Rebecca Pask

742 total citations
6 papers, 499 citations indexed

About

Rebecca Pask is a scholar working on Genetics, Surgery and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Rebecca Pask has authored 6 papers receiving a total of 499 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Surgery and 2 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Rebecca Pask's work include Diabetes and associated disorders (3 papers), Genetic Associations and Epidemiology (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Rebecca Pask is often cited by papers focused on Diabetes and associated disorders (3 papers), Genetic Associations and Epidemiology (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Rebecca Pask collaborates with scholars based in United Kingdom and United States. Rebecca Pask's co-authors include John A. Todd, Sarah Nutland, Neil Walker, Joanna M. M. Howson, Jason D. Cooper, David Clayton, Alexander Lam, Luc J Smink, Lisa M. Maier and Deborah J. Smyth and has published in prestigious journals such as Nature Genetics, Diabetes and The American Journal of Human Genetics.

In The Last Decade

Rebecca Pask

6 papers receiving 489 citations

Peers

Rebecca Pask

GENET

MB

IMMUN

SURGE

EDM

Allan Daly United Kingdom

Sanghoon Moon South Korea

Ramesh Ram Australia

Yibing Han China

Hanni Ke China

Prashantha Hebbar Kuwait

Tara Willson United States

Ariadna González‐del Angel Mexico

Kwang Ho Pyun South Korea

Suzanne K. Cordovado United States

Allan Daly United Kingdom

Rebecca Pask

179 ×0.5

GENET

275 ×1.7

MB

49 ×0.7

IMMUN

79 ×1.6

SURGE

47 ×1.2

EDM

Citations per year, relative to Rebecca Pask Rebecca Pask (= 1×) peers Allan Daly

Countries citing papers authored by Rebecca Pask

Since Specialization

Citations

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

Fields of papers citing papers by Rebecca Pask

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca Pask

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

All Works

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6 of 6 papers shown

1.

Pask, Rebecca, Jason D. Cooper, Neil Walker, et al.. (2006). No evidence for a major effect of two common polymorphisms of the catalase gene in type 1 diabetes susceptibility. Diabetes/Metabolism Research and Reviews. 22(5). 356–360. 31 indexed citations

2.

Maier, Lisa M., Juliet Chapman, Joanna M. M. Howson, et al.. (2005). No Evidence of Association or Interaction between the IL4RA, IL4, and IL13 Genes in Type 1 Diabetes. The American Journal of Human Genetics. 76(3). 517–521. 38 indexed citations

3.

Clayton, David, Neil Walker, Deborah J. Smyth, et al.. (2005). Population structure, differential bias and genomic control in a large-scale, case-control association study. Nature Genetics. 37(11). 1243–1246. 354 indexed citations

4.

Pask, Rebecca, Helen Rance, Bryan J. Barratt, et al.. (2004). Investigating the utility of combining Φ29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray™ genotyping. BMC Biotechnology. 4(1). 15–15. 30 indexed citations

5.

Jamieson, Sarra E., Jacqueline K. White, Joanna M. M. Howson, et al.. (2004). Candidate gene association study of solute carrier family 11a members 1 (SLC11A1) and 2 (SLC11A2) genes in Alzheimer's disease. Neuroscience Letters. 374(2). 124–128. 24 indexed citations

6.

Payne, Felicity, Deborah J. Smyth, Rebecca Pask, et al.. (2004). Haplotype Tag Single Nucleotide Polymorphism Analysis of the Human Orthologues of the Rat Type 1 Diabetes GenesIan4(Lyp/Iddm1) andCblb. Diabetes. 53(2). 505–509. 22 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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