S.A. Rundle

4.3k total citations · 1 hit paper
19 papers, 1.2k citations indexed

About

S.A. Rundle is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, S.A. Rundle has authored 19 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in S.A. Rundle's work include Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (5 papers) and RNA modifications and cancer (2 papers). S.A. Rundle is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (5 papers) and RNA modifications and cancer (2 papers). S.A. Rundle collaborates with scholars based in United Kingdom, United States and Netherlands. S.A. Rundle's co-authors include J. David Brook, William Reardon, David E. Housman, Alan Buckler, D J Shaw, Peter S. Harper, H G Harley, Steve Crow, Peter S. Harper and Duncan J. Shaw and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

S.A. Rundle

19 papers receiving 1.2k citations

Hit Papers

Expansion of an unstable DNA region and phenotypic variat... 1992 2026 2003 2014 1992 100 200 300 400 500
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.

  1. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
    1992 587 citations J. David Brook, S.A. Rundle et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S.A. Rundle United Kingdom 13 889 881 372 255 124 19 1.2k
Deborah E. Schuback United States 18 495 0.6× 446 0.5× 536 1.4× 412 1.6× 247 2.0× 30 1.3k
Lu‐Shiun Her Taiwan 11 628 0.7× 769 0.9× 208 0.6× 116 0.5× 108 0.9× 15 1.2k
Margaret J. Velardo United States 3 256 0.3× 416 0.5× 52 0.1× 315 1.2× 60 0.5× 4 704
B. Wilburn United States 9 552 0.6× 607 0.7× 228 0.6× 95 0.4× 74 0.6× 12 921
Ramya Sundararajan United States 10 136 0.2× 597 0.7× 125 0.3× 131 0.5× 106 0.9× 10 810
Ole Wiskow United States 7 265 0.3× 638 0.7× 263 0.7× 60 0.2× 58 0.5× 9 1.1k
John Monahan Japan 10 118 0.1× 350 0.4× 44 0.1× 276 1.1× 57 0.5× 13 555
Michael G. Kearse United States 13 192 0.2× 747 0.8× 138 0.4× 211 0.8× 23 0.2× 23 952
Nathalie Dutheil France 11 104 0.1× 255 0.3× 202 0.5× 214 0.8× 96 0.8× 19 562
Anneloor L.M.A. ten Asbroek Netherlands 14 125 0.1× 657 0.7× 111 0.3× 51 0.2× 399 3.2× 26 1.0k

Countries citing papers authored by S.A. Rundle

Since Specialization
Citations

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

Fields of papers citing papers by S.A. Rundle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S.A. Rundle. 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 S.A. Rundle. The network helps show where S.A. Rundle may publish in the future.

Co-authorship network of co-authors of S.A. Rundle

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

All Works

19 of 19 papers shown
1.
2.
Shaw, Duncan J., Mila E. McCurrach, S.A. Rundle, et al.. (1993). Genomic organization and transcriptional units at the myotonic dystrophy locus. Genomics. 18(3). 673–679. 56 indexed citations
3.
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
4.
Shaw, Duncan J., Shaista Chaudhary, S.A. Rundle, et al.. (1993). A study of DNA methylation in myotonic dystrophy.. Journal of Medical Genetics. 30(3). 189–192. 32 indexed citations
5.
Brook, J. David, S.A. Rundle, William Reardon, et al.. (1992). Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy. Nature. 355(6360). 545–546. 587 indexed citations breakdown →
6.
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
7.
Crow, Steve, H G Harley, J. David Brook, S.A. Rundle, & Duncan J. Shaw. (1992). Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat. Human Molecular Genetics. 1(6). 451–451. 8 indexed citations
8.
Brook, J. David, Boris V. Zemelman, Michael J. Siciliano, et al.. (1992). Radiation-reduced hybrids for the myotonic dystrophy locus. Genomics. 13(2). 243–250. 16 indexed citations
9.
Mitchell, Anna L., A. Bale, Dolph L. Hatfield, et al.. (1992). Regional localization of the selenocysteine tRNA gene (TRSP) on human chromosome 19. Cytogenetic and Genome Research. 61(2). 117–120. 6 indexed citations
10.
Reardon, William, H G Harley, J. David Brook, et al.. (1992). Minimal expression of myotonic dystrophy: a clinical and molecular analysis.. Journal of Medical Genetics. 29(11). 770–773. 26 indexed citations
11.
Harley, H G, K.V. Walsh, S.A. Rundle, et al.. (1991). Localisation of the myotonic dystrophy locus to 19q13.2?19q13.3 and its relationship to twelve polymorphic loci on 19q. Human Genetics. 87(1). 73–80. 26 indexed citations
12.
Brook, J. David, Samantha J.L. Knight, Susan Roberts, et al.. (1991). The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments. Human Genetics. 87(1). 65–72. 12 indexed citations
13.
Leib, David A., Kari C. Nadeau, S.A. Rundle, & P A Schaffer. (1991). The promoter of the latency-associated transcripts of herpes simplex virus type 1 contains a functional cAMP-response element: role of the latency-associated transcripts and cAMP in reactivation of viral latency.. Proceedings of the National Academy of Sciences. 88(1). 48–52. 128 indexed citations
14.
Harley, H G, J. David Brook, S.A. Rundle, et al.. (1991). Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.. PubMed. 49(1). 68–75. 80 indexed citations
15.
Brook, J. David, H G Harley, K.V. Walsh, et al.. (1991). Identification of new DNA markers close to the myotonic dystrophy locus.. Journal of Medical Genetics. 28(2). 84–88. 17 indexed citations
16.
Brook, J. David, K.V. Walsh, H G Harley, S.A. Rundle, & Duncan J. Shaw. (1990). A polymorphic DNA clone which maps to 19q13.2 - 19qter (D19S62). Nucleic Acids Research. 18(4). 1086–1086. 5 indexed citations
17.
Brook, J. David, Meena Upadhyaya, S.A. Rundle, et al.. (1990). A HindIII polymorphism identified by a DNA clone which maps to chromosome 17 (D17S245). Nucleic Acids Research. 18(4). 1085–1085. 3 indexed citations
18.
Brook, J. David, H G Harley, S.A. Rundle, K.V. Walsh, & Duncan J. Shaw. (1990). RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63). Nucleic Acids Research. 18(4). 1085–1085. 2 indexed citations
19.
Johnson, Keith, Peggy Shelbourne, June Davies, et al.. (1990). A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.. PubMed. 46(6). 1073–81. 45 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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