Loren E. Hough

2.0k total citations
47 papers, 1.5k citations indexed

About

Loren E. Hough is a scholar working on Molecular Biology, Cell Biology and Electronic, Optical and Magnetic Materials. According to data from OpenAlex, Loren E. Hough has authored 47 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 11 papers in Cell Biology and 9 papers in Electronic, Optical and Magnetic Materials. Recurrent topics in Loren E. Hough's work include RNA Research and Splicing (16 papers), Liquid Crystal Research Advancements (9 papers) and Nuclear Structure and Function (9 papers). Loren E. Hough is often cited by papers focused on RNA Research and Splicing (16 papers), Liquid Crystal Research Advancements (9 papers) and Nuclear Structure and Function (9 papers). Loren E. Hough collaborates with scholars based in United States, Germany and United Kingdom. Loren E. Hough's co-authors include Noel A. Clark, Matthew A. Glaser, Michi Nakata, David M. Walba, Eva Körblová, Meredith D. Betterton, Joseph E. Maclennan, Michael P. Rout, Dong Chen and Jaclyn Tetenbaum-Novatt and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Physical Review Letters.

In The Last Decade

Loren E. Hough

45 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Loren E. Hough United States	21	733	604	312	257	252	47	1.5k
Giuliano Zanchetta Italy	21	869 1.2×	417 0.7×	206 0.7×	291 1.1×	82 0.3×	49	1.6k
Marco Buscaglia Italy	24	752 1.0×	555 0.9×	137 0.4×	433 1.7×	120 0.5×	58	1.6k
Seok‐Cheol Hong South Korea	21	560 0.8×	286 0.5×	130 0.4×	418 1.6×	334 1.3×	64	1.9k
K. Tompa Hungary	18	455 0.6×	153 0.3×	117 0.4×	452 1.8×	167 0.7×	119	1.3k
Wojciech T. Góźdź Poland	21	465 0.6×	102 0.2×	288 0.9×	475 1.8×	23 0.1×	66	1.2k
Zoher Gueroui France	20	689 0.9×	153 0.3×	73 0.2×	250 1.0×	31 0.1×	31	1.3k
V. G. Nazarenko Ukraine	19	305 0.4×	1.4k 2.3×	428 1.4×	513 2.0×	236 0.9×	78	1.7k
H.J. Deuling Germany	13	517 0.7×	364 0.6×	161 0.5×	129 0.5×	67 0.3×	17	1.2k
Józef K. Mościcki Poland	17	193 0.3×	347 0.6×	185 0.6×	484 1.9×	309 1.2×	67	1.2k

Countries citing papers authored by Loren E. Hough

Since Specialization

Citations

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

Fields of papers citing papers by Loren E. Hough

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Loren E. Hough. 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 Loren E. Hough. The network helps show where Loren E. Hough may publish in the future.

Co-authorship network of co-authors of Loren E. Hough

This figure shows the co-authorship network connecting the top 25 collaborators of Loren E. Hough. A scholar is included among the top collaborators of Loren E. Hough 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 Loren E. Hough. Loren E. Hough 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

Ramirez, Dominique, Loren E. Hough, & Michael R. Shirts. (2024). Coiled-coil domains are sufficient to drive liquid-liquid phase separation in protein models. Biophysical Journal. 123(6). 703–717. 26 indexed citations

Whited, Allison M., Irwin Jungreis, Jonathan M. Mudge, et al.. (2024). Biophysical characterization of high-confidence, small human proteins. SHILAP Revista de lepidopterología. 4(3). 100167–100167. 1 indexed citations

Ramirez, Dominique, Loren E. Hough, & Michael R. Shirts. (2023). Coiled-coil domains can drive liquid-liquid phase separation. Biophysical Journal. 122(3). 209a–209a. 1 indexed citations

Lewis, Karen A., et al.. (2023). ParSe 2.0: A web tool to identify drivers of protein phase separation at the proteome level. Protein Science. 32(9). e4756–e4756. 9 indexed citations

Correia, John J., et al.. (2022). Intrinsically disordered regions that drive phase separation form a robustly distinct protein class. Journal of Biological Chemistry. 299(1). 102801–102801. 44 indexed citations

Correia, John J., et al.. (2021). Beta turn propensity and a model polymer scaling exponent identify intrinsically disordered phase-separating proteins. Journal of Biological Chemistry. 297(5). 101343–101343. 24 indexed citations

Lee, Thomas, et al.. (2020). C-Terminal Tail Polyglycylation and Polyglutamylation Alter Microtubule Mechanical Properties. Biophysical Journal. 119(11). 2219–2230. 10 indexed citations

Lee, Thomas, et al.. (2020). C-Terminal Tail Polyglycylation and Polyglutamylation Alter Microtubule Mechanical Properties. Biophysical Journal. 118(3). 597a–597a. 1 indexed citations

Betterton, Meredith D., et al.. (2019). Bound-State Diffusion due to Binding to Flexible Polymers in a Selective Biofilter. Biophysical Journal. 118(2). 376–385. 6 indexed citations

10.

Betterton, Meredith D., et al.. (2019). Design principles of selective transport through biopolymer barriers. Physical review. E. 100(4). 42414–42414. 13 indexed citations

11.

Hough, Loren E., et al.. (2018). In-Cell NMR within Budding Yeast Reveals Cytoplasmic Masking of Hydrophobic Residues of FG Repeats. Biophysical Journal. 115(9). 1690–1695. 15 indexed citations

12.

Blackwell, Robert N., C. J. Edelmaier, Zachary R. Gergely, et al.. (2017). Physical Determinants of Bipolar Mitotic Spindle Assembly and Stability in Fission Yeast. Biophysical Journal. 112(3). 432a–432a.

13.

Vernerey, Franck J., et al.. (2017). Effects of soft interactions and bound mobility on diffusion in crowded environments: a model of sticky and slippery obstacles. Physical Biology. 14(4). 45008–45008. 10 indexed citations

14.

Blackwell, Robert N., C. J. Edelmaier, Zachary R. Gergely, et al.. (2017). Physical determinants of bipolar mitotic spindle assembly and stability in fission yeast. Science Advances. 3(1). e1601603–e1601603. 44 indexed citations

15.

Gergely, Zachary R., et al.. (2016). Kinesin-8 effects on mitotic microtubule dynamics contribute to spindle function in fission yeast. Molecular Biology of the Cell. 27(22). 3490–3514. 28 indexed citations

16.

Blackwell, Robert N., et al.. (2015). Hysteresis, reentrance, and glassy dynamics in systems of self-propelled rods. Physical Review E. 92(6). 60501–60501. 12 indexed citations

17.

Tetenbaum-Novatt, Jaclyn, Loren E. Hough, Roxana Mironska, Anna Sophia McKenney, & Michael P. Rout. (2012). Nucleocytoplasmic Transport: A Role for Nonspecific Competition in Karyopherin-Nucleoporin Interactions. Molecular & Cellular Proteomics. 11(5). 31–46. 49 indexed citations

18.

Hough, Loren E., Anne Schwabe, Matthew A. Glaser, J. Richard McIntosh, & Meredith D. Betterton. (2009). Microtubule Depolymerization by the Kinesin-8 Motor Kip3p: A Mathematical Model. Biophysical Journal. 96(8). 3050–3064. 33 indexed citations

19.

Hough, Loren E., Chenhui Zhu, Michi Nakata, et al.. (2007). Optical Activity Produced by Layer Chirality in Bent-Core Liquid Crystals. Physical Review Letters. 98(3). 37802–37802. 21 indexed citations

20.

Prosperi, Davide, Carlo Morasso, Francesco Mantegazza, et al.. (2006). Phantom Nanoparticles as Probes of Biomolecular Interactions. Small. 2(8-9). 1060–1067. 16 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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