Janel Johnson

7.9k total citations
15 papers, 585 citations indexed

About

Janel Johnson is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Janel Johnson has authored 15 papers receiving a total of 585 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 10 papers in Cellular and Molecular Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Janel Johnson's work include Parkinson's Disease Mechanisms and Treatments (11 papers), Nuclear Receptors and Signaling (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Janel Johnson is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (11 papers), Nuclear Receptors and Signaling (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Janel Johnson collaborates with scholars based in United States, United Kingdom and Italy. Janel Johnson's co-authors include Andrew Singleton, Dena Hernández, John Hardy, Katrina Gwinn, Paola Giunti, Henry Houlden, Nicholas Wood, Melissa Hanson, Stephen Hague and Bernard Ravina and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Janel Johnson

14 papers receiving 573 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Janel Johnson United States	10	389	290	235	141	121	15	585
Magali Periquet France	7	591 1.5×	411 1.4×	183 0.8×	165 1.2×	97 0.8×	7	696
Shamol Saha United States	10	444 1.1×	229 0.8×	404 1.7×	121 0.9×	209 1.7×	13	849
Ana Gorostidi Spain	20	607 1.6×	204 0.7×	303 1.3×	224 1.6×	228 1.9×	30	891
Shabnam Salehi‐Rad Canada	11	457 1.2×	211 0.7×	249 1.1×	164 1.2×	217 1.8×	13	660
Philippe Pals Belgium	11	376 1.0×	191 0.7×	206 0.9×	188 1.3×	140 1.2×	15	573
Robert Hering Germany	6	360 0.9×	279 1.0×	137 0.6×	101 0.7×	65 0.5×	8	471
Christoph B. Lücking Germany	9	385 1.0×	286 1.0×	155 0.7×	127 0.9×	55 0.5×	11	502
Christan F. Rohé Netherlands	6	656 1.7×	264 0.9×	227 1.0×	256 1.8×	223 1.8×	6	783
Louisa C. Johnston United States	11	374 1.0×	329 1.1×	147 0.6×	83 0.6×	82 0.7×	12	669
Etsuro Ohta Japan	14	591 1.5×	197 0.7×	324 1.4×	199 1.4×	251 2.1×	23	764

Countries citing papers authored by Janel Johnson

Since Specialization

Citations

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

Fields of papers citing papers by Janel Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janel Johnson

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

All Works

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15 of 15 papers shown

Perkins, Katie, Katherine G. Meilleur, Līvija Medne, et al.. (2011). P3.48 Exome sequencing with linkage analysis identifies a novel ACTA1 variant in a large family with progressive muscle weakness. Neuromuscular Disorders. 21(9-10). 696–697. 1 indexed citations

Stévanin, Giovanni, Sylvie Forlani, C. Cazeneuve, et al.. (2009). Conventional mutations are associated with a different phenotype than polyglutamine expansions in spinocerebellar ataxias. 16. 284–284. 5 indexed citations

Johnson, Janel, Nicholas Wood, Paola Giunti, & Henry Houlden. (2008). Clinical and genetic analysis of spinocerebellar ataxia type 11. The Cerebellum. 7(2). 159–164. 19 indexed citations

Houlden, Henry, Janel Johnson, Christopher Gardner‐Thorpe, et al.. (2007). Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11. Nature Genetics. 39(12). 1434–1436. 130 indexed citations

Johnson, Janel, Coro Paisán‐Ruíz, Grisel Lopez, et al.. (2007). Comprehensive Screening of a North American Parkinson’s Disease Cohort for <i>LRRK2</i> Mutation. Neurodegenerative Diseases. 4(5). 386–391. 21 indexed citations

Johnson, Janel, Nicholas Wood, Paola Giunti, & Henry Houlden. (2007). Clinical and genetic analysis of spinocerebellar ataxia type 11. The Cerebellum. 1–6.

Xiromerisiou, Georgia, et al.. (2006). Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants. European Journal of Neurology. 14(1). 7–11. 41 indexed citations

Clarimón, Jordi, Janel Johnson, Ruth Djaldetti, et al.. (2005). Mutation of the Parkin gene in a Persian family: Clinical progression over a 40‐year period. Movement Disorders. 20(7). 887–890. 4 indexed citations

Clarimón, Jordi, Janel Johnson, Okan Doğu, et al.. (2005). Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 133B(1). 120–123. 18 indexed citations

10.

Hernández, Dena, Coro Paisán‐Ruíz, Aideen McInerney‐Leo, et al.. (2005). Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Annals of Neurology. 57(3). 453–456. 84 indexed citations

11.

Johnson, Janel, Lars Lannfelt, Anna Glaser, et al.. (2004). No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found. Neuroscience Letters. 363(2). 99–101. 5 indexed citations

12.

Doğu, Okan, Janel Johnson, Dena Hernández, et al.. (2004). A consanguineous Turkish family with early‐onset Parkinson's disease and an exon 4 parkin deletion. Movement Disorders. 19(7). 812–816. 24 indexed citations

13.

Bruno, Michiko Kimura, Bernard Ravina, Gaëtan Garraux, et al.. (2003). Exercise‐induced dystonia as a preceding symptom of familial Parkinson's disease. Movement Disorders. 19(2). 228–230. 18 indexed citations

14.

Hague, Stephen, Ekaterina Rogaeva, Dena G. Hernandez, et al.. (2003). Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation. Annals of Neurology. 54(2). 271–274. 190 indexed citations

15.

Eerola, Johanna, D. G. Hernandez, Jyrki Launes, et al.. (2003). Assessment of a DJ-1 ( PARK7 ) polymorphism in Finnish PD. Neurology. 61(7). 1000–1002. 25 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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