Arthur I. Skoultchi

15.9k total citations · 1 hit paper
148 papers, 9.8k citations indexed

About

Arthur I. Skoultchi is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Arthur I. Skoultchi has authored 148 papers receiving a total of 9.8k indexed citations (citations by other indexed papers that have themselves been cited), including 133 papers in Molecular Biology, 18 papers in Genetics and 15 papers in Oncology. Recurrent topics in Arthur I. Skoultchi's work include Genomics and Chromatin Dynamics (47 papers), Epigenetics and DNA Methylation (36 papers) and RNA Research and Splicing (35 papers). Arthur I. Skoultchi is often cited by papers focused on Genomics and Chromatin Dynamics (47 papers), Epigenetics and DNA Methylation (36 papers) and RNA Research and Splicing (35 papers). Arthur I. Skoultchi collaborates with scholars based in United States, Czechia and Japan. Arthur I. Skoultchi's co-authors include Yuhong Fan, Herbert M. Lachman, Christopher L. Woodcock, Farshid Radparvar, Tomáš Stopka, Natasha Rekhtman, Igor Matushansky, Dmitry V. Fyodorov, Carl L. Schildkraut and Allen Sirotkin and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Arthur I. Skoultchi

145 papers receiving 9.6k citations

Hit Papers

1 papers align trajectories

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.

Emerging roles of linker histones in regulating chromatin structure and function

2017 322 citations Dmitry V. Fyodorov, Bing‐Rui Zhou et al. Nature Reviews Molecular Cell Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Arthur I. Skoultchi United States	55	8.1k	1.5k	897	884	839	148	9.8k
David I. K. Martin United States	52	9.1k 1.1×	2.8k 1.9×	987 1.1×	576 0.7×	1.1k 1.3×	94	11.5k
Merlin Crossley Australia	52	6.8k 0.8×	1.5k 1.0×	807 0.9×	509 0.6×	516 0.6×	138	8.8k
Michael Fry United Kingdom	46	8.7k 1.1×	872 0.6×	1.0k 1.1×	1.3k 1.5×	460 0.5×	99	10.8k
Denise Sheer United Kingdom	51	6.0k 0.7×	1.9k 1.3×	1.4k 1.5×	2.1k 2.4×	625 0.7×	178	10.9k
Anna Jauch Germany	43	5.2k 0.6×	1.6k 1.1×	621 0.7×	1.6k 1.8×	1.0k 1.2×	194	7.7k
Peter Laslo United States	17	7.4k 0.9×	1.1k 0.8×	2.0k 2.3×	757 0.9×	847 1.0×	20	9.9k
Thomas B. Shows United States	54	6.9k 0.8×	2.3k 1.6×	1.5k 1.7×	1.1k 1.3×	296 0.4×	175	10.9k
Miguel Vidal Spain	41	8.6k 1.1×	2.0k 1.3×	495 0.6×	647 0.7×	557 0.7×	93	9.9k
Bruce M. Paterson United States	33	5.9k 0.7×	936 0.6×	820 0.9×	2.4k 2.7×	497 0.6×	56	8.7k
Lynne E. Maquat United States	73	15.7k 1.9×	1.7k 1.2×	756 0.8×	568 0.6×	992 1.2×	161	18.2k

Countries citing papers authored by Arthur I. Skoultchi

Since Specialization

Citations

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

Fields of papers citing papers by Arthur I. Skoultchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arthur I. Skoultchi. 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 Arthur I. Skoultchi. The network helps show where Arthur I. Skoultchi may publish in the future.

Co-authorship network of co-authors of Arthur I. Skoultchi

This figure shows the co-authorship network connecting the top 25 collaborators of Arthur I. Skoultchi. A scholar is included among the top collaborators of Arthur I. Skoultchi 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 Arthur I. Skoultchi. Arthur I. Skoultchi 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

Kozmík, Zbyněk, Zbyněk Kozmík, Jan Pačes, et al.. (2023). Chromatin Remodeling Enzyme Snf2h Is Essential for Retinal Cell Proliferation and Photoreceptor Maintenance. Cells. 12(7). 1035–1035. 3 indexed citations

Andreyeva, Evgeniya N., Alexander Emelyanov, Lu Sun, et al.. (2022). Drosophila SUMM4 complex couples insulator function and DNA replication control. eLife. 11. 2 indexed citations

Pinto, Hugo, Laxmi Mishra, Justin C. Wheat, et al.. (2020). H1 linker histones silence repetitive elements by promoting both histone H3K9 methylation and chromatin compaction. Proceedings of the National Academy of Sciences. 117(25). 14251–14258. 53 indexed citations

Fyodorov, Dmitry V., Bing‐Rui Zhou, Arthur I. Skoultchi, & Yawen Bai. (2017). Emerging roles of linker histones in regulating chromatin structure and function. Nature Reviews Molecular Cell Biology. 19(3). 192–206. 322 indexed citations breakdown →

He, Shuying, Rebecca McGreal, Qing Xie, et al.. (2016). Chromatin remodeling enzyme Snf2h regulates embryonic lens differentiation and denucleation. Development. 143(11). 1937–1947. 43 indexed citations

Gökhan, Şölen, et al.. (2014). The Role of H1 Linker Histone Subtypes in Preserving the Fidelity of Elaboration of Mesendodermal and Neuroectodermal Lineages during Embryonic Development. PLoS ONE. 9(5). e96858–e96858. 6 indexed citations

Wontakal, Sandeep N., Xingyi Guo, Cameron Smith, et al.. (2012). A core erythroid transcriptional network is repressed by a master regulator of myelo-lymphoid differentiation. Proceedings of the National Academy of Sciences. 109(10). 3832–3837. 59 indexed citations

Burda, Pavel, Juraj Kokavec, Petra Bašová, et al.. (2009). PU.1 Activation Relieves GATA-1–Mediated Repression of Cebpa and Cbfb during Leukemia Differentiation. Molecular Cancer Research. 7(10). 1693–1703. 21 indexed citations

Yang, Ying, Tomáš Stopka, Nady Golestaneh, et al.. (2006). Regulation of αA‐crystallin via Pax6, c‐Maf, CREB and a broad domain of lens‐specific chromatin. The EMBO Journal. 25(10). 2107–2118. 91 indexed citations

10.

Yang, Yaw-Ching, Tomáš Stopka, Nady Golestaneh, et al.. (2005). Developmentally Regulated Tissue–specific Expression of the Mouse A–crystallin Requires Establishment of a Broad H3K9 Acetylation Domain Including the Upstream Region DCR1, Activated via FGF2 Signaling. Investigative Ophthalmology & Visual Science. 46(13). 3483–3483. 1 indexed citations

11.

Stopka, Tomáš, Derek F. Amanatullah, Michael Papetti, & Arthur I. Skoultchi. (2005). PU.1 inhibits the erythroid program by binding to GATA‐1 on DNA and creating a repressive chromatin structure. The EMBO Journal. 24(21). 3712–3723. 119 indexed citations

12.

Rekhtman, Natasha, Kevin S. Choe, Igor Matushansky, et al.. (2003). PU.1 and pRB Interact and Cooperate To Repress GATA-1 and Block Erythroid Differentiation. Molecular and Cellular Biology. 23(21). 7460–7474. 85 indexed citations

13.

Starck, Joëlle, Sandrine Sarrazin, C. Gonnet, et al.. (1999). Spi-1/PU.1 Is a Positive Regulator of the Fli-1 Gene Involved in Inhibition of Erythroid Differentiation in Friend Erythroleukemic Cell Lines. Molecular and Cellular Biology. 19(1). 121–135. 68 indexed citations

14.

Rekhtman, Natasha, Farshid Radparvar, Todd Evans, & Arthur I. Skoultchi. (1999). Direct interaction of hematopoietic transcription factors PU.1 and GATA-1: functional antagonism in erythroid cells. Genes & Development. 13(11). 1398–1411. 391 indexed citations

15.

Funke, Birgit, Bruno Saint-Jore, Anne Puech, et al.. (1997). Characterization and Mutation Analysis of Goosecoid-like (GSCL), a Homeodomain-Containing Gene That Maps to the Critical Region for VCFS/DGS on 22q11. Genomics. 46(3). 364–372. 21 indexed citations

16.

Rao, Govinda, Leila Alland, Peter Guida, et al.. (1996). Mouse Sin3A interacts with and can functionally substitute for the amino-terminal repression of the Myc antagonist Mxi1.. PubMed. 12(5). 1165–72. 36 indexed citations

17.

Schreiber‐Agus, Nicole, Ken Chen, Richard Torres, et al.. (1995). An amino-terminal domain of Mxi1 mediates anti-myc oncogenic activity and interacts with a homolog of the Yeast Transcriptional Repressor SIN3. Cell. 80(5). 777–786. 327 indexed citations

18.

Liu, Ta-Jen, et al.. (1989). The Efficiency of 3′-End Formation Contributes to the Relative Levels of Different Histone mRNAs. Molecular and Cellular Biology. 9(8). 3499–3508. 15 indexed citations

19.

Hickey, Robert J., Arthur I. Skoultchi, Peter W. Gunning, & Larry Kedes. (1986). Regulation of a Human Cardiac Actin Gene Introduced Into Rat L6 Myoblasts Suggests a Defect in Their Myogenic Program. Molecular and Cellular Biology. 6(9). 3287–3290. 13 indexed citations

20.

Sprecher, Cindy A., et al.. (1985). Regulated Expression of a Chimeric Histone Gene Introduced into Mouse Fibroblasts. Molecular and Cellular Biology. 5(9). 2316–2324. 18 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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