Janel O. Johnson

9.5k total citations
11 papers, 364 citations indexed

About

Janel O. Johnson is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Janel O. Johnson has authored 11 papers receiving a total of 364 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Neurology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Molecular Biology. Recurrent topics in Janel O. Johnson's work include Genetic Neurodegenerative Diseases (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Janel O. Johnson is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Janel O. Johnson collaborates with scholars based in United States, United Kingdom and Italy. Janel O. Johnson's co-authors include Bryan J. Traynor, Andrew Singleton, J. Raphael Gibbs, Yevgeniya Abramzon, Sampath Arepalli, Sonja W. Scholz, Gabriella Restagno, Gabriele Mora, Andrea Calvo and Dena Hernández and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and Neurology.

In The Last Decade

Janel O. Johnson

11 papers receiving 345 citations

Peers

Janel O. Johnson

NEURO

CMN

GENET

NEURO

Yevgeniya Abramzon United States

Amelie Pandraud United Kingdom

Stéphanie Efthymiou United Kingdom

Milena Janković Serbia

Stefania Magri Italy

Jennifer Müller vom Hagen Germany

Elena Sánchez-Ferrero Spain

Mustafa Batbayli Denmark

Claire Guissart France

Chiara Reale Italy

Yevgeniya Abramzon United States

Janel O. Johnson

327 ×2.0

NEURO

216 ×1.4

71 ×0.8

CMN

161 ×2.2

GENET

112 ×1.7

NEURO

Citations per year, relative to Janel O. Johnson Janel O. Johnson (= 1×) peers Yevgeniya Abramzon

Countries citing papers authored by Janel O. Johnson

Since Specialization

Citations

This map shows the geographic impact of Janel O. 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 O. 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 O. Johnson more than expected).

Fields of papers citing papers by Janel O. Johnson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janel O. Johnson

This figure shows the co-authorship network connecting the top 25 collaborators of Janel O. Johnson. A scholar is included among the top collaborators of Janel O. 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 O. Johnson. Janel O. 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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11 of 11 papers shown

Caress, James B., Janel O. Johnson, Yevgeniya Abramzon, et al.. (2016). Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy. Muscle & Nerve. 56(5). 1001–1005. 5 indexed citations

Rollinson, Sara, Janis Bennion Callister, Kate Young, et al.. (2014). A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD. Neurobiology of Aging. 36(3). 1601.e1–1601.e5. 18 indexed citations

Johnson, Janel O., Giovanni Stévanin, Joyce van de Leemput, et al.. (2014). A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome. Movement Disorders. 30(2). 262–266. 22 indexed citations

Landouré, Guida, Melanie A. Knight, Horia Stanescu, et al.. (2012). A candidate gene for autoimmune myasthenia gravis. Neurology. 79(4). 342–347. 17 indexed citations

Johnson, Janel O., J. Raphael Gibbs, André Mégarbané, et al.. (2012). Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. Brain. 135(9). 2875–2882. 99 indexed citations

Abramzon, Yevgeniya, Janel O. Johnson, Sonja W. Scholz, et al.. (2012). Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis. Neurobiology of Aging. 33(9). 2231.e1–2231.e6. 84 indexed citations

Landouré, Guida, Jeremy M. Sullivan, Janel O. Johnson, et al.. (2012). Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family. Neurology. 79(2). 192–194. 23 indexed citations

Sailer, Anna, Sonja W. Scholz, J. Raphael Gibbs, et al.. (2012). Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases. Neurology. 79(2). 127–131. 28 indexed citations

Traynor, Bryan J., Michael A. Nalls, J. Raphael Gibbs, et al.. (2010). Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients. Proceedings of the National Academy of Sciences. 107(27). 12335–12338. 22 indexed citations

10.

Hanağası, Haşmet, Andrew J. Lees, Janel O. Johnson, Andrew Singleton, & Murat Emre. (2006). Smoking‐responsive juvenile‐onset Parkinsonism. Movement Disorders. 22(1). 115–119. 19 indexed citations

11.

Khan, Naheed L., L. H. Eunson, Elizabeth Graham, et al.. (2005). Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow‐up over 10 years. Movement Disorders. 20(4). 479–484. 27 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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