Tiffany Grider

1.2k total citations
16 papers, 267 citations indexed

About

Tiffany Grider is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Tiffany Grider has authored 16 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 7 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in Tiffany Grider's work include Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (8 papers) and Botulinum Toxin and Related Neurological Disorders (4 papers). Tiffany Grider is often cited by papers focused on Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (8 papers) and Botulinum Toxin and Related Neurological Disorders (4 papers). Tiffany Grider collaborates with scholars based in United States, United Kingdom and Italy. Tiffany Grider's co-authors include Michael E. Shy, Mary M. Reilly, Shawna Feely, Nivedita U. Jerath, Chelsea Bacon, Yunhong Bai, Xingyao Wu, Ludwig Gutmann, Sinéad M. Murphy and Christopher D. J. Sinclair and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Journal of Virology.

In The Last Decade

Tiffany Grider

14 papers receiving 266 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tiffany Grider United States 10 213 118 66 59 47 16 267
Katherine Berry United States 7 174 0.8× 89 0.8× 73 1.1× 74 1.3× 29 0.6× 8 288
Ana I. Seixas Portugal 8 189 0.9× 80 0.7× 32 0.5× 192 3.3× 34 0.7× 13 286
Chelsea Bacon United States 6 160 0.8× 110 0.9× 48 0.7× 78 1.3× 47 1.0× 7 253
Ruxu Zhang China 11 190 0.9× 82 0.7× 71 1.1× 193 3.3× 38 0.8× 40 375
Pedro José Tomaselli Brazil 11 256 1.2× 102 0.9× 87 1.3× 160 2.7× 56 1.2× 35 382
Menelaos Pipis United Kingdom 7 214 1.0× 74 0.6× 79 1.2× 90 1.5× 41 0.9× 10 289
Jana Haberlová Czechia 11 156 0.7× 48 0.4× 64 1.0× 105 1.8× 45 1.0× 24 297
Helle Høyer Norway 8 243 1.1× 96 0.8× 105 1.6× 97 1.6× 50 1.1× 17 329
Dagmara Kabzińska Poland 13 329 1.5× 104 0.9× 140 2.1× 210 3.6× 73 1.6× 50 482
H.M.E. Bienfait Netherlands 9 187 0.9× 77 0.7× 57 0.9× 105 1.8× 102 2.2× 10 306

Countries citing papers authored by Tiffany Grider

Since Specialization
Citations

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

Fields of papers citing papers by Tiffany Grider

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tiffany Grider

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

All Works

16 of 16 papers shown
1.
White, Amy, Tiffany Grider, Josef Alawneh, et al.. (2024). P004: Urine polyols for diagnosis of sorbitol dehydrogenase (SORD) deficiency-related peripheral neuropathy*. SHILAP Revista de lepidopterología. 2. 100881–100881.
2.
Crowe, Louis, Tiffany Grider, Melanie Shepherd, et al.. (2024). Timed Up and Go, Fall Risk and Foot Deformities in Charcot-Marie-Tooth Patients: A Retrospective Review. Foot & Ankle Orthopaedics. 9(4).
3.
Wang, Hongge, Matt Davison, Katherine M. Call, et al.. (2021). MicroRNAs as Biomarkers of Charcot-Marie-Tooth Disease Type 1A. Neurology. 97(5). e489–e500. 18 indexed citations
4.
Feely, Shawna, Tiffany Grider, Marina Scarlato, et al.. (2021). Loss of function MPZ mutation causes milder CMT1B neuropathy. Journal of the Peripheral Nervous System. 26(2). 177–183. 16 indexed citations
5.
Wang, Hongge, Matt Davison, Martin Kramer, et al.. (2019). Transmembrane protease serine 5: a novel Schwann cell plasma marker for CMT1A. Annals of Clinical and Translational Neurology. 7(1). 69–82. 35 indexed citations
6.
Holte, Lenore, et al.. (2019). The audiologic profile of patients with Charcot-Marie Tooth neuropathy can be characterised by both cochlear and neural deficits. International Journal of Audiology. 58(12). 902–912. 14 indexed citations
7.
Morrow, Jasper M., Matthew R. Evans, Tiffany Grider, et al.. (2018). Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A. Neurology. 91(12). e1125–e1129. 48 indexed citations
8.
Wang, David S., Xingyao Wu, Yunhong Bai, et al.. (2017). PMP22 exon 4 deletion causes ER retention of PMP22 and a gain‐of‐function allele in CMT1E. Annals of Clinical and Translational Neurology. 4(4). 236–245. 9 indexed citations
9.
Jerath, Nivedita U., Steven A. Moore, Michael E. Shy, et al.. (2015). Rare Manifestation of a c.290 C>T, p.Gly97GluVCPMutation. SHILAP Revista de lepidopterología. 2015. 1–5. 16 indexed citations
10.
Jerath, Nivedita U., Tiffany Grider, & Michael E. Shy. (2015). Progressive Lower Extremity Weakness and Axonal Sensorimotor Polyneuropathy from a Mutation inKIF5A(c.611G>A;p.Arg204Gln). SHILAP Revista de lepidopterología. 2015. 1–5. 3 indexed citations
11.
Pisciotta, Chiara, Yunhong Bai, Kathryn M. Brennan, et al.. (2015). Reduced neurofilament expression in cutaneous nerve fibers of patients with CMT2E. Neurology. 85(3). 228–234. 25 indexed citations
12.
Jerath, Nivedita U., John Kamholz, Tiffany Grider, et al.. (2015). Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2‐p12) deletion. Muscle & Nerve. 52(5). 905–908. 6 indexed citations
13.
Jerath, Nivedita U., Michael E. Shy, Tiffany Grider, & Ludwig Gutmann. (2015). A case of neuromyotonia and axonal motor neuropathy: A report of a HINT1 mutation in the United States. Muscle & Nerve. 52(6). 1110–1113. 18 indexed citations
14.
Grider, Tiffany, David Cuthbertson, Shawna Feely, & Michael E. Shy. (2014). Health-Related Quality Of Life By SF-36 in Patients with HNPP Compared To Those With CMT1A (P2.067). Neurology. 82(10_supplement). 1 indexed citations
15.
Sadjadi, Reza, Mary M. Reilly, Michael E. Shy, et al.. (2014). Psychometrics evaluation of Charcot‐Marie‐Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis. Journal of the Peripheral Nervous System. 19(3). 192–196. 53 indexed citations
16.
Lipkin, Steven M., Tiffany Grider, Richard A. Heyman, Christopher K. Glass, & Fred H. Gage. (1996). Constitutive retinoid receptors expressed from adenovirus vectors that specifically activate chromosomal target genes required for differentiation of promyelocytic leukemia and teratocarcinoma cells. Journal of Virology. 70(10). 7182–7189. 5 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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2026