J Myring

940 total citations
11 papers, 636 citations indexed

About

J Myring is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, J Myring has authored 11 papers receiving a total of 636 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 7 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in J Myring's work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Ubiquitin and proteasome pathways (2 papers). J Myring is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers) and Ubiquitin and proteasome pathways (2 papers). J Myring collaborates with scholars based in United Kingdom, United States and Brazil. J Myring's co-authors include William Reardon, Steve Crow, J. David Brook, J. MacMillan, Duncan J. Shaw, P S Harper, Iain Fenton, Peter S. Harper, H G Harley and S.A. Rundle and has published in prestigious journals such as The Lancet, Human Molecular Genetics and British Journal of Cancer.

In The Last Decade

J Myring

11 papers receiving 618 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
J Myring United Kingdom	9	452	445	227	93	91	11	636
James F. Gusella United States	10	670 1.5×	606 1.4×	498 2.2×	113 1.2×	42 0.5×	16	1.0k
Colleen Callahan United States	8	512 1.1×	518 1.2×	204 0.9×	122 1.3×	18 0.2×	10	715
Dong-Hui Chen United States	9	370 0.8×	277 0.6×	127 0.6×	83 0.9×	25 0.3×	10	579
K Leys United Kingdom	9	425 0.9×	266 0.6×	463 2.0×	30 0.3×	42 0.5×	13	782
Jason Myers United States	13	483 1.1×	205 0.5×	72 0.3×	70 0.8×	31 0.3×	19	649
Moreno Ferrarini Italy	16	249 0.6×	353 0.8×	223 1.0×	49 0.5×	45 0.5×	31	607
Yorck Hellenbroich Germany	17	661 1.5×	527 1.2×	235 1.0×	277 3.0×	31 0.3×	44	952
Edith Lopez United States	7	579 1.3×	506 1.1×	147 0.6×	76 0.8×	15 0.2×	8	681
David S. Lynch United Kingdom	13	346 0.8×	145 0.3×	97 0.4×	66 0.7×	104 1.1×	30	578
Esra Battaloğlu Türkiye	14	231 0.5×	229 0.5×	85 0.4×	61 0.7×	19 0.2×	33	457

Countries citing papers authored by J Myring

Since Specialization

Citations

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

Fields of papers citing papers by J Myring

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J Myring

This figure shows the co-authorship network connecting the top 25 collaborators of J Myring. A scholar is included among the top collaborators of J Myring 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 J Myring. J Myring is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Phillips, Margaret, Mark T. Rogers, Rebecca A. Barnetson, et al.. (1998). PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness. Neuromuscular Disorders. 8(7). 439–446. 24 indexed citations

Gray, J., J Myring, Curtis Gumbs, et al.. (1998). BRCA1 and BRCA2 in breast cancer families from Wales: moderate mutation frequency and two recurrent mutations in BRCA1. British Journal of Cancer. 78(11). 1417–1420. 8 indexed citations

Maheshwar, Magitha M., Jeremy P. Cheadle, Adriane C. Jones, et al.. (1997). The GAP-Related Domain of Tuberin, the Product of the TSC2 Gene, is a Target for Missense Mutations in Tuberous Sclerosis. Human Molecular Genetics. 6(11). 1991–1996. 109 indexed citations

Lazarou, L., Andrea L. Meredith, J Myring, et al.. (1993). Huntington's disease: predictive testing and the molecular genetics laboratory. Clinical Genetics. 43(3). 150–156. 2 indexed citations

Reardon, William, J. MacMillan, J Myring, et al.. (1993). Cataract and myotonic dystrophy: the role of molecular diagnosis.. British Journal of Ophthalmology. 77(9). 579–583. 13 indexed citations

MacMillan, J., J Myring, J. David Brook, et al.. (1993). Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy.. PubMed. 52(6). 1164–74. 303 indexed citations

Harley, H G, S.A. Rundle, William Reardon, et al.. (1992). Unstable DNA sequence in myotonic dystrophy. The Lancet. 339(8802). 1125–1128. 143 indexed citations

MacMillan, J., J Myring, H G Harley, et al.. (1992). Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders. Neuromuscular Disorders. 2(5-6). 405–411. 1 indexed citations

Reardon, William, et al.. (1992). Five years experience of predictive testing for myotonic dystrophy using linked DNA markers. American Journal of Medical Genetics. 43(6). 1006–1011. 9 indexed citations

10.

Cheadle, Jeremy P., J Myring, Layla N. Al-Jader, & Linda Meredith. (1992). Mutation analysis of 184 cystic fibrosis families in Wales.. Journal of Medical Genetics. 29(9). 642–646. 10 indexed citations

11.

Myring, J, Andrea L. Meredith, H G Harley, et al.. (1992). Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.. Journal of Medical Genetics. 29(11). 785–788. 14 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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