Barry Moore

6.6k total citations · 2 hit papers
36 papers, 2.9k citations indexed

About

Barry Moore is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Barry Moore has authored 36 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Barry Moore's work include Genomics and Phylogenetic Studies (11 papers), Genomics and Rare Diseases (10 papers) and RNA and protein synthesis mechanisms (7 papers). Barry Moore is often cited by papers focused on Genomics and Phylogenetic Studies (11 papers), Genomics and Rare Diseases (10 papers) and RNA and protein synthesis mechanisms (7 papers). Barry Moore collaborates with scholars based in United States, Poland and United Kingdom. Barry Moore's co-authors include Mark Yandell, Carson Holt, Genı́s Parra, Sofia Robb, Eric Ross, Ian Korf, Alejandro Sánchez Alvarado, Brandi L. Cantarel, Michael S. Campbell and Martin G. Reese and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Barry Moore

34 papers receiving 2.9k 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.

MAKER: An easy-to-use annotation pipeline designed for emerging model organism genomes

2007 1.3k citations Brandi L. Cantarel, Ian Korf et al. Genome Research profile →
Genome Annotation and Curation Using MAKER and MAKER‐P

2014 451 citations Michael S. Campbell, Carson Holt et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Barry Moore United States	21	1.8k	881	825	271	227	36	2.9k
Maja Tarailo‐Graovac Canada	20	2.1k 1.2×	1.1k 1.2×	945 1.1×	234 0.9×	206 0.9×	58	3.3k
Harm Nijveen Netherlands	20	1.7k 1.0×	1.4k 1.5×	734 0.9×	299 1.1×	265 1.2×	54	3.7k
Robert Vaser Croatia	5	1.8k 1.0×	761 0.9×	667 0.8×	481 1.8×	136 0.6×	10	2.9k
Rémy Bruggmann Switzerland	37	1.6k 0.9×	816 0.9×	799 1.0×	246 0.9×	211 0.9×	116	3.9k
Matthew A. Campbell United States	26	1.8k 1.0×	1.6k 1.8×	790 1.0×	263 1.0×	266 1.2×	81	3.4k
Terence D. Murphy United States	20	1.9k 1.1×	731 0.8×	495 0.6×	193 0.7×	131 0.6×	41	2.7k
Maria Nattestad United States	11	2.7k 1.5×	1.6k 1.8×	1.1k 1.3×	444 1.6×	280 1.2×	17	3.9k
Weidong Bao United States	15	2.1k 1.2×	1.6k 1.8×	643 0.8×	254 0.9×	246 1.1×	25	3.0k
Răzvan Sultana United States	18	1.9k 1.1×	813 0.9×	595 0.7×	236 0.9×	156 0.7×	23	3.2k

Countries citing papers authored by Barry Moore

Since Specialization

Citations

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

Fields of papers citing papers by Barry Moore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barry Moore

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

Peterson, Bennet, Edgar J. Hernández, Charlotte A. Hobbs, et al.. (2023). Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning. Genome Medicine. 15(1). 18–18. 10 indexed citations

Wen, Ting, Andrew Farrell, Rong Mao, et al.. (2022). Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome. Molecular Case Studies. 8(7). a006242–a006242. 5 indexed citations

Simeone, Christopher A., Joseph L. Wilkerson, Annelise M. Poss, et al.. (2022). A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia. npj Genomic Medicine. 7(1). 43–43. 11 indexed citations

Farrell, Andrew, Julia Wynn, Barry Moore, et al.. (2020). Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias. SHILAP Revista de lepidopterología. 1(1). 100008–100008. 5 indexed citations

Flygare, Steven, Edgar J. Hernández, Lon Phan, et al.. (2018). The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool. BMC Bioinformatics. 19(1). 57–57. 25 indexed citations

Al-Agha, Abdulmoein Eid, Esther Nuebel, Barry Moore, et al.. (2017). Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation. The Journal of Clinical Endocrinology & Metabolism. 103(2). 555–563. 44 indexed citations

Cunningham, Fiona, et al.. (2015). Improving the Sequence Ontology terminology for genomic variant annotation. Journal of Biomedical Semantics. 6(1). 32–32. 20 indexed citations

Manuck, Tracy A., W. Scott Watkins, Barry Moore, et al.. (2014). Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth prevention. American Journal of Obstetrics and Gynecology. 210(4). 321.e1–321.e21. 24 indexed citations

Flygare, Steven, et al.. (2013). ImagePlane: An Automated Image Analysis Pipeline for High-Throughput Screens Using the Planarian Schmidtea mediterranea. Journal of Computational Biology. 20(8). 583–592. 1 indexed citations

10.

Moore, Barry, et al.. (2012). Using GVF for Clinical Annotation of Personal Genomes..

11.

Lluisma, Arturo O., Brett Milash, Barry Moore, Baldomero M. Olivera, & Pradip K. Bandyopadhyay. (2012). Novel venom peptides from the cone snail Conus pulicarius discovered through next-generation sequencing of its venom duct transcriptome. Marine Genomics. 5. 43–51. 55 indexed citations

12.

Yandell, Mark, Chad Huff, Hao Hu, et al.. (2011). A probabilistic disease-gene finder for personal genomes. Genome Research. 21(9). 1529–1542. 138 indexed citations

13.

Moore, Barry, Gaofeng Fan, & Karen Eilbeck. (2010). SOBA: sequence ontology bioinformatics analysis. Nucleic Acids Research. 38(Web Server). W161–W164. 6 indexed citations

14.

Reese, Martin G., Barry Moore, Colin Batchelor, et al.. (2010). A standard variation file format for human genome sequences. Genome biology. 11(8). R88–R88. 61 indexed citations

15.

Eilbeck, Karen, Barry Moore, Carson Holt, & Mark Yandell. (2009). Quantitative measures for the management and comparison of annotated genomes. BMC Bioinformatics. 10(1). 67–67. 96 indexed citations

16.

Cantarel, Brandi L., Ian Korf, Sofia Robb, et al.. (2007). MAKER: An easy-to-use annotation pipeline designed for emerging model organism genomes. Genome Research. 18(1). 188–196. 1257 indexed citations breakdown →

17.

Matveeva, O. V., Yury D. Nechipurenko, Leonardo Rossi, et al.. (2007). Comparison of approaches for rational siRNA design leading to a new efficient and transparent method. Nucleic Acids Research. 35(8). e63–e63. 116 indexed citations

18.

Wills, Norma M., et al.. (2006). A Functional –1 Ribosomal Frameshift Signal in the Human Paraneoplastic Ma3 Gene. Journal of Biological Chemistry. 281(11). 7082–7088. 66 indexed citations

19.

Moore, Barry, Britt C. Persson, Chad Nelson, Raymond F. Gesteland, & John F. Atkins. (2000). Quadruplet codons: implications for code expansion and the specification of translation step size. Journal of Molecular Biology. 298(2). 195–209. 54 indexed citations

20.

Moore, Barry. (2000). Decoding of tandem quadruplets by adjacent tRNAs with eight-base anticodon loops. Nucleic Acids Research. 28(18). 3615–3624. 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.

Explore authors with similar magnitude of impact