Philip A. Leighton

5.4k total citations · 1 hit paper
46 papers, 3.3k citations indexed

About

Philip A. Leighton is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Philip A. Leighton has authored 46 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 21 papers in Genetics and 10 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Philip A. Leighton's work include Animal Genetics and Reproduction (15 papers), CRISPR and Genetic Engineering (11 papers) and Monoclonal and Polyclonal Antibodies Research (10 papers). Philip A. Leighton is often cited by papers focused on Animal Genetics and Reproduction (15 papers), CRISPR and Genetic Engineering (11 papers) and Monoclonal and Polyclonal Antibodies Research (10 papers). Philip A. Leighton collaborates with scholars based in United States, Germany and Chile. Philip A. Leighton's co-authors include Shirley M. Tilghman, Robert S. Ingram, Jonathan Eggenschwiler, Argiris Efstratiadis, Marie‐Cecile van de Lavoir, Jennifer Saam, Jeremy K. M. Sanders, R. J. Etches, S M Tilghman and Colin L. Stewart and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Philip A. Leighton

45 papers receiving 3.2k citations

Hit Papers

Disruption of imprinting caused by deletion of the H19 ge... 1995 2026 2005 2015 1995 200 400 600

Peers

Philip A. Leighton
Neil Vargesson United Kingdom
Christopher J. Ward United States
Yinghua Shen United States
Peggy S. Eis United States
Christopher S. Navara United States
W. J. Hage Netherlands
Larry L. Deaven United States
James McGrath United States
Andrew E. H. Elia United States
Neil Vargesson United Kingdom
Philip A. Leighton
Citations per year, relative to Philip A. Leighton Philip A. Leighton (= 1×) peers Neil Vargesson

Countries citing papers authored by Philip A. Leighton

Since Specialization
Citations

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

Fields of papers citing papers by Philip A. Leighton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip A. Leighton

This figure shows the co-authorship network connecting the top 25 collaborators of Philip A. Leighton. A scholar is included among the top collaborators of Philip A. Leighton 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 A. Leighton. Philip A. Leighton 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.
Ching, Kathryn H., Darlene Pedersen, Alba T. Macias, et al.. (2021). Common light chain chickens produce human antibodies of high affinity and broad epitope coverage for the engineering of bispecifics. mAbs. 13(1). 1862451–1862451. 7 indexed citations
2.
Cameron, Béatrice, Tarik Dabdoubi, F Soubrier, et al.. (2020). Complementary epitopes and favorable developability of monoclonal anti-LAMP1 antibodies generated using two transgenic animal platforms. PLoS ONE. 15(7). e0235815–e0235815. 6 indexed citations
3.
Ching, Kathryn H., et al.. (2020). Expression of human lambda expands the repertoire of OmniChickens. PLoS ONE. 15(1). e0228164–e0228164. 5 indexed citations
4.
Collarini, Ellen J., Philip A. Leighton, & Marie‐Cecile van de Lavoir. (2018). Production of Transgenic Chickens Using Cultured Primordial Germ Cells and Gonocytes. Methods in molecular biology. 1874. 403–430. 20 indexed citations
5.
Leighton, Philip A., et al.. (2018). V(D)J Rearrangement Is Dispensable for Producing CDR-H3 Sequence Diversity in a Gene Converting Species. Frontiers in Immunology. 9. 1317–1317. 6 indexed citations
6.
Dimitrov, Lazar, Darlene Pedersen, Kathryn H. Ching, et al.. (2016). Germline Gene Editing in Chickens by Efficient CRISPR-Mediated Homologous Recombination in Primordial Germ Cells. PLoS ONE. 11(4). e0154303–e0154303. 84 indexed citations
7.
Leighton, Philip A., Darlene Pedersen, Kathryn H. Ching, et al.. (2016). Generation of chickens expressing Cre recombinase. Transgenic Research. 25(5). 609–616. 11 indexed citations
8.
Leighton, Philip A., et al.. (2015). A Diverse Repertoire of Human Immunoglobulin Variable Genes in a Chicken B Cell Line is Generated by Both Gene Conversion and Somatic Hypermutation. Frontiers in Immunology. 6. 126–126. 18 indexed citations
9.
Schusser, Benjamin, Ellen J. Collarini, Shelley Izquierdo, et al.. (2013). Harnessing Gene Conversion in Chicken B Cells to Create a Human Antibody Sequence Repertoire. PLoS ONE. 8(11). e80108–e80108. 25 indexed citations
10.
Schusser, Benjamin, Ellen J. Collarini, Shelley Izquierdo, et al.. (2013). Immunoglobulin knockout chickens via efficient homologous recombination in primordial germ cells. Proceedings of the National Academy of Sciences. 110(50). 20170–20175. 122 indexed citations
11.
Lavoir, Marie‐Cecile van de, Ellen J. Collarini, Philip A. Leighton, et al.. (2012). Interspecific Germline Transmission of Cultured Primordial Germ Cells. PLoS ONE. 7(5). e35664–e35664. 57 indexed citations
12.
Leighton, Philip A., et al.. (2008). Genetic modification of primordial germ cells by gene trapping, gene targeting, and ϕC31 integrase. Molecular Reproduction and Development. 75(7). 1163–1175. 50 indexed citations
13.
Lavoir, Marie‐Cecile van de, Philip A. Leighton, Babette S. Heyer, et al.. (2006). Germline transmission of genetically modified primordial germ cells. Nature. 441(7094). 766–769. 355 indexed citations
14.
Lavoir, Marie‐Cecile van de, Philip A. Leighton, Babette S. Heyer, et al.. (2005). High-grade transgenic somatic chimeras from chicken embryonic stem cells. Mechanisms of Development. 123(1). 31–41. 86 indexed citations
15.
Leighton, Philip A., Kevin J. Mitchell, Lisa V. Goodrich, et al.. (2001). Defining brain wiring patterns and mechanisms through gene trapping in mice. Nature. 410(6825). 174–179. 338 indexed citations
16.
Mitchell, Kevin J., Olivia Kelly, Jane Brennan, et al.. (2001). Functional analysis of secreted and transmembrane proteins critical to mouse development. Nature Genetics. 28(3). 241–249. 341 indexed citations
17.
Eggenschwiler, Jonathan, Thomas Ludwig, Peter Fisher, et al.. (1997). Mouse mutant embryos overexpressing IGF-II exhibit phenotypic features of the Beckwith–Wiedemann and Simpson–Golabi–Behmel syndromes. Genes & Development. 11(23). 3128–3142. 270 indexed citations
18.
Leighton, Philip A., Jennifer Saam, Robert S. Ingram, & Shirley M. Tilghman. (1996). Genomic Imprinting in Mice: Its Function and Mechanism1. Biology of Reproduction. 54(2). 273–278. 45 indexed citations
19.
Tilghman, S M, Marisa S. Bartolomei, Andrea L. Webber, et al.. (1993). Parental Imprinting of the H19 and Igf2 Genes in the Mouse. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 287–295. 19 indexed citations
20.
Leighton, Philip A. & Pei‐Hua Lu. (1987). .lambda. cro Repressor complex with OR3 DNA: nitrogen-15 NMR observations. Biochemistry. 26(23). 7262–7271. 30 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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