R. Mountford

2.8k total citations
27 papers, 1.2k citations indexed

About

R. Mountford is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, R. Mountford has authored 27 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in R. Mountford's work include Muscle Physiology and Disorders (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and RNA Research and Splicing (5 papers). R. Mountford is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Neurogenetic and Muscular Disorders Research (6 papers) and RNA Research and Splicing (5 papers). R. Mountford collaborates with scholars based in United Kingdom, United States and South Africa. R. Mountford's co-authors include Andrew Read, Glyn Stanway, G. C. Schild, P. Reeve, Ian S. Roberts, G J Boulnois, Klaus Jann, Kay E. Davies, Pamela Hughes and J. W. Almond and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

R. Mountford

27 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Mountford United Kingdom 16 612 349 269 257 191 27 1.2k
Geoffrey Y. Akita United States 19 778 1.3× 130 0.4× 275 1.0× 108 0.4× 304 1.6× 27 1.7k
Misa Onishi Japan 12 382 0.6× 181 0.5× 173 0.6× 51 0.2× 287 1.5× 16 1.0k
Steffen Schubert Germany 23 1.4k 2.3× 126 0.4× 194 0.7× 19 0.1× 65 0.3× 78 2.1k
Boyan C. Goumnerov United States 8 849 1.4× 39 0.1× 302 1.1× 69 0.3× 66 0.3× 8 1.6k
Manuela Mura Italy 21 746 1.2× 285 0.8× 162 0.6× 102 0.4× 77 0.4× 48 1.5k
Sheila Connelly United States 31 1.8k 2.9× 74 0.2× 1.0k 3.7× 49 0.2× 305 1.6× 69 2.5k
Loretta Pappan United States 11 397 0.6× 65 0.2× 96 0.4× 35 0.1× 71 0.4× 12 1.1k
Bernard Conrad Switzerland 15 657 1.1× 96 0.3× 556 2.1× 19 0.1× 127 0.7× 24 1.8k
Bruno Dallagiovanna Brazil 22 823 1.3× 133 0.4× 49 0.2× 164 0.6× 44 0.2× 79 1.4k
Luis Ugozzoli United States 12 726 1.2× 37 0.1× 286 1.1× 126 0.5× 76 0.4× 24 1.5k

Countries citing papers authored by R. Mountford

Since Specialization
Citations

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

Fields of papers citing papers by R. Mountford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Mountford

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

All Works

20 of 20 papers shown
1.
Dawood, F., R. Mountford, R. G. Farquharson, & Siobhan Quenby. (2007). Genetic polymorphisms on the factor V gene in women with recurrent miscarriage and acquired APCR. Human Reproduction. 22(9). 2546–2553. 13 indexed citations
2.
Bolton‐Maggs, Paula, Hava Peretz, Rachel Butler, et al.. (2004). A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency. Journal of Thrombosis and Haemostasis. 2(6). 918–924. 53 indexed citations
3.
Butler, Rachel, et al.. (2003). Eleven novel mutations in non-Jewish factor XI deficient kindreds detected by SSCP with heteroduplex analysis followed by sequencing. Journal of Thrombosis and Haemostasis. 1. P1687–P1687. 8 indexed citations
4.
Stewart, Helen, Andrew J. Wallace, Julie McGaughran, R. Mountford, & Helen Kingston. (1998). Molecular diagnosis of spinal muscular atrophy. Archives of Disease in Childhood. 78(6). 531–535. 12 indexed citations
5.
Talbot, Kevin, Chris P. Ponting, Aspasia Theodosiou, et al.. (1997). Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?. Human Molecular Genetics. 6(3). 497–500. 126 indexed citations
6.
7.
Rowe, Peter, J.N. Goulding, Tina C. Summerfield, et al.. (1996). The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE). Human Genetics. 97(3). 345–352. 37 indexed citations
8.
Rowe, Peter, J.N. Goulding, Andrew Read, et al.. (1993). New markers for linkage analysis of X-linked hypophosphataemic rickets. Human Genetics. 91(6). 571–5. 14 indexed citations
9.
Helliwell, Timothy R., J M Ellis, R. Mountford, Richard Appleton, & Glenn E. Morris. (1992). A truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane.. PubMed. 50(3). 508–14. 59 indexed citations
10.
Love, Donald R., Sarah England, Andreas Speer, et al.. (1991). Sequences of junction fragments in the deletion-prone region of the dystrophin gene. Genomics. 10(1). 57–67. 48 indexed citations
11.
Read, Andrew, R. Mountford, S. M. Forrest, et al.. (1988). Patterns of exon deletions in Duchenne and Becker muscular dystrophy. Human Genetics. 80(2). 152–156. 36 indexed citations
12.
Roberts, Ian S., R. Mountford, Rachel Hodge, Klaus Jann, & G J Boulnois. (1988). Common organization of gene clusters for production of different capsular polysaccharides (K antigens) in Escherichia coli. Journal of Bacteriology. 170(3). 1305–1310. 101 indexed citations
13.
Donnai, Dian, R. Mountford, & Andrew Read. (1988). Norrie disease resulting from a gene deletion: clinical features and DNA studies.. Journal of Medical Genetics. 25(2). 73–78. 62 indexed citations
14.
Forrest, S. M., Gareth Cross, Nick Thomas, et al.. (1987). EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY. The Lancet. 330(8571). 1294–1297. 40 indexed citations
15.
Read, Andrew, Rajesh V. Thakker, K.E. Davies, et al.. (1986). Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis. Human Genetics. 73(3). 267–270. 53 indexed citations
16.
Roberts, Ian S., R. Mountford, D Bitter-Suermann, et al.. (1986). Molecular cloning and analysis of genes for production of K5, K7, K12, and K92 capsular polysaccharides in Escherichia coli. Journal of Bacteriology. 168(3). 1228–1233. 93 indexed citations
17.
Read, Andrew, L Kerzin-Storrar, R. Mountford, R Elles, & R Harris. (1986). A register based system for gene tracking in Duchenne muscular dystrophy.. Journal of Medical Genetics. 23(6). 581–586. 15 indexed citations
18.
Stanway, Glyn, Pamela Hughes, R. Mountford, et al.. (1984). Comparison of the complete nucleotide sequences of the genomes of the neurovirulent poliovirus P3/Leon/37 and its attenuated Sabin vaccine derivative P3/Leon 12a1b.. Proceedings of the National Academy of Sciences. 81(5). 1539–1543. 153 indexed citations
19.
Minor, Philip D., G. C. Schild, Janet S. Bootman, et al.. (1983). Location and primary structure of a major antigenic site for poliovirus neutralization. Nature. 301(5902). 674–679. 156 indexed citations
20.
Hauptmann, R, et al.. (1983). Nucleotide Sequence of the Haemagglutinin Gene of Influenza Virus A/England/321/77. Journal of General Virology. 64(1). 215–220. 6 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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