Judith Cossins

2.8k total citations
47 papers, 1.8k citations indexed

About

Judith Cossins is a scholar working on Neurology, Molecular Biology and Cell Biology. According to data from OpenAlex, Judith Cossins has authored 47 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Neurology, 23 papers in Molecular Biology and 13 papers in Cell Biology. Recurrent topics in Judith Cossins's work include Myasthenia Gravis and Thymoma (37 papers), Peripheral Neuropathies and Disorders (13 papers) and Cellular transport and secretion (12 papers). Judith Cossins is often cited by papers focused on Myasthenia Gravis and Thymoma (37 papers), Peripheral Neuropathies and Disorders (13 papers) and Cellular transport and secretion (12 papers). Judith Cossins collaborates with scholars based in United Kingdom, United States and Austria. Judith Cossins's co-authors include Angela Vincent, David Beeson, Susan Maxwell, Inga Koneczny, Patrick Waters, Richard Webster, Pedro M. Rodríguez Cruz, David Beeson, Wei Wei Liu and Jacqueline Palace and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Experimental Medicine and PLoS ONE.

In The Last Decade

Judith Cossins

47 papers receiving 1.8k citations

Peers

Countries citing papers authored by Judith Cossins

Since Specialization

Citations

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

Fields of papers citing papers by Judith Cossins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Cossins

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Cossins. A scholar is included among the top collaborators of Judith Cossins 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 Judith Cossins. Judith Cossins 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	Dose escalation pre-clinical trial of novel DOK7-AAV in mouse model of DOK7 congenital myasthenia 2024 ·Brain Communications ·Judith Cossins, (unknown), Claudia Canzonetta, (unknown), David Beeson, Patricio V. Sepulveda, Yin Yao Dong	1
2	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
3	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
4	Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series 2019 ·Genome Medicine ·John Taylor, (unknown), E Blair, Sarah Wordsworth, David Beeson, Saleel Chandratre, Judith Cossins, Tracy Lester, Andrea H. Németh, Elizabeth Ormondroyd, Smita Y. Patel, Alistair T. Pagnamenta, Jenny C. Taylor, Kate Thomson, Hugh Watkins, Andrew O.M. Wilkie, Julian C. Knight	21
5	A rare c.183_187dupCTCAC mutation of the acetylcholine receptor CHRNE gene in a South Asian female with congenital myasthenic syndrome: a case report 2016 ·BMC Neurology ·Thashi Chang, Judith Cossins, David Beeson	11
6	Silencing of Dok-7 in Adult Rat Muscle Increases Susceptibility to Passive Transfer Myasthenia Gravis 2016 ·American Journal Of Pathology ·Alejandro M. Gomez, Jo Stevens, Marina Mané-Damas, Peter Molenaar, Hans Duimel, Fons Verheyen, Judith Cossins, David Beeson, Marc H. De Baets, Mario Losen, Pilar Martínez‐Martínez	11
7	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
8	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
9	Clinical features of congenital myasthenic syndrome due to mutations inDPAGT1 2013 ·Journal of Neurology Neurosurgery & Psychiatry ·Sarah Finlayson, Jacqueline Palace, Katsiaryna Belaya, Timothy J. Walls, Fiona Norwood, Georgina Burke, Janice L. Holton, Samuel Ignacio Pascual Pascual, Judith Cossins, David Beeson	34
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	A mouse model of the slow channel myasthenic syndrome: Neuromuscular physiology and effects of ephedrine treatment 2013 ·Experimental Neurology ·Richard Webster, Judith Cossins, Daniel Lashley, (unknown), Wei Wei Liu, James R. Wickens, Pilar Martínez‐Martínez, Marc De Baets, David Beeson	24
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	Antibodies identified by cell‐based assays in myasthenia gravis and associated diseases 2012 ·Annals of the New York Academy of Sciences ·Angela Vincent, Patrick Waters, Maria Isabel Leite, Leslie Jacobson, Inga Koneczny, Judith Cossins, David Beeson	34
14	Presence and Pathogenic Relevance of Antibodies to Clustered Acetylcholine Receptor in Ocular and Generalized Myasthenia Gravis 2012 ·Archives of Neurology ·Saiju Jacob, Stuart Viegas, Maria Isabel Leite, Richard Webster, Judith Cossins, Robin P. Kennett, David Hilton‐Jones, B. Paul Morgan, Angela Vincent	104
15	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
16	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
17	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
18	Antibodies to AChRs in seronegative myasthenia gravis 2006 ·Journal of Neuroimmunology ·Maria Isabel Leite, Judith Cossins, David Beeson, Nick Willcox, Angela Vincent	1
19	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
20	Identification of MMP-18, a Putative Novel Human Matrix Metalloproteinase 1996 ·Biochemical and Biophysical Research Communications ·Judith Cossins, (unknown), Graham Catlin, A. J. H. Gearing, (unknown)	105

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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