David J. McBride

17.2k total citations
12 papers, 835 citations indexed

About

David J. McBride is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, David J. McBride has authored 12 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in David J. McBride's work include Genomic variations and chromosomal abnormalities (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genomics and Chromatin Dynamics (2 papers). David J. McBride is often cited by papers focused on Genomic variations and chromosomal abnormalities (2 papers), Cancer Genomics and Diagnostics (2 papers) and Genomics and Chromatin Dynamics (2 papers). David J. McBride collaborates with scholars based in United Kingdom, United States and Australia. David J. McBride's co-authors include Jay R. Shapiro, Alan R. Shuldiner, Richard Wenstrup, Muriel T. Davisson, S. C. Marks, Stewart D. Chipman, David W. Rowe, Michael G. Dunn, Mark T. Ross and Zoya Kingsbury and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

David J. McBride

12 papers receiving 825 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David J. McBride United Kingdom	9	343	306	284	151	149	12	835
Francesco Albano Italy	25	771 2.2×	122 0.4×	279 1.0×	238 1.6×	236 1.6×	140	1.8k
Barbara Bernasconi Italy	21	441 1.3×	127 0.4×	192 0.7×	251 1.7×	418 2.8×	47	1.1k
Azim Mohamedali United Kingdom	18	499 1.5×	165 0.5×	208 0.7×	164 1.1×	160 1.1×	37	1.4k
Luisa Anelli Italy	23	563 1.6×	121 0.4×	260 0.9×	161 1.1×	149 1.0×	87	1.3k
Antonella Zagaria Italy	23	504 1.5×	117 0.4×	242 0.9×	146 1.0×	132 0.9×	80	1.2k
Yuka Harada Japan	23	1.0k 3.0×	131 0.4×	229 0.8×	111 0.7×	203 1.4×	106	2.0k
D Arthur United States	19	785 2.3×	192 0.6×	127 0.4×	171 1.1×	212 1.4×	29	2.0k
Remco M. Hoogenboezem Netherlands	20	530 1.5×	99 0.3×	141 0.5×	47 0.3×	225 1.5×	51	1.2k
Nathalie Douet‐Guilbert France	23	703 2.0×	629 2.1×	124 0.4×	147 1.0×	122 0.8×	109	1.8k
Bartlomiej Przychodzen United States	20	834 2.4×	122 0.4×	177 0.6×	217 1.4×	144 1.0×	105	1.7k

Countries citing papers authored by David J. McBride

Since Specialization

Citations

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

Fields of papers citing papers by David J. McBride

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David J. McBride

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

All Works

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12 of 12 papers shown

Berri, Stefano, John F. Peden, Claire Fielding, et al.. (2025). A dedicated caller for DUX4 rearrangements from whole-genome sequencing data. BMC Medical Genomics. 18(1). 24–24. 1 indexed citations

McBride, David J., Claire Fielding, Alexandra Vatsiou, et al.. (2023). Whole-Genome Sequencing Can Identify Clinically Relevant Variants from a Single Sub-Punch of a Dried Blood Spot Specimen. International Journal of Neonatal Screening. 9(3). 52–52. 4 indexed citations

Lau, Edmund, Fairleigh Reeves, Ken Chow, et al.. (2020). Detection of ctDNA in plasma of patients with clinically localised prostate cancer is associated with rapid disease progression. Genome Medicine. 12(1). 72–72. 42 indexed citations

Graymore, Michelle & David J. McBride. (2013). Socio-ecological value of wetlands: the dilemma of balancing human and ecological water needs. Australasian Journal of Environmental Management. 20(3). 225–241. 9 indexed citations

Schuh, Anna, Jennifer Becq, Sean Humphray, et al.. (2012). Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns. Blood. 120(20). 4191–4196. 214 indexed citations

McBride, David J., Adam Buckle, Veronica van Heyningen, & Dirk A. Kleinjan. (2011). DNaseI Hypersensitivity and Ultraconservation Reveal Novel, Interdependent Long-Range Enhancers at the Complex Pax6 Cis-Regulatory Region. PLoS ONE. 6(12). e28616–e28616. 45 indexed citations

McBride, David J., Arto Orpana, Christos Sotiriou, et al.. (2010). Use of cancer‐specific genomic rearrangements to quantify disease burden in plasma from patients with solid tumors. Genes Chromosomes and Cancer. 49(11). 1062–1069. 151 indexed citations

Streeten, Elizabeth A., Thomas Beck, Jeffery R. O’Connell, et al.. (2008). Autosome-wide linkage analysis of hip structural phenotypes in the Old Order Amish. Bone. 43(3). 607–612. 8 indexed citations

Burton, Peter, David J. McBride, Jonathan Wilkes, J. David Barry, & Richard McCulloch. (2007). Ku Heterodimer-Independent End Joining inTrypanosoma bruceiCell Extracts Relies upon Sequence Microhomology. Eukaryotic Cell. 6(10). 1773–1781. 49 indexed citations

10.

McBride, David J.. (2004). Rounding up active cis-elements in the triple C corral: Combining conservation, cleavage and conformation capture for the analysis of regulatory gene domains. Briefings in Functional Genomics and Proteomics. 3(3). 267–279. 4 indexed citations

11.

McBride, David J., Jay R. Shapiro, & Michael G. Dunn. (1998). Bone Geometry and Strength Measurements in Aging Mice with the oim Mutation. Calcified Tissue International. 62(2). 172–176. 51 indexed citations

12.

Chipman, Stewart D., David J. McBride, Muriel T. Davisson, et al.. (1993). Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta.. Proceedings of the National Academy of Sciences. 90(5). 1701–1705. 257 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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