Matthew Harms

13.5k total citations · 1 hit paper
27 papers, 1.9k citations indexed

About

Matthew Harms is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Matthew Harms has authored 27 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 8 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Matthew Harms's work include Amyotrophic Lateral Sclerosis Research (13 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Neurological diseases and metabolism (3 papers). Matthew Harms is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (13 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Neurological diseases and metabolism (3 papers). Matthew Harms collaborates with scholars based in United States, United Kingdom and Spain. Matthew Harms's co-authors include Liqun Luo, Barry J. Dickson, Yan Sun, J. Ng, Georg Dietzl, Julia Tzu, Satoko Hakeda‐Suzuki, Timothy M. Miller, Masahiko Kuroda and Jana Mahadevan and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Neuroscience.

In The Last Decade

Matthew Harms

26 papers receiving 1.8k 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.

Small GTPases Rac and Rho in the Maintenance of Dendritic Spines and Branches in Hippocampal Pyramidal Neurons

2000 600 citations Matthew Harms, Liqun Luo et al. Journal of Neuroscience profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew Harms United States	13	1.0k	824	511	322	170	27	1.9k
Kevin L. Seburn United States	23	1.3k 1.3×	663 0.8×	303 0.6×	287 0.9×	221 1.3×	48	2.2k
Hiroshi Nishimune United States	23	1.2k 1.2×	738 0.9×	520 1.0×	560 1.7×	264 1.6×	50	2.1k
Weichun Lin United States	24	1.7k 1.7×	1.1k 1.4×	685 1.3×	294 0.9×	151 0.9×	46	2.5k
Keren Ben‐Yaakov Israel	13	927 0.9×	765 0.9×	329 0.6×	142 0.4×	109 0.6×	17	1.7k
Stuart J. Rabin United States	19	972 1.0×	831 1.0×	187 0.4×	225 0.7×	112 0.7×	25	1.7k
Takahiro Gotow Japan	24	1.0k 1.0×	632 0.8×	604 1.2×	205 0.6×	70 0.4×	56	2.1k
Josep E. Esquerda Spain	26	806 0.8×	648 0.8×	170 0.3×	416 1.3×	411 2.4×	66	1.7k
Dario Bonanomi Italy	21	1.7k 1.6×	990 1.2×	559 1.1×	93 0.3×	81 0.5×	33	2.6k
Amar N. Kar United States	25	1.2k 1.2×	410 0.5×	171 0.3×	177 0.5×	119 0.7×	32	1.6k
Kristien Verhoeven Belgium	17	814 0.8×	737 0.9×	480 0.9×	313 1.0×	105 0.6×	27	1.9k

Countries citing papers authored by Matthew Harms

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Harms

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Harms

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

All Works

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20 of 20 papers shown

Berry, James D., Sabrina Paganoni, Matthew Harms, et al.. (2024). Access for ALL in ALS: A large‐scale, inclusive, collaborative consortium to unlock the molecular and genetic mechanisms of amyotrophic lateral sclerosis. Muscle & Nerve. 70(6). 1140–1150. 1 indexed citations

McElhiney, Martin, et al.. (2024). Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis. Journal of Genetic Counseling. 34(1). e1890–e1890. 3 indexed citations

Roggenbuck, Jennifer, et al.. (2024). The Answer ALS return of results study: Answering the duty to disclose. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(7-8). 743–750. 1 indexed citations

Soták, Matúš, Matthew Harms, Jamie Kraft, et al.. (2022). Lipoxins reduce obesity-induced adipose tissue inflammation in 3D-cultured human adipocytes and explant cultures. iScience. 25(7). 104602–104602. 9 indexed citations

Zoghbi, Anthony W., Ryan S. Dhindsa, Terry E. Goldberg, et al.. (2021). High-impact rare genetic variants in severe schizophrenia. Proceedings of the National Academy of Sciences. 118(51). 33 indexed citations

O’Rourke, Jacqueline G., Alberto Yáñez, Janet L. Markman, et al.. (2020). C9orf72 in myeloid cells suppresses STING-induced inflammation. Nature. 585(7823). 96–101. 203 indexed citations

Gregory, Jenna M., Delphine Fagegaltier, Hemali Phatnani, & Matthew Harms. (2020). Genetics of Amyotrophic Lateral Sclerosis. Aberdeen University Research Archive (Aberdeen University). 8(4). 121–131. 46 indexed citations

Gelfman, Sahar, Janice McCarthy, Matthew Harms, et al.. (2020). Incorporating external information to improve sparse signal detection in rare‐variant gene‐set‐based analyses. Genetic Epidemiology. 44(4). 330–338. 4 indexed citations

Leighton, Danielle, Cristiane Araújo Martins Moreno, Suvankar Pal, et al.. (2019). Assessing ACMG Criteria for the Classification of Reported ALS Gene Mutations: Utility, Pitfalls and Recommendations (N2.001). Neurology. 92(15_supplement). 2 indexed citations

10.

Moreno, Cristiane Araújo Martins, Eduardo de Paula Estephan, Soledad Monges, et al.. (2019). Congenital fiber type disproportion caused by TPM3 mutation: A report of two atypical cases. Neuromuscular Disorders. 30(1). 54–58. 6 indexed citations

11.

Ly, Cindy V., L. Randall Koenig, Jon Christensen, et al.. (2019). Tau positron emission tomography imaging in C9orf72 repeat expansion carriers. European Journal of Neurology. 26(9). 1235–1239. 2 indexed citations

12.

Kanekura, Kohsuke, Takuya Yagi, Alexander J. Cammack, et al.. (2016). Poly-dipeptides encoded by the C9ORF72 repeats block global protein translation. Human Molecular Genetics. 25(9). 1803–1813. 125 indexed citations

13.

Leighton, Danielle, Elaine Cleary, Laura Stephenson, et al.. (2016). Genetic epidemiology of motor neuron disease-associated variants in the Scottish population. Neurobiology of Aging. 51. 178.e11–178.e20. 33 indexed citations

14.

Haller, Gabe, David M. Alvarado, Kevin McCall, et al.. (2015). A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis. Human Molecular Genetics. 25(1). 202–209. 51 indexed citations

15.

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

16.

Harms, Matthew. (2011). Inpatient Management of Guillain-Barré Syndrome. The Neurohospitalist. 1(2). 78–84. 30 indexed citations

17.

Hakeda‐Suzuki, Satoko, J. Ng, Julia Tzu, et al.. (2002). Rac function and regulation during Drosophila development. Nature. 416(6879). 438–442. 297 indexed citations

18.

Ng, J., Matthew Harms, Julia Tzu, et al.. (2002). Rac GTPases control axon growth, guidance and branching. Nature. 416(6879). 442–447. 283 indexed citations

19.

Harms, Matthew, et al.. (2000). Small GTPases Rac and Rho in the Maintenance of Dendritic Spines and Branches in Hippocampal Pyramidal Neurons. Journal of Neuroscience. 20(14). 5329–5338. 600 indexed citations breakdown →

20.

Harms, Matthew. (1999). Forces measured during spinal manipulative procedures in two age groups. British journal of rheumatology. 38(3). 267–274. 33 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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