Radoje Drmanac

7.2k total citations · 2 hit papers
50 papers, 2.7k citations indexed

About

Radoje Drmanac is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Radoje Drmanac has authored 50 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Plant Science. Recurrent topics in Radoje Drmanac's work include Genomics and Phylogenetic Studies (15 papers), RNA and protein synthesis mechanisms (11 papers) and Genomics and Rare Diseases (10 papers). Radoje Drmanac is often cited by papers focused on Genomics and Phylogenetic Studies (15 papers), RNA and protein synthesis mechanisms (11 papers) and Genomics and Rare Diseases (10 papers). Radoje Drmanac collaborates with scholars based in China, United States and United Kingdom. Radoje Drmanac's co-authors include Leroy Hood, Snezana Drmanac, Ivan Labat, Krishna Prasad Pant, Radomir Crkvenjakov, Gustavo Glusman, Chad D. Huff, Lynn B. Jorde, Jay Shendure and Lee Rowen and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Radoje Drmanac

48 papers receiving 2.6k 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.

Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing

2010 722 citations Jared C. Roach, Gustavo Glusman et al. Science profile →
Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

2014 388 citations Radoje Drmanac et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Radoje Drmanac China	20	1.7k	1.0k	305	295	163	50	2.7k
Adam Ameur Sweden	32	2.4k 1.4×	738 0.7×	485 1.6×	264 0.9×	124 0.8×	96	3.7k
Robert J. Lipshutz United States	11	3.0k 1.8×	1.2k 1.1×	228 0.7×	267 0.9×	288 1.8×	14	4.3k
Liuda Ziaugra United States	6	2.0k 1.2×	964 0.9×	236 0.8×	261 0.9×	196 1.2×	8	3.8k
Erin N. Smith United States	26	1.9k 1.1×	1.0k 1.0×	238 0.8×	248 0.8×	63 0.4×	60	2.9k
Jessica Severin Japan	17	2.0k 1.2×	661 0.6×	219 0.7×	296 1.0×	81 0.5×	25	2.8k
Zheng Li China	36	2.0k 1.2×	652 0.6×	335 1.1×	310 1.1×	101 0.6×	185	3.5k
John A. Capra United States	33	3.8k 2.3×	918 0.9×	267 0.9×	398 1.3×	48 0.3×	111	4.9k
Zhenglong Gu United States	29	2.9k 1.7×	923 0.9×	243 0.8×	1.0k 3.5×	83 0.5×	101	4.0k
Marian M. de Pancorbo Spain	26	1.1k 0.7×	1.2k 1.1×	203 0.7×	77 0.3×	113 0.7×	209	2.6k

Countries citing papers authored by Radoje Drmanac

Since Specialization

Citations

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

Fields of papers citing papers by Radoje Drmanac

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Radoje Drmanac

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

All Works

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20 of 20 papers shown

Drmanac, Radoje. (2023). Methods and compositions for efficient nucleic acid sequencing. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information).

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

Chen, Ying, Hui Wang, Jin Min Yang, et al.. (2021). Reusable and sensitive exonuclease III activity detection on DNB nanoarrays based on cPAS sequencing technology. Enzyme and Microbial Technology. 150. 109878–109878. 3 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

Mu, Weixue, Jinpu Wei, Ting Yang, et al.. (2020). The draft genome assembly of the critically endangered Nyssa yunnanensis, a plant species with extremely small populations endemic to Yunnan Province, China. SHILAP Revista de lepidopterología. 2020. 1–12. 4 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

Patterson, Jordan, Eric Carpenter, Zhenzhen Zhu, et al.. (2019). Impact of sequencing depth and technology on de novo RNA-Seq assembly. BMC Genomics. 20(1). 604–604. 45 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.

Drmanac, Radoje. (2012). The Ultimate Genetic Test. Science. 336(6085). 1110–1112. 24 indexed citations

15.

Carnevali, P., Aaron L. Halpern, Geoffrey B. Nilsen, et al.. (2011). Computational Techniques for Human Genome Resequencing Using Mated Gapped Reads. Journal of Computational Biology. 19(3). 279–292. 57 indexed citations

16.

Roach, Jared C., Gustavo Glusman, Arian F. A. Smit, et al.. (2010). Analysis of Genetic Inheritance in a Family Quartet by Whole-Genome Sequencing. Science. 328(5978). 636–639. 722 indexed citations breakdown →

17.

Schirinzi, Annalisa, Snezana Drmanac, Bruno Dallapiccola, et al.. (2006). Combinatorial Sequencing-by-Hybridization: Analysis of the NF1 Gene. Genetic Testing. 10(1). 8–17. 5 indexed citations

18.

Cowie, Shannon, Snezana Drmanac, Donald A. Swanson, et al.. (2004). Identification ofAPCgene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization. Human Mutation. 24(3). 261–271. 14 indexed citations

19.

Drmanac, Radoje, Ivan Labat, & Radomir Crkvenjakov. (1991). An Algorithm for the DNA Sequence Generation from k-Tuple Word Contents of the Minimal Number of Random Fragments. Journal of Biomolecular Structure and Dynamics. 8(5). 1085–1102. 18 indexed citations

20.

Drmanac, Radoje, Žaklina Strezoska, Ivan Labat, Snezana Drmanac, & Radomir Crkvenjakov. (1990). Reliable Hybridization of Oligonucleotides as Short as Six Nucleotides. DNA and Cell Biology. 9(7). 527–534. 49 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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