Meg Byron

3.6k total citations · 1 hit paper
26 papers, 2.8k citations indexed

About

Meg Byron is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Meg Byron has authored 26 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Meg Byron's work include Genomics and Chromatin Dynamics (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and RNA Research and Splicing (8 papers). Meg Byron is often cited by papers focused on Genomics and Chromatin Dynamics (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and RNA Research and Splicing (8 papers). Meg Byron collaborates with scholars based in United States, Germany and Ireland. Meg Byron's co-authors include Jeanne B. Lawrence, Lisa L. Hall, Kelly P. Smith, John A. McNeil, Katherine A. Fitzgerald, Brian G. Monks, Pallavi Gandhi, Luke O'neill, Maninjay Atianand and Emiliano P. Ricci and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Meg Byron

25 papers receiving 2.8k citations

Hit Papers

A Long Noncoding RNA Mediates Both Activation and Repress... 2013 2026 2017 2021 2013 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Meg Byron United States 22 2.4k 929 692 357 276 26 2.8k
Lisa L. Hall United States 24 2.3k 1.0× 1.1k 1.2× 791 1.1× 309 0.9× 272 1.0× 32 2.8k
Stefan L. Ameres Austria 23 3.9k 1.6× 1.9k 2.1× 308 0.4× 515 1.4× 228 0.8× 40 4.5k
J. Mauro Calabrese United States 20 4.2k 1.8× 2.0k 2.2× 574 0.8× 259 0.7× 157 0.6× 35 4.5k
Fan Lai United States 20 3.0k 1.3× 1.8k 1.9× 234 0.3× 295 0.8× 169 0.6× 33 3.7k
Iris H. Jonkers Netherlands 21 2.1k 0.9× 336 0.4× 673 1.0× 174 0.5× 223 0.8× 41 2.7k
Cameron S. Osborne United Kingdom 23 3.1k 1.3× 318 0.3× 625 0.9× 593 1.7× 338 1.2× 40 3.6k
Sihem Cheloufi United States 16 4.0k 1.7× 2.1k 2.3× 251 0.4× 502 1.4× 293 1.1× 24 4.5k
Shona Murphy United Kingdom 37 3.6k 1.5× 384 0.4× 294 0.4× 250 0.7× 412 1.5× 71 4.2k
Grace Teng United States 14 3.6k 1.5× 1.3k 1.4× 303 0.4× 1.0k 2.9× 607 2.2× 16 4.4k

Countries citing papers authored by Meg Byron

Since Specialization
Citations

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

Fields of papers citing papers by Meg Byron

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meg Byron

This figure shows the co-authorship network connecting the top 25 collaborators of Meg Byron. A scholar is included among the top collaborators of Meg Byron 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 Meg Byron. Meg Byron 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.
Byron, Meg, et al.. (2023). Early chromosome condensation by XIST builds A-repeat RNA density that facilitates gene silencing. Cell Reports. 42(7). 112686–112686. 6 indexed citations
2.
Wang, Feng, Ana Bošković, Xiaochun Zhu, et al.. (2017). Rlim-Dependent and -Independent Pathways for X Chromosome Inactivation in Female ESCs. Cell Reports. 21(13). 3691–3699. 17 indexed citations
3.
Hall, Lisa L., Meg Byron, Dawn M. Carone, et al.. (2017). Demethylated HSATII DNA and HSATII RNA Foci Sequester PRC1 and MeCP2 into Cancer-Specific Nuclear Bodies. Cell Reports. 18(12). 2943–2956. 67 indexed citations
4.
Wang, Feng, Jongdae Shin, Jeremy M. Shea, et al.. (2016). Regulation of X-linked gene expression during early mouse development by Rlim. eLife. 5. 39 indexed citations
5.
Shin, Jongdae, Mary C. Wallingford, Judith Gallant, et al.. (2014). RLIM is dispensable for X-chromosome inactivation in the mouse embryonic epiblast. Nature. 511(7507). 86–89. 48 indexed citations
6.
Hall, Lisa L., Dawn M. Carone, Alvin Gomez, et al.. (2014). Stable C0T-1 Repeat RNA Is Abundant and Is Associated with Euchromatic Interphase Chromosomes. Cell. 156(5). 907–919. 143 indexed citations
7.
Carpenter, Susan, Maninjay Atianand, Emiliano P. Ricci, et al.. (2013). A Long Noncoding RNA Mediates Both Activation and Repression of Immune Response Genes. Science. 341(6147). 789–792. 776 indexed citations breakdown →
8.
Jiang, Jun, Gregory J. Cost, Allison M. Cotton, et al.. (2013). Translating dosage compensation to trisomy 21. Nature. 500(7462). 296–300. 250 indexed citations
9.
Jiao, Baowei, Hong Ma, Maxim N. Shokhirev, et al.. (2012). Paternal RLIM/Rnf12 Is a Survival Factor for Milk-Producing Alveolar Cells. Cell. 149(3). 630–641. 24 indexed citations
10.
Shin, Jongdae, Michael Bossenz, Young Sun Chung, et al.. (2010). Maternal Rnf12/RLIM is required for imprinted X-chromosome inactivation in mice. Nature. 467(7318). 977–981. 135 indexed citations
11.
Baù, Davide, Amartya Sanyal, Bryan R. Lajoie, et al.. (2010). The three-dimensional folding of the α-globin gene domain reveals formation of chromatin globules. Nature Structural & Molecular Biology. 18(1). 107–114. 222 indexed citations
12.
Hall, Lisa L., et al.. (2009). AURKB-mediated effects on chromatin regulate binding versus release of XIST RNA to the inactive chromosome. The Journal of Cell Biology. 186(4). 491–507. 39 indexed citations
13.
Hall, Lisa L., Meg Byron, John T. Butler, et al.. (2008). X‐inactivation reveals epigenetic anomalies in most hESC but identifies sublines that initiate as expected. Journal of Cellular Physiology. 216(2). 445–452. 91 indexed citations
14.
Hall, Lisa L., Kelly P. Smith, Meg Byron, & Jeanne B. Lawrence. (2006). Molecular anatomy of a speckle. The Anatomical Record Part A Discoveries in Molecular Cellular and Evolutionary Biology. 288A(7). 664–675. 190 indexed citations
15.
Smith, Kelly P., Meg Byron, Christine Clemson, & Jeanne B. Lawrence. (2004). Ubiquitinated proteins including uH2A on the human and mouse inactive X chromosome: enrichment in gene rich bands. Chromosoma. 113(6). 324–335. 56 indexed citations
16.
Smith, Kelly P., Meg Byron, Brenda O’Connell, et al.. (2004). c‐Myc localization within the nucleus: Evidence for association with the PML nuclear body. Journal of Cellular Biochemistry. 93(6). 1282–1296. 23 indexed citations
17.
Moen, Phillip T., Carol V. Johnson, Meg Byron, et al.. (2003). Repositioning of Muscle-specific Genes Relative to the Periphery of SC-35 Domains during Skeletal Myogenesis. Molecular Biology of the Cell. 15(1). 197–206. 74 indexed citations
18.
Hall, Lisa L., Meg Byron, Kosuke Sakai, et al.. (2002). An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells. Proceedings of the National Academy of Sciences. 99(13). 8677–8682. 119 indexed citations
19.
Shopland, Lindsay S., Meg Byron, Janet L. Stein, et al.. (2001). Replication-dependent Histone Gene Expression Is Related to Cajal Body (CB) Association but Does Not Require Sustained CB Contact. Molecular Biology of the Cell. 12(3). 565–576. 67 indexed citations
20.
Larsen, Melinda, Steven J. Ressler, Michael J. Gerdes, et al.. (2000). The WFDC1 gene encoding ps20 localizes to 16q24, a region of LOH in multiple cancers. Mammalian Genome. 11(9). 767–773. 29 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026