Janet E. Sowden

1.5k total citations
23 papers, 577 citations indexed

About

Janet E. Sowden is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Janet E. Sowden has authored 23 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 12 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in Janet E. Sowden's work include Hereditary Neurological Disorders (14 papers), Botulinum Toxin and Related Neurological Disorders (10 papers) and Genetic Neurodegenerative Diseases (5 papers). Janet E. Sowden is often cited by papers focused on Hereditary Neurological Disorders (14 papers), Botulinum Toxin and Related Neurological Disorders (10 papers) and Genetic Neurodegenerative Diseases (5 papers). Janet E. Sowden collaborates with scholars based in United States, Australia and United Kingdom. Janet E. Sowden's co-authors include David N. Herrmann, Rabi Tawil, Melanie Ehrlich, Koji Tsumagari, Michael E. Shy, Michelle Lacey, Nicholas E. Johnson, Nuran Dilek, Gregory E. Crawford and Chad Heatwole and has published in prestigious journals such as Nucleic Acids Research, Neurology and The American Journal of Human Genetics.

In The Last Decade

Janet E. Sowden

23 papers receiving 572 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janet E. Sowden United States 12 298 213 184 91 76 23 577
Teodora Chamova Bulgaria 13 416 1.4× 161 0.8× 59 0.3× 105 1.2× 130 1.7× 41 598
Matthew Wicklund United States 12 223 0.7× 127 0.6× 111 0.6× 31 0.3× 83 1.1× 34 412
Dan Cox United Kingdom 11 221 0.7× 71 0.3× 111 0.6× 98 1.1× 25 0.3× 18 389
Henk Veldman Netherlands 16 182 0.6× 163 0.8× 199 1.1× 64 0.7× 44 0.6× 20 484
Claudia Castiglioni Chile 15 320 1.1× 111 0.5× 61 0.3× 54 0.6× 125 1.6× 47 566
Paulo Victor Sgobbi de Souza Brazil 14 250 0.8× 240 1.1× 277 1.5× 55 0.6× 179 2.4× 82 707
José Castro Portugal 9 186 0.6× 52 0.2× 252 1.4× 68 0.7× 188 2.5× 28 513
M. Al-Lozi United States 6 175 0.6× 67 0.3× 67 0.4× 88 1.0× 93 1.2× 10 361
H. Grehl Germany 12 215 0.7× 325 1.5× 245 1.3× 66 0.7× 32 0.4× 32 616
Kay‐Marie Lamar United States 8 342 1.1× 128 0.6× 46 0.3× 33 0.4× 48 0.6× 8 406

Countries citing papers authored by Janet E. Sowden

Since Specialization
Citations

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

Fields of papers citing papers by Janet E. Sowden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janet E. Sowden. 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 Janet E. Sowden. The network helps show where Janet E. Sowden may publish in the future.

Co-authorship network of co-authors of Janet E. Sowden

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

All Works

20 of 20 papers shown
1.
Dilek, Nuran, Janet E. Sowden, Katy Eichinger, et al.. (2024). Patient‐reported disease burden in the Accelerate Clinical Trials in Charcot–Marie–Tooth Disease Study. Journal of the Peripheral Nervous System. 29(4). 487–493. 1 indexed citations
2.
Dinesh, Karthik, Lindsay B. Baker, Janet E. Sowden, et al.. (2023). Disease‐specific wearable sensor algorithms for profiling activity, gait, and balance in individuals with Charcot–Marie–Tooth disease type 1A. Journal of the Peripheral Nervous System. 28(3). 368–381. 5 indexed citations
3.
Eichinger, Katy, Janet E. Sowden, Joshua Burns, et al.. (2022). Accelerate Clinical Trials in Charcot-Marie-Tooth Disease (ACT-CMT): A Protocol to Address Clinical Trial Readiness in CMT1A. Frontiers in Neurology. 13. 6 indexed citations
4.
Sowden, Janet E., et al.. (2021). In Vivo Reflectance Microscopy of Meissner Corpuscles and Bedside Measures of Large Fiber Sensory Function. Neurology. 98(7). e750–e758. 5 indexed citations
5.
Bray, Paula, Kayla Cornett, Davide Pareyson, et al.. (2020). Reliability of the Charcot‐Marie‐Tooth functional outcome measure. Journal of the Peripheral Nervous System. 25(3). 288–291. 9 indexed citations
6.
Sowden, Janet E., et al.. (2019). Measuring peripheral nerve involvement in Friedreich’s ataxia. Annals of Clinical and Translational Neurology. 6(9). 1718–1727. 11 indexed citations
7.
Estilow, Tim, Joshua Burns, Emanuela Pagliano, et al.. (2019). Balance impairment in pediatric charcot–marie–tooth disease. Muscle & Nerve. 60(3). 242–249. 1 indexed citations
8.
Eichinger, Katy, Joshua Burns, Kayla Cornett, et al.. (2018). The Charcot-Marie-Tooth Functional Outcome Measure (CMT-FOM). Neurology. 91(15). e1381–e1384. 26 indexed citations
9.
McDermott, Michael, et al.. (2017). In-vivo reflectance confocal microscopy of Meissner's corpuscles in diabetic distal symmetric polyneuropathy. Journal of the Neurological Sciences. 378. 213–219. 10 indexed citations
10.
Lemmers, Richard J.L.F., Patrick J. van der Vliet, Judit Balog, et al.. (2017). Deep characterization of a common D4Z4 variant identifies biallelic DUX4 expression as a modifier for disease penetrance in FSHD2. European Journal of Human Genetics. 26(1). 94–106. 20 indexed citations
11.
Herrmann, D., Rita Horváth, Janet E. Sowden, et al.. (2014). Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy. The American Journal of Human Genetics. 95(4). 472–472. 2 indexed citations
12.
Johnson, Nicholas E., Chad Heatwole, Nuran Dilek, et al.. (2014). Quality-of-life in Charcot–Marie–Tooth disease: The patient’s perspective. Neuromuscular Disorders. 24(11). 1018–1023. 67 indexed citations
13.
Herrmann, D., Rita Horváth, Janet E. Sowden, et al.. (2014). Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy. The American Journal of Human Genetics. 95(3). 332–339. 81 indexed citations
14.
Johnson, Nicholas E., Janet E. Sowden, Nuran Dilek, et al.. (2014). Prospective study of muscle cramps in Charcot‐Marie‐Tooth disease. Muscle & Nerve. 51(4). 485–488. 19 indexed citations
15.
Johnson, Nicholas E., et al.. (2013). Patient Identification of the Symptomatic Impact of Charcot–Marie–Tooth Disease Type 1A. Journal of Clinical Neuromuscular Disease. 15(1). 19–23. 13 indexed citations
16.
Tsumagari, Koji, Michelle Lacey, Carl Baribault, et al.. (2011). Gene expression during normal and FSHD myogenesis. BMC Medical Genomics. 4(1). 67–67. 81 indexed citations
17.
Klooster, Rinse, Kirsten R. Straasheijm, Bharati Shah, et al.. (2009). Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level. European Journal of Human Genetics. 17(12). 1615–1624. 51 indexed citations
18.
Xu, Xueqing, Koji Tsumagari, Janet E. Sowden, et al.. (2009). DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2. Nucleic Acids Research. 37(22). 7381–7393. 17 indexed citations
19.
Tsumagari, Koji, Lixin Qi, Chunbo Shao, et al.. (2008). Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers. Nucleic Acids Research. 36(7). 2196–2207. 48 indexed citations
20.
Sowden, Janet E.. (2005). Genotype-phenotype correlation in a family with late onset CMT and an MPZ lys236del mutation. Journal of Neurology Neurosurgery & Psychiatry. 76(3). 442–444. 9 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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