Bosl Noh

3.6k total citations
29 papers, 2.9k citations indexed

About

Bosl Noh is a scholar working on Plant Science, Molecular Biology and Ecology, Evolution, Behavior and Systematics. According to data from OpenAlex, Bosl Noh has authored 29 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Plant Science, 21 papers in Molecular Biology and 1 paper in Ecology, Evolution, Behavior and Systematics. Recurrent topics in Bosl Noh's work include Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (11 papers) and Plant Gene Expression Analysis (10 papers). Bosl Noh is often cited by papers focused on Plant Molecular Biology Research (22 papers), Plant Reproductive Biology (11 papers) and Plant Gene Expression Analysis (10 papers). Bosl Noh collaborates with scholars based in South Korea, United States and Ethiopia. Bosl Noh's co-authors include Edgar P. Spalding, Angus Murphy, Yoo‐Sun Noh, Richard M. Amasino, Richard D. Vierstra, Anindita Bandyopadhyay, Wendy Ann Peer, Soon‐Ki Han, Young‐Min Jeong and Min‐Jeong Kang and has published in prestigious journals such as Nature, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Bosl Noh

28 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bosl Noh South Korea	24	2.6k	2.2k	97	72	62	29	2.9k
Keith Earley United States	11	2.6k 1.0×	2.3k 1.0×	74 0.8×	87 1.2×	64 1.0×	14	3.1k
Nathalie Frangne France	19	1.6k 0.6×	1.3k 0.6×	79 0.8×	38 0.5×	53 0.9×	25	1.9k
Boosaree Titapiwatanakun United States	12	1.9k 0.7×	1.5k 0.7×	30 0.3×	80 1.1×	50 0.8×	13	2.1k
John McElver United States	12	1.2k 0.4×	1.5k 0.7×	98 1.0×	45 0.6×	30 0.5×	14	1.9k
Ing‐Feng Chang Taiwan	19	1.2k 0.4×	1.1k 0.5×	33 0.3×	54 0.8×	30 0.5×	29	1.7k
Ming Luo China	25	2.5k 1.0×	2.1k 1.0×	83 0.9×	86 1.2×	25 0.4×	28	2.9k
Santiago Mora‐García Argentina	17	2.4k 0.9×	1.8k 0.8×	82 0.8×	31 0.4×	49 0.8×	27	2.7k
Ursula Halfter United States	14	2.9k 1.1×	1.7k 0.8×	67 0.7×	20 0.3×	30 0.5×	16	3.2k
Vincent Vincenzetti Switzerland	16	1.2k 0.5×	1.3k 0.6×	34 0.4×	53 0.7×	35 0.6×	21	1.7k
Hee Jin Park South Korea	25	1.5k 0.6×	967 0.4×	41 0.4×	30 0.4×	47 0.8×	42	1.8k

Countries citing papers authored by Bosl Noh

Since Specialization

Citations

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

Fields of papers citing papers by Bosl Noh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bosl Noh

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

Khan, Irfan Ullah, et al.. (2024). Genomic overview of INA-induced NPR1 targeting and transcriptional cascades in Arabidopsis. Nucleic Acids Research. 52(7). 3572–3588. 4 indexed citations

Noh, Bosl, et al.. (2022). Negative evidence on the transgenerational inheritance of defense priming in Arabidopsis thaliana. BMB Reports. 55(7). 342–347. 7 indexed citations

Choi, Myunghwan, et al.. (2020). De Novo Shoot Regeneration Controlled by HEN1 and TCP3/4 in Arabidopsis. Plant and Cell Physiology. 61(9). 1600–1613. 24 indexed citations

Kim, Ji Yun, et al.. (2018). Epigenetic reprogramming by histone acetyltransferase HAG1/AtGCN5 is required for pluripotency acquisition in Arabidopsis. The EMBO Journal. 37(20). 113 indexed citations

Kim, Ji Yun, Jee Eun Oh, Yoo‐Sun Noh, & Bosl Noh. (2015). Epigenetic control of juvenile‐to‐adult phase transition by the Arabidopsis SAGA‐like complex. The Plant Journal. 83(3). 537–545. 36 indexed citations

Cho, Jungnam, Jee-Youn Ryu, Young‐Min Jeong, et al.. (2012). Control of Seed Germination by Light-Induced Histone Arginine Demethylation Activity. Developmental Cell. 22(4). 736–748. 125 indexed citations

Song, Hae‐Ryong, Soon‐Ki Han, Muho Han, et al.. (2012). HDA19 is required for the repression of salicylic acid biosynthesis and salicylic acid‐mediated defense responses in Arabidopsis. The Plant Journal. 71(1). 135–146. 151 indexed citations

Hyun, Y., et al.. (2011). Identification of regulators required for the reactivation of FLOWERING LOCUS C during Arabidopsis reproduction. Planta. 234(6). 1237–1250. 23 indexed citations

Ko, Jonghyun, Irina Mitina, Yosuke Tamada, et al.. (2010). Growth habit determination by the balance of histone methylation activities in Arabidopsis. The EMBO Journal. 29(18). 3208–3215. 78 indexed citations

10.

Jeong, Young‐Min, et al.. (2009). Temporal and Spatial Expression Patterns of Nine Arabidopsis Genes Encoding Jumonji C-Domain Proteins. Molecules and Cells. 27(4). 481–490. 27 indexed citations

11.

Song, Hae-Ryong, et al.. (2009). The RNA Binding Protein ELF9 Directly ReducesSUPPRESSOR OF OVEREXPRESSION OF CO1Transcript Levels inArabidopsis, Possibly via Nonsense-Mediated mRNA Decay. The Plant Cell. 21(4). 1195–1211. 27 indexed citations

12.

Jeong, Juhee, Hae-Ryong Song, Jonghyun Ko, et al.. (2009). Repression of FLOWERING LOCUS T Chromatin by Functionally Redundant Histone H3 Lysine 4 Demethylases in Arabidopsis. PLoS ONE. 4(11). e8033–e8033. 132 indexed citations

13.

Choi, Jean, Y. Hyun, Min Jeong Kang, et al.. (2008). Resetting and regulation of FLOWERING LOCUS C expression during Arabidopsis reproductive development. The Plant Journal. 57(5). 918–931. 125 indexed citations

14.

Walker, Joseph, et al.. (2006). Multiple Heme Oxygenase Family Members Contribute to the Biosynthesis of the Phytochrome Chromophore in Arabidopsis. PLANT PHYSIOLOGY. 140(3). 856–868. 106 indexed citations

15.

Han, Soon‐Ki, et al.. (2006). Role of plant CBP/p300‐like genes in the regulation of flowering time. The Plant Journal. 49(1). 103–114. 85 indexed citations

16.

Froehlich, Allan C., Bosl Noh, Richard D. Vierstra, Jennifer Loros, & Jay Dunlap. (2005). Genetic and Molecular Analysis of Phytochromes from the Filamentous Fungus Neurospora crassa. Eukaryotic Cell. 4(12). 2140–2152. 131 indexed citations

17.

Noh, Bosl, Seunghee Lee, Hyun‐Jin Kim, et al.. (2004). Divergent Roles of a Pair of Homologous Jumonji/Zinc-Finger–Class Transcription Factor Proteins in the Regulation of Arabidopsis Flowering Time. The Plant Cell. 16(10). 2601–2613. 228 indexed citations

18.

Noh, Bosl, Anindita Bandyopadhyay, Wendy Ann Peer, Edgar P. Spalding, & Angus Murphy. (2003). Enhanced gravi- and phototropism in plant mdr mutants mislocalizing the auxin efflux protein PIN1. Nature. 423(6943). 999–1002. 211 indexed citations

19.

Noh, Bosl, Angus Murphy, & Edgar P. Spalding. (2001). Multidrug Resistance –like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development. The Plant Cell. 13(11). 2441–2454. 426 indexed citations

20.

Noh, Bosl, Angus Murphy, & Edgar P. Spalding. (2001). Multidrug Resistance-Like Genes of Arabidopsis Required for Auxin Transport and Auxin-Mediated Development. The Plant Cell. 13(11). 2441–2441. 107 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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