. Strain United States 10 476 0.5× 375 0.7× 277 0.7× 188 0.5× 115 0.4× 10 883
Kelly M. Hinkle United States 15 759 0.7× 329 0.6× 323 0.8× 269 0.7× 372 1.4× 18 1.1k
Sarah Morgan Germany 20 515 0.5× 428 0.8× 271 0.6× 202 0.5× 150 0.6× 38 1.1k
Ingrid Goebel Germany 13 675 0.7× 310 0.6× 619 1.5× 307 0.8× 315 1.2× 18 1.4k
Lasse Pihlstrøm Norway 18 549 0.5× 284 0.5× 310 0.7× 229 0.6× 222 0.8× 49 904

Countries citing papers authored by Cheryl Halter

Since Specialization
Citations

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

Fields of papers citing papers by Cheryl Halter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cheryl Halter

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

All Works

18 of 18 papers shown
1.
Foroud, Tatiana, Danielle Smith, Cheryl Halter, et al.. (2015). Novel recruitment strategy to enrich forLRRK2mutation carriers. Molecular Genetics & Genomic Medicine. 3(5). 404–412. 12 indexed citations
2.
Pankratz, Nathan, Alexandra Dumitriu, Kurt N. Hetrick, et al.. (2011). Copy Number Variation in Familial Parkinson Disease. PLoS ONE. 6(8). e20988–e20988. 54 indexed citations
3.
Latourelle, Jeanne C., Audrey E. Hendricks, Nathan Pankratz, et al.. (2011). Genomewide linkage study of modifiers of LRRK2‐related Parkinson's disease. Movement Disorders. 26(11). 2039–2044. 4 indexed citations
4.
Simon, David K., Nathan Pankratz, Diane Kissell, et al.. (2010). Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. BMC Medical Genetics. 11(1). 53–53. 26 indexed citations
5.
Pankratz, Nathan, William C. Nichols, Michael W. Pauciulo, et al.. (2009). Alpha‐synuclein and familial Parkinson's disease. Movement Disorders. 24(8). 1125–1131. 33 indexed citations
6.
Latourelle, Jeanne C., Nathan Pankratz, Alexandra Dumitriu, et al.. (2009). Genomewide association study for onset age in Parkinson disease. BMC Medical Genetics. 10(1). 98–98. 88 indexed citations
7.
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
8.
Pankratz, Nathan, Jemma B. Wilk, Jeanne C. Latourelle, et al.. (2008). Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Human Genetics. 124(6). 593–605. 342 indexed citations
9.
Nichols, William C., Michael W. Pauciulo, Nathan Pankratz, et al.. (2006). R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation. Movement Disorders. 22(2). 254–256. 8 indexed citations
10.
Pankratz, Nathan, Michael W. Pauciulo, Cheryl Halter, et al.. (2006). Mutations in DJ-1 are rare in familial Parkinson disease. Neuroscience Letters. 408(3). 209–213. 41 indexed citations
11.
Nichols, William C., Nathan Pankratz, Dena Hernández, et al.. (2005). Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. The Lancet. 365(9457). 410–412. 347 indexed citations
12.
Pankratz, Nathan, Cheryl Halter, Alice Rudolph, et al.. (2005). Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia. Movement Disorders. 21(1). 45–49. 92 indexed citations
13.
Nichols, William C., Nathan Pankratz, Terry Reed, et al.. (2004). Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Movement Disorders. 19(6). 649–655. 29 indexed citations
14.
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
15.
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
16.
Reider, Carson, Cheryl Halter, Peter Castelluccio, et al.. (2002). Reliability of reported age at onset for Parkinson's disease. Movement Disorders. 18(3). 275–279. 28 indexed citations
17.
Halter, Cheryl, et al.. (1992). How treatment of persons with serious mental illness is portrayed in undergraduate psychology textbooks. Community Mental Health Journal. 28(1). 29–42. 9 indexed citations
18.
Rajecki, D. W., et al.. (1991). Documentation of Media Reflections of the Patriotic Revival in the United States in the 1980s. The Journal of Social Psychology. 131(3). 401–411. 3 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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