Janel O. Johnson

9.5k citations

11 papers · 364 indexed · h-index 10

Co-authors: Bryan J. Traynor Andrew Singleton J. Raphael Gibbs Yevgeniya Abramzon Sampath Arepalli Sonja W. Scholz Gabriella Restagno Gabriele Mora
Topics: Genetic Neurodegenerative Diseases (4 papers)Neurogenetic and Muscular Disorders Research (3 papers)Parkinson's Disease Mechanisms and Treatments (3 papers)
Cited by: Neurology Clinical Biochemistry
Journals: Proceedings of the National Academy of Sciences Brain Neurology
Partner nations: United States United Kingdom Italy

In The Last Decade

Janel O. Johnson

11 papers receiving 345 citations

Peers

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

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

#	Work	Indexed citations
1	Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar‐onset neuropathy 2016 ·Muscle & Nerve ·James B. Caress,Janel O. Johnson,Yevgeniya Abramzon,Gregory A. Hawkins,J. Raphael Gibbs,Elizabeth Sullivan,(unknown),Bryan J. Traynor	5
2	A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD 2014 ·Neurobiology of Aging ·Sara Rollinson,Janis Bennion Callister,Kate Young,Sarah Ryan,Ronald Druyeh,Jonathan D. Rohrer,Julie S. Snowden,Anna Richardson,Matt Jones,Jenny Harris,Yvonne S. Davidson,Andrew Robinson,John Ealing,Janel O. Johnson,Bryan J. Traynor,Simon Mead,David Mann,Stuart Pickering‐Brown	18
3	A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome 2014 ·Movement Disorders ·Janel O. Johnson,Giovanni Stévanin,Joyce van de Leemput,Dena G. Hernandez,Sampath Arepalli,Sylvie Forlani,Reza Zonozi,J. Raphael Gibbs,Alexis Brice,Alexandra Dürr,Andrew B. Singleton	22
4	A candidate gene for autoimmune myasthenia gravis 2012 ·Neurology ·Guida Landouré,Melanie A. Knight,Horia Stanescu,(unknown),Yijun Shi,(unknown),Janel O. Johnson,Dena Hernandez,Bryan J. Traynor,Leslie G. Biesecker,Abdel Elkahloun,Carlo Rinaldi,Angela Vincent,Nick Willcox,Robert Kleta,Kenneth H. Fischbeck,Barrington G. Burnett	17
5	Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease 2012 ·Brain ·Janel O. Johnson,J. Raphael Gibbs,André Mégarbané,J. Andoni Urtizberea,Dena Hernández,A. Reghan Foley,Sampath Arepalli,Amelie Pandraud,Javier Simón‐Sánchez,Peter T. Clayton,Mary M. Reilly,Francesco Muntoni,Yevgeniya Abramzon,Henry Houlden,Andrew Singleton	99
6	Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis 2012 ·Neurobiology of Aging ·Yevgeniya Abramzon,Janel O. Johnson,Sonja W. Scholz,J. Paul Taylor,Maura Brunetti,Andrea Calvo,Jessica Mandrioli,Michael Benatar,Gabriele Mora,Gabriella Restagno,Adriano Chiò,Bryan J. Traynor	84
7	Exome sequencing identifies a novel TRPV4 mutation in a CMT2C family 2012 ·Neurology ·Guida Landouré,Jeremy M. Sullivan,Janel O. Johnson,Clare H. Munns,Yijun Shi,(unknown),J. Raphael Gibbs,Rachelle Gaudet,Christy L. Ludlow,Kenneth H. Fischbeck,Bryan J. Traynor,Barrington G. Burnett,Charlotte J. Sumner	23
8	Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases 2012 ·Neurology ·Anna Sailer,Sonja W. Scholz,J. Raphael Gibbs,Arianna Tucci,Janel O. Johnson,Nicholas Wood,Vincent Plagnol,Holger Hummerich,Jinhui Ding,Dena Hernández,John Hardy,Howard J. Federoff,Bryan J. Traynor,Andrew Singleton,Henry Houlden	28
9	Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients 2010 ·Proceedings of the National Academy of Sciences ·Bryan J. Traynor,Michael A. Nalls,(unknown),J. Raphael Gibbs,Jennifer C. Schymick,Sampath Arepalli,Dena Hernandez,Marcel P. van der Brug,Janel O. Johnson,Allissa Dillman,Mark Cookson,Cristina Moglia,Andrea Calvo,Gabriella Restagno,Gabriele Mora,Adriano Chiò	22
10	Smoking‐responsive juvenile‐onset Parkinsonism 2006 ·Movement Disorders ·Haşmet Hanağası,Andrew J. Lees,Janel O. Johnson,Andrew Singleton,Murat Emre	19
11	Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow‐up over 10 years 2005 ·Movement Disorders ·Naheed L. Khan,(unknown),L. H. Eunson,Elizabeth Graham,Janel O. Johnson,(unknown),Mary B. Davis,Andrew Singleton,Nicholas Wood,Andrew J. Lees	27

About Janel O. Johnson

Janel O. Johnson is a scholar working on Neurology, Genetics and Cellular and Molecular Neuroscience, having authored 11 papers that have together received 364 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (4 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). The work is most often cited by research in Neurology (163 citations), Clinical Biochemistry (60 citations) and Neurology (66 citations). Janel O. Johnson has collaborated with scholars based in United States, United Kingdom and Italy. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Brain and Neurology.

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.

Explore authors with similar magnitude of impact