B. Czech

9.9k total citations · 6 hit papers
53 papers, 5.8k citations indexed

About

B. Czech is a scholar working on Molecular Biology, Plant Science and Nuclear and High Energy Physics. According to data from OpenAlex, B. Czech has authored 53 papers receiving a total of 5.8k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 23 papers in Plant Science and 21 papers in Nuclear and High Energy Physics. Recurrent topics in B. Czech's work include Nuclear physics research studies (20 papers), Chromosomal and Genetic Variations (20 papers) and CRISPR and Genetic Engineering (15 papers). B. Czech is often cited by papers focused on Nuclear physics research studies (20 papers), Chromosomal and Genetic Variations (20 papers) and CRISPR and Genetic Engineering (15 papers). B. Czech collaborates with scholars based in United States, Poland and Ukraine. B. Czech's co-authors include Gregory J. Hannon, Detlef Weigel, Jiawei Wang, Norbert Perrimon, Julius Brennecke, Rui Zhou, Jonathan Preall, Erica Mica, Rebecca Schwab and Marzia Munafò and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

B. Czech

52 papers receiving 5.8k citations

Hit Papers

miR156-Regulated SPL Transcription Factors Define an Endo... 2008 2026 2014 2020 2009 2011 2008 2010 2018 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Czech United States 25 4.5k 3.2k 906 433 292 53 5.8k
Asifa Akhtar Germany 45 7.1k 1.6× 1.1k 0.4× 1.3k 1.5× 1.3k 3.0× 484 1.7× 92 8.0k
M. Mar Albà Spain 39 4.0k 0.9× 942 0.3× 727 0.8× 850 2.0× 521 1.8× 80 5.7k
Brenda Bass United States 44 7.2k 1.6× 679 0.2× 963 1.1× 328 0.8× 608 2.1× 87 8.2k
Yukihide Tomari Japan 47 9.8k 2.2× 2.4k 0.7× 3.9k 4.3× 824 1.9× 687 2.4× 98 11.3k
Todd Richmond United States 39 5.4k 1.2× 4.0k 1.2× 476 0.5× 2.3k 5.4× 175 0.6× 69 8.5k
Prim B. Singh United Kingdom 45 5.5k 1.2× 1.4k 0.4× 254 0.3× 1.1k 2.6× 424 1.5× 115 6.6k
Marjori Matzke Austria 60 10.5k 2.3× 10.7k 3.3× 1.4k 1.6× 1.3k 3.0× 264 0.9× 141 15.4k
Manyuan Long United States 48 5.8k 1.3× 3.4k 1.0× 305 0.3× 2.6k 6.0× 359 1.2× 132 8.0k
Thomas R. Bürglin Sweden 37 3.8k 0.8× 1.2k 0.4× 326 0.4× 816 1.9× 200 0.7× 71 5.2k
Shintaro Iwasaki Japan 36 3.8k 0.8× 687 0.2× 986 1.1× 237 0.5× 228 0.8× 154 5.3k

Countries citing papers authored by B. Czech

Since Specialization
Citations

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

Fields of papers citing papers by B. Czech

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Czech

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

All Works

20 of 20 papers shown
1.
Bornelöv, Susanne, B. Czech, & Gregory J. Hannon. (2022). An evolutionarily conserved stop codon enrichment at the 5′ ends of mammalian piRNAs. Nature Communications. 13(1). 2118–2118. 5 indexed citations
2.
Eastwood, Evelyn L., Susanne Bornelöv, Marzia Munafò, et al.. (2021). Dimerisation of the PICTS complex via LC8/Cut-up drives co-transcriptional transposon silencing in Drosophila. eLife. 10. 30 indexed citations
3.
Munafò, Marzia, Alessandro Passera, Susanne Bornelöv, et al.. (2021). Channel nuclear pore complex subunits are required for transposon silencing in Drosophila. eLife. 10. 19 indexed citations
4.
Kneuss, Emma, Marzia Munafò, Evelyn L. Eastwood, et al.. (2019). Specialization of the Drosophila nuclear export family protein Nxf3 for piRNA precursor export. Genes & Development. 33(17-18). 1208–1220. 42 indexed citations
5.
Munafò, Marzia, Ashley Sawle, Emma Kneuss, et al.. (2019). Daedalus and Gasz recruit Armitage to mitochondria, bringing piRNA precursors to the biogenesis machinery. Genes & Development. 33(13-14). 844–856. 32 indexed citations
6.
Czech, B. & Gregory J. Hannon. (2016). One Loop to Rule Them All: The Ping-Pong Cycle and piRNA-Guided Silencing. Trends in Biochemical Sciences. 41(4). 324–337. 335 indexed citations breakdown →
7.
Teixeira, Felipe Karam, B. Czech, Jonathan Preall, et al.. (2015). Regulation of Ribosome Biogenesis and Protein Synthesis Controls Germline Stem Cell Differentiation. Cell stem cell. 18(2). 276–290. 169 indexed citations
8.
Teixeira, Felipe Karam, Thomas R. Hurd, B. Czech, et al.. (2015). ATP synthase promotes germ cell differentiation independent of oxidative phosphorylation. Nature Cell Biology. 17(5). 689–696. 92 indexed citations
9.
Czech, B., Jonathan Preall, Jon McGinn, & Gregory J. Hannon. (2013). A Transcriptome-wide RNAi Screen in the Drosophila Ovary Reveals Factors of the Germline piRNA Pathway. Molecular Cell. 50(5). 749–761. 191 indexed citations
10.
Preall, Jonathan, B. Czech, Paloma M. Guzzardo, Felix Muerdter, & Gregory J. Hannon. (2012). shutdown is a component of the Drosophila piRNA biogenesis machinery. RNA. 18(8). 1446–1457. 67 indexed citations
11.
Wang, Jianbin, B. Czech, Amanda E. Crunk, et al.. (2011). Deep small RNA sequencing from the nematodeAscarisreveals conservation, functional diversification, and novel developmental profiles. Genome Research. 21(9). 1462–1477. 140 indexed citations
12.
Ni, Jian-Quan, Rui Zhou, B. Czech, et al.. (2011). A genome-scale shRNA resource for transgenic RNAi in Drosophila. Nature Methods. 8(5). 405–407. 605 indexed citations breakdown →
13.
Muerdter, Felix, Ivan Olovnikov, Antoine Molaro, et al.. (2011). Production of artificial piRNAs in flies and mice. RNA. 18(1). 42–52. 84 indexed citations
14.
Rudchik, A.T., K. W. Kemper, О.А. Ponkratenko, et al.. (2009). 8Li optical potential from 7Li(18O, 17O)8Li reaction analysis. Nuclear Physics A. 831(3-4). 139–149. 5 indexed citations
15.
Wang, Jiawei, B. Czech, & Detlef Weigel. (2009). miR156-Regulated SPL Transcription Factors Define an Endogenous Flowering Pathway in Arabidopsis thaliana. Cell. 138(4). 738–749. 1159 indexed citations breakdown →
16.
Czech, B., Rui Zhou, Yaniv Erlich, et al.. (2009). Hierarchical Rules for Argonaute Loading in Drosophila. Molecular Cell. 36(3). 445–456. 205 indexed citations
17.
Wang, Jiawei, Rebecca Schwab, B. Czech, Erica Mica, & Detlef Weigel. (2008). Dual Effects of miR156-Targeted SPL Genes and CYP78A5/KLUH on Plastochron Length and Organ Size in Arabidopsis thaliana    . The Plant Cell. 20(5). 1231–1243. 424 indexed citations
18.
Kirakosyan, V. V., А. Симоненко, V.A. Karnaukhov, et al.. (2008). The upgraded FASA setup for studying nuclear multifragmentation. Instruments and Experimental Techniques. 51(2). 159–165. 2 indexed citations
19.
Czech, B., Colin D. Malone, Rui Zhou, et al.. (2008). An endogenous small interfering RNA pathway in Drosophila. Nature. 453(7196). 798–802. 546 indexed citations breakdown →
20.
Siwek, A., A. Budzanowski, A. Fomichev, et al.. (2002). Incomplete energy deposition in long CsI(Tl) crystals. Nukleonika. 47. 141–145. 1 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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