Lorna Taylor

2.4k total citations · 1 hit paper
24 papers, 1.8k citations indexed

About

Lorna Taylor is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Lorna Taylor has authored 24 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Lorna Taylor's work include CRISPR and Genetic Engineering (16 papers), Animal Genetics and Reproduction (16 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Lorna Taylor is often cited by papers focused on CRISPR and Genetic Engineering (16 papers), Animal Genetics and Reproduction (16 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Lorna Taylor collaborates with scholars based in United Kingdom, United States and Iceland. Lorna Taylor's co-authors include Debra Rose Wilson, Michael J. McGrew, Milton J. Finegold, Ching N. Ou, Allan Bradley, Gretchen J. Darlington, Margaret Wilde, Adrian Sherman, Helen Sang and James D. Glover and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Lorna Taylor

24 papers receiving 1.7k citations

Hit Papers

Impaired Energy Homeostasis in C/EBPα Knockout Mice 1995 2026 2005 2015 1995 250 500 750

Peers

Lorna Taylor
Elena Grigorieva United Kingdom
Heidi Dorward United States
Scott A. Ochsner United States
Darryl L. Hadsell United States
Amiya K. Ghosh United States
Lorin K. Johnson United States
Elena Grigorieva United Kingdom
Lorna Taylor
Citations per year, relative to Lorna Taylor Lorna Taylor (= 1×) peers Elena Grigorieva

Countries citing papers authored by Lorna Taylor

Since Specialization
Citations

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

Fields of papers citing papers by Lorna Taylor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lorna Taylor. 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 Lorna Taylor. The network helps show where Lorna Taylor may publish in the future.

Co-authorship network of co-authors of Lorna Taylor

This figure shows the co-authorship network connecting the top 25 collaborators of Lorna Taylor. A scholar is included among the top collaborators of Lorna Taylor 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 Lorna Taylor. Lorna Taylor 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.
Doddamani, Dadakhalandar, et al.. (2025). Propagation of goose primordial germ cells in vitro relies on FGF and BMP signalling pathways. Communications Biology. 8(1). 301–301. 1 indexed citations
2.
Doddamani, Dadakhalandar, Daniel F. Carlson, Lynn McTeir, et al.. (2025). PRDM14 is essential for vertebrate gastrulation and safeguards avian germ cell identity. Developmental Biology. 521. 129–137. 1 indexed citations
3.
Sheffield, David, et al.. (2024). Musculoskeletal pain and working practices in the UK early childhood education workforce. Safety Science. 178. 106592–106592. 1 indexed citations
4.
Doddamani, Dadakhalandar, Mark Woodcock, Lorna Taylor, et al.. (2023). The Transcriptome of Chicken Migratory Primordial Germ Cells Reveals Intrinsic Sex Differences and Expression of Hallmark Germ Cell Genes. Cells. 12(8). 1151–1151. 4 indexed citations
5.
Idoko-Akoh, Alewo, Daniel H. Goldhill, Carol Sheppard, et al.. (2023). Creating resistance to avian influenza infection through genome editing of the ANP32 gene family. Nature Communications. 14(1). 45 indexed citations
6.
Taylor, Lorna, Tuanjun Hu, Dominique Meunier, et al.. (2021). Avian Primordial Germ Cells Are Bipotent for Male or Female Gametogenesis. Frontiers in Cell and Developmental Biology. 9. 726827–726827. 13 indexed citations
7.
Woodcock, Mark, Dadakhalandar Doddamani, Tuanjun Hu, et al.. (2021). Direct allele introgression into pure chicken breeds using Sire Dam Surrogate (SDS) mating. Nature Communications. 12(1). 659–659. 63 indexed citations
8.
Woodcock, Mark, Almas Gheyas, Andrew S. Mason, et al.. (2019). Reviving rare chicken breeds using genetically engineered sterility in surrogate host birds. Proceedings of the National Academy of Sciences. 116(42). 20930–20937. 57 indexed citations
9.
Idoko-Akoh, Alewo, Lorna Taylor, Helen Sang, & Michael J. McGrew. (2018). High fidelity CRISPR/Cas9 increases precise monoallelic and biallelic editing events in primordial germ cells. Scientific Reports. 8(1). 15126–15126. 37 indexed citations
10.
Taylor, Lorna, et al.. (2016). Cryopreservation of specialized chicken lines using cultured primordial germ cells. Poultry Science. 95(8). 1905–1911. 44 indexed citations
11.
Whyte, Jemima, James D. Glover, Mark Woodcock, et al.. (2015). FGF, Insulin, and SMAD Signaling Cooperate for Avian Primordial Germ Cell Self-Renewal. Stem Cell Reports. 5(6). 1171–1182. 142 indexed citations
12.
Glover, James D., Jemima Whyte, Joanna Brzeszczyńska, et al.. (2014). Culturing avian primordial germ cells and novel transposon vectors for transgenesis. Transgenic Research. 23(1). 193–193. 2 indexed citations
13.
Glover, James D., et al.. (2013). A Novel Piggybac Transposon Inducible Expression System Identifies a Role for Akt Signalling in Primordial Germ Cell Migration. PLoS ONE. 8(11). e77222–e77222. 24 indexed citations
14.
Macdonald, Joni, Lorna Taylor, Helen Sang, & Mike J. McGrew. (2012). Genetic Modification of the chicken genome using transposable elements. Transgenic Research. 21(4). 912–913. 4 indexed citations
15.
Macdonald, Joni, Lorna Taylor, Adrian Sherman, et al.. (2012). Efficient genetic modification and germ-line transmission of primordial germ cells using piggyBac and Tol2 transposons. Proceedings of the National Academy of Sciences. 109(23). E1466–72. 136 indexed citations
16.
Macdonald, Joni, James D. Glover, Lorna Taylor, Helen Sang, & Michael J. McGrew. (2010). Characterisation and Germline Transmission of Cultured Avian Primordial Germ Cells. PLoS ONE. 5(11). e15518–e15518. 127 indexed citations
17.
McGrew, Michael J., Adrian Sherman, Simon Lillico, Lorna Taylor, & Helen Sang. (2010). Functional conservation between rodents and chicken of regulatory sequences driving skeletal muscle gene expression in transgenic chickens. BMC Developmental Biology. 10(1). 26–26. 13 indexed citations
18.
Lilliendahl, Kristján, Jón Sólmundsson, Guðmundur A. Guðmundsson, & Lorna Taylor. (2003). Can Surveillance Radar be used to Monitor the Foraging Distribution of Colonially Breeding Alcids?. Ornithological Applications. 105(1). 145–150. 2 indexed citations
19.
Lilliendahl, Kristján, Jón Sólmundsson, Guðmundur A. Guðmundsson, & Lorna Taylor. (2003). CAN SURVEILLANCE RADAR BE USED TO MONITOR THE FORAGING DISTRIBUTION OF COLONIALLY BREEDING ALCIDS?. Ornithological Applications. 105(1). 145–145. 4 indexed citations
20.
Ning, Yujie, et al.. (1992). Isolation of monochromosomal hybrids following fusion of human diploid fibroblast-derived microcells with mouse A9 cells. Cytogenetic and Genome Research. 60(1). 79–80. 13 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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