Helen Sang

4.3k total citations
59 papers, 3.1k citations indexed

About

Helen Sang is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Helen Sang has authored 59 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Molecular Biology, 35 papers in Genetics and 11 papers in Immunology. Recurrent topics in Helen Sang's work include Animal Genetics and Reproduction (32 papers), CRISPR and Genetic Engineering (28 papers) and Virus-based gene therapy research (8 papers). Helen Sang is often cited by papers focused on Animal Genetics and Reproduction (32 papers), CRISPR and Genetic Engineering (28 papers) and Virus-based gene therapy research (8 papers). Helen Sang collaborates with scholars based in United Kingdom, United States and Australia. Helen Sang's co-authors include Michael J. McGrew, Adrian Sherman, Simon Lillico, Hazel Gilhooley, Lorna Taylor, Kyriacos Mitrophanous, Fiona M. Ellard, Christine M. Mather, Joni Macdonald and Margaret M. Perry and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Helen Sang

59 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Helen Sang United Kingdom 30 2.2k 1.7k 267 241 228 59 3.1k
Scott C. Fahrenkrug United States 35 3.2k 1.4× 2.3k 1.4× 398 1.5× 267 1.1× 513 2.3× 88 4.5k
Isaäc J. Nijman Netherlands 36 2.6k 1.2× 1.9k 1.1× 388 1.5× 384 1.6× 549 2.4× 81 5.1k
Simon Lillico United Kingdom 28 2.4k 1.1× 2.0k 1.2× 161 0.6× 90 0.4× 299 1.3× 66 3.2k
Kumiko Ui‐Tei Japan 34 3.9k 1.8× 696 0.4× 484 1.8× 362 1.5× 501 2.2× 105 5.0k
Xiaoxiang Hu China 33 1.5k 0.7× 1.7k 1.0× 416 1.6× 196 0.8× 297 1.3× 175 3.5k
Moisés Mallo Portugal 35 3.3k 1.5× 1.2k 0.7× 460 1.7× 241 1.0× 155 0.7× 78 4.5k
M. C. T. Penedo United States 28 762 0.3× 1.2k 0.7× 229 0.9× 341 1.4× 87 0.4× 88 2.6k
Cord Drögemüller Switzerland 37 2.3k 1.0× 2.7k 1.6× 139 0.5× 717 3.0× 327 1.4× 349 5.4k
Daniel F. Carlson United States 24 2.6k 1.2× 1.6k 1.0× 90 0.3× 257 1.1× 374 1.6× 50 3.2k
Michael J. McGrew United Kingdom 24 2.5k 1.1× 1.3k 0.8× 88 0.3× 245 1.0× 189 0.8× 37 2.9k

Countries citing papers authored by Helen Sang

Since Specialization
Citations

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

Fields of papers citing papers by Helen Sang

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helen Sang

This figure shows the co-authorship network connecting the top 25 collaborators of Helen Sang. A scholar is included among the top collaborators of Helen Sang 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 Helen Sang. Helen Sang 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.
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
2.
Long, Jason S., Alewo Idoko-Akoh, Bhakti Mistry, et al.. (2019). Species specific differences in use of ANP32 proteins by influenza A virus. eLife. 8. 67 indexed citations
3.
Flight, Monica Hoyos, et al.. (2017). Genome Editing and the Future of Farming meeting report. Transgenic Research. 26(2). 319–321. 2 indexed citations
4.
Rozbicki, Emil, Manli Chuai, Antti Karjalainen, et al.. (2015). Myosin-II-mediated cell shape changes and cell intercalation contribute to primitive streak formation. Nature Cell Biology. 17(4). 397–408. 146 indexed citations
5.
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
6.
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
7.
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
8.
Valášek, Petr, Susanne Theis, April DeLaurier, et al.. (2011). Cellular and molecular investigations into the development of the pectoral girdle. Developmental Biology. 357(1). 108–116. 58 indexed citations
9.
Towers, Matthew, Jason Signolet, Adrian Sherman, Helen Sang, & Cheryll Tickle. (2011). Insights into bird wing evolution and digit specification from polarizing region fate maps. Nature Communications. 2(1). 426–426. 64 indexed citations
10.
Sherman, Adrian, et al.. (2010). The Roslin Institute Transgenic Chicken Facility: developments in chicken transgenesis. Transgenic Research. 19(1). 151–151. 1 indexed citations
11.
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
12.
McGrew, Michael J., Adrian Sherman, Simon Lillico, et al.. (2008). Localised axial progenitor cell populations in the avian tail bud are not committed to a posterior Hox identity. Development. 135(13). 2289–2299. 124 indexed citations
13.
Bru, Thierry, et al.. (2008). Rapid induction of pluripotency genes after exposure of human somatic cells to mouse ES cell extracts. Experimental Cell Research. 314(14). 2634–2642. 61 indexed citations
14.
Das, Raman M, Gareth R. Howell, Elizabeth R. Farrell, et al.. (2006). A robust system for RNA interference in the chicken using a modified microRNA operon. Developmental Biology. 294(2). 554–563. 172 indexed citations
15.
16.
McGrew, Michael J., Adrian Sherman, Fiona M. Ellard, et al.. (2004). Efficient production of germline transgenic chickens using lentiviral vectors. EMBO Reports. 5(7). 728–733. 292 indexed citations
17.
Sang, Helen. (2004). Prospects for transgenesis in the chick. Mechanisms of Development. 121(9). 1179–1186. 84 indexed citations
18.
Gaunt, Stephen J., Wendy Dean, Helen Sang, & Robert D. Burton. (1999). Evidence that Hoxa expression domains are evolutionarily transposed in spinal ganglia, and are established by forward spreading in paraxial mesoderm. Mechanisms of Development. 82(1-2). 109–118. 26 indexed citations
19.
Perry, Margaret M. & Helen Sang. (1993). Transgenesis in chickens. Transgenic Research. 2(3). 125–133. 25 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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