G. Rowley

436 total citations
10 papers, 318 citations indexed

About

G. Rowley is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, G. Rowley has authored 10 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Hematology. Recurrent topics in G. Rowley's work include Cancer-related gene regulation (3 papers), RNA modifications and cancer (2 papers) and Hemophilia Treatment and Research (2 papers). G. Rowley is often cited by papers focused on Cancer-related gene regulation (3 papers), RNA modifications and cancer (2 papers) and Hemophilia Treatment and Research (2 papers). G. Rowley collaborates with scholars based in United Kingdom and Canada. G. Rowley's co-authors include Jane Cole, Alan R. Lehmann, Herdis Steingrimsdottir, G. Dorado, F. Giannelli, Sara Teresinha Olalla Saad, David Beare, Isabella Ceccherini, Peter M. Green and Cathryn M. Lewis and has published in prestigious journals such as Nucleic Acids Research, Gastroenterology and The American Journal of Human Genetics.

In The Last Decade

G. Rowley

10 papers receiving 314 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Rowley United Kingdom	6	247	55	53	41	28	10	318
N G Copeland United States	7	215 0.9×	22 0.4×	91 1.7×	42 1.0×	20 0.7×	8	350
Lynn Lehmann United States	8	317 1.3×	26 0.5×	47 0.9×	13 0.3×	29 1.0×	9	406
Giorgia Montano Sweden	13	319 1.3×	43 0.8×	45 0.8×	35 0.9×	17 0.6×	17	435
Marika Pla France	9	184 0.7×	35 0.6×	26 0.5×	49 1.2×	12 0.4×	15	375
Sayaka Nagao-Sato Japan	5	202 0.8×	50 0.9×	25 0.5×	34 0.8×	8 0.3×	8	349
Qianli Zhuang Canada	8	252 1.0×	15 0.3×	47 0.9×	39 1.0×	15 0.5×	11	368
Magdalena Medrzycki United States	11	341 1.4×	77 1.4×	32 0.6×	26 0.6×	53 1.9×	17	425
L. Faggioli Italy	11	189 0.8×	80 1.5×	36 0.7×	30 0.7×	9 0.3×	18	379
Daniela Ulgiati Australia	13	167 0.7×	29 0.5×	33 0.6×	22 0.5×	7 0.3×	28	328
Jacqueline Dickson United Kingdom	6	358 1.4×	53 1.0×	78 1.5×	35 0.9×	17 0.6×	7	426

Countries citing papers authored by G. Rowley

Since Specialization

Citations

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

Fields of papers citing papers by G. Rowley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Rowley

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

All Works

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10 of 10 papers shown

1.

Allen, M H, Cathryn M. Lewis, Scott Fisher, et al.. (2000). Corneodesmosin (S) gene association with psoriasis vulgaris. Journal of Investigative Dermatology. 115(3). 576–576. 2 indexed citations

2.

Mirza, Muddassar M., G. Rowley, Jochen Hampe, et al.. (2000). Analysis of single nucleotide polymorphisms in the NRAMP2 gene, for association with inflammatory bowel disease. Gastroenterology. 118(4). A594–A595. 1 indexed citations

3.

Green, Peter M., et al.. (1999). DNA Variation in a 5-Mb Region of the X Chromosome and Estimates of Sex-Specific/Type-Specific Mutation Rates. The American Journal of Human Genetics. 64(2). 508–517. 25 indexed citations

4.

Morgan, Gareth, et al.. (1997). Further evidence for the importance of an androgen response element in the factor IX promoter. British Journal of Haematology. 98(1). 79–85. 16 indexed citations

5.

Tagliavacca, Luigina, et al.. (1997). Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their families. Haemophilia. 3(3). 177–182. 4 indexed citations

6.

Rowley, G., et al.. (1997). ChemInform Abstract: Multiplex Solid‐Phase Fluorescent ‐ Chemical Cleavage. ChemInform. 28(20). 1 indexed citations

7.

Rowley, G., et al.. (1995). Ultrarapid Mutation Detection by Multiplex, Solid-Phase Chemical Cleavage. Genomics. 30(3). 574–582. 68 indexed citations

8.

Curry, John, G. Rowley, Vera Aparecida Saddi, et al.. (1995). Determination of hprt mutant and mutation frequencies and the molecular characterization of human derived in vivo T‐lymphocyte mutants. Environmental and Molecular Mutagenesis. 25(3). 169–179. 21 indexed citations

9.

Steingrimsdottir, Herdis, G. Rowley, David Beare, et al.. (1993). Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donors. Mutation Research/DNA Repair. 294(1). 29–41. 46 indexed citations

10.

Steingrimsdottir, Herdis, G. Rowley, G. Dorado, Jane Cole, & Alan R. Lehmann. (1992). Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene. Nucleic Acids Research. 20(6). 1201–1208. 134 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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