Dean P. Staus

3.9k total citations · 1 hit paper
29 papers, 2.6k citations indexed

About

Dean P. Staus is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Dean P. Staus has authored 29 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 17 papers in Cellular and Molecular Neuroscience and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Dean P. Staus's work include Receptor Mechanisms and Signaling (23 papers), Neuropeptides and Animal Physiology (16 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Dean P. Staus is often cited by papers focused on Receptor Mechanisms and Signaling (23 papers), Neuropeptides and Animal Physiology (16 papers) and Monoclonal and Polyclonal Antibodies Research (6 papers). Dean P. Staus collaborates with scholars based in United States, Belgium and Japan. Dean P. Staus's co-authors include Robert J. Lefkowitz, Laura M. Wingler, Andrew C. Kruse, Naomi R. Latorraca, Brian K. Kobilka, A.L.W. Kleinhenz, Ron O. Dror, Biswaranjan Pani, Conor McMahon and Seungkirl Ahn and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Dean P. Staus

29 papers receiving 2.6k citations

Hit 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.

Structure of the M2 muscarinic receptor–β-arrestin complex in a lipid nanodisc

2020 250 citations Dean P. Staus, A.L.W. Kleinhenz et al. Nature profile →

Peers

Countries citing papers authored by Dean P. Staus

Since Specialization

Citations

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

Fields of papers citing papers by Dean P. Staus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dean P. Staus. 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 Dean P. Staus. The network helps show where Dean P. Staus may publish in the future.

Co-authorship network of co-authors of Dean P. Staus

This figure shows the co-authorship network connecting the top 25 collaborators of Dean P. Staus. A scholar is included among the top collaborators of Dean P. Staus 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 Dean P. Staus. Dean P. Staus 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

#	Work	Indexed citations
1	Antibodies expand the scope of angiotensin receptor pharmacology 2024 ·Nature Chemical Biology ·Meredith A. Skiba, Sarah M. Sterling, Shaun Rawson, Shuhao Zhang, Huixin Xu, (unknown), (unknown), Morgan S. A. Gilman, (unknown), Peng‐Xiang Shen, Dean P. Staus, Ji‐Hee Kim, Conor McMahon, Maria K. Lehtinen, Howard A. Rockman, Patrick Barth, Laura M. Wingler, Andrew C. Kruse	13
2	Phosphorylation patterns in the AT1R C-terminal tail specify distinct downstream signaling pathways 2024 ·Science Signaling ·Clarice Gareri, (unknown), (unknown), João A. Paulo, Steven P. Gygi, Uyen Pham, (unknown), Laura M. Wingler, Dean P. Staus, Tomasz Maciej Stępniewski, Jana Selent, (unknown), (unknown), Sudarshan Rajagopal, Howard A. Rockman	6
3	Noncanonical scaffolding of G _αi and β-arrestin by G protein–coupled receptors 2021 ·Science ·Jeffrey S. Smith, Thomas F. Pack, Asuka Inoue, (unknown), (unknown), Issac Choi, Dylan Scott Eiger, Anmol Warman, Xinyu Xiong, Zhiyuan Ma, Gayathri Viswanathan, (unknown), Lauren K. Rochelle, Dean P. Staus, Joshua C. Snyder, Alem W. Kahsai, Marc G. Caron, Sudarshan Rajagopal	73
4	Unique Positive Cooperativity Between the β-Arrestin–Biased β-Blocker Carvedilol and a Small Molecule Positive Allosteric Modulator of the β2-Adrenergic Receptor 2021 ·Molecular Pharmacology ·Biswaranjan Pani, Seungkirl Ahn, Paula Rambarat, (unknown), Alem W. Kahsai, (unknown), (unknown), Dean P. Staus, Tommaso Costa, Robert J. Lefkowitz	16
5	Synthetic nanobodies as angiotensin receptor blockers 2020 ·Proceedings of the National Academy of Sciences ·Conor McMahon, Dean P. Staus, Laura M. Wingler, Jialu Wang, Meredith A. Skiba, Matthias Elgeti, Wayne L. Hubbell, Howard A. Rockman, Andrew C. Kruse, Robert J. Lefkowitz	38
6	Molecular mechanism of biased signaling in a prototypical G protein–coupled receptor 2020 ·Science ·Carl‐Mikael Suomivuori, Naomi R. Latorraca, Laura M. Wingler, Stephan Eismann, Matthew C. King, A.L.W. Kleinhenz, Meredith A. Skiba, Dean P. Staus, Andrew C. Kruse, Robert J. Lefkowitz, Ron O. Dror	167
7	Allosteric activation of proto-oncogene kinase Src by GPCR–beta-arrestin complexes 2020 ·Journal of Biological Chemistry ·Natalia Pakharukova, Ali Masoudi, Biswaranjan Pani, Dean P. Staus, Robert J. Lefkowitz	31
8	Molecular Mechanism of Biased Signaling in a Prototypical G-protein-coupled Receptor 2020 ·Biophysical Journal ·Carl‐Mikael Suomivuori, Naomi R. Latorraca, Laura M. Wingler, Stephan Eismann, Matthew C. King, A.L.W. Kleinhenz, Meredith A. Skiba, Dean P. Staus, Andrew C. Kruse, Robert J. Lefkowitz, Ron O. Dror	17
9	Mechanism of β ₂ AR regulation by an intracellular positive allosteric modulator 2019 ·Science ·Xiangyu Liu, Ali Masoudi, Alem W. Kahsai, Li-Yin Huang, Biswaranjan Pani, Dean P. Staus, Paul J. Shim, Kunio Hirata, (unknown), (unknown), Paula Rambarat, Seungkirl Ahn, Robert J. Lefkowitz, Brian K. Kobilka	90
10	Detergent- and phospholipid-based reconstitution systems have differential effects on constitutive activity of G-protein–coupled receptors 2019 ·Journal of Biological Chemistry ·Dean P. Staus, Laura M. Wingler, Dmitry Pichugin, R. Scott Prosser, Robert J. Lefkowitz	36
11	Angiotensin Analogs with Divergent Bias Stabilize Distinct Receptor Conformations 2019 ·Cell ·Laura M. Wingler, Matthias Elgeti, Daniel Hilger, Naomi R. Latorraca, Michael T. Lerch, Dean P. Staus, Ron O. Dror, Brian K. Kobilka, Wayne L. Hubbell, Robert J. Lefkowitz	191
12	Distinctive Activation Mechanism for Angiotensin Receptor Revealed by a Synthetic Nanobody 2019 ·Cell ·Laura M. Wingler, Conor McMahon, Dean P. Staus, Robert J. Lefkowitz, Andrew C. Kruse	135
13	G protein–coupled receptor kinases (GRKs) orchestrate biased agonism at the β ₂ -adrenergic receptor 2018 ·Science Signaling ·Minjung Choi, Dean P. Staus, Laura M. Wingler, Seungkirl Ahn, Biswaranjan Pani, W. Darrell Capel, Robert J. Lefkowitz	52
14	Small-Molecule Positive Allosteric Modulators of the β2-Adrenoceptor Isolated from DNA-Encoded Libraries 2018 ·Molecular Pharmacology ·Seungkirl Ahn, Biswaranjan Pani, Alem W. Kahsai, (unknown), (unknown), M. Vestergaard, Lei Jin, Shuai Zhao, Laura M. Wingler, Paula Rambarat, (unknown), (unknown), Lillian Sun, Paul J. Shim, Dean P. Staus, Li-Yin Huang, Thomas Franch, Xin Chen, Robert J. Lefkowitz	65
15	Multidimensional Tracking of GPCR Signaling via Peroxidase-Catalyzed Proximity Labeling 2017 ·Cell ·(unknown), Marian Kalocsay, Dean P. Staus, Laura M. Wingler, Roberta Pascolutti, João A. Paulo, Steven P. Gygi, Andrew C. Kruse	188
16	Gαi is required for carvedilol-induced β1 adrenergic receptor β-arrestin biased signaling 2017 ·Nature Communications ·Jialu Wang, Kenji Hanada, Dean P. Staus, Michael Makara, Giri Raj Dahal, Qiang Chen, Andrea Ahles, Stefan Engelhardt, Howard A. Rockman	77
17	Conformationally selective RNA aptamers allosterically modulate the β2-adrenoceptor 2016 ·Nature Chemical Biology ·Alem W. Kahsai, James W. Wisler, Jungmin Lee, Seungkirl Ahn, Thomas J. Cahill, S. Moses Dennison, Dean P. Staus, A. Thomsen, Kara Anasti, Biswaranjan Pani, Laura M. Wingler, Hemant Desai, Kristin M. Bompiani, Ryan T. Strachan, Xiaoxia Qin, (unknown), Bruce A. Sullenger, Robert J. Lefkowitz	66
18	Structure of active β-arrestin-1 bound to a G-protein-coupled receptor phosphopeptide 2013 ·Nature ·Arun K. Shukla, Aashish Manglik, Andrew C. Kruse, Kunhong Xiao, Rosana I. Reis, (unknown), Dean P. Staus, Daniel Hilger, Serdar Uysal, Li-Yin Huang, Marcin Paduch, (unknown), Akiko Koide, Shohei Koide, William I. Weis, Anthony A. Kossiakoff, Brian K. Kobilka, Robert J. Lefkowitz	353
19	Regulation of β2-Adrenergic Receptor Function by Conformationally Selective Single-Domain Intrabodies 2013 ·Molecular Pharmacology ·Dean P. Staus, Laura M. Wingler, Ryan T. Strachan, Søren G. F. Rasmussen, Els Pardon, Seungkirl Ahn, Jan Steyaert, Brian K. Kobilka, Robert J. Lefkowitz	110
20	Sphingosine 1-Phosphate Receptor 2 Signals Through Leukemia-Associated RhoGEF (LARG), to Promote Smooth Muscle Cell Differentiation 2010 ·Arteriosclerosis Thrombosis and Vascular Biology ·(unknown), Dean P. Staus, Adi D. Dubash, Joan M. Taylor, Christopher P. Mack	45

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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