Anna D. Senft

610 total citations
8 papers, 342 citations indexed

About

Anna D. Senft is a scholar working on Molecular Biology, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Anna D. Senft has authored 8 papers receiving a total of 342 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Plant Science and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Anna D. Senft's work include Epigenetics and DNA Methylation (5 papers), CRISPR and Genetic Engineering (4 papers) and RNA modifications and cancer (2 papers). Anna D. Senft is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), CRISPR and Genetic Engineering (4 papers) and RNA modifications and cancer (2 papers). Anna D. Senft collaborates with scholars based in United Kingdom, United States and Germany. Anna D. Senft's co-authors include Todd S. Macfarlan, Ita Costello, Elizabeth K. Bikoff, Elizabeth J. Robertson, Frédéric Koch, Hamish W. King, Arne W. Mould, Lars Wittler, Phillip Grote and Bernhard G. Herrmann and has published in prestigious journals such as Nature Communications, Nature Genetics and Nature Cell Biology.

In The Last Decade

Anna D. Senft

8 papers receiving 336 citations

Peers

Anna D. Senft

MB

PS

GENET

CR

IMMUN

Patricia E. Carreira Australia

Hendrik Schultheis Germany

Emmanuelle Szenker‐Ravi France

Melodi Tastemel United States

Lizhi Yi China

Uwe Schwartz Germany

Sarah G. Swygert United States

Chuan-Wei Jang United States

Aditya Sankar Denmark

Soizik Berlivet Canada

Patricia E. Carreira Australia

Anna D. Senft

221 ×0.7

MB

163 ×1.6

PS

50 ×1.1

GENET

24 ×0.8

CR

36 ×1.4

IMMUN

Citations per year, relative to Anna D. Senft Anna D. Senft (= 1×) peers Patricia E. Carreira

Countries citing papers authored by Anna D. Senft

Since Specialization

Citations

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

Fields of papers citing papers by Anna D. Senft

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna D. Senft. 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 Anna D. Senft. The network helps show where Anna D. Senft may publish in the future.

Co-authorship network of co-authors of Anna D. Senft

This figure shows the co-authorship network connecting the top 25 collaborators of Anna D. Senft. A scholar is included among the top collaborators of Anna D. Senft 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 Anna D. Senft. Anna D. Senft is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Xie, Guojia, Ji‐Eun Lee, Anna D. Senft, et al.. (2023). MLL3/MLL4 methyltransferase activities control early embryonic development and embryonic stem cell differentiation in a lineage-selective manner. Nature Genetics. 55(4). 693–705. 35 indexed citations

2.

Sun, Ming‐an, Gernot Wolf, Yejun Wang, et al.. (2021). Endogenous Retroviruses Drive Lineage-Specific Regulatory Evolution across Primate and Rodent Placentae. Molecular Biology and Evolution. 38(11). 4992–5004. 30 indexed citations

3.

Harland, Luke, Claire Simon, Anna D. Senft, et al.. (2021). The T-box transcription factor Eomesodermin governs haemogenic competence of yolk sac mesodermal progenitors. Nature Cell Biology. 23(1). 61–74. 21 indexed citations

4.

Senft, Anna D. & Todd S. Macfarlan. (2021). Transposable elements shape the evolution of mammalian development. Nature Reviews Genetics. 22(11). 691–711. 147 indexed citations

5.

Senft, Anna D., Elizabeth K. Bikoff, Elizabeth J. Robertson, & Ita Costello. (2019). Genetic dissection of Nodal and Bmp signalling requirements during primordial germ cell development in mouse. Nature Communications. 10(1). 1089–1089. 39 indexed citations

6.

Senft, Anna D., Ita Costello, Hamish W. King, et al.. (2018). Combinatorial Smad2/3 Activities Downstream of Nodal Signaling Maintain Embryonic/Extra-Embryonic Cell Identities during Lineage Priming. Cell Reports. 24(8). 1977–1985.e7. 24 indexed citations

7.

Beisaw, Arica, Pavel Tsaytler, Frédéric Koch, et al.. (2017). BRACHYURY directs histone acetylation to target loci during mesoderm development. EMBO Reports. 19(1). 118–134. 23 indexed citations

8.

Sudheer, Smita, Jinhua Liu, Frédéric Koch, et al.. (2016). Different Concentrations of FGF Ligands, FGF2 or FGF8 Determine Distinct States of WNT-Induced Presomitic Mesoderm. Stem Cells. 34(7). 1790–1800. 23 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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