Philip J. Gage

4.6k total citations
52 papers, 3.7k citations indexed

About

Philip J. Gage is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Philip J. Gage has authored 52 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Philip J. Gage's work include Developmental Biology and Gene Regulation (16 papers), Growth Hormone and Insulin-like Growth Factors (8 papers) and Congenital heart defects research (7 papers). Philip J. Gage is often cited by papers focused on Developmental Biology and Gene Regulation (16 papers), Growth Hormone and Insulin-like Growth Factors (8 papers) and Congenital heart defects research (7 papers). Philip J. Gage collaborates with scholars based in United States, Canada and Sweden. Philip J. Gage's co-authors include Sally A. Camper, Hoonkyo Suh, Michael Levine, Joseph C. Glorioso, Tord Hjalt, Amanda L. Zacharias, Amanda Evans, Sandra K. Prucka, William Rhoades and Jacques Drouin and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Blood.

In The Last Decade

Philip J. Gage

52 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip J. Gage United States 31 2.4k 1.0k 529 514 445 52 3.7k
Peter Colosi United States 28 2.6k 1.1× 2.1k 2.0× 197 0.4× 259 0.5× 195 0.4× 46 3.5k
Nicola Ragge United Kingdom 29 1.1k 0.4× 1.2k 1.1× 288 0.5× 277 0.5× 75 0.2× 74 2.6k
Charlene J. Williams United States 28 1.2k 0.5× 933 0.9× 97 0.2× 320 0.6× 255 0.6× 64 3.2k
Hélène Dollfus France 42 4.8k 2.0× 3.0k 2.8× 344 0.7× 177 0.3× 84 0.2× 178 6.7k
Giorgio Corte Italy 38 2.7k 1.1× 501 0.5× 341 0.6× 108 0.2× 99 0.2× 69 4.3k
Sylvia Hu United States 19 2.0k 0.8× 516 0.5× 505 1.0× 167 0.3× 118 0.3× 32 3.4k
K. Reed Clark United States 29 3.2k 1.3× 1.9k 1.9× 189 0.4× 451 0.9× 24 0.1× 40 4.3k
Masaru Tamura Japan 29 1.6k 0.7× 516 0.5× 237 0.4× 217 0.4× 54 0.1× 121 2.9k
Iqbal Ahmad United States 37 3.2k 1.3× 335 0.3× 664 1.3× 84 0.2× 80 0.2× 106 3.9k
Nancy A. Jenkins United States 27 3.7k 1.5× 1.0k 1.0× 161 0.3× 185 0.4× 113 0.3× 44 5.0k

Countries citing papers authored by Philip J. Gage

Since Specialization
Citations

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

Fields of papers citing papers by Philip J. Gage

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip J. Gage

This figure shows the co-authorship network connecting the top 25 collaborators of Philip J. Gage. A scholar is included among the top collaborators of Philip J. Gage 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 J. Gage. Philip J. Gage 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.
Seo, Seungwoon, Sam Li‐Sheng Chen, Wenzhong Liu, et al.. (2017). Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development. Investigative Ophthalmology & Visual Science. 58(3). 1368–1368. 42 indexed citations
2.
Alam, Denise Al, Frédéric Sala, Soula Danopoulos, et al.. (2012). FGF9–Pitx2–FGF10 signaling controls cecal formation in mice. Developmental Biology. 369(2). 340–348. 22 indexed citations
3.
Bassett, Erin A., Trevor Williams, Amanda L. Zacharias, et al.. (2010). AP-2α knockout mice exhibit optic cup patterning defects and failure of optic stalk morphogenesis. Human Molecular Genetics. 19(9). 1791–1804. 50 indexed citations
4.
Zacharias, Amanda L., Mark Lewandoski, Michael A. Rudnicki, & Philip J. Gage. (2010). Pitx2 is an upstream activator of extraocular myogenesis and survival. Developmental Biology. 349(2). 395–405. 47 indexed citations
5.
Davis, Shannon W., et al.. (2009). Loss of β-catenin in the Wnt1 expression domain results in an expansion of Rathke's pouch. Developmental Biology. 331(2). 491–491. 1 indexed citations
6.
Gage, Philip J. & Amanda L. Zacharias. (2009). Signaling “cross‐talk” is integrated by transcription factors in the development of the anterior segment in the eye. Developmental Dynamics. 238(9). 2149–2162. 40 indexed citations
7.
Qian, Min, et al.. (2008). Pitx2 is critical for the survival and specification of extraocular muscles. Developmental Biology. 319(2). 536–536. 3 indexed citations
8.
L’honoré, Aurore, Vincent Coulon, Alexandre Marcil, et al.. (2007). Sequential expression and redundancy of Pitx2 and Pitx3 genes during muscle development. Developmental Biology. 307(2). 421–433. 70 indexed citations
9.
Nowotschin, Sonja, Jun Liao, Philip J. Gage, et al.. (2006). Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development. 133(8). 1565–1573. 108 indexed citations
10.
Ai, Di, Wei Liu, Lijiang Ma, et al.. (2006). Pitx2 regulates cardiac left–right asymmetry by patterning second cardiac lineage-derived myocardium. Developmental Biology. 296(2). 437–449. 96 indexed citations
11.
Evans, Amanda & Philip J. Gage. (2006). The essential role of Pitx2 in extraocular muscle development. Developmental Biology. 295(1). 384–385. 2 indexed citations
12.
Skidmore, Jennifer, et al.. (2006). Nestin-Cre mediated deletion ofPitx2 in the mouse. genesis. 44(7). 336–344. 36 indexed citations
13.
Berry, Fred B., Matthew A. Lines, Tim Footz, et al.. (2006). Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld–Rieger syndrome and anterior segment dysgenesis. Human Molecular Genetics. 15(6). 905–919. 7 indexed citations
14.
Degar, Barbara, et al.. (2006). Hematopoiesis following disruption of the Pitx2 homeodomain gene. Experimental Hematology. 34(2). 167–178. 6 indexed citations
15.
Gage, Philip J. & Amanda Evans. (2005). Pitx2 Function in Neural Crest Is Required for Specific Intrinsic and Extrinsic Functions During Eye Development. Investigative Ophthalmology & Visual Science. 46(13). 3129–3129. 1 indexed citations
16.
Gage, Philip J., William Rhoades, Sandra K. Prucka, & Tord Hjalt. (2005). Fate Maps of Neural Crest and Mesoderm in the Mammalian Eye. Investigative Ophthalmology & Visual Science. 46(11). 4200–4200. 289 indexed citations
17.
Swaroop, Anand, Masayuki Akimoto, Elena V. Filippova, & Philip J. Gage. (2003). Transgenic Mice Lines Expressing Cre-Recombinase Specifically in the Photoreceptors or Retinal Pigment Epithelium: Towards Somatic Mutagenesis in Retinal Cell Types. Investigative Ophthalmology & Visual Science. 44(13). 4526–4526. 2 indexed citations
18.
Martin, Donna M., Jennifer Skidmore, Claudia Vieira, et al.. (2003). PITX2 is required for normal development of neurons in the mouse subthalamic nucleus and midbrain. Developmental Biology. 267(1). 93–108. 87 indexed citations
19.
Gage, Philip J. & Hoonkyo Suh. (1999). The bicoid -related Pitx gene family in development. Mammalian Genome. 10(2). 197–200. 127 indexed citations
20.

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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