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, Bethan Lang, Sarosh R. Irani, Michael S. Zandi, Manuel A. Friese, Dimitri M. Kullmann and Ian Galea 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

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.

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 →

Peers

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

#	Work	Indexed citations
1	Structures of the human adult muscle-type nicotinic receptor in resting and desensitized states 2025 ·Cell Reports ·Anna Li, A.C.W. Pike, Richard Webster, Susan Maxwell, Wei Wei Liu, (unknown), Jacqueline Palace, David Beeson, David B. Sauer, Yin Yao Dong	0
2	Unraveling the molecular interactions between α7 nicotinic receptor and a RIC3 variant associated with backward speech 2024 ·Cellular and Molecular Life Sciences ·(unknown), (unknown), (unknown), Edward Rea, (unknown), Julia S. Scott, (unknown), Susan Maxwell, Richard Webster, David Beeson, Yin Yao Dong, Stefan Preković, Isabel Bermúdez, Dianne F. Newbury	3
3	IgG1-3 MuSK Antibodies Inhibit AChR Cluster Formation, Restored by SHP2 Inhibitor, Despite Normal MuSK, DOK7, or AChR Subunit Phosphorylation 2023 ·Neurology Neuroimmunology & Neuroinflammation ·Michelangelo Cao, Wei Wei Liu, Susan Maxwell, Saif Huda, Richard Webster, Amelia Evoli, David Beeson, Judith Cossins, Angela Vincent	6
4	Congenital myasthenic syndrome due to a TOR1AIP1 mutation: a new disease pathway for impaired synaptic transmission 2020 ·Brain Communications ·Judith Cossins, Richard Webster, Susan Maxwell, Pedro M. Rodríguez Cruz, (unknown), J. Llewelyn, Ji‐Yeon Shin, Jacqueline Palace, David Beeson	14
5	A rare mutation in the COLQ gene causing congenital myasthenic syndrome with remarkable improvement to fluoxetine: A case report 2020 ·Neuromuscular Disorders ·(unknown), (unknown), (unknown), (unknown), (unknown), Susan Maxwell, Judith Cossins, David Beeson, Thashi Chang	2
6	Novel mutations in the C-terminal region of GMPPB causing limb-girdle muscular dystrophy overlapping with congenital myasthenic syndrome 2017 ·Neuromuscular Disorders ·Sushan Luo, Shuang Cai, Susan Maxwell, (unknown), Wenhua Zhu, Kai Qiao, Zhen Zhu, Lei Zhou, Jianying Xi, Jiahong Lu, David Beeson, Chongbo Zhao	26
7	Clinical features of the myasthenic syndrome arising from mutations in GMPPB 2016 ·Journal of Neurology Neurosurgery & Psychiatry ·Pedro M. Rodríguez Cruz, Katsiaryna Belaya, Keivan Basiri, Maryam Sedghi, Maria Elena Farrugia, Janice L. Holton, Wei Wei Liu, Susan Maxwell, Richard Petty, Timothy J. Walls, Robin P. Kennett, Matthew Pitt, Anna Sárközy, Matt Parton, Hanns Lochmüller, Francesco Muntoni, Jacqueline Palace, David Beeson	44
8	Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain 2015 ·The American Journal of Human Genetics ·Clare V. Logan, Judith Cossins, Pedro M. Rodríguez Cruz, David Parry, Susan Maxwell, Pilar Martínez‐Martínez, Joey Riepsaame, Zakia A. Abdelhamed, (unknown), María Morán, S. Robb, Gabriel Chow, Caroline A. Sewry, Philip M. Hopkins, Eamonn Sheridan, Sandeep Jayawant, Jacqueline Palace, Colin A. Johnson, David Beeson	55
9	Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR 2013 ·Human Molecular Genetics ·Katarzyna Marta Zoltowska, Richard Webster, Sarah Finlayson, Susan Maxwell, Judith Cossins, (unknown), Hanns Lochmüller, David Beeson	42
10	Congenital myasthenic syndromes due to mutations inALG2andALG14 2013 ·Brain ·Judith Cossins, Katsiaryna Belaya, Debbie Hicks, Mustafa A. Salih, Sarah Finlayson, Nicola Carboni, Wei Wei Liu, Susan Maxwell, Katarzyna Marta Zoltowska, (unknown), Steven H. Laval, (unknown), Peter Donnelly, David Bentley, Simon J. McGowan, (unknown), Jacqueline Palace, Hanns Lochmüller, David Beeson	89
11	Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1 2013 ·Neuromuscular Disorders ·Keivan Basiri, Katsiaryna Belaya, Wei Wei Liu, Susan Maxwell, Maryam Sedghi, David Beeson	27
12	The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome 2012 ·Human Molecular Genetics ·Judith Cossins, Wei Wei Liu, Katsiaryna Belaya, Susan Maxwell, Michael Oldridge, Tracy Lester, S. Robb, David Beeson	50
13	Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates 2012 ·The American Journal of Human Genetics ·Katsiaryna Belaya, Sarah Finlayson, Clarke R. Slater, Judith Cossins, Wei Wei Liu, Susan Maxwell, Simon J. McGowan, Siarhei Maslau, Stephen R.F. Twigg, Timothy J. Walls, Samuel Ignacio Pascual Pascual, Jacqueline Palace, David Beeson	101
14	Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome 2012 ·Annals of the New York Academy of Sciences ·Katsiaryna Belaya, Sarah Finlayson, Judith Cossins, Wei Wei Liu, Susan Maxwell, Jacqueline Palace, David Beeson	27
15	Aquaporin-4 Antibodies in Neuromyelitis Optica and Longitudinally Extensive Transverse Myelitis 2008 ·Archives of Neurology ·Patrick Waters, Sven Jarius, Edward Littleton, Maria Isabel Leite, Saiju Jacob, (unknown), Ruth Geraldes, Thomas R. Vale, Anu Jacob, Jacqueline Palace, Susan Maxwell, David Beeson, Angela Vincent	232
16	Congenital Myasthenic Syndromes and the Formation of the Neuromuscular Junction 2008 ·Annals of the New York Academy of Sciences ·David Beeson, Richard Webster, Judith Cossins, Daniel Lashley, Hayley Spearman, Susan Maxwell, Clarke R. Slater, John Newsom–Davis, Jacqueline Palace, Angela Vincent	20
17	A novel sensitive assay for aqueporin-4 antibodies (NMO-IgG) 2007 ·Journal of Neurology Neurosurgery & Psychiatry ·Patrick Waters, Sven Jarius, Edward Littleton, Jacqueline Palace, Susan Maxwell, David Beeson, A. Vincent	1
18	Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy 2006 ·Science ·David Beeson, Osamu Higuchi, Jackie Palace, Judy Cossins, Hayley Spearman, Susan Maxwell, John Newsom–Davis, Georgina Burke, P. Fawcett, Masakatsu Motomura, Juliane S. Müller, Hanns Lochmüller, Clarke R. Slater, Angela Vincent, Yuji Yamanashi	201
19	A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition 2004 ·Human Molecular Genetics ·Judy Cossins, Richard Webster, Susan Maxwell, Georgina Burke, Angela Vincent, David Beeson	27
20	Distinct phenotypes of congenital acetylcholine receptor deficiency 2004 ·Neuromuscular Disorders ·Georgina Burke, Judith Cossins, Susan Maxwell, S. Robb, Michael Nicolle, Angela Vincent, John Newsom–Davis, Jackie Palace, David Beeson	47

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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