Della Yee

5.6k total citations · 2 hit papers
36 papers, 4.4k citations indexed

About

Della Yee is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Della Yee has authored 36 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Immunology. Recurrent topics in Della Yee's work include Epigenetics and DNA Methylation (13 papers), Pluripotent Stem Cells Research (12 papers) and Genomics and Chromatin Dynamics (9 papers). Della Yee is often cited by papers focused on Epigenetics and DNA Methylation (13 papers), Pluripotent Stem Cells Research (12 papers) and Genomics and Chromatin Dynamics (9 papers). Della Yee collaborates with scholars based in United States, France and Netherlands. Della Yee's co-authors include Terry Magnuson, Joshua Starmer, Stormy J. Chamberlain, David W. Threadgill, Raymond C. Harris, Laura A. Hansen, Stuart H. Yuspa, Robert J. Coffey, Andrzej A. Dlugosz and Karl Herrup and has published in prestigious journals such as Science, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Della Yee

35 papers receiving 4.4k citations

Hit Papers

Targeted Disruption of Mouse EGF receptor: Effect of Gene... 1995 2026 2005 2015 1995 2000 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Della Yee United States 25 3.4k 864 518 393 392 36 4.4k
Paul S. Knoepfler United States 43 4.5k 1.3× 726 0.8× 677 1.3× 254 0.6× 516 1.3× 88 5.8k
Anne K. Voss Australia 45 4.1k 1.2× 981 1.1× 475 0.9× 367 0.9× 553 1.4× 113 5.6k
Corrinne G. Lobe Canada 31 3.4k 1.0× 871 1.0× 522 1.0× 536 1.4× 504 1.3× 48 5.3k
Kunio Kitamura Japan 32 2.1k 0.6× 556 0.6× 487 0.9× 538 1.4× 123 0.3× 92 3.4k
A. Paula Monaghan United States 30 4.0k 1.2× 1.2k 1.3× 314 0.6× 484 1.2× 537 1.4× 42 5.4k
Sergio Ottolenghi Italy 44 3.9k 1.1× 1.0k 1.2× 415 0.8× 342 0.9× 609 1.6× 137 6.1k
Giorgio R. Merlo Italy 39 3.0k 0.9× 1.1k 1.3× 914 1.8× 301 0.8× 488 1.2× 87 4.1k
Siew‐Lan Ang United States 37 4.4k 1.3× 988 1.1× 452 0.9× 640 1.6× 250 0.6× 48 6.2k
Shigemi Hayashi United States 11 3.2k 0.9× 832 1.0× 279 0.5× 460 1.2× 241 0.6× 12 4.1k
Andrei Glinka Germany 15 5.0k 1.5× 1.1k 1.3× 671 1.3× 514 1.3× 177 0.5× 21 5.8k

Countries citing papers authored by Della Yee

Since Specialization
Citations

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

Fields of papers citing papers by Della Yee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Della Yee

This figure shows the co-authorship network connecting the top 25 collaborators of Della Yee. A scholar is included among the top collaborators of Della Yee 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 Della Yee. Della Yee 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.
Mu, Weipeng, Noel Murcia, Keriayn N. Smith, et al.. (2022). RBBP4 dysfunction reshapes the genomic landscape of H3K27 methylation and acetylation and disrupts gene expression. G3 Genes Genomes Genetics. 12(6). 13 indexed citations
2.
Mu, Weipeng, Joshua Starmer, Della Yee, & Terry Magnuson. (2018). EZH2 variants differentially regulate polycomb repressive complex 2 in histone methylation and cell differentiation. Epigenetics & Chromatin. 11(1). 71–71. 31 indexed citations
3.
Mu, Weipeng, Joshua Starmer, Yoichiro Shibata, Della Yee, & Terry Magnuson. (2017). EZH1 in germ cells safeguards the function of PRC2 during spermatogenesis. Developmental Biology. 424(2). 198–207. 32 indexed citations
4.
Chandler, Ronald L., Jeffrey S. Damrauer, Jesse R. Raab, et al.. (2015). Coexistent ARID1A–PIK3CA mutations promote ovarian clear-cell tumorigenesis through pro-tumorigenic inflammatory cytokine signalling. Nature Communications. 6(1). 6118–6118. 230 indexed citations
5.
Jang, Chuan-Wei, Yoichiro Shibata, Joshua Starmer, Della Yee, & Terry Magnuson. (2015). Histone H3.3 maintains genome integrity during mammalian development. Genes & Development. 29(13). 1377–1392. 135 indexed citations
6.
Mu, Weipeng, Joshua Starmer, Andrew Fedoriw, Della Yee, & Terry Magnuson. (2014). Repression of the soma-specific transcriptome by Polycomb-repressive complex 2 promotes male germ cell development. Genes & Development. 28(18). 2056–2069. 83 indexed citations
7.
Starmer, Joshua, Joshua W. Mugford, J. Mauro Calabrese, et al.. (2014). fourSig: a method for determining chromosomal interactions in 4C-Seq data. Nucleic Acids Research. 42(8). e68–e68. 31 indexed citations
8.
Mugford, Joshua W., Joshua Starmer, J. Mauro Calabrese, et al.. (2014). Evidence for Local Regulatory Control of Escape from Imprinted X Chromosome Inactivation. Genetics. 197(2). 715–723. 19 indexed citations
9.
Calabrese, J. Mauro, Wei Sun, Lingyun Song, et al.. (2012). Site-Specific Silencing of Regulatory Elements as a Mechanism of X Inactivation. Cell. 151(5). 951–963. 152 indexed citations
10.
Fedoriw, Andrew, J. Mauro Calabrese, Weipeng Mu, Della Yee, & Terry Magnuson. (2012). Differentiation-Driven Nucleolar Association of the Mouse Imprinted Kcnq1 Locus. G3 Genes Genomes Genetics. 2(12). 1521–1528. 19 indexed citations
11.
Chamberlain, Stormy J., Della Yee, & Terry Magnuson. (2008). Polycomb Repressive Complex 2 Is Dispensable for Maintenance of Embryonic Stem Cell Pluripotency. Stem Cells. 26(6). 1496–1505. 259 indexed citations
12.
Li, Manyu, Della Yee, Terry Magnuson, Oliver Smithies, & Kathleen M. Caron. (2006). Reduced maternal expression of adrenomedullin disrupts fertility, placentation, and fetal growth in mice. Journal of Clinical Investigation. 116(10). 2653–2662. 79 indexed citations
13.
Kalantry, Sundeep, et al.. (2006). The Polycomb group protein Eed protects the inactive X-chromosome from differentiation-induced reactivation. Nature Cell Biology. 8(2). 195–202. 119 indexed citations
14.
Montgomery, Nathan D., Della Yee, Andrew Chen, et al.. (2005). The Murine Polycomb Group Protein Eed Is Required for Global Histone H3 Lysine-27 Methylation. Current Biology. 15(10). 942–947. 280 indexed citations
15.
Vivian, Jay L., Yijing Chen, Della Yee, Elizabeth Schneider, & Terry Magnuson. (2002). An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N -ethyl- N - nitrosourea-mutagenized mouse embryonic stem cells. Proceedings of the National Academy of Sciences. 99(24). 15542–15547. 45 indexed citations
16.
Reiter, Jill L., David W. Threadgill, Greg Eley, et al.. (2001). Comparative Genomic Sequence Analysis and Isolation of Human and Mouse Alternative EGFR Transcripts Encoding Truncated Receptor Isoforms. Genomics. 71(1). 1–20. 91 indexed citations
17.
Bultman, Scott J., Della Yee, Jackie Nicholson, et al.. (2000). A Brg1 Null Mutation in the Mouse Reveals Functional Differences among Mammalian SWI/SNF Complexes. Molecular Cell. 6(6). 1287–1295. 653 indexed citations breakdown →
18.
Threadgill, David W., Andrzej A. Dlugosz, Laura A. Hansen, et al.. (1995). Targeted Disruption of Mouse EGF receptor: Effect of Genetic Background on Mutant Phenotype. Science. 269(5221). 230–234. 1177 indexed citations breakdown →
19.
Tomasiewicz, Henry, Katsuhiko Ono, Della Yee, et al.. (1993). Genetic deletion of a neural cell adhesion molecule variant (N-CAM-180) produces distinct defects in the central nervous system. Neuron. 11(6). 1163–1174. 409 indexed citations
20.
Niswander, Lee, Della Yee, Eugene M. Rinchik, Liane B. Russell, & Terry Magnuson. (1989). The albino–deletion complex in the mouse defines genes necessary for development of embryonic and extraembryonic ectoderm*. Development. 105(1). 175–182. 47 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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