Peggy Allred

2.2k total citations · 1 hit paper
18 papers, 1.4k citations indexed

About

Peggy Allred is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Peggy Allred has authored 18 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 11 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Peggy Allred's work include Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (11 papers) and biodegradable polymer synthesis and properties (3 papers). Peggy Allred is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (12 papers), Neurogenetic and Muscular Disorders Research (11 papers) and biodegradable polymer synthesis and properties (3 papers). Peggy Allred collaborates with scholars based in United States, United Kingdom and Mexico. Peggy Allred's co-authors include Alan Pestronk, Robert H. Baloh, Matthew B. Harms, Timothy M. Miller, Stanley H. Appel, Ericka Simpson, Alison Goate, Janet Cady, John Ravits and David Schoenfeld and has published in prestigious journals such as Neurology, Annals of Neurology and The Lancet Neurology.

In The Last Decade

Peggy Allred

18 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study

2013 492 citations Timothy M. Miller, Alan Pestronk et al. The Lancet Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peggy Allred United States	12	694	663	566	343	267	18	1.4k
Ericka Simpson United States	15	552 0.8×	757 1.1×	518 0.9×	313 0.9×	255 1.0×	26	1.6k
Serena Lattante Italy	23	771 1.1×	1.2k 1.8×	764 1.3×	422 1.2×	209 0.8×	54	1.8k
Melissa McAlonis‐Downes United States	16	807 1.2×	1.3k 2.0×	793 1.4×	327 1.0×	321 1.2×	18	1.8k
Shibi Likhite United States	15	928 1.3×	1.0k 1.5×	778 1.4×	364 1.1×	306 1.1×	36	1.9k
Jianwen Deng China	19	810 1.2×	651 1.0×	254 0.4×	162 0.5×	395 1.5×	85	1.4k
Nicole Hersmus Belgium	14	610 0.9×	644 1.0×	446 0.8×	179 0.5×	240 0.9×	19	1.2k
Basar Cenik United States	10	733 1.1×	930 1.4×	440 0.8×	148 0.4×	115 0.4×	13	1.4k
Giulietta Riboldi Italy	19	846 1.2×	432 0.7×	393 0.7×	133 0.4×	353 1.3×	43	1.4k
Sorana Ciura France	13	427 0.6×	726 1.1×	398 0.7×	156 0.5×	177 0.7×	19	1.1k
Jiasheng Zhang United States	13	590 0.9×	484 0.7×	126 0.2×	253 0.7×	178 0.7×	18	1.2k

Countries citing papers authored by Peggy Allred

Since Specialization

Citations

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

Fields of papers citing papers by Peggy Allred

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peggy Allred

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

All Works

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18 of 18 papers shown

Diaz, Frank, John S. Thornton, Stephen Wastling, et al.. (2024). Longitudinal Quantitative MRI Provides Responsive Outcome Measures for Early and Late Muscle Changes in ALS. Muscle & Nerve. 71(2). 171–182. 2 indexed citations

Ly, Cindy V., Wade Self, James Bollinger, et al.. (2023). Protein kinetics of superoxide dismutase‐1 in familial and sporadic amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 10(6). 1012–1024. 7 indexed citations

Clawson, Lora, Merit Cudkowicz, Lisa S. Krivickas, et al.. (2017). A randomized controlled trial of resistance and endurance exercise in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 19(3-4). 250–258. 47 indexed citations

Rushton, David J., Patricia L. Andres, Peggy Allred, Robert H. Baloh, & Clive N. Svendsen. (2017). Patients with ALS show highly correlated progression rates in left and right limb muscles. Neurology. 89(2). 196–206. 12 indexed citations

Weihl, Conrad C., Robert H. Baloh, Youjin Lee, et al.. (2015). Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis. Neuromuscular Disorders. 25(4). 289–296. 49 indexed citations

Paganoni, Sabrina, Amy M. Shui, Peggy Allred, et al.. (2015). Pre‐morbid type 2 diabetes mellitus is not a prognostic factor in amyotrophic lateral sclerosis. Muscle & Nerve. 52(3). 339–343. 27 indexed citations

Harms, Matthew, Janet Cady, Erica Koval, et al.. (2014). The TREM2 Variant p.R47H is a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis (I5-2.002). Neurology. 82(10_supplement). 1 indexed citations

Cady, Janet, Erica Koval, Bruno A. Benítez, et al.. (2014). TREM2Variant p.R47H as a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis. JAMA Neurology. 71(4). 449–449. 214 indexed citations

Harms, Matthew, Janet Cady, Erica Koval, et al.. (2014). The TREM2 Variant p.R47H is a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis (I5-2.002). 82. 1 indexed citations

10.

Cady, Janet, Peggy Allred, Taha Bali, et al.. (2014). Amyotrophic lateral sclerosis onset is influenced by the burden of rare variants in known amyotrophic lateral sclerosis genes. Annals of Neurology. 77(1). 100–113. 150 indexed citations

11.

Miller, Timothy M., Alan Pestronk, William David, et al.. (2013). An antisense oligonucleotide against SOD1 delivered intrathecally for patients with SOD1 familial amyotrophic lateral sclerosis: a phase 1, randomised, first-in-man study. The Lancet Neurology. 12(5). 435–442. 492 indexed citations breakdown →

12.

Harms, Matthew B., Janet Cady, Craig M. Zaidman, et al.. (2013). Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis. Neurobiology of Aging. 34(9). 2234.e13–2234.e19. 58 indexed citations

13.

Sommerville, R. Brian, Peggy Allred, Shaughn Bell, et al.. (2012). Exome Sequencing Reveals DNAJB6 Mutations in Dominantly-Inherited Myopathy (S55.004). Neurology. 78(Meeting Abstracts 1). S55.004–S55.004. 2 indexed citations

14.

Harms, Matthew B., Kassandra M Ori-McKenney, Mariacristina Scoto, et al.. (2012). Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy. Neurology. 78(22). 1714–1720. 148 indexed citations

15.

Miller, Timothy M., Richard Smith, William David, et al.. (2012). Results of a Phase 1, Double-Blind, Placebo-Controlled, Dose-Escalation Study of the Safety, Tolerability, and Pharmacokinetics of ISIS 333611 Administered Intrathecally to Patients with Familial ALS Due to SOD1 Gene Mutations (S25.001). Neurology. 78(Meeting Abstracts 1). S25.001–S25.001. 4 indexed citations

16.

Harms, Matthew B., R. Brian Sommerville, Peggy Allred, et al.. (2011). Exome sequencing reveals DNAJB6 mutations in dominantly‐inherited myopathy. Annals of Neurology. 71(3). 407–416. 124 indexed citations

17.

Lopate, Glenn, Robert H. Baloh, Muhammad Al‐Lozi, et al.. (2010). Familial ALS with extreme phenotypic variability due to the I113T SOD1 mutation. Amyotrophic Lateral Sclerosis. 11(1-2). 232–236. 30 indexed citations

18.

Harms, Matthew B., Peggy Allred, R. J. M. Gardner, et al.. (2010). Dominant spinal muscular atrophy with lower extremity predominance. Neurology. 75(6). 539–546. 44 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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