Ian A. Hope

5.5k total citations · 1 hit paper
57 papers, 4.4k citations indexed

About

Ian A. Hope is a scholar working on Aging, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ian A. Hope has authored 57 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Aging, 32 papers in Molecular Biology and 8 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ian A. Hope's work include Genetics, Aging, and Longevity in Model Organisms (38 papers), CRISPR and Genetic Engineering (16 papers) and Malaria Research and Control (6 papers). Ian A. Hope is often cited by papers focused on Genetics, Aging, and Longevity in Model Organisms (38 papers), CRISPR and Genetic Engineering (16 papers) and Malaria Research and Control (6 papers). Ian A. Hope collaborates with scholars based in United Kingdom, United States and Switzerland. Ian A. Hope's co-authors include Kevin Struhl, David E. Hill, S. Mahadevan, Jennifer P. Macke, Albertha J.M. Walhout, John Reece-Hoyes, John G. Scaife, John E. Hyde, Christian A Grove and Colin T. Dolphin and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Ian A. Hope

57 papers receiving 4.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Functional dissection of a eukaryotic transcriptional activator protein, GCN4 of Yeast

1986 815 citations Ian A. Hope, Kevin Struhl Cell profile →

Peers

Ian A. Hope

MB

AGING

GENET

PHEOH

PS

Asako Sugimoto Japan

Erich M. Schwarz United States

James J. Moresco United States

Igor Antoshechkin United States

Jean Vandenhaute Belgium

Alejandro Chavez United States

Peter R. Boag Australia

Jérôme Reboul France

Carlos B. Hirschberg United States

A. Francis Stewart Germany

Asako Sugimoto Japan

Ian A. Hope

2.6k ×0.8

MB

1.1k ×1.1

AGING

522 ×0.7

GENET

272 ×0.6

PHEOH

700 ×1.6

PS

Citations per year, relative to Ian A. Hope Ian A. Hope (= 1×) peers Asako Sugimoto

Countries citing papers authored by Ian A. Hope

Since Specialization

Citations

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

Fields of papers citing papers by Ian A. Hope

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ian A. Hope. 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 Ian A. Hope. The network helps show where Ian A. Hope may publish in the future.

Co-authorship network of co-authors of Ian A. Hope

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

All Works

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20 of 20 papers shown

1.

Hope, Ian A., et al.. (2013). The Caenorhabditis elegans homeobox gene ceh‐19 is required for MC motorneuron function. genesis. 51(3). 163–178. 4 indexed citations

2.

Dolphin, Colin T., et al.. (2013). The significance of alternative transcripts for Caenorhabditis eleganstranscription factor genes, based on expression pattern analysis. BMC Genomics. 14(1). 249–249. 9 indexed citations

3.

Hirani, Nisha, et al.. (2013). A simplified counter-selection recombineering protocol for creating fluorescent protein reporter constructs directly from C. elegans fosmid genomic clones. BMC Biotechnology. 13(1). 1–1. 118 indexed citations

4.

Hope, Ian A., et al.. (2011). Expression Pattern Analysis of Regulatory Transcription Factors in Caenorhabditis elegans. Methods in molecular biology. 786. 21–50. 6 indexed citations

5.

Sait, Steven M., et al.. (2011). DAF-16 and Δ9 Desaturase Genes Promote Cold Tolerance in Long-Lived Caenorhabditis elegans age-1 Mutants. PLoS ONE. 6(9). e24550–e24550. 42 indexed citations

6.

Westenberg, Marcel, et al.. (2010). Escherichia coli MW005: lambda Red-mediated recombineering and copy-number induction of oriV-equipped constructs in a single host. BMC Biotechnology. 10(1). 27–27. 18 indexed citations

7.

Schuster, Eugene F., Joshua McElwee, Jennifer M. A. Tullet, et al.. (2010). DamID in C. elegans reveals longevity‐associated targets of DAF‐16/FoxO. Molecular Systems Biology. 6(1). 399–399. 105 indexed citations

8.

Hope, Ian A., et al.. (2010). Determination of the mobility of novel and established Caenorhabditis elegans sarcomeric proteins in vivo. European Journal of Cell Biology. 89(6). 437–448. 15 indexed citations

9.

Hope, Ian A., et al.. (2009). The Caenorhabditis elegans sirtuin gene, sir-2.1, is widely expressed and induced upon caloric restriction. Mechanisms of Ageing and Development. 130(11-12). 762–770. 25 indexed citations

10.

Reece-Hoyes, John, Denis Dupuy, Christian A Grove, et al.. (2007). Insight into transcription factor gene duplication from Caenorhabditis elegans Promoterome-driven expression patterns. BMC Genomics. 8(1). 27–27. 106 indexed citations

11.

Deplancke, Bart, Arnab Mukhopadhyay, Wanyuan Ao, et al.. (2006). A Gene-Centered C. elegans Protein-DNA Interaction Network. Cell. 125(6). 1193–1205. 189 indexed citations

12.

Hope, Ian A., Jonathan Stevens, Josie Hayes, et al.. (2004). Feasibility of Genome-Scale Construction of Promoter::Reporter Gene Fusions for Expression in Caenorhabditis elegans Using a MultiSite Gateway Recombination System. Genome Research. 14(10b). 2070–2075. 37 indexed citations

13.

Dupuy, Denis, Qianru Li, Bart Deplancke, et al.. (2004). A First Version of the Caenorhabditis elegans Promoterome. Genome Research. 14(10b). 2169–2175. 137 indexed citations

14.

Hope, Ian A.. (2003). The forkhead gene family of Caenorhabditis elegans. Gene. 304. 43–55. 37 indexed citations

15.

Inoue, Takao, David R. Sherwood, Gudrun Aspöck, et al.. (2002). Gene expression markers for Caenorhabditis elegans vulval cells. Mechanisms of Development. 119. S203–S209. 75 indexed citations

16.

Bauer, Petra, et al.. (2002). Evidence Suggesting That a Fifth of Annotated Caenorhabditis elegans Genes May Be Pseudogenes. Genome Research. 12(5). 770–775. 68 indexed citations

17.

Hope, Ian A., et al.. (1998). Promoter trapping identifies real genes in C. elegans. Molecular and General Genetics MGG. 260(2-3). 300–308. 14 indexed citations

18.

Briggs, David, et al.. (1995). Developmental expression pattern screen for genes predicted in the C. elegans genome sequencing project. Nature Genetics. 11(3). 309–313. 45 indexed citations

19.

Hope, Ian A., et al.. (1993). Molecular markers of differentiation in Caenorhabditis elegans obtained by promoter trapping. Developmental Dynamics. 196(2). 124–132. 16 indexed citations

20.

Hope, Ian A., S. Mahadevan, & Kevin Struhl. (1988). Structural and functional characterization of the short acidic transcriptional activation region of yeast GCN4 protein. Nature. 333(6174). 635–640. 284 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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