G F Saunders

3.1k total citations
60 papers, 2.6k citations indexed

About

G F Saunders is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, G F Saunders has authored 60 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in G F Saunders's work include Renal and related cancers (18 papers), RNA modifications and cancer (9 papers) and RNA and protein synthesis mechanisms (8 papers). G F Saunders is often cited by papers focused on Renal and related cancers (18 papers), RNA modifications and cancer (9 papers) and RNA and protein synthesis mechanisms (8 papers). G F Saunders collaborates with scholars based in United States, France and Netherlands. G F Saunders's co-authors include Louise C. Strong, Peter T. Lomedico, Stephen M. Hewitt, Gail Fraizer, Vicki Huff, W. T. Schroeder, Marsha L. Frazier, Linda C. Lopez, Vincent M. Riccardi and Hugo A. Barrera‐Saldaña and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

G F Saunders

60 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G F Saunders United States 29 2.0k 557 311 274 249 60 2.6k
K L Ramachandran United States 14 1.6k 0.8× 477 0.9× 62 0.2× 141 0.5× 294 1.2× 15 3.0k
SH Orkin United States 32 3.4k 1.7× 992 1.8× 243 0.8× 52 0.2× 207 0.8× 50 6.0k
Somayyeh Fahiminiya Canada 27 1.2k 0.6× 811 1.5× 106 0.3× 166 0.6× 226 0.9× 52 2.2k
Małgorzata Bielińska United States 29 1.7k 0.9× 857 1.5× 57 0.2× 195 0.7× 519 2.1× 41 2.4k
C. Jones United States 30 1.3k 0.7× 586 1.1× 83 0.3× 55 0.2× 128 0.5× 66 2.3k
Sabra C. Goff United States 21 1.8k 0.9× 676 1.2× 360 1.2× 29 0.1× 106 0.4× 26 4.0k
Julie A. DeLoia United States 30 1.2k 0.6× 553 1.0× 302 1.0× 39 0.1× 209 0.8× 63 2.9k
M L Law United States 23 1.6k 0.8× 579 1.0× 77 0.2× 55 0.2× 129 0.5× 40 2.2k
Manas K. Ray United States 26 1.4k 0.7× 577 1.0× 42 0.1× 83 0.3× 191 0.8× 52 2.1k
N Odartchenko Switzerland 23 721 0.4× 226 0.4× 83 0.3× 100 0.4× 103 0.4× 53 1.7k

Countries citing papers authored by G F Saunders

Since Specialization
Citations

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

Fields of papers citing papers by G F Saunders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G F Saunders. 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 G F Saunders. The network helps show where G F Saunders may publish in the future.

Co-authorship network of co-authors of G F Saunders

This figure shows the co-authorship network connecting the top 25 collaborators of G F Saunders. A scholar is included among the top collaborators of G F Saunders 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 G F Saunders. G F Saunders 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.
Fraizer, Gail, et al.. (1999). WT1 and GATA1 expression in myelodysplastic syndrome and acute leukemia. Leukemia. 13(6). 891–900. 47 indexed citations
2.
Li, Chao, et al.. (1997). Functional Analysis of Paired Box Missense Mutations in The PAX6 Gene. Human Molecular Genetics. 6(3). 381–386. 62 indexed citations
3.
Ferrell, R E, et al.. (1994). Paired box mutations in familial and sporadic aniridia predicts truncated aniridia proteins.. PubMed. 54(5). 801–11. 50 indexed citations
4.
Fraizer, Gail, Ying Wu, Stephen M. Hewitt, et al.. (1994). Transcriptional regulation of the human Wilms' tumor gene (WT1). Cell type-specific enhancer and promiscuous promoter.. Journal of Biological Chemistry. 269(12). 8892–8900. 74 indexed citations
5.
Kass, David H., et al.. (1993). Examination of DNA methylation of chromosomal hot spots associated with breast cancer.. PubMed. 13(5A). 1245–51. 6 indexed citations
6.
Miwa, Hiroto, Gail E. Tomlinson, Charles F. Timmons, et al.. (1992). RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology. JNCI Journal of the National Cancer Institute. 84(3). 181–187. 39 indexed citations
7.
Mannens, M., J.M.N. Hoovers, E. M. Bleeker‐Wagemakers, et al.. (1991). The distal region of 11p13 and associated genetic diseases. Genomics. 11(2). 284–293. 19 indexed citations
8.
Verbraak, Frank D., et al.. (1991). DNA diagnosis in a family with autosomal dominant aniridia. Ophthalmic Paediatrics and Genetics. 12(4). 165–170. 3 indexed citations
9.
Jeanpierre, Marc, Corinne Antignac, Christophe Béroud, et al.. (1990). Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor. Genomics. 7(3). 434–438. 18 indexed citations
10.
Selvanayagam, P, Louise C. Strong, G F Saunders, & Bart Barlogie. (1990). A rare Bc/l RFLP in the putative oncogene bcl-1 locus. Nucleic Acids Research. 18(6). 1665–1665. 1 indexed citations
11.
Stellrecht, Christine M., et al.. (1987). Localization of an abundant myeloid mRNA to individual leukocytes in mixed cell populations.. PubMed. 1(3). 167–72. 10 indexed citations
12.
Huff, Vicki, et al.. (1987). AnEcoRl polymorphism associated with a human genomic clone from band 11p13. Nucleic Acids Research. 15(18). 7651–7651. 8 indexed citations
13.
Stellrecht, Christine M., et al.. (1987). Localization of an Abundant Myeloid-Related Sequence. Acta Haematologica. 78(1). 11–17. 2 indexed citations
14.
Lopez, Linda C., Wen‐Hsiung Li, Marsha L. Frazier, C C Luo, & G F Saunders. (1984). Evolution of glucagon genes.. Molecular Biology and Evolution. 1(4). 335–44. 31 indexed citations
15.
Lopez, Linda C., Marsha L. Frazier, C J Su, Ashwani Kumar, & G F Saunders. (1983). Mammalian pancreatic preproglucagon contains three glucagon-related peptides.. Proceedings of the National Academy of Sciences. 80(18). 5485–5489. 180 indexed citations
16.
Kidd, Vincent J. & G F Saunders. (1982). Linkage arrangement of human placental lactogen and growth hormone genes.. Journal of Biological Chemistry. 257(18). 10673–10680. 21 indexed citations
17.
Kuo, M. Tien, William Meinke, & G F Saunders. (1975). Localization of cytoplasmic-membrane-associated DNA in human chromosomes.. Proceedings of the National Academy of Sciences. 72(12). 5004–5006. 5 indexed citations
18.
Shirakawa, S & G F Saunders. (1971). In Vivo Methylation of DNA in Human Leukocytes. Experimental Biology and Medicine. 138(1). 369–372. 1 indexed citations
19.
McLaughlin, C S, J. Dondon, M. Grunberg‐Manago, A.M. Michelson, & G F Saunders. (1968). Stability of the messenger RNA-transfer RNA-ribosome complex. Journal of Molecular Biology. 32(3). 521–542. 30 indexed citations
20.
Miller, Jonathan D., Jon Hughes, G F Saunders, & L. Leon Campbell. (1968). Physiological and Biochemical Characteristics of Some Strains of Sulphate-reducing Bacteria. Journal of General Microbiology. 52(2). 173–179. 9 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by K L Ramachandran Breakdown of academic impact, for papers by SH Orkin Breakdown of academic impact, for papers by Somayyeh Fahiminiya Breakdown of academic impact, for papers by Małgorzata Bielińska Breakdown of academic impact, for papers by C. Jones Breakdown of academic impact, for papers by Sabra C. Goff Breakdown of academic impact, for papers by Julie A. DeLoia Breakdown of academic impact, for papers by M L Law Breakdown of academic impact, for papers by Manas K. Ray Breakdown of academic impact, for papers by N Odartchenko
Rankless by CCL
2026