Brock A. Peters

8.0k total citations · 1 hit paper
37 papers, 2.7k citations indexed

About

Brock A. Peters is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Brock A. Peters has authored 37 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 15 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Brock A. Peters's work include Genomics and Phylogenetic Studies (11 papers), Genomics and Rare Diseases (9 papers) and Genomic variations and chromosomal abnormalities (7 papers). Brock A. Peters is often cited by papers focused on Genomics and Phylogenetic Studies (11 papers), Genomics and Rare Diseases (9 papers) and Genomic variations and chromosomal abnormalities (7 papers). Brock A. Peters collaborates with scholars based in China, United States and United Kingdom. Brock A. Peters's co-authors include Janine Ptak, Victor E. Velculescu, Natalie Silliman, Steve Szabo, Kenneth W. Kinzler, Bert Vogelstein, Radoje Drmanac, Pedram Argani, Kurtis E. Bachman and Hiroyuki Konishi and has published in prestigious journals such as Science, Nucleic Acids Research and Nature Medicine.

In The Last Decade

Brock A. Peters

36 papers receiving 2.7k citations

Hit Papers

align trajectories sort by overperformance

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.

The PIK3CA gene is mutated with high frequency in human breast cancers

2004 519 citations Kurtis E. Bachman, Pedram Argani et al. Cancer Biology & Therapy profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Brock A. Peters China	16	2.0k	690	686	535	273	37	2.7k
Howard H. Yang United States	28	2.1k 1.1×	641 0.9×	562 0.8×	484 0.9×	293 1.1×	81	2.9k
Subhajyoti De United States	33	2.6k 1.3×	1.1k 1.6×	676 1.0×	712 1.3×	224 0.8×	89	3.8k
Lluís Morey United States	26	4.1k 2.0×	684 1.0×	436 0.6×	595 1.1×	222 0.8×	41	4.6k
Roslin Russell United Kingdom	22	1.5k 0.8×	645 0.9×	977 1.4×	469 0.9×	216 0.8×	30	2.7k
Xiaole Shirley Liu United States	19	2.6k 1.3×	802 1.2×	593 0.9×	445 0.8×	229 0.8×	25	3.3k
Jakob Lovén United States	15	2.5k 1.3×	636 0.9×	435 0.6×	365 0.7×	113 0.4×	17	3.1k
Bernat Gel Spain	22	1.6k 0.8×	965 1.4×	319 0.5×	364 0.7×	229 0.8×	48	2.4k
Matthew N. Bainbridge United States	30	2.4k 1.2×	595 0.9×	279 0.4×	1.3k 2.5×	206 0.8×	62	3.8k
Dirce Maria Carraro Brazil	33	1.8k 0.9×	1.0k 1.5×	929 1.4×	585 1.1×	435 1.6×	188	3.4k
Véronique Voisin Canada	21	1.8k 0.9×	655 0.9×	500 0.7×	172 0.3×	244 0.9×	46	2.9k

Countries citing papers authored by Brock A. Peters

Since Specialization

Citations

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

Fields of papers citing papers by Brock A. Peters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Brock A. Peters. 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 Brock A. Peters. The network helps show where Brock A. Peters may publish in the future.

Co-authorship network of co-authors of Brock A. Peters

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

McElwain, Mark A. & Brock A. Peters. (2022). Accurate Sequencing and Haplotyping from 10 Cells Using Long Fragment Read (LFR) Technology. Methods in molecular biology. 2590. 71–84. 1 indexed citations

Wang, Ou, Xiaofang Cheng, Radoje Drmanac, & Brock A. Peters. (2022). A Simple Cost-Effective Method for Whole-Genome Sequencing, Haplotyping, and Assembly. Methods in molecular biology. 2590. 101–125. 3 indexed citations

Hong, Jiaxu, Xiaoqing Liu, Hao Gu, et al.. (2021). A Novel Hierarchical Deep Learning Framework for Diagnosing Multiple Visual Impairment Diseases in the Clinical Environment. Frontiers in Medicine. 8. 654696–654696. 8 indexed citations

Weng, Jiancong, Tian Chen, Yinlong Xie, et al.. (2020). IterCluster: a barcode clustering algorithm for long fragment read analysis. PeerJ. 8. e8431–e8431. 1 indexed citations

Murigneux, Valentine, Agnelo Furtado, Timothy J. C. Bruxner, et al.. (2020). Comparison of long-read methods for sequencing and assembly of a plant genome. GigaScience. 9(12). 67 indexed citations

Leng, Lizhi, Jiya Sun, Jinrong Huang, et al.. (2019). Single-Cell Transcriptome Analysis of Uniparental Embryos Reveals Parent-of-Origin Effects on Human Preimplantation Development. Cell stem cell. 25(5). 697–712.e6. 70 indexed citations

Liu, Chuanyu, Mingyue Wang, Xiaoyu Wei, et al.. (2019). An ATAC-seq atlas of chromatin accessibility in mouse tissues. Scientific Data. 6(1). 65–65. 67 indexed citations

Mao, Qing, Robert Chin, Weiwei Xie, et al.. (2018). Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid. Clinical Chemistry. 64(4). 715–725. 9 indexed citations

McElwain, Mark A., Rebecca Yu Zhang, Radoje Drmanac, & Brock A. Peters. (2017). Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping. Methods in molecular biology. 1551. 191–205. 4 indexed citations

10.

Walker, Richard F., Qing Mao, Robert Chin, et al.. (2017). Clinical and genetic analysis of a rare syndrome associated with neoteny. Genetics in Medicine. 20(5). 495–502. 4 indexed citations

11.

Mao, Qing, Rebecca Yu Zhang, Mad Price Ball, et al.. (2016). The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes. GigaScience. 5(1). 42–42. 12 indexed citations

12.

Peters, Brock A., Bahram G. Kermani, Misha R. Agarwal, et al.. (2015). Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing. Genome Research. 25(3). 426–434. 37 indexed citations

13.

Schaaf, Christian P., Manuel L. Gonzalez‐Garay, Fan Xia, et al.. (2013). Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism. Nature Genetics. 45(11). 1405–1408. 210 indexed citations

14.

Hu, Xiaolan, Howard M. Stern, Lin Ge, et al.. (2009). Genetic Alterations and Oncogenic Pathways Associated with Breast Cancer Subtypes. Molecular Cancer Research. 7(4). 511–522. 177 indexed citations

15.

Kaminker, Joshua S., Yan Zhang, Peter M. Haverty, et al.. (2007). Distinguishing Cancer-Associated Missense Mutations from Common Polymorphisms. Cancer Research. 67(2). 465–473. 104 indexed citations

16.

Peters, Brock A., Brad St. Croix, Tobias Sjöblom, et al.. (2007). Large-scale identification of novel transcripts in the human genome. Genome Research. 17(3). 287–292. 14 indexed citations

17.

Peters, Brock A., Luis A. Díaz, Kornélia Polyák, et al.. (2005). Contribution of bone marrow–derived endothelial cells to human tumor vasculature. Nature Medicine. 11(3). 261–262. 377 indexed citations

18.

Wang, Zhenghe, Dong Shen, D. Williams Parsons, et al.. (2004). Mutational Analysis of the Tyrosine Phosphatome in Colorectal Cancers. Science. 304(5674). 1164–1166. 412 indexed citations

19.

Bachman, Kurtis E., Pedram Argani, Yardena Samuels, et al.. (2004). The PIK3CA gene is mutated with high frequency in human breast cancers. Cancer Biology & Therapy. 3(8). 772–775. 519 indexed citations breakdown →

20.

Holland, Elizabeth A., Therese M. Becker, Brock A. Peters, et al.. (1995). Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds.. PubMed. 11(11). 2289–94. 87 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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