Anthony Renwick

9.2k total citations · 3 hit papers
21 papers, 3.2k citations indexed

About

Anthony Renwick is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Anthony Renwick has authored 21 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Anthony Renwick's work include BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (6 papers) and Genetic factors in colorectal cancer (5 papers). Anthony Renwick is often cited by papers focused on BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (6 papers) and Genetic factors in colorectal cancer (5 papers). Anthony Renwick collaborates with scholars based in United Kingdom, United States and France. Anthony Renwick's co-authors include Sheila Seal, Nazneen Rahman, Michael R. Stratton, Douglas F. Easton, Rita Barfoot, D. Gareth Evans, Diana Eccles, Hiran Jayatilake, Lesley McGuffog and Deborah J. Thompson and has published in prestigious journals such as Nature Communications, Nature Genetics and Scientific Reports.

In The Last Decade

Anthony Renwick

21 papers receiving 3.1k 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.

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

2006 689 citations Nazneen Rahman, Sheila Seal et al. Nature Genetics profile →
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

2006 513 citations Sheila Seal, Deborah J. Thompson et al. Nature Genetics profile →
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

2006 511 citations Anthony Renwick, Deborah J. Thompson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anthony Renwick United Kingdom	17	1.7k	1.7k	694	632	476	21	3.2k
Claire Domon–Dell France	24	2.5k 1.4×	1.2k 0.7×	270 0.4×	118 0.2×	312 0.7×	40	3.5k
Annemieke W. Plug United States	16	3.6k 2.1×	1.2k 0.7×	800 1.2×	625 1.0×	644 1.4×	18	4.2k
Dmitri Loukinov United States	28	3.1k 1.8×	1.1k 0.6×	350 0.5×	284 0.4×	105 0.2×	44	3.6k
Sean M. Baker United States	15	2.6k 1.5×	741 0.4×	1.6k 2.3×	251 0.4×	3.1k 6.4×	20	4.5k
Hiroshi Fukamachi Japan	27	1.5k 0.9×	387 0.2×	483 0.7×	255 0.4×	186 0.4×	109	2.7k
Kornelia Neveling Netherlands	25	2.2k 1.3×	814 0.5×	630 0.9×	197 0.3×	209 0.4×	60	2.8k
Mark T.A. Donoghue United States	23	1.8k 1.0×	457 0.3×	914 1.3×	1.1k 1.7×	120 0.3×	58	3.1k
Martin F. Arlt United States	22	2.1k 1.2×	1.2k 0.7×	291 0.4×	314 0.5×	91 0.2×	37	2.7k
Agnel Sfeir United States	31	4.5k 2.6×	380 0.2×	343 0.5×	594 0.9×	81 0.2×	47	5.4k
Elizabeth A. Chavez Canada	24	1.9k 1.1×	335 0.2×	219 0.3×	304 0.5×	297 0.6×	41	2.9k

Countries citing papers authored by Anthony Renwick

Since Specialization

Citations

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

Fields of papers citing papers by Anthony Renwick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anthony Renwick

This figure shows the co-authorship network connecting the top 25 collaborators of Anthony Renwick. A scholar is included among the top collaborators of Anthony Renwick 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 Anthony Renwick. Anthony Renwick 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

Ruark, Elise, Márton Münz, Matthew Clarke, et al.. (2016). OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis. Scientific Reports. 6(1). 31029–31029. 4 indexed citations

Loveday, Chey, Katrina Tatton‐Brown, Matthew Clarke, et al.. (2015). Mutations in the PP2A regulatory subunit B family genesPPP2R5B,PPP2R5CandPPP2R5Dcause human overgrowth. Human Molecular Genetics. 24(17). 4775–4779. 62 indexed citations

Münz, Márton, Elise Ruark, Anthony Renwick, et al.. (2015). CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting. Genome Medicine. 7(1). 76–76. 29 indexed citations

Litchfield, Kevin, Brenda Summersgill, Shawn Yost, et al.. (2015). Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours. Nature Communications. 6(1). 5973–5973. 132 indexed citations

Ruark, Elise, Márton Münz, Anthony Renwick, et al.. (2015). The ICR1000 UK exome series: a resource of gene variation in an outbred population [version 1; referees: 2 approved]. 4. 2 indexed citations

Snape, Katie, Elise Ruark, Patrick Tarpey, et al.. (2012). Predisposition gene identification in common cancers by exome sequencing: insights from familial breast cancer. Breast Cancer Research and Treatment. 134(1). 429–433. 36 indexed citations

Hadsell, Darryl L., Jerry Wei, Anthony Renwick, et al.. (2012). In silico QTL mapping of maternal nurturing ability with the mouse diversity panel. Physiological Genomics. 44(16). 787–798. 7 indexed citations

Turnbull, Clare, Elizabeth Rapley, Sheila Seal, et al.. (2010). Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer. Nature Genetics. 42(7). 604–607. 235 indexed citations

Turnbull, Clare, Sarah Hines, Anthony Renwick, et al.. (2010). Mutation and association analysis of GEN1 in breast cancer susceptibility. Breast Cancer Research and Treatment. 124(1). 283–288. 14 indexed citations

10.

Rapley, Elizabeth, Clare Turnbull, Ali Amin Al Olama, et al.. (2009). A genome-wide association study of testicular germ cell tumor. Nature Genetics. 41(7). 807–810. 233 indexed citations

11.

Rahman, Nazneen, Sheila Seal, Deborah J. Thompson, et al.. (2006). PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nature Genetics. 39(2). 165–167. 689 indexed citations breakdown →

12.

Renwick, Anthony, Deborah J. Thompson, Sheila Seal, et al.. (2006). ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nature Genetics. 38(8). 873–875. 511 indexed citations breakdown →

13.

Seal, Sheila, Deborah J. Thompson, Anthony Renwick, et al.. (2006). Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nature Genetics. 38(11). 1239–1241. 513 indexed citations breakdown →

14.

Thompson, Deborah J., Sheila Seal, Mieke Schutte, et al.. (2006). A Multicenter Study of Cancer Incidence in CHEK2 1100delC Mutation Carriers. Cancer Epidemiology Biomarkers & Prevention. 15(12). 2542–2545. 41 indexed citations

15.

Tommiska, Johanna, Sheila Seal, Anthony Renwick, et al.. (2005). Evaluation of RAD50 in familial breast cancer predisposition. International Journal of Cancer. 118(11). 2911–2916. 47 indexed citations

16.

Seal, Sheila, Rita Barfoot, Hiran Jayatilake, et al.. (2003). Evaluation of Fanconi Anemia genes in familial breast cancer predisposition.. PubMed. 63(24). 8596–9. 50 indexed citations

17.

Timms‐Wilson, T. M., Richard J. Ellis, Anthony Renwick, et al.. (2000). Chromosomal Insertion of Phenazine-1-Carboxylic Acid Biosynthetic Pathway Enhances Efficacy of Damping-off Disease Control by Pseudomonas fluorescens. Molecular Plant-Microbe Interactions. 13(12). 1293–1300. 58 indexed citations

18.

Ellis, Richard J., T. M. Timms‐Wilson, J. E. Beringer, et al.. (1999). Ecological basis for biocontrol of damping-off disease by Pseudomonas fluorescens 54/96. Journal of Applied Microbiology. 87(3). 454–463. 35 indexed citations

19.

Skinner, Wendy, Andy M. Bailey, Anthony Renwick, et al.. (1998). A single amino-acid substitution in the iron-sulphur protein subunit of succinate dehydrogenase determines resistance to carboxin in Mycosphaerella graminicola. Current Genetics. 34(5). 393–398. 99 indexed citations

20.

Renwick, Anthony, et al.. (1990). Biological control of soil-borne plant pathogens.. 1. 227–231. 299 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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