Susan Maxwell

3.8k total citations · 1 hit paper
39 papers, 2.4k citations indexed

About

Susan Maxwell is a scholar working on Neurology, Molecular Biology and Cell Biology. According to data from OpenAlex, Susan Maxwell has authored 39 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Neurology, 27 papers in Molecular Biology and 15 papers in Cell Biology. Recurrent topics in Susan Maxwell's work include Myasthenia Gravis and Thymoma (27 papers), Cellular transport and secretion (14 papers) and Ion channel regulation and function (14 papers). Susan Maxwell is often cited by papers focused on Myasthenia Gravis and Thymoma (27 papers), Cellular transport and secretion (14 papers) and Ion channel regulation and function (14 papers). Susan Maxwell collaborates with scholars based in United Kingdom, United States and Austria. Susan Maxwell's co-authors include David Beeson, Angela Vincent, Patrick Waters, Judith Cossins, Sarosh R. Irani, Bethan Lang, Christian G. Bien, Luigi Zuliani, Manuel A. Friese and Dimitri M. Kullmann and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Brain.

In The Last Decade

Susan Maxwell

38 papers receiving 2.4k citations

Hit Papers

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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.

N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes

2010 784 citations Patrick Waters, Susan Maxwell et al. Brain profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Susan Maxwell	1.9k	770	431	387	274	39	2.4k
Luigi Zuliani	2.7k 1.5×	619 0.8×	299 0.7×	604 1.6×	543 2.0×	38	3.0k
David Beeson	2.5k 1.4×	1.1k 1.5×	545 1.3×	229 0.6×	308 1.1×	79	3.7k
Jesús Planagumà	1.9k 1.0×	773 1.0×	274 0.6×	604 1.6×	610 2.2×	48	3.0k
Helena Ariño	1.9k 1.0×	279 0.4×	182 0.4×	395 1.0×	408 1.5×	37	2.2k
Αναστασία Ζεκερίδου	1.7k 0.9×	403 0.5×	127 0.3×	273 0.7×	228 0.8×	99	2.3k
Bastien Joubert	2.0k 1.1×	415 0.5×	156 0.4×	352 0.9×	500 1.8×	104	2.6k
Haruo Shimazaki	1.8k 1.0×	852 1.1×	131 0.3×	598 1.5×	858 3.1×	73	2.9k
Jaime Masjuan	1.8k 0.9×	309 0.4×	93 0.2×	569 1.5×	305 1.1×	6	2.0k
Virginie Desestret	1.6k 0.9×	481 0.6×	98 0.2×	322 0.8×	367 1.3×	71	2.5k
Jean‐Christophe Antoine	1.7k 0.9×	302 0.4×	117 0.3×	327 0.8×	454 1.7×	64	2.1k

Countries citing papers authored by Susan Maxwell

Since Specialization

Citations

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

Fields of papers citing papers by Susan Maxwell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Susan Maxwell

This figure shows the co-authorship network connecting the top 25 collaborators of Susan Maxwell. A scholar is included among the top collaborators of Susan Maxwell 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 Susan Maxwell. Susan Maxwell 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

Li, Anna, A.C.W. Pike, Richard Webster, et al.. (2025). Structures of the human adult muscle-type nicotinic receptor in resting and desensitized states. Cell Reports. 44(5). 115581–115581.

Rea, Edward, Julia S. Scott, Susan Maxwell, et al.. (2024). Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech. Cellular and Molecular Life Sciences. 81(1). 129–129. 3 indexed citations

Cao, Michelangelo, Wei Wei Liu, Susan Maxwell, et al.. (2023). IgG1-3 MuSK Antibodies Inhibit AChR Cluster Formation, Restored by SHP2 Inhibitor, Despite Normal MuSK, DOK7, or AChR Subunit Phosphorylation. Neurology Neuroimmunology & Neuroinflammation. 10(6). 6 indexed citations

Cossins, Judith, Richard Webster, Susan Maxwell, et al.. (2020). Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission. Brain Communications. 2(2). fcaa174–fcaa174. 14 indexed citations

Çetin, Hakan, Richard Webster, Wei Wei Liu, et al.. (2020). Myasthenia gravis AChR antibodies inhibit function of rapsyn-clustered AChRs. Journal of Neurology Neurosurgery & Psychiatry. 91(5). 526–532. 16 indexed citations

Luo, Sushan, Shuang Cai, Susan Maxwell, et al.. (2017). Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome. Neuromuscular Disorders. 27(6). 557–564. 26 indexed citations

Cruz, Pedro M. Rodríguez, Katsiaryna Belaya, Keivan Basiri, et al.. (2016). Clinical features of the myasthenic syndrome arising from mutations in GMPPB. Journal of Neurology Neurosurgery & Psychiatry. 87(8). 802–809. 44 indexed citations

Logan, Clare V., Judith Cossins, Pedro M. Rodríguez Cruz, et al.. (2015). Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain. The American Journal of Human Genetics. 97(6). 878–885. 55 indexed citations

Basiri, Keivan, Katsiaryna Belaya, Wei Wei Liu, et al.. (2013). Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1. Neuromuscular Disorders. 23(6). 469–472. 27 indexed citations

10.

Zoltowska, Katarzyna Marta, Richard Webster, Sarah Finlayson, et al.. (2013). Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR. Human Molecular Genetics. 22(14). 2905–2913. 42 indexed citations

11.

Webster, Richard, Susan Maxwell, Hayley Spearman, et al.. (2012). A novel congenital myasthenic syndrome due to decreased acetylcholine receptor ion-channel conductance. Brain. 135(4). 1070–1080. 14 indexed citations

12.

Belaya, Katsiaryna, Sarah Finlayson, Clarke R. Slater, et al.. (2012). Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates. The American Journal of Human Genetics. 91(1). 193–201. 101 indexed citations

13.

Cossins, Judith, Wei Wei Liu, Katsiaryna Belaya, et al.. (2012). The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome. Human Molecular Genetics. 21(17). 3765–3775. 50 indexed citations

14.

Waters, Patrick, Sven Jarius, Edward Littleton, et al.. (2008). Aquaporin-4 Antibodies in Neuromyelitis Optica and Longitudinally Extensive Transverse Myelitis. Archives of Neurology. 65(7). 913–9. 232 indexed citations

15.

Beeson, David, Richard Webster, Judith Cossins, et al.. (2008). Congenital Myasthenic Syndromes and the Formation of the Neuromuscular Junction. Annals of the New York Academy of Sciences. 1132(1). 99–103. 20 indexed citations

16.

Waters, Patrick, Sven Jarius, Edward Littleton, et al.. (2007). A novel sensitive assay for aqueporin-4 antibodies (NMO-IgG). Journal of Neurology Neurosurgery & Psychiatry. 78. 1030–1030. 1 indexed citations

17.

Palace, Jacqueline, Daniel Lashley, John Newsom–Davis, et al.. (2007). Clinical features of the DOK7 neuromuscular junction synaptopathy. Brain. 130(6). 1507–1515. 91 indexed citations

18.

Beeson, David, Osamu Higuchi, Jackie Palace, et al.. (2006). Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy. Science. 313(5795). 1975–1978. 201 indexed citations

19.

Cossins, Judy, Richard Webster, Susan Maxwell, et al.. (2004). A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition. Human Molecular Genetics. 13(23). 2947–2957. 27 indexed citations

20.

Burke, Georgina, Judith Cossins, Susan Maxwell, et al.. (2004). Distinct phenotypes of congenital acetylcholine receptor deficiency. Neuromuscular Disorders. 14(6). 356–364. 47 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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