Andrew Dearlove

2.8k total citations · 1 hit paper
17 papers, 1.9k citations indexed

About

Andrew Dearlove is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Andrew Dearlove has authored 17 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Genetics. Recurrent topics in Andrew Dearlove's work include Neurogenetic and Muscular Disorders Research (4 papers), Hereditary Neurological Disorders (4 papers) and Neurological diseases and metabolism (3 papers). Andrew Dearlove is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Hereditary Neurological Disorders (4 papers) and Neurological diseases and metabolism (3 papers). Andrew Dearlove collaborates with scholars based in United Kingdom, United States and Singapore. Andrew Dearlove's co-authors include Tom Vulliamy, Monica Bessler, Philip J. Mason, Inderjeet Dokal, Anna Marrone, Frederick D. Goldman, Evan Reid, David C. Rubinsztein, Michael D. Rhodes and Ingrid K. Svenson and has published in prestigious journals such as Nature, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Andrew Dearlove

16 papers receiving 1.8k citations

Hit Papers

The RNA component of telomerase is mutated in autosomal d... 2001 2026 2009 2017 2001 200 400 600
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.

  1. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
    2001 705 citations Tom Vulliamy, Anna Marrone et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Dearlove United Kingdom 13 846 605 357 247 234 17 1.9k
Qiji Liu China 22 899 1.1× 232 0.4× 109 0.3× 174 0.7× 90 0.4× 87 1.6k
Manae S. Kurokawa Japan 23 785 0.9× 147 0.2× 123 0.3× 130 0.5× 168 0.7× 82 1.8k
Turgut Tükel Türkiye 14 510 0.6× 730 1.2× 217 0.6× 114 0.5× 167 0.7× 18 1.5k
Henning B. Boldt Denmark 23 833 1.0× 112 0.2× 107 0.3× 275 1.1× 154 0.7× 44 2.2k
Candace L. Kerr United States 27 851 1.0× 141 0.2× 176 0.5× 168 0.7× 97 0.4× 53 1.7k
Laurent Metzinger France 27 2.0k 2.3× 362 0.6× 257 0.7× 123 0.5× 36 0.2× 51 2.6k
Tanya Lehky United States 21 566 0.7× 259 0.4× 336 0.9× 382 1.5× 55 0.2× 57 2.2k
Martin C. Wapenaar Netherlands 24 1.4k 1.6× 164 0.3× 208 0.6× 238 1.0× 64 0.3× 45 2.2k
Emanuele Azzoni Italy 14 1.0k 1.2× 267 0.4× 79 0.2× 301 1.2× 514 2.2× 24 2.5k
Satomi Mitsuhashi Japan 28 1.8k 2.2× 249 0.4× 375 1.1× 299 1.2× 51 0.2× 99 2.4k

Countries citing papers authored by Andrew Dearlove

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Dearlove

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Dearlove

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

All Works

17 of 17 papers shown
1.
Ching, Yung‐Hao, Tushar K. Ghosh, Elizabeth A. Packham, et al.. (2005). Mutation in myosin heavy chain 6 causes atrial septal defect. Nature Genetics. 37(4). 423–428. 195 indexed citations
2.
Kennedy, Ann, Masaki Inada, Stephen M. Krane, et al.. (2005). MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMDMO). Journal of Clinical Investigation. 115(10). 2832–2842. 75 indexed citations
3.
Ching, Yung‐Hao, Tushar K. Ghosh, Elizabeth A. Packham, et al.. (2005). Ching, Y. H. et al. Mutation in myosin heavy chain 6 causes atrial septal defect. Nature Genet. 37, 423-428. 1 indexed citations
4.
Aung, Tin, Richard Bowman, Paul Chew, et al.. (2003). Genome-wide Linkage Scan for Primary Angle Closure Glaucoma. Investigative Ophthalmology & Visual Science. 44(13). 3224–3224.
5.
Moodie, Simon, Jocelyn Fraser, David Curtis, et al.. (2003). Coeliac disease: investigation of proposed causal variants in the CTLA4 gene region. European Journal of Immunogenetics. 30(6). 427–432. 37 indexed citations
6.
Kennedy, Ann, Paul T. Christie, Brian Harding, et al.. (2003). Matrix metalloproteinase 13 (MMP13) mutation causes spondyloepimetaphyseal dysplasia (SEMD), Missouri variant. 5(18). 25–6. 2 indexed citations
7.
Reid, Evan, Mark Kloos, Allison E. Ashley‐Koch, et al.. (2002). A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10). The American Journal of Human Genetics. 71(5). 1189–1194. 377 indexed citations
8.
Dearlove, Andrew. (2002). High throughput genotyping technologies. Briefings in Functional Genomics and Proteomics. 1(2). 139–150. 19 indexed citations
9.
Vulliamy, Tom, Anna Marrone, Frederick D. Goldman, et al.. (2001). The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature. 413(6854). 432–435. 705 indexed citations breakdown →
10.
Fraser, Jocelyn, Simon Moodie, David Curtis, et al.. (2001). Coeliac disease: follow‐up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11. Annals of Human Genetics. 65(4). 377–386. 33 indexed citations
11.
Brockington, Martin, Caroline A. Sewry, R. Herrmann, et al.. (2000). Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42. The American Journal of Human Genetics. 66(2). 428–435. 56 indexed citations
12.
Brett, Peter, David Curtis, Michelle Morris, et al.. (2000). A genome‐wide family‐based linkage study of coeliac disease. Annals of Human Genetics. 64(6). 479–490. 65 indexed citations
13.
Reid, Evan, Andrew Dearlove, Olivia Osborn, Mark T. Rogers, & David C. Rubinsztein. (2000). A Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Maps to Chromosome 19q13. The American Journal of Human Genetics. 66(2). 728–732. 52 indexed citations
14.
Ohadi, Mina, M. R. A. LALLOZ, Pak C. Sham, et al.. (1999). Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping. The American Journal of Human Genetics. 64(1). 165–171. 138 indexed citations
15.
Reid, Evan, Andrew Dearlove, Michael D. Rhodes, & David C. Rubinsztein. (1999). A New Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Mapping to Chromosome 12q13, and Evidence for Further Genetic Heterogeneity. The American Journal of Human Genetics. 65(3). 757–763. 65 indexed citations
16.
Reid, Evan, Andrew Dearlove, Margo L. Whiteford, Michael D. Rhodes, & David C. Rubinsztein. (1999). Autosomal dominant spastic paraplegia. Neurology. 53(8). 1844–1844. 21 indexed citations
17.
Rhodes, Michael D., et al.. (1997). High-throughput microsatellite analysis using fluorescent dUTPs for high-resolution genetic mapping of the mouse genome.. Genome Research. 7(1). 81–86. 9 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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