Susan Maxwell

3.9k citations

39 papers · 2.4k · 1 hit paper · h-index 22

Impact in

Neurology top 0.5%
- Autoimmune Neurological Disorders and Treatments
- Myasthenia Gravis and Thymoma
- Peripheral Neuropathies and Disorders
- Neuroblastoma Research and Treatments
Cell Biology top 5%
- Cellular transport and secretion

Papers in

Neurology 29
- Myasthenia Gravis and Thymoma 27
- Autoimmune Neurological Disorders and Treatments 3
- Peripheral Neuropathies and Disorders 3
Molecular Biology 22
- Ion channel regulation and function 11
- Glycosylation and Glycoproteins Research 5
- Nicotinic Acetylcholine Receptors Study 3
- Muscle Physiology and Disorders 3

Co-authors: David Beeson (25 shared papers)Angela Vincent (15 shared papers)Patrick Waters (6 shared papers)Judith Cossins (22 shared papers)Bethan Lang (2 shared papers)Sarosh R. Irani (2 shared papers)Christian G. Bien (1 shared paper)Katarzyna D. Bera (1 shared paper)
Journals: Neuromuscular Disorders (5 papers)Brain (5 papers)Human Molecular Genetics (4 papers)Annals of the New York Academy of Sciences (4 papers)Journal of Neurology Neurosurgery & Psychiatry (3 papers)
Partner nations: United Kingdom United States Austria

In The Last Decade

Susan Maxwell

39 papers receiving 2.4k citations

Susan Maxwell's Hit Papers

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N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes 2010 · 787 citations

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-authors

The 25 scholars most cited alongside Susan Maxwell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Susan Maxwell Line = papers co-authored together Susan Maxwell links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes Brain ·Sarosh R. Irani, Katarzyna D. Bera, Patrick Waters, Luigi Zuliani, Susan Maxwell, Michael S. Zandi, Manuel A. Friese, Ian Galea, Dimitri M. Kullmann, David Beeson, Bethan Lang, Christian G. Bien, Angela Vincent Hit paper breakdown →	2010	787
2	Aquaporin-4 Antibodies in Neuromyelitis Optica and Longitudinally Extensive Transverse Myelitis Archives of Neurology ·Patrick Waters, Sven Jarius, Edward Littleton, Maria Isabel Leite, Saiju Jacob, Bryony Gray, Ruth Geraldes, Thomas R. Vale, Anu Jacob, Jacqueline Palace, Susan Maxwell, David Beeson, Angela Vincent	2008	234
3	Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy 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	2006	201
4	Antibodies to GABA _A receptor α1 and γ2 subunits Neurology ·Philippa Pettingill, Holger Kramer, Jan Coebergh, R Pettingill, Susan Maxwell, Anjan Nibber, Andrea Malaspina, Anu Jacob, Sarosh R. Irani, Camilla Buckley, David Beeson, Bethan Lang, Patrick Waters, Angela Vincent	2015	142
5	Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates 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	2012	103
6	Clinical features of the DOK7 neuromuscular junction synaptopathy Brain ·Jacqueline Palace, Daniel Lashley, John Newsom–Davis, Judith Cossins, Susan Maxwell, Roger H. Kennett, Sandeep Jayawant, Yuji Yamanashi, D Beeson	2007	92
7	Congenital myasthenic syndromes due to mutations inALG2andALG14 Brain ·Judith Cossins, Katsiaryna Belaya, Debbie Hicks, Mustafa A. Salih, Sarah Finlayson, Nicola Carboni, Wei Wei Liu, Susan Maxwell, Katarzyna Marta Zoltowska, Golara Torabi Farsani, Steven H. Laval, M.Z. Seidhamed, Peter Donnelly, David Bentley, Simon J. McGowan, Juliane Müller, Jacqueline Palace, Hanns Lochmüller, David Beeson	2013	91
8	Rapsyn mutations in hereditary myasthenia Neurology ·Georgina Burke, Judith Cossins, Susan Maxwell, Gregory L. Owens, Angela Vincent, S. Robb, Michael Nicolle, David Hilton‐Jones, John Newsom–Davis, Jackie Palace, David Beeson	2003	90
9	The search for new antigenic targets in myasthenia gravis Annals of the New York Academy of Sciences ·Judith Cossins, Katsiaryna Belaya, Katarzyna Marta Zoltowska, Inga Koneczny, Susan Maxwell, Leslie Jacobson, Maria Isabel Leite, Patrick Waters, Angela Vincent, David Beeson	2012	64
10	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 ·Clare V. Logan, Judith Cossins, Pedro M. Rodríguez Cruz, David Parry, Susan Maxwell, Pilar Martínez‐Martínez, Joey Riepsaame, Zakia A. Abdelhamed, Alice V. R. Lake, María Morán, S. Robb, Gabriel Chow, Caroline A. Sewry, Philip M. Hopkins, Eamonn Sheridan, Sandeep Jayawant, Jacqueline Palace, Colin A. Johnson, David Beeson	2015	56
11	The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome Human Molecular Genetics ·Judith Cossins, Wei Wei Liu, Katsiaryna Belaya, Susan Maxwell, Michael Oldridge, Tracy Lester, S. Robb, David Beeson	2012	50
12	Germline mutation in DOK7 associated with fetal akinesia deformation sequence Journal of Medical Genetics ·Julie Vogt, Neil V. Morgan, Tamás Marton, Susan Maxwell, Benjamin J. Harrison, David Beeson, Eamonn R. Maher	2009	47
13	Distinct phenotypes of congenital acetylcholine receptor deficiency Neuromuscular Disorders ·Georgina Burke, Judith Cossins, Susan Maxwell, S. Robb, Michael Nicolle, Angela Vincent, John Newsom–Davis, Jackie Palace, David Beeson	2004	47
14	Clinical features of the myasthenic syndrome arising from mutations in GMPPB 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	2016	45
15	Mutations in GFPT1 that underlie limb-girdle congenital myasthenic syndrome result in reduced cell-surface expression of muscle AChR Human Molecular Genetics ·Katarzyna Marta Zoltowska, Richard Webster, Sarah Finlayson, Susan Maxwell, Judith Cossins, Juliane Müller, Hanns Lochmüller, David Beeson	2013	43
16	β2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structure Brain ·An Vanhaesebrouck, Richard Webster, Susan Maxwell, Pedro M. Rodríguez Cruz, Judith Cossins, James R. Wickens, Wei Wei Liu, Hakan Çetin, Jonathan Cheung, H. Ramjattan, Jacqueline Palace, David Beeson	2019	35
17	Non-radioactive serological diagnosis of myasthenia gravis and clinical features of patients from Tianjin, China Journal of the Neurological Sciences ·Li Yang, Susan Maxwell, Maria Isabel Leite, Patrick Waters, Linda Clover, Xin Fan, Daqi Zhang, Chun‐Sheng Yang, David Beeson, Angela Vincent	2010	33
18	Clinical features in a large Iranian family with a limb-girdle congenital myasthenic syndrome due to a mutation in DPAGT1 Neuromuscular Disorders ·Keivan Basiri, Katsiaryna Belaya, Wei Wei Liu, Susan Maxwell, Maryam Sedghi, David Beeson	2013	29
19	Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome Annals of the New York Academy of Sciences ·Katsiaryna Belaya, Sarah Finlayson, Judith Cossins, Wei Wei Liu, Susan Maxwell, Jacqueline Palace, David Beeson	2012	28
20	A mouse model of AChR deficiency syndrome with a phenotype reflecting the human condition Human Molecular Genetics ·Judy Cossins, Richard Webster, Susan Maxwell, Georgina Burke, Angela Vincent, David Beeson	2004	27

About Susan Maxwell

Susan Maxwell is a scholar working on Neurology, Molecular Biology, Cell Biology, Pharmacology and Genetics, having authored 39 papers that have together received 2.4k indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (27 papers), Cellular transport and secretion (13 papers), Ion channel regulation and function (11 papers), Glycosylation and Glycoproteins Research (5 papers), Nicotinic Acetylcholine Receptors Study (3 papers), Autoimmune Neurological Disorders and Treatments (3 papers), Muscle Physiology and Disorders (3 papers) and Peripheral Neuropathies and Disorders (3 papers). The work is most often cited by research in Neurology (1.8k citations), Cell Biology (361 citations), Biological Psychiatry (34 citations), Pathology and Forensic Medicine (219 citations) and Genetics (126 citations). Susan Maxwell has collaborated with scholars based in United Kingdom, United States and Austria. Frequent co-authors include David Beeson, Angela Vincent, Patrick Waters, Judith Cossins, Bethan Lang, Sarosh R. Irani, Christian G. Bien, Katarzyna D. Bera, Ian Galea and Luigi Zuliani. Their work appears in journals such as Neuromuscular Disorders, Brain, Human Molecular Genetics, Annals of the New York Academy of Sciences and Journal of Neurology Neurosurgery & Psychiatry.

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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