Andrew D. Stephens

3.9k total citations · 1 hit paper
38 papers, 2.1k citations indexed

About

Andrew D. Stephens is a scholar working on Molecular Biology, Cell Biology and Plant Science. According to data from OpenAlex, Andrew D. Stephens has authored 38 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 20 papers in Cell Biology and 8 papers in Plant Science. Recurrent topics in Andrew D. Stephens's work include Genomics and Chromatin Dynamics (24 papers), Nuclear Structure and Function (17 papers) and RNA Research and Splicing (14 papers). Andrew D. Stephens is often cited by papers focused on Genomics and Chromatin Dynamics (24 papers), Nuclear Structure and Function (17 papers) and RNA Research and Splicing (14 papers). Andrew D. Stephens collaborates with scholars based in United States, Malaysia and Belgium. Andrew D. Stephens's co-authors include John F. Marko, Edward J. Banigan, Stephen A. Adam, Robert D. Goldman, Kerry Bloom, Jan Lammerding, Sylvain Gabriele, Yohalie Kalukula, Julian Haase and Patrick Z. Liu and has published in prestigious journals such as Nature Communications, Nature Genetics and Nature Reviews Molecular Cell Biology.

In The Last Decade

Andrew D. Stephens

38 papers receiving 2.1k citations

Hit Papers

Mechanics and functional consequences of nuclear deformat... 2022 2026 2023 2024 2022 50 100 150 200

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew D. Stephens United States 23 1.7k 976 296 132 97 38 2.1k
Amy Shaub Maddox United States 22 1.2k 0.7× 1.2k 1.3× 203 0.7× 116 0.9× 101 1.0× 46 2.0k
Monika Zwerger United States 19 1.8k 1.0× 540 0.6× 101 0.3× 121 0.9× 101 1.0× 28 2.1k
U. Serdar Tulu United States 12 1.1k 0.6× 1.1k 1.2× 141 0.5× 159 1.2× 270 2.8× 16 1.6k
Jérémie Gaillard France 18 1.2k 0.7× 1.4k 1.4× 305 1.0× 54 0.4× 73 0.8× 29 1.8k
Melissa K. Gardner United States 28 1.9k 1.1× 1.9k 1.9× 465 1.6× 55 0.4× 106 1.1× 53 2.4k
James J. Hartman United States 17 1.1k 0.6× 879 0.9× 95 0.3× 75 0.6× 54 0.6× 28 1.8k
Ivo A. Telley Germany 17 976 0.6× 997 1.0× 154 0.5× 233 1.8× 46 0.5× 31 1.5k
Wei‐Lih Lee United States 20 1.1k 0.6× 1.1k 1.2× 127 0.4× 46 0.3× 71 0.7× 28 1.5k
Ekaterina L. Grishchuk United States 28 2.3k 1.4× 2.5k 2.6× 600 2.0× 54 0.4× 41 0.4× 60 2.9k

Countries citing papers authored by Andrew D. Stephens

Since Specialization
Citations

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

Fields of papers citing papers by Andrew D. Stephens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew D. Stephens. 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 Andrew D. Stephens. The network helps show where Andrew D. Stephens may publish in the future.

Co-authorship network of co-authors of Andrew D. Stephens

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew D. Stephens. A scholar is included among the top collaborators of Andrew D. Stephens 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 Andrew D. Stephens. Andrew D. Stephens 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.
Almassalha, Luay M., et al.. (2025). Nuclear blebs are associated with destabilized chromatin-packing domains. Journal of Cell Science. 138(3). 3 indexed citations
2.
Manning, Gerard, et al.. (2024). DNA damage causes ATM-dependent heterochromatin loss leading to nuclear softening, blebbing, and rupture. Molecular Biology of the Cell. 36(3). br6–br6. 4 indexed citations
3.
Chiu, Katherine, et al.. (2023). Actin contraction controls nuclear blebbing and rupture independent of actin confinement. Molecular Biology of the Cell. 35(2). ar19–ar19. 14 indexed citations
4.
Kalukula, Yohalie, Andrew D. Stephens, Jan Lammerding, & Sylvain Gabriele. (2022). Mechanics and functional consequences of nuclear deformations. Nature Reviews Molecular Cell Biology. 23(9). 583–602. 246 indexed citations breakdown →
5.
Belaghzal, Houda, Tyler Borrman, Andrew D. Stephens, et al.. (2021). Liquid chromatin Hi-C characterizes compartment-dependent chromatin interaction dynamics. Nature Genetics. 53(3). 367–378. 76 indexed citations
6.
Strom, Amy R., Ronald Biggs, Edward J. Banigan, et al.. (2021). HP1α is a chromatin crosslinker that controls nuclear and mitotic chromosome mechanics. eLife. 10. 86 indexed citations
7.
Amitai, Assaf, Jason D. Buenrostro, Aditi Chakrabarti, et al.. (2020). Advances in Chromatin and Chromosome Research: Perspectives from Multiple Fields. Molecular Cell. 79(6). 881–901. 38 indexed citations
8.
Matthews, James, Qiao Zhang, Kalina R. Atanasova, et al.. (2020). High-throughput gene screen reveals modulators of nuclear shape. Molecular Biology of the Cell. 31(13). 1392–1402. 28 indexed citations
9.
Stephens, Andrew D., Patrick Z. Liu, Viswajit Kandula, et al.. (2019). Physicochemical mechanotransduction alters nuclear shape and mechanics via heterochromatin formation. Molecular Biology of the Cell. 30(17). 2320–2330. 80 indexed citations
10.
Gladstein, Scott, Luay M. Almassalha, Lusik Cherkezyan, et al.. (2019). Multimodal interference-based imaging of nanoscale structure and macromolecular motion uncovers UV induced cellular paroxysm. Nature Communications. 10(1). 1652–1652. 12 indexed citations
11.
Hobson, Chad M., et al.. (2019). Nuclear Deformation with Combined AFM and 3D Multi-Color Live-Cell Line Bessel Sheet Imaging. Biophysical Journal. 116(3). 24a–24a. 1 indexed citations
12.
Stephens, Andrew D., Patrick Z. Liu, Viswajit Kandula, et al.. (2019). Physicochemical mechanotransduction alters nuclear shape and mechanics via heterochromatin formation. Molecular Biology of the Cell. mbc.E19–5. 12 indexed citations
13.
Stephens, Andrew D., Edward J. Banigan, Stephen A. Adam, Robert D. Goldman, & John F. Marko. (2017). Chromatin and lamin A determine two different mechanical response regimes of the cell nucleus. Molecular Biology of the Cell. 28(14). 1984–1996. 321 indexed citations
14.
Stephens, Andrew D., Patrick Z. Liu, Edward J. Banigan, et al.. (2017). Chromatin histone modifications and rigidity affect nuclear morphology independent of lamins. Molecular Biology of the Cell. 29(2). 220–233. 239 indexed citations
15.
Banigan, Edward J., Andrew D. Stephens, & John F. Marko. (2017). Mechanics and Buckling of Biopolymeric Shells and Cell Nuclei. Biophysical Journal. 113(8). 1654–1663. 40 indexed citations
16.
Verdaasdonk, Jolien S., Andrew D. Stephens, Julian Haase, & Kerry Bloom. (2013). Bending the Rules: Widefield Microscopy and the Abbe Limit of Resolution. Journal of Cellular Physiology. 229(2). 132–138. 31 indexed citations
17.
Haase, Julian, Prashant Mishra, Andrew D. Stephens, et al.. (2013). A 3D Map of the Yeast Kinetochore Reveals the Presence of Core and Accessory Centromere-Specific Histone. Current Biology. 23(19). 1939–1944. 49 indexed citations
18.
Stephens, Andrew D., et al.. (2013). The spatial segregation of pericentric cohesin and condensin in the mitotic spindle. Molecular Biology of the Cell. 24(24). 3909–3919. 30 indexed citations
19.
Stephens, Andrew D., Julian Haase, Leandra Vicci, Russell M. Taylor, & Kerry Bloom. (2011). Cohesin, condensin, and the intramolecular centromere loop together generate the mitotic chromatin spring. The Journal of Cell Biology. 193(7). 1167–1180. 112 indexed citations
20.
Bekker, Janine M., Andrew D. Stephens, William T. Clarke, et al.. (2007). Direct interaction of Gas11 with microtubules: Implications for the dynein regulatory complex. Cell Motility and the Cytoskeleton. 64(6). 461–473. 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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