David Bentley

110.7k total citations · 5 hit papers
131 papers, 12.3k citations indexed

About

David Bentley is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, David Bentley has authored 131 papers receiving a total of 12.3k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 41 papers in Genetics and 32 papers in Cellular and Molecular Neuroscience. Recurrent topics in David Bentley's work include Neurobiology and Insect Physiology Research (24 papers), Genomics and Rare Diseases (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). David Bentley is often cited by papers focused on Neurobiology and Insect Physiology Research (24 papers), Genomics and Rare Diseases (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). David Bentley collaborates with scholars based in United Kingdom, United States and Sweden. David Bentley's co-authors include Haig Keshishian, Panos Deloukas, Sarah Hunt, Martin Bobrow, Ronald R. Hoy, Gil McVean, Carlos Caldas, Tim Forshew, Nitzan Rosenfeld and Dana W.Y. Tsui and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

David Bentley

126 papers receiving 11.9k citations

Hit Papers

5 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.

Analysis of Circulating Tumor DNA to Monitor Metastatic Breast Cancer

2013 1.6k citations Sean Humphray, David Bentley et al. profile →
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

1993 1.1k citations David Vetrie, Igor Vořechovský et al. profile →
Noninvasive Identification and Monitoring of Cancer Mutations by Targeted Deep Sequencing of Plasma DNA

2012 975 citations David Bentley et al. profile →
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome

2004 707 citations Gil McVean, Sarah Hunt et al. profile →
Whole-genome re-sequencing

2006 538 citations David Bentley profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Bentley United Kingdom	52	5.1k	2.9k	2.7k	2.3k	1.7k	131	12.3k
Stanley F. Nelson United States	72	11.0k 2.1×	3.8k 1.3×	2.2k 0.8×	1.4k 0.6×	1.0k 0.6×	208	18.8k
William D. Richardson United Kingdom	80	13.4k 2.6×	2.6k 0.9×	3.5k 1.3×	5.3k 2.3×	1.7k 1.0×	165	25.0k
Nadia Rosenthal United States	74	13.5k 2.6×	2.1k 0.7×	1.2k 0.4×	1.4k 0.6×	2.0k 1.2×	239	20.7k
André Rosenthal Germany	52	6.6k 1.3×	2.1k 0.7×	1.2k 0.5×	999 0.4×	871 0.5×	139	10.1k
Kāri Stefánsson Iceland	80	6.5k 1.3×	6.1k 2.1×	920 0.3×	1.5k 0.7×	1.5k 0.9×	246	17.8k
Han G. Brunner Netherlands	65	11.9k 2.3×	9.2k 3.2×	1.3k 0.5×	1.6k 0.7×	1.4k 0.8×	278	20.9k
John D. McPherson United States	52	6.7k 1.3×	2.2k 0.8×	1.8k 0.7×	539 0.2×	854 0.5×	145	11.4k
David Fitzpatrick United Kingdom	65	6.9k 1.4×	5.4k 1.9×	894 0.3×	812 0.4×	2.6k 1.5×	271	14.3k
Samuel Aparício Canada	63	11.1k 2.2×	3.4k 1.2×	3.7k 1.4×	937 0.4×	887 0.5×	168	17.2k
Jonathan A. Epstein United States	92	17.1k 3.4×	3.1k 1.1×	1.9k 0.7×	1.9k 0.8×	1.3k 0.8×	263	23.9k

Countries citing papers authored by David Bentley

Since Specialization

Citations

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

Fields of papers citing papers by David Bentley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Bentley

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Ryan, Sarra, John F. Peden, Zoya Kingsbury, et al.. (2023). Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia. Leukemia. 37(3). 518–528. 41 indexed citations

Shen, Fei, Nina Gonzaludo, Alka Malhotra, et al.. (2021). Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data. The Pharmacogenomics Journal. 21(2). 251–261. 54 indexed citations

Sanchis‐Juan, Alba, Courtney E. French, Isabelle Delon, et al.. (2020). Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data. Genetics in Medicine. 22(5). 945–953. 79 indexed citations

Dolzhenko, Egor, Mark F. Bennett, Phillip A. Richmond, et al.. (2020). ExpansionHunter Denovo: a computational method for locating known and novel repeat expansions in short-read sequencing data. Genome biology. 21(1). 102–102. 95 indexed citations

Ross, Mark T., David Bentley, Margarida Mendes Lopes, et al.. (2018). Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in PAX6 in a South African family.. PubMed. 24. 407–413. 19 indexed citations

Eberle, Michael A., Epameinondas Fritzilas, Peter Krusche, et al.. (2016). A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree. Genome Research. 27(1). 157–164. 220 indexed citations

Vetrie, David, Igor Vořechovský, Paschalis Sideras, et al.. (2012). Pillars Article: The Gene Involved in X-linked Agammaglobulinaemia Is a Member of the Src Family of Protein-Tyrosine Kinases. Nature. 1993. 361: 226–233. The Journal of Immunology. 188(7). 2948–2955. 2 indexed citations

Leschziner, Guy, Alison J. Coffey, Toby Andrew, et al.. (2011). Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS). Epilepsy Research. 96(1-2). 109–115. 15 indexed citations

Bentley, David & Brenda Murphy. (2006). Power, Praxis and the Métis of Kelly Lake, Canada. 26(2). 289. 2 indexed citations

10.

Dawson, Elisabeth, Yuan Chen, Sarah Hunt, et al.. (2001). A SNP Resource for Human Chromosome 22: Extracting Dense Clusters of SNPs From the Genomic Sequence. Genome Research. 11(1). 170–178. 59 indexed citations

11.

Göttgens, Berthold, Linda Barton, James Gilbert, et al.. (2000). Analysis of vertebrate SCL loci identifies conserved enhancers. Nature Biotechnology. 18(2). 181–186. 151 indexed citations

12.

Bentley, David, Kim D. Pruitt, Panos Deloukas, Greg Schuler, & Jim Ostell. (1998). Coordination of human genome sequencing via a consensus framework map. Trends in Genetics. 14(10). 381–384. 9 indexed citations

13.

Bentley, David & Timothy P. O’Connor. (1994). Cytoskeletal events in growth cone steering. Current Opinion in Neurobiology. 4(1). 43–48. 156 indexed citations

14.

Bentley, David, et al.. (1992). Project Management: Keys to Success. Civil engineering. 62(4). 58–59. 12 indexed citations

15.

Cole, Charlotte G., Ketan Patel, Janet Shipley, et al.. (1992). Identification of region-specific yeast artificial chromosomes using pools of Alu element-mediated polymerase chain reaction probes labeled via linear amplification. Genomics. 14(4). 931–938. 6 indexed citations

16.

Flomen, Rachel, et al.. (1992). Detection of point mutations and a gross deletion in six Hunter Syndrome patients. Genomics. 13(3). 543–550. 56 indexed citations

17.

Green, Peter M., et al.. (1990). The incidence and distribution of CpG←Tpg transitions in the coagulation factor IX gene. A fresh look at CPG mutitional hospots. Nucleic Acids Research. 18(11). 3227–3231. 69 indexed citations

18.

Lefcort, Frances, et al.. (1989). Selective recognition between embryonic afferent neurons of grasshopper appendages in vitro. Developmental Biology. 135(2). 221–230. 5 indexed citations

19.

Bentley, David, et al.. (1989). Pre‐axonogenesis migration of afferent pioneer cells in the grasshopper embryo. Journal of Experimental Zoology. 251(2). 217–223. 5 indexed citations

20.

Bentley, David, et al.. (1964). The Atmospheric Pressure Wave Generated by a Nuclear Explosion.. PhDT. 1 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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