Andrew S. Peterson

12.2k total citations · 1 hit paper
65 papers, 6.1k citations indexed

About

Andrew S. Peterson is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Andrew S. Peterson has authored 65 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 16 papers in Genetics and 12 papers in Surgery. Recurrent topics in Andrew S. Peterson's work include Hedgehog Signaling Pathway Studies (11 papers), Lipoproteins and Cardiovascular Health (7 papers) and Monoclonal and Polyclonal Antibodies Research (7 papers). Andrew S. Peterson is often cited by papers focused on Hedgehog Signaling Pathway Studies (11 papers), Lipoproteins and Cardiovascular Health (7 papers) and Monoclonal and Polyclonal Antibodies Research (7 papers). Andrew S. Peterson collaborates with scholars based in United States, France and Australia. Andrew S. Peterson's co-authors include R Myers, Andres V. Maricq, David Julius, Anthony J. Brake, Scott May, Brian Seed, Deepti Bhat, Amir M. Ashique, Steven J. Burakoff and Nila Patil and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Andrew S. Peterson

64 papers receiving 5.9k citations

Hit Papers

Primary Structure And Functional Expression of the 5HT 3 ... 1991 2026 2002 2014 1991 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew S. Peterson United States 39 4.0k 1.4k 1.3k 733 641 65 6.1k
Kirk R. Thomas United States 31 5.6k 1.4× 2.1k 1.5× 937 0.7× 630 0.9× 575 0.9× 46 7.5k
Norbert B. Ghyselinck France 54 6.3k 1.6× 2.6k 1.8× 719 0.5× 686 0.9× 1.1k 1.7× 114 8.9k
Tom Glaser United States 31 5.9k 1.5× 1.8k 1.2× 716 0.5× 637 0.9× 291 0.5× 51 7.7k
Douglas Forrest United States 46 3.9k 1.0× 1.5k 1.0× 1.5k 1.1× 426 0.6× 302 0.5× 113 7.8k
Christina Thaller United States 38 5.6k 1.4× 2.7k 1.9× 952 0.7× 627 0.9× 501 0.8× 67 7.1k
Philip M. Smallwood United States 37 5.4k 1.3× 1.1k 0.7× 1.2k 0.9× 879 1.2× 209 0.3× 52 6.5k
Rashmi Kothary Canada 50 5.1k 1.3× 1.1k 0.8× 1.1k 0.8× 1.2k 1.6× 354 0.6× 195 7.3k
Stefano Stifani Canada 47 4.6k 1.2× 975 0.7× 675 0.5× 479 0.7× 697 1.1× 99 7.1k
Yue Feng United States 43 4.9k 1.2× 2.4k 1.7× 1.3k 1.0× 545 0.7× 237 0.4× 115 7.1k
Norma J. Nowak United States 41 5.1k 1.3× 2.6k 1.8× 948 0.7× 571 0.8× 352 0.5× 140 8.4k

Countries citing papers authored by Andrew S. Peterson

Since Specialization
Citations

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

Fields of papers citing papers by Andrew S. Peterson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew S. Peterson

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew S. Peterson. A scholar is included among the top collaborators of Andrew S. Peterson 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 S. Peterson. Andrew S. Peterson 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.
Davies, C., Simon E. Vidal, Lilian Phu, et al.. (2021). Antibody toolkit reveals N-terminally ubiquitinated substrates of UBE2W. Nature Communications. 12(1). 4608–4608. 17 indexed citations
2.
Ultsch, Mark, Wenyan Li, Charles Eigenbrot, et al.. (2019). Identification of a Helical Segment within the Intrinsically Disordered Region of the PCSK9 Prodomain. Journal of Molecular Biology. 431(5). 885–903. 9 indexed citations
3.
Speca, David J., James S. Trimmer, Andrew S. Peterson, & Elva Dı́az. (2017). Whole exome sequencing reveals a functional mutation in the GAIN domain of the Bai2 receptor underlying a forward mutagenesis hyperactivity QTL. Mammalian Genome. 28(11-12). 465–475. 2 indexed citations
4.
Solloway, Mark J., Azadeh Madjidi, Chunyan Gu, et al.. (2015). Glucagon Couples Hepatic Amino Acid Catabolism to mTOR-Dependent Regulation of α-Cell Mass. Cell Reports. 12(3). 495–510. 144 indexed citations
5.
Zhang, Yingnan, Charles Eigenbrot, Lijuan Zhou, et al.. (2013). Identification of a Small Peptide That Inhibits PCSK9 Protein Binding to the Low Density Lipoprotein Receptor. Journal of Biological Chemistry. 289(2). 942–955. 127 indexed citations
6.
Zhang, Yingnan, Lijuan Zhou, Monica Kong-Beltran, et al.. (2012). Calcium-Independent Inhibition of PCSK9 by Affinity-Improved Variants of the LDL Receptor EGF(A) Domain. Journal of Molecular Biology. 422(5). 685–696. 31 indexed citations
7.
Phamluong, Khanhky, Wei Lin, Kai Barck, et al.. (2012). Chondroitin sulfate synthase 1 (Chsy1) is required for bone development and digit patterning. Developmental Biology. 363(2). 413–425. 67 indexed citations
8.
Lipari, Michael T., Wei Li, Paul Moran, et al.. (2012). Furin-cleaved Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Is Active and Modulates Low Density Lipoprotein Receptor and Serum Cholesterol Levels. Journal of Biological Chemistry. 287(52). 43482–43491. 75 indexed citations
9.
Phamluong, Khanhky, Li Li, Mei Sun, et al.. (2011). Global defects in collagen secretion in a Mia3/TANGO1 knockout mouse. The Journal of Cell Biology. 193(5). 935–951. 148 indexed citations
10.
Coulter, Sally, Christopher Liddle, Anne Wong, et al.. (2011). FGF19 Regulates Cell Proliferation, Glucose and Bile Acid Metabolism via FGFR4-Dependent and Independent Pathways. PLoS ONE. 6(3). e17868–e17868. 150 indexed citations
11.
Endoh‐Yamagami, Setsu, Kameel M. Karkar, Scott May, et al.. (2010). A mutation in the pericentrin gene causes abnormal interneuron migration to the olfactory bulb in mice. Developmental Biology. 340(1). 41–53. 29 indexed citations
12.
Vilhais-Neto, Gonçalo C., Karen Smith, Andrew S. Peterson, Jerry L. Workman, & Olivier Pourquié. (2009). 13-P031 Rere (Atrophin2) controls retinoic acid signaling and somite bilateral symmetry. Mechanisms of Development. 126. S203–S204.
13.
Evangelista, Marie, James Lee, Leon Parker, et al.. (2008). Kinome siRNA Screen Identifies Regulators of Ciliogenesis and Hedgehog Signal Transduction. Science Signaling. 1(39). ra7–ra7. 64 indexed citations
14.
Zarbalis, Konstantinos, Scott May, Yiguo Shen, et al.. (2004). A Focused and Efficient Genetic Screening Strategy in the Mouse: Identification of Mutations That Disrupt Cortical Development. PLoS Biology. 2(8). e219–e219. 104 indexed citations
15.
Zoltewicz, J. Susie, et al.. (2003). Atrophin 2 recruits histone deacetylase and is required for the function of multiple signaling centers during mouse embryogenesis. Development. 131(1). 3–14. 82 indexed citations
16.
Womack, Mary D., Kevin Thompson, Erika E. Fanselow, George J. Augustine, & Andrew S. Peterson. (1998). Elevated intracellular calcium levels in cerebellar granule neurons of weaver mice. Neuroreport. 9(15). 3391–3395. 5 indexed citations
17.
Macrae, Alexander D., Richard T. Premont, Mohamed Jaber, Andrew S. Peterson, & Robert J. Lefkowitz. (1996). Cloning, characterization, and chromosomal localization of rec1.3, a member of the G-protein-coupled receptor family highly expressed in brain. Molecular Brain Research. 42(2). 245–254. 35 indexed citations
18.
Patil, Nila, David R. Cox, Deepti Bhat, et al.. (1995). A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nature Genetics. 11(2). 126–129. 437 indexed citations
19.
Bulfone, Alessandro, Susan Smiga, Kenji Shimamura, et al.. (1995). T-Brain-1: A homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex. Neuron. 15(1). 63–78. 364 indexed citations
20.
Ratnofsky, S, Andrew S. Peterson, J L Greenstein, & Steven J. Burakoff. (1987). Expression and function of CD8 in a murine T cell hybridoma.. The Journal of Experimental Medicine. 166(6). 1747–1757. 54 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026