R Croxen

1.7k total citations
22 papers, 595 citations indexed

About

R Croxen is a scholar working on Molecular Biology, Neurology and Cell Biology. According to data from OpenAlex, R Croxen has authored 22 papers receiving a total of 595 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Neurology and 9 papers in Cell Biology. Recurrent topics in R Croxen's work include Myasthenia Gravis and Thymoma (14 papers), Ion channel regulation and function (10 papers) and Cellular transport and secretion (8 papers). R Croxen is often cited by papers focused on Myasthenia Gravis and Thymoma (14 papers), Ion channel regulation and function (10 papers) and Cellular transport and secretion (8 papers). R Croxen collaborates with scholars based in United Kingdom, Netherlands and United States. R Croxen's co-authors include John Newsom–Davis, Angela Vincent, David Beeson, David Beeson, Claire Newland, M Brydson, G Chauplannaz, Harry Oosterhuis, Richard Webster and Sharon Brownlow and has published in prestigious journals such as Journal of Clinical Investigation, Brain and Neurology.

In The Last Decade

R Croxen

22 papers receiving 574 citations

Peers

Countries citing papers authored by R Croxen

Since Specialization

Citations

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

Fields of papers citing papers by R Croxen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Croxen

This figure shows the co-authorship network connecting the top 25 collaborators of R Croxen. A scholar is included among the top collaborators of R Croxen 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 R Croxen. R Croxen 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	The Translocation of an Autologous Free RPE and Choroid Graft: An Organ Culture 2005 ·Investigative Ophthalmology & Visual Science ·R Croxen, Kristel Maaijwee, (unknown), (unknown), Antonia M. Joussen, Bernd Kirchhof, Joris Meurs	1
2	Somatostatin in diabetic retinopathy. 2004 ·PubMed ·R Croxen, G. S. Baarsma, Robert W. A. M. Kuijpers, P. Martin van Hagen	6
3	Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome 2004 ·Neurology ·Richard Webster, M Brydson, R Croxen, John Newsom–Davis, Angela Vincent, David Beeson	26
4	Structural Abnormalities of the AChR Caused by Mutations Underlying Congenital Myasthenic Syndromes 2003 ·Annals of the New York Academy of Sciences ·David Beeson, Richard Webster, John Ealing, R Croxen, Sharon Brownlow, M Brydson, John Newsom–Davis, Clarke R. Slater, C. J. Hatton, Chris Shelley, David Colquhoun, Angela Vincent	9
5	The role of somatostatin and somatostatin analogs in the pathophysiology of the human immune system. 2003 ·PubMed ·Virgil A. S. H. Dalm, Leo J. Hofland, Diego Ferone, R Croxen, Steven W. J. Lamberts, P. Martin van Hagen	14
6	Recessive inheritance and variable pentrance of slow channel myasthenic syndromes 2002 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), R Croxen, C. J. Hatton, Chris Shelley, David Colquhoun, G Chauplannaz, Harry Oosterhuis, John Newsom–Davis, Ajoy Vincent	2
7	Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes 2002 ·Neurology ·R Croxen, C. J. Hatton, Chris Shelley, M Brydson, G Chauplannaz, Harry Oosterhuis, Angela Vincent, John Newsom–Davis, David Colquhoun, David Beeson	60
8	Myasthenia gravis in a woman with congenital AChR deficiency due to ε-subunit mutations 2002 ·Neurology ·R Croxen, Angela Vincent, John Newsom–Davis, David Beeson	23
9	Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene loci 2001 ·International Journal of Molecular Medicine ·Fangyuan Li, (unknown), R Croxen, (unknown), Qiuping Yuan, Kerstin Lindblad, Martin Schalling, Sámuel Komoly, David Beeson, Catharina Larsson	5
10	End-plate gamma- and varepsilon-subunit mRNA levels in AChR deficiency syndrome due to varepsilon-subunit null mutations 2001 ·Brain ·R Croxen	47
11	Acetylcholine receptor δ subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita 2001 ·Journal of Clinical Investigation ·Sharon Brownlow, Richard Webster, R Croxen, M Brydson, Brian Neville, Jean‐Pierre Lin, Angela Vincent, John Newsom–Davis, David Beeson	60
12	Acetylcholine receptor δ subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita 2001 ·Journal of Clinical Investigation ·Sharon Brownlow, Richard Webster, R Croxen, M Brydson, Brian Neville, Jean‐Pierre Lin, Angela Vincent, John Newsom–Davis, David Beeson	58
13	Splice-site mutations in the achr epsilon subunit gene associated with congenital myasthenic syndrome 2000 ·European Journal of Neuroscience ·R Croxen, Ajoy Vincent, John Newsom–Davis, (unknown)	5
14	Novel functional ?-subunit polypeptide generated by a single nucleotide deletion in acetylcholine receptor deficiency congenital myasthenic syndrome 1999 ·Annals of Neurology ·R Croxen, Claire Newland, Maria Betty, A. Vincent, John Newsom–Davis, David Beeson	38
15	Mutation of the acetylcholine receptor ?-subunit promoter in congenital myasthenic syndrome 1999 ·Annals of Neurology ·(unknown), R Croxen, Angela Vincent, (unknown), Michael Hutchinson, John Newsom–Davis, David Beeson	65
16	Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24 1999 ·Neurology ·(unknown), (unknown), R Croxen, Karl Morten, Waney Squier, John Newsom–Davis, David Beeson, Catharina Larsson	26
17	Congenital Myasthenic Syndromes: Studies of the AChR and Other Candidate Genes^a 1998 ·Annals of the New York Academy of Sciences ·David Beeson, Claire Newland, R Croxen, (unknown), (unknown), Catharina Larsson, Muhammad Bilal Tariq, Angela Vincent, John Newsom–Davis	7
18	A Single Nucleotide Deletion in the ɛ Subunit of the Acetylcholine Receptor (AChR) in Five Congenital Myasthenic Syndrome Patients with AChR Deficiency^a 1998 ·Annals of the New York Academy of Sciences ·R Croxen, David Beeson, Claire Newland, Maria Betty, A. Vincent, (unknown)	7
19	Mutations in Different Functional Domains of the Human Muscle Acetylcholine Receptor Subunit in Patients with the Slow-Channel congenital Myasthenic Syndrome 1997 ·Human Molecular Genetics ·R Croxen, Claire Newland, David Beeson, Harry Oosterhuis, G Chauplannaz, Angela Vincent, John Newsom–Davis	116
20	Isolation of an Ustilago maydis gene encoding 3-hydroxy-3-methylglutaryl-coenzyme A reductase and expression of a C-terminal-truncated form in Escherichia coli 1994 ·Microbiology ·R Croxen, Michael W. Goosey, J. P. R. Keon, John A. Hargreaves	13

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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