R.T. Taggart

2.6k total citations
53 papers, 2.0k citations indexed

About

R.T. Taggart is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, R.T. Taggart has authored 53 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 13 papers in Surgery and 7 papers in Genetics. Recurrent topics in R.T. Taggart's work include Glycosylation and Glycoproteins Research (14 papers), RNA and protein synthesis mechanisms (10 papers) and Helicobacter pylori-related gastroenterology studies (10 papers). R.T. Taggart is often cited by papers focused on Glycosylation and Glycoproteins Research (14 papers), RNA and protein synthesis mechanisms (10 papers) and Helicobacter pylori-related gastroenterology studies (10 papers). R.T. Taggart collaborates with scholars based in United States, Japan and Netherlands. R.T. Taggart's co-authors include Uta Francke, T. Mohandas, Takeshi Azuma, I. Michael Samloff, Michael H. Lehmann, Elizabeth Allen, Larry J. Shapiro, Arthur J. Moss, Pauline H. Yen and Jeffrey A. Towbin and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

R.T. Taggart

53 papers receiving 2.0k 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.T. Taggart United States 26 1.3k 455 413 236 206 53 2.0k
Tony Antakly Canada 22 851 0.7× 303 0.7× 441 1.1× 239 1.0× 276 1.3× 43 1.9k
Paul Hossenlopp France 23 1.7k 1.4× 377 0.8× 616 1.5× 322 1.4× 141 0.7× 29 3.4k
Katrina Rothblum United States 20 1.2k 0.9× 324 0.7× 198 0.5× 119 0.5× 136 0.7× 28 1.8k
Katherine A. Gollahon United States 26 1.4k 1.1× 170 0.4× 319 0.8× 157 0.7× 329 1.6× 41 2.7k
Francis James Grant United States 22 1.5k 1.2× 88 0.2× 373 0.9× 335 1.4× 246 1.2× 33 3.1k
Göran Levan Sweden 26 1.5k 1.2× 129 0.3× 874 2.1× 162 0.7× 416 2.0× 121 2.6k
Takashi Katayama Japan 23 734 0.6× 102 0.2× 180 0.4× 252 1.1× 297 1.4× 157 1.9k
Henrike Maatz Germany 10 994 0.8× 760 1.7× 160 0.4× 175 0.7× 104 0.5× 17 1.8k
J.‐C. Kaplan France 22 988 0.8× 139 0.3× 279 0.7× 110 0.5× 120 0.6× 54 1.5k
Anthony N. Corps United Kingdom 29 902 0.7× 89 0.2× 236 0.6× 606 2.6× 169 0.8× 47 2.3k

Countries citing papers authored by R.T. Taggart

Since Specialization
Citations

This map shows the geographic impact of R.T. Taggart'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.T. Taggart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites R.T. Taggart more than expected).

Fields of papers citing papers by R.T. Taggart

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R.T. Taggart

This figure shows the co-authorship network connecting the top 25 collaborators of R.T. Taggart. A scholar is included among the top collaborators of R.T. Taggart 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.T. Taggart. R.T. Taggart 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.
Azaiez, Héla, Sai Prasad, R.T. Taggart, et al.. (2004). GJB2: The spectrum of deafness-causing allele variants and their phenotype. Human Mutation. 24(4). 305–311. 63 indexed citations
2.
Vladutiu, Georgirene D., Michael J. Bennett, David Smail, et al.. (2000). A Variable Myopathy Associated with Heterozygosity for the R503C Mutation in the Carnitine Palmitoyltransferase II Gene. Molecular Genetics and Metabolism. 70(2). 134–141. 44 indexed citations
3.
Lehmann, Michael H., Katherine W. Timothy, Barbara S. Fromm, et al.. (1997). Age-Gender Influence on the Rate-Corrected QT Interval and the QT-Heart Rate Relation in Families With Genotypically Characterized Long QT Syndrome. Journal of the American College of Cardiology. 29(1). 93–99. 134 indexed citations
4.
Lehmann, Michael H., Fumio Suzuki, Barbara S. Fromm, et al.. (1994). T wave “humps” as a potential electrocardiographic marker of the long QT syndrome. Journal of the American College of Cardiology. 24(3). 746–754. 83 indexed citations
5.
Jiang, Changan, Donald L. Atkinson, Jeffrey A. Towbin, et al.. (1994). Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity. Nature Genetics. 8(2). 141–147. 193 indexed citations
6.
Pang, J T, C Wooding, R.T. Taggart, et al.. (1993). MOLECULAR-GENETIC MAPPING OF 13 MARKERS FROM CHROMOSOME-11Q13 IN 33 FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1. Journal of Bone and Mineral Research. 8. 1 indexed citations
7.
Azuma, Takeshi, Takanobu Hayakumo, Keishu Yasuda, et al.. (1993). Pepsinogen C gene polymorphisms associated with gastric body ulcer.. Gut. 34(4). 450–455. 6 indexed citations
8.
Krebs, Christopher J., Joseph Horton, Chadwick Mullins, William Paradee, & R.T. Taggart. (1993). D11S971 CATT polymorphism (RC27) located near the MEN1 locus at 11q13. Human Molecular Genetics. 2(6). 825–825. 5 indexed citations
9.
Ginzinger, David G., Viji Shridhar, Antonio Baldini, et al.. (1992). The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3.. PubMed. 50(4). 826–33. 8 indexed citations
10.
Bowcock, A., Takeshi Azuma, Robert I. Barnes, et al.. (1992). Detection of a polymorphism within the pepsinogen C gene with PCR: Construction of a linkage map around PGC from 6p11–6p21.3. Genomics. 14(2). 398–402. 3 indexed citations
11.
Taggart, R.T., Takeshi Azuma, Shengbiao Wu, Graeme I. Bell, & A. Bowcock. (1991). A Highly Informative Polymorphism of the Pepsinogen C Gene Detected by Polymerase Chain Reaction. Advances in experimental medicine and biology. 306. 95–99. 4 indexed citations
12.
Azuma, Takeshi, et al.. (1990). Assignment of cathepsin E (CTSE) to human chromosome region 1q31 by in situ hybridization and analysis of somatic cell hybrids. Cytogenetic and Genome Research. 53(2-3). 137–139. 8 indexed citations
13.
Habu, Yasuki, Takeshi Azuma, Keiichi Kawai, & R.T. Taggart. (1990). Restriction analysis of pepsinogen C gene in Japanese. Gastroenterologia Japonica. 25(2). 270–270. 1 indexed citations
14.
Taggart, R.T., et al.. (1989). Human Pepsinogen C (Progastriesin). Journal of Biological Chemistry. 264(1). 375–379. 43 indexed citations
15.
Azuma, Takeshi, Hideto Inokuchi, Sotaro Fujimoto, et al.. (1989). Carboxyl terminal glycine extended progastrin (gastrin-G) in human gastric mucosa and gastrinomas. Clinica Chimica Acta. 179(2). 201–203. 2 indexed citations
16.
Pals, Gerard, Takeshi Azuma, T. Mohandas, et al.. (1989). Human pepsinogen C (progastricsin) polymorphism: Evidence for a single locus located at 6p21.1-pter. Genomics. 4(2). 137–145. 28 indexed citations
17.
Azuma, Takeshi, Gerard Pals, & R.T. Taggart. (1988). RFLP for the human pepsinogen C gene (PGC). Nucleic Acids Research. 16(19). 9372–9372. 11 indexed citations
18.
Samloff, I. Michael, R.T. Taggart, Tadashi Shiraishi, et al.. (1987). Slow moving proteinase. Gastroenterology. 93(1). 77–84. 12 indexed citations
19.
Taggart, R.T. & I. Michael Samloff. (1987). Immunochemical, Electrophoretic, and Genetic Heterogeneity of Pepsinogen I. Gastroenterology. 92(1). 143–150. 6 indexed citations
20.
Nakai, H., M.G. Byers, T.B. Shows, & R.T. Taggart. (1986). Assignment of the pepsinogen gene complex (<i>PGA</i>) to human chromosome region llql3 by in situ hybridization. Cytogenetic and Genome Research. 43(3-4). 215–217. 36 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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