Robert J. Hardwick

871 total citations
8 papers, 494 citations indexed

About

Robert J. Hardwick is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Robert J. Hardwick has authored 8 papers receiving a total of 494 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Robert J. Hardwick's work include Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers) and Chromosomal and Genetic Variations (2 papers). Robert J. Hardwick is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (3 papers) and Chromosomal and Genetic Variations (2 papers). Robert J. Hardwick collaborates with scholars based in United Kingdom, United States and Tanzania. Robert J. Hardwick's co-authors include David J. Porteous, Andrew D. Morris, Michael R. Stratton, Ludmil B. Alexandrov, Anna F. Dominiczak, Raheleh Rahbari, Matthew E. Hurles, Sarah Lindsay, Blair H. Smith and Arthur Wüster and has published in prestigious journals such as Nature Genetics, Bioinformatics and PLoS ONE.

In The Last Decade

Robert J. Hardwick

8 papers receiving 490 citations

Peers

Robert J. Hardwick

MB

GENET

CR

PPCH

PS

Sabita K. Murthy Canada

Marco Garieri Switzerland

Rajini Haraksingh United States

Corinne Fasquelle Belgium

Ko–ichiro Yoshiura Japan

Chee Seng Ku Sweden

Sjors Middelkamp Netherlands

M. F. Croquette France

Jesper Eisfeldt Sweden

Quan Chen China

Sabita K. Murthy Canada

Robert J. Hardwick

371 ×1.4

MB

196 ×0.7

GENET

83 ×0.7

CR

61 ×1.3

PPCH

39 ×0.8

PS

Citations per year, relative to Robert J. Hardwick Robert J. Hardwick (= 1×) peers Sabita K. Murthy

Countries citing papers authored by Robert J. Hardwick

Since Specialization

Citations

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

Fields of papers citing papers by Robert J. Hardwick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert J. Hardwick. 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 Robert J. Hardwick. The network helps show where Robert J. Hardwick may publish in the future.

Co-authorship network of co-authors of Robert J. Hardwick

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

All Works

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8 of 8 papers shown

1.

Zuccherato, Luciana W., Eduardo Tarazona‐Santos, Robert J. Hardwick, et al.. (2017). Population genetics of immune-related multilocus copy number variation in Native Americans. Journal of The Royal Society Interface. 14(128). 20170057–20170057. 5 indexed citations

2.

Rahbari, Raheleh, Arthur Wüster, Sarah Lindsay, et al.. (2015). Timing, rates and spectra of human germline mutation. Nature Genetics. 48(2). 126–133. 381 indexed citations

3.

Aklillu, Eleni, Linda Odenthal-Hesse, Abiy Habtewold, et al.. (2013). CCL3L1 copy number, HIV load, and immune reconstitution in sub-Saharan Africans. BMC Infectious Diseases. 13(1). 536–536. 15 indexed citations

4.

Veal, Colin, Hang Xu, Robert C. Free, et al.. (2013). Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation. Bioinformatics. 29(16). 1997–2003. 8 indexed citations

5.

Kaess, Bernhard M., Maciej Tomaszewski, Peter S. Braund, et al.. (2011). Large-Scale Candidate Gene Analysis of HDL Particle Features. PLoS ONE. 6(1). e14529–e14529. 27 indexed citations

6.

Jespersgaard, Cathrine, Robert J. Hardwick, Michael Theisen, et al.. (2011). Determination of Beta-Defensin Genomic Copy Number in Different Populations: A Comparison of Three Methods. PLoS ONE. 6(2). e16768–e16768. 36 indexed citations

7.

Hardwick, Robert J., M. V. Tretyakov, & Yuri E. Dubrova. (2009). Age-Related Accumulation of Mutations Supports a Replication-Dependent Mechanism of Spontaneous Mutation at Tandem Repeat DNA Loci in Mice. Molecular Biology and Evolution. 26(11). 2647–2654. 20 indexed citations

8.

Ahuja, A. K., Ruth Barber, Robert J. Hardwick, et al.. (2008). The effects of Atm haploinsufficiency on mutation rate in the mouse germ line and somatic tissue. Mutagenesis. 23(5). 367–370. 2 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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