Jeffrey A. Nickerson

8.3k total citations · 1 hit paper
86 papers, 6.3k citations indexed

About

Jeffrey A. Nickerson is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Jeffrey A. Nickerson has authored 86 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Molecular Biology, 10 papers in Cell Biology and 6 papers in Oncology. Recurrent topics in Jeffrey A. Nickerson's work include Genomics and Chromatin Dynamics (32 papers), RNA Research and Splicing (32 papers) and Nuclear Structure and Function (20 papers). Jeffrey A. Nickerson is often cited by papers focused on Genomics and Chromatin Dynamics (32 papers), RNA Research and Splicing (32 papers) and Nuclear Structure and Function (20 papers). Jeffrey A. Nickerson collaborates with scholars based in United States, Chile and Canada. Jeffrey A. Nickerson's co-authors include Sheldon Penman, Andrew H. Fischer, Daniele Zink, Anthony N. Imbalzano, Dian He, Janet L. Stein, Jane B. Lian, André J. van Wijnen, Katherine M. Wan and Benjamin J. Blencowe and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Jeffrey A. Nickerson

86 papers receiving 6.2k citations

Hit Papers

Nuclear structure in cancer cells 2004 2026 2011 2018 2004 250 500 750

Peers

Jeffrey A. Nickerson
Michael D. Henry United States
Jamison L. Nourse United States
Franz Oswald Germany
Suzie J. Scales United States
Michael D. Henry United States
Jeffrey A. Nickerson
Citations per year, relative to Jeffrey A. Nickerson Jeffrey A. Nickerson (= 1×) peers Michael D. Henry

Countries citing papers authored by Jeffrey A. Nickerson

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey A. Nickerson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeffrey A. Nickerson

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey A. Nickerson. A scholar is included among the top collaborators of Jeffrey A. Nickerson 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 Jeffrey A. Nickerson. Jeffrey A. Nickerson 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.
Nickerson, Jeffrey A. & Fatemeh Momen‐Heravi. (2024). Long non-coding RNAs: roles in cellular stress responses and epigenetic mechanisms regulating chromatin. Nucleus. 15(1). 2350180–2350180. 11 indexed citations
2.
Lin, Yen‐Chen, Nandini Ramesh, Eric N. Anderson, et al.. (2021). Interactions between ALS-linked FUS and nucleoporins are associated with defects in the nucleocytoplasmic transport pathway. Nature Neuroscience. 24(8). 1077–1088. 63 indexed citations
3.
Zaidi, Sayyed K., Andrew J. Fritz, Kirsten M. Tracy, et al.. (2018). Nuclear organization mediates cancer-compromised genetic and epigenetic control. Advances in Biological Regulation. 69. 1–10. 10 indexed citations
4.
Padilla‐Benavides, Teresita, et al.. (2017). Casein kinase 2-mediated phosphorylation of Brahma-related gene 1 controls myoblast proliferation and contributes to SWI/SNF complex composition. Journal of Biological Chemistry. 292(45). 18592–18607. 24 indexed citations
5.
Barutcu, A. Rasim, Bryan R. Lajoie, Andrew J. Fritz, et al.. (2016). SMARCA4 regulates gene expression and higher-order chromatin structure in proliferating mammary epithelial cells. Genome Research. 26(9). 1188–1201. 76 indexed citations
6.
Neelam, Srujana, T. J. Chancellor, Yuan Li, et al.. (2015). Direct force probe reveals the mechanics of nuclear homeostasis in the mammalian cell. Proceedings of the National Academy of Sciences. 112(18). 5720–5725. 102 indexed citations
7.
Tran, Hélène, Sandra Almeida, Jill E. Moore, et al.. (2015). Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS. Neuron. 87(6). 1207–1214. 144 indexed citations
8.
Quaresma, Alexandre J.C., et al.. (2013). Regulation of mRNA export by the PI3 kinase/AKT signal transduction pathway. Molecular Biology of the Cell. 24(8). 1208–1221. 16 indexed citations
9.
Baron, Desiree M., Catherine L. Ward, Reddy Ranjith K. Sama, et al.. (2013). Amyotrophic lateral sclerosis-linked FUS/TLS alters stress granule assembly and dynamics. Molecular Neurodegeneration. 8(1). 30–30. 120 indexed citations
10.
Tortelote, Giovane G., J. Manuel Hernández‐Hernández, Alexandre J.C. Quaresma, et al.. (2012). Wnt3 function in the epiblast is required for the maintenance but not the initiation of gastrulation in mice. Developmental Biology. 374(1). 164–173. 54 indexed citations
11.
Goel, Hira Lal, Jean M. Underwood, Jeffrey A. Nickerson, Chung‐Cheng Hsieh, & Lucia R. Languino. (2010). β1 integrins mediate cell proliferation in three‐dimensional cultures by regulating expression of the sonic hedgehog effector protein, GLI1. Journal of Cellular Physiology. 224(1). 210–217. 28 indexed citations
12.
Pockwinse, Shirwin M., Krishna P. Kota, Alexandre J.C. Quaresma, et al.. (2010). Live cell imaging of the cancer‐related transcription factor RUNX2 during mitotic progression. Journal of Cellular Physiology. 226(5). 1383–1389. 15 indexed citations
13.
Zaidi, Sayyed K., Ricardo Medina, Shirwin M. Pockwinse, et al.. (2010). Subnuclear Localization and Intranuclear Trafficking of Transcription Factors. Methods in molecular biology. 647. 77–93. 2 indexed citations
14.
Pratap, Jitesh, Jean M. Underwood, Jacqueline Akech, et al.. (2009). Ectopic Runx2 Expression in Mammary Epithelial Cells Disrupts Formation of Normal Acini Structure: Implications for Breast Cancer Progression. Cancer Research. 69(17). 6807–6814. 74 indexed citations
15.
Heisterkamp, Alexander, Iva Maxwell, Eric Mazur, et al.. (2005). Pulse energy dependence of subcellular dissection by femtosecond laser pulses. Optics Express. 13(10). 3690–3690. 121 indexed citations
16.
Vradii, Diana, Stefan Wagner, Jeffrey A. Nickerson, et al.. (2005). Brg1, the ATPase subunit of the SWI/SNF chromatin remodeling complex, is required for myeloid differentiation to granulocytes. Journal of Cellular Physiology. 206(1). 112–118. 41 indexed citations
17.
McCracken, Susan, Dáša Longman, Edyta Marcon, et al.. (2005). Proteomic Analysis of SRm160-containing Complexes Reveals a Conserved Association with Cohesin. Journal of Biological Chemistry. 280(51). 42227–42236. 27 indexed citations
18.
Herbert, Alan, Stefan Wagner, & Jeffrey A. Nickerson. (2002). Induction of Protein Translation by ADAR1 within Living Cell Nuclei Is Not Dependent on RNA Editing. Molecular Cell. 10(5). 1235–1246. 30 indexed citations
19.
Blencowe, Benjamin J., Göran Baurén, Adam G. Eldridge, et al.. (2000). The SRm160/300 splicing coactivator subunits. RNA. 6(1). 111–120. 89 indexed citations
20.
Issner, Robbyn, et al.. (1998). A coactivator of pre-mRNA splicing. Genes & Development. 12(7). 996–1009. 185 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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