Philip M. Smallwood

9.9k total citations · 2 hit papers
52 papers, 6.5k citations indexed

About

Philip M. Smallwood is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Philip M. Smallwood has authored 52 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 15 papers in Cell Biology and 14 papers in Cellular and Molecular Neuroscience. Recurrent topics in Philip M. Smallwood's work include Wnt/β-catenin signaling in development and cancer (23 papers), Retinal Development and Disorders (11 papers) and Axon Guidance and Neuronal Signaling (10 papers). Philip M. Smallwood is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (23 papers), Retinal Development and Disorders (11 papers) and Axon Guidance and Neuronal Signaling (10 papers). Philip M. Smallwood collaborates with scholars based in United States, France and China. Philip M. Smallwood's co-authors include Jeremy Nathans, Amir Rattner, Yanshu Wang, John Williams, John C. Williams, Debra J. Gilbert, Yulian Zhou, Chris Cho, Jennifer P. Macke and Hui Sun and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Philip M. Smallwood

51 papers receiving 6.4k citations

Hit Papers

Vascular Development in the Retina and Inner Ear 1999 2026 2008 2017 2004 1999 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip M. Smallwood United States 37 5.4k 1.2k 1.1k 879 611 52 6.5k
Amir Rattner United States 33 4.1k 0.8× 951 0.8× 645 0.6× 607 0.7× 540 0.9× 62 5.3k
Dennis S. Rice United States 30 2.9k 0.5× 1.8k 1.4× 551 0.5× 858 1.0× 400 0.7× 55 5.0k
Paola Bovolenta Spain 51 5.2k 1.0× 2.5k 2.0× 1.2k 1.2× 1.2k 1.3× 333 0.5× 125 7.3k
Frederick J. Livesey United Kingdom 42 6.2k 1.2× 2.0k 1.6× 907 0.9× 795 0.9× 493 0.8× 73 8.3k
Ruth Ashery‐Padan Israel 44 4.7k 0.9× 905 0.7× 1.1k 1.0× 781 0.9× 219 0.4× 80 6.0k
Takahisa Furukawa Japan 46 7.1k 1.3× 2.5k 2.0× 1.3k 1.3× 1.2k 1.4× 188 0.3× 130 8.4k
Hannie Kremer Netherlands 44 5.1k 1.0× 697 0.6× 1.2k 1.1× 728 0.8× 1.1k 1.7× 188 8.0k
Valeria Marigo Italy 35 4.3k 0.8× 791 0.6× 1.1k 1.0× 638 0.7× 133 0.2× 88 5.0k
Chyuan‐Sheng Lin United States 31 4.3k 0.8× 778 0.6× 1.3k 1.2× 540 0.6× 255 0.4× 70 6.5k
Josseline Kaplan France 41 6.9k 1.3× 911 0.7× 1.4k 1.3× 1.0k 1.2× 393 0.6× 172 9.0k

Countries citing papers authored by Philip M. Smallwood

Since Specialization
Citations

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

Fields of papers citing papers by Philip M. Smallwood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip M. Smallwood. 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 Philip M. Smallwood. The network helps show where Philip M. Smallwood may publish in the future.

Co-authorship network of co-authors of Philip M. Smallwood

This figure shows the co-authorship network connecting the top 25 collaborators of Philip M. Smallwood. A scholar is included among the top collaborators of Philip M. Smallwood 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 Philip M. Smallwood. Philip M. Smallwood 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.
Zhu, Ningyu, Philip M. Smallwood, Amir Rattner, et al.. (2024). Utility of protein–protein binding surfaces composed of anti-parallel alpha-helices and beta-sheets selected by phage display. Journal of Biological Chemistry. 300(5). 107283–107283.
2.
Wang, Yanshu, Arjun K. Venkatesh, Jiajia Xu, et al.. (2022). The WNT7A/WNT7B/GPR124/RECK signaling module plays an essential role in mammalian limb development. Development. 149(9). 6 indexed citations
3.
Williams, John, et al.. (2019). Defining the binding interface of Amyloid Precursor Protein (APP) and Contactin3 (CNTN3) by site-directed mutagenesis. PLoS ONE. 14(7). e0219384–e0219384. 3 indexed citations
4.
Wang, Yanshu, Chris Cho, John Williams, et al.. (2018). Interplay of the Norrin and Wnt7a/Wnt7b signaling systems in blood–brain barrier and blood–retina barrier development and maintenance. Proceedings of the National Academy of Sciences. 115(50). E11827–E11836. 107 indexed citations
6.
Chang, Hao, Philip M. Smallwood, John S. Williams, & Jeremy Nathans. (2017). Intramembrane Proteolysis of Astrotactins. Journal of Biological Chemistry. 292(8). 3506–3516. 5 indexed citations
7.
Zhou, Yulian, John Williams, Philip M. Smallwood, & Jeremy Nathans. (2015). Sox7, Sox17, and Sox18 Cooperatively Regulate Vascular Development in the Mouse Retina. PLoS ONE. 10(12). e0143650–e0143650. 70 indexed citations
8.
Chang, Hao, Hugh Cahill, Philip M. Smallwood, Yanshu Wang, & Jeremy Nathans. (2015). Identification of Astrotactin2 as a Genetic Modifier That Regulates the Global Orientation of Mammalian Hair Follicles. PLoS Genetics. 11(9). e1005532–e1005532. 18 indexed citations
9.
Hua, Zhong L., Hao Chang, Yanshu Wang, Philip M. Smallwood, & Jeremy Nathans. (2014). Partial interchangeability of Fz3 and Fz6 in tissue polarity signaling for epithelial orientation and axon growth and guidance. Development. 141(20). 3944–3954. 25 indexed citations
10.
Badea, Tudor C., et al.. (2012). Combinatorial Expression of Brn3 Transcription Factors in Somatosensory Neurons: Genetic and Morphologic Analysis. Journal of Neuroscience. 32(3). 995–1007. 68 indexed citations
11.
Wang, Yanshu, Amir Rattner, Yulian Zhou, et al.. (2012). Norrin/Frizzled4 Signaling in Retinal Vascular Development and Blood Brain Barrier Plasticity. Cell. 151(6). 1332–1344. 286 indexed citations
12.
Ye, Xin, Yanshu Wang, Hugh Cahill, et al.. (2009). Norrin, Frizzled-4, and Lrp5 Signaling in Endothelial Cells Controls a Genetic Program for Retinal Vascularization. Cell. 139(2). 285–298. 346 indexed citations
13.
Liu, Chunqiao, Yanshu Wang, Philip M. Smallwood, & Jeremy Nathans. (2008). An Essential Role for Frizzled5 in Neuronal Survival in the Parafascicular Nucleus of the Thalamus. Journal of Neuroscience. 28(22). 5641–5653. 53 indexed citations
14.
Rotolo, Thomas, Philip M. Smallwood, John Williams, & Jeremy Nathans. (2008). Genetically-Directed, Cell Type-Specific Sparse Labeling for the Analysis of Neuronal Morphology. PLoS ONE. 3(12). e4099–e4099. 61 indexed citations
15.
Liu, Chunqiao, Yanshu Wang, Philip M. Smallwood, & Jeremy Nathans. (2008). An essential role for Frizzled5 in neuronal survival in the parafascicular nucleus of the thalamus. Developmental Biology. 319(2). 536–536. 6 indexed citations
16.
Rattner, Amir, Philip M. Smallwood, John C. Williams, et al.. (2001). A Photoreceptor-Specific Cadherin Is Essential for the Structural Integrity of the Outer Segment and for Photoreceptor Survival. Neuron. 32(5). 775–786. 106 indexed citations
17.
Sun, Hui, Philip M. Smallwood, & Jeremy Nathans. (2000). Biochemical defects in ABCR protein variants associated with human retinopathies. Nature Genetics. 26(2). 242–246. 164 indexed citations
18.
Sun, Hui, et al.. (1997). Identification and characterization of a conserved family of protein serine/threonine phosphatases homologous to Drosophila retinal degeneration C (rdgC). Proceedings of the National Academy of Sciences. 94(21). 11639–11644. 45 indexed citations
19.
Johns, Donald R., David Valle, Charles Eil, et al.. (1990). Mutation in the Gene Encoding the Stimulatory G Protein of Adenylate Cyclase in Albright's Hereditary Osteodystrophy. New England Journal of Medicine. 322(20). 1412–1419. 288 indexed citations
20.
Levine, Michael A., Keith D. Kaufman, Philip M. Smallwood, et al.. (1988). Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.. Proceedings of the National Academy of Sciences. 85(2). 617–621. 99 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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