Barbara C. Byth

1.5k total citations
14 papers, 1.2k citations indexed

About

Barbara C. Byth is a scholar working on Molecular Biology, Physiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Barbara C. Byth has authored 14 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Physiology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Barbara C. Byth's work include Muscle Physiology and Disorders (6 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Barbara C. Byth is often cited by papers focused on Muscle Physiology and Disorders (6 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Barbara C. Byth collaborates with scholars based in Canada, United Kingdom and United States. Barbara C. Byth's co-authors include Donald R. Love, Yvonne H. Edwards, Kay E. Davies, Jonathon M. Tinsley, Derek J. Blake, Diane F. Hill, George Dickson, Frank S. Walsh, N.K. Spurr and John Kendrick‐Jones and has published in prestigious journals such as Nature, Nucleic Acids Research and Human Molecular Genetics.

In The Last Decade

Barbara C. Byth

14 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara C. Byth Canada 9 1.1k 289 287 222 208 14 1.2k
Rosie Fisher United Kingdom 8 1.4k 1.2× 279 1.0× 128 0.4× 313 1.4× 253 1.2× 12 1.5k
Joseph X. DiMario United States 18 1.2k 1.0× 135 0.5× 156 0.5× 141 0.6× 207 1.0× 41 1.3k
J.G. Dickson United Kingdom 11 937 0.8× 224 0.8× 87 0.3× 118 0.5× 186 0.9× 22 1.1k
E Ozawa Japan 17 1.3k 1.2× 386 1.3× 110 0.4× 145 0.7× 337 1.6× 21 1.4k
BJ Petrof Canada 6 873 0.8× 89 0.3× 109 0.4× 207 0.9× 304 1.5× 6 1.1k
Michele Hadhazy United States 20 1.4k 1.2× 176 0.6× 157 0.5× 115 0.5× 266 1.3× 30 1.6k
Christian Pastoret France 10 753 0.7× 118 0.4× 95 0.3× 198 0.9× 196 0.9× 13 812
Andrew Weir United Kingdom 6 886 0.8× 159 0.6× 75 0.3× 157 0.7× 244 1.2× 8 1.1k
L M Kunkel United States 12 755 0.7× 142 0.5× 128 0.4× 57 0.3× 217 1.0× 19 914
M. Wehling United States 8 912 0.8× 84 0.3× 99 0.3× 258 1.2× 370 1.8× 12 1.1k

Countries citing papers authored by Barbara C. Byth

Since Specialization
Citations

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

Fields of papers citing papers by Barbara C. Byth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara C. Byth. 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 Barbara C. Byth. The network helps show where Barbara C. Byth may publish in the future.

Co-authorship network of co-authors of Barbara C. Byth

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

All Works

14 of 14 papers shown
1.
Byth, Barbara C., et al.. (1995). Molecular analysis of three patients with interstitial deletions of chromosome band 14q31.. Journal of Medical Genetics. 32(7). 564–567. 19 indexed citations
2.
Byth, Barbara C., Gordon R. Thomas, Nandy Hofland, & Diane W. Cox. (1994). Application of inverse PCR to isolation of end probes from cosmids. Nucleic Acids Research. 22(9). 1766–1767. 2 indexed citations
3.
Blake, Derek J., Jonathon M. Tinsley, Barbara C. Byth, et al.. (1993). The utrophin and dystrophin genes share similarities in genomic structure. Human Molecular Genetics. 2(11). 1765–1772. 84 indexed citations
4.
Byth, Barbara C., et al.. (1993). Polymorphism of the protein C inhibitor (PCI) gene on chromosome 14. Human Molecular Genetics. 2(1). 92–92. 1 indexed citations
5.
Passos‐Bueno, Maria Rita, Barbara C. Byth, Reinaldo Issao Takata, et al.. (1993). Severe nonspecific X‐linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X‐linked mental retardation?. American Journal of Medical Genetics. 46(2). 172–175. 20 indexed citations
6.
Byth, Barbara C. & Diane W. Cox. (1993). Two consecutive dinucleotide repeats constitute an informative marker at the α1-antichymotrypsin (AACT) locus. Human Molecular Genetics. 2(7). 1085–1085. 5 indexed citations
7.
Love, Donald R., Barbara C. Byth, Jonathon M. Tinsley, Derek J. Blake, & Kay E. Davies. (1993). Dystrophin and dystrophin-related proteins: A review of protein and RNA studies. Neuromuscular Disorders. 3(1). 5–21. 51 indexed citations
8.
Byth, Barbara C., Joost C.M. Meijers, & Diane W. Cox. (1993). A (CA)n repeat polymorphism in the protein C inhibitor (PCI) gene. Human Molecular Genetics. 2(10). 1752–1752. 11 indexed citations
9.
Byth, Barbara C. & Diane W. Cox. (1993). A (CA)n repeat polymorphism at the 5′ end of the α1antitrypsin gene (PI). Human Molecular Genetics. 2(10). 1752–1752. 11 indexed citations
10.
Tinsley, Jonathon M., Derek J. Blake, A. Roche, et al.. (1992). Primary structure of dystrophin-related protein. Nature. 360(6404). 591–593. 339 indexed citations
11.
Byth, Barbara C., Donald R. Love, J. Murray, & K E Davies. (1992). Localization of two new DNA markers on the linkage map of human chromosome 6q. Cytogenetic and Genome Research. 60(3-4). 216–218. 1 indexed citations
12.
Passos‐Bueno, Maria Rita, Barbara C. Byth, Donald R. Love, et al.. (1991). Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27. Journal of the Neurological Sciences. 102(2). 206–208. 1 indexed citations
13.
Gilliam, T. Conrad, Linda M. Brzustowicz, Lucio H. Castilla, et al.. (1990). Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Nature. 345(6278). 823–825. 257 indexed citations
14.
Love, Donald R., Diane F. Hill, George Dickson, et al.. (1989). An autosomal transcript in skeletal muscle with homology to dystrophin. Nature. 339(6219). 55–58. 437 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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