Brett Copeland

2.2k total citations
6 papers, 351 citations indexed

About

Brett Copeland is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Brett Copeland has authored 6 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Nephrology. Recurrent topics in Brett Copeland's work include Genomics and Rare Diseases (3 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Phylogenetic Studies (2 papers). Brett Copeland is often cited by papers focused on Genomics and Rare Diseases (3 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Phylogenetic Studies (2 papers). Brett Copeland collaborates with scholars based in United States, Australia and Italy. Brett Copeland's co-authors include David B. Goldstein, Ryan S. Dhindsa, Andrew S. Allen, Ayal B. Gussow, William H. Majoros, Quanli Wang, Slavé Petrovski, Anthony M. Mustoe, Alicia Guemez‐Gamboa and Gary W. Mathern and has published in prestigious journals such as Nature Medicine, Annals of Internal Medicine and PLoS ONE.

In The Last Decade

Brett Copeland

6 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brett Copeland United States	6	175	136	35	22	21	6	351
Mélanie Fradin France	10	170 1.0×	149 1.1×	14 0.4×	76 3.5×	10 0.5×	23	334
Angela J. Churchill United States	6	380 2.2×	115 0.8×	30 0.9×	6 0.3×	15 0.7×	6	500
David Mansfield United Kingdom	9	324 1.9×	176 1.3×	21 0.6×	6 0.3×	42 2.0×	25	541
Roberta Caccia Italy	11	272 1.6×	86 0.6×	5 0.1×	12 0.5×	10 0.5×	12	381
Xiaomeng Yang China	11	172 1.0×	76 0.6×	6 0.2×	6 0.3×	47 2.2×	43	356
Ranga N. Parthasarathy United States	12	198 1.1×	85 0.6×	4 0.1×	22 1.0×	35 1.7×	21	439
Patrícia Maria Abreu Machado Brazil	10	86 0.5×	98 0.7×	4 0.1×	29 1.3×	10 0.5×	31	339
Qian Pan China	10	298 1.7×	86 0.6×	3 0.1×	24 1.1×	11 0.5×	56	485
Verayuth Praphanphoj Thailand	12	181 1.0×	138 1.0×	3 0.1×	28 1.3×	35 1.7×	20	328

Countries citing papers authored by Brett Copeland

Since Specialization

Citations

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

Fields of papers citing papers by Brett Copeland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brett Copeland

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

All Works

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6 of 6 papers shown

1.

Dhindsa, Ryan S., Brett Copeland, Anthony M. Mustoe, & David B. Goldstein. (2020). Natural Selection Shapes Codon Usage in the Human Genome. The American Journal of Human Genetics. 107(1). 83–95. 41 indexed citations

2.

Hayeck, Tristan J., Nicholas Stong, Charles J. Wolock, et al.. (2019). Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance. The American Journal of Human Genetics. 104(2). 299–309. 21 indexed citations

3.

Rasouly, Hila Milo, Emily Groopman, David Fasel, et al.. (2018). The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing. Annals of Internal Medicine. 170(1). 11–21. 46 indexed citations

4.

Gussow, Ayal B., Brett Copeland, Ryan S. Dhindsa, et al.. (2017). Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics. PLoS ONE. 12(8). e0181604–e0181604. 135 indexed citations

5.

Zhu, Xiaolin, Brett Copeland, Joshua Bridgers, et al.. (2017). A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations. PLoS Genetics. 13(11). e1007104–e1007104. 17 indexed citations

6.

Baek, Seung Tae, Brett Copeland, Eun-Jin Yun, et al.. (2015). An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development. Nature Medicine. 21(12). 1445–1454. 91 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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