Bernhard Payer

5.3k total citations · 2 hit papers
38 papers, 3.9k citations indexed

About

Bernhard Payer is a scholar working on Molecular Biology, Genetics and Aging. According to data from OpenAlex, Bernhard Payer has authored 38 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 19 papers in Genetics and 2 papers in Aging. Recurrent topics in Bernhard Payer's work include CRISPR and Genetic Engineering (15 papers), Pluripotent Stem Cells Research (14 papers) and Epigenetics and DNA Methylation (14 papers). Bernhard Payer is often cited by papers focused on CRISPR and Genetic Engineering (15 papers), Pluripotent Stem Cells Research (14 papers) and Epigenetics and DNA Methylation (14 papers). Bernhard Payer collaborates with scholars based in United States, Spain and United Kingdom. Bernhard Payer's co-authors include Jeannie T. Lee, Mitinori Saitou, M. Azim Surani, Sheila C. Barton, Yasuhide Ohinata, Dónal O’Carroll, Katia Ancelin, Yukiko Ono, Joseph Avruch and Dawang Zhou and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Bernhard Payer

36 papers receiving 3.9k citations

Hit Papers

Blimp1 is a critical determinant of the germ cell lineage... 2005 2026 2012 2019 2005 2009 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
Bernhard Payer United States 24 3.1k 1.2k 794 488 408 38 3.9k
Ian R. Adams United Kingdom 29 3.2k 1.0× 809 0.7× 535 0.7× 378 0.8× 173 0.4× 55 3.7k
Tristan A. Rodríguez United Kingdom 28 2.8k 0.9× 594 0.5× 567 0.7× 289 0.6× 371 0.9× 48 3.5k
Fredrik Lanner Sweden 31 3.5k 1.1× 529 0.4× 318 0.4× 605 1.2× 398 1.0× 60 4.0k
Ira Daar United States 31 2.9k 0.9× 554 0.5× 1.2k 1.5× 527 1.1× 151 0.4× 79 3.9k
Anna Philpott United Kingdom 37 3.6k 1.1× 638 0.5× 862 1.1× 251 0.5× 404 1.0× 97 4.4k
Masami Kanai‐Azuma Japan 33 2.7k 0.9× 1.1k 0.9× 340 0.4× 396 0.8× 525 1.3× 82 3.7k
Michel Cohen‐Tannoudji France 32 2.6k 0.8× 756 0.6× 338 0.4× 183 0.4× 217 0.5× 73 3.5k
Amy Ralston United States 24 3.8k 1.2× 619 0.5× 915 1.2× 946 1.9× 136 0.3× 45 4.3k
Jaime A. Rivera‐Pérez United States 27 2.5k 0.8× 751 0.6× 241 0.3× 212 0.4× 184 0.5× 47 2.9k
Lídia Pérez Spain 17 3.6k 1.2× 736 0.6× 679 0.9× 202 0.4× 330 0.8× 25 4.3k

Countries citing papers authored by Bernhard Payer

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard Payer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Payer

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Payer. A scholar is included among the top collaborators of Bernhard Payer 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 Bernhard Payer. Bernhard Payer 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.
Maqueda, María, Joan Bertran, Damiana Álvarez‐Errico, et al.. (2025). Chromatin activity of IκBα mediates the exit from naïve pluripotency. eLife. 14.
2.
Neguembor, Maria Victoria, Elliot A. Hershberg, Ruslan I. Sadreyev, et al.. (2023). Cohesin controls X chromosome structure remodeling and X-reactivation during mouse iPSC-reprogramming. Proceedings of the National Academy of Sciences. 120(4). e2213810120–e2213810120. 6 indexed citations
3.
Cozzuto, Luca, Patricia Lorden, Norio Hamada, et al.. (2022). Controlled X‐chromosome dynamics defines meiotic potential of female mouse in vitro germ cells. The EMBO Journal. 41(12). e109457–e109457. 14 indexed citations
4.
Llonch, Sílvia, Montserrat Barragán, Paula Nieto, et al.. (2021). Single human oocyte transcriptome analysis reveals distinct maturation stage‐dependent pathways impacted by age. Aging Cell. 20(5). e13360–e13360. 67 indexed citations
5.
Jiang, Zhisheng, et al.. (2021). A conserved expression signature predicts growth rate and reveals cell & lineage-specific differences. PLoS Computational Biology. 17(11). e1009582–e1009582. 6 indexed citations
6.
Vivori, Claudia, Panagiotis Papasaikas, Ralph Stadhouders, et al.. (2021). Dynamics of alternative splicing during somatic cell reprogramming reveals functions for RNA-binding proteins CPSF3, hnRNP UL1, and TIA1. Genome biology. 22(1). 171–171. 16 indexed citations
7.
Vidal, Enrique, Eduard Zorita, Nil Üresin, et al.. (2021). Chromosome compartments on the inactive X guide TAD formation independently of transcription during X-reactivation. Nature Communications. 12(1). 3499–3499. 30 indexed citations
8.
Sripathy, Smitha, Vid Leko, Taylor K. Loe, et al.. (2017). Screen for reactivation of MeCP2 on the inactive X chromosome identifies the BMP/TGF-β superfamily as a regulator of XIST expression. Proceedings of the National Academy of Sciences. 114(7). 1619–1624. 49 indexed citations
9.
Payer, Bernhard. (2016). Developmental regulation of X-chromosome inactivation. Seminars in Cell and Developmental Biology. 56. 88–99. 31 indexed citations
10.
Beringer, Malte, Valerio Di Carlo, Enrique Blanco, et al.. (2016). EPOP Functionally Links Elongin and Polycomb in Pluripotent Stem Cells. Molecular Cell. 64(4). 645–658. 108 indexed citations
11.
Froberg, John E., Chunyao Wei, Hongjae Sunwoo, et al.. (2015). A comprehensive Xist interactome reveals cohesin repulsion and an RNA-directed chromosome conformation. Science. 349(6245). 357 indexed citations
12.
Anguera, Montserrat C., Ruslan I. Sadreyev, Zhaoqing Zhang, et al.. (2012). Molecular Signatures of Human Induced Pluripotent Stem Cells Highlight Sex Differences and Cancer Genes. Cell stem cell. 11(1). 75–90. 129 indexed citations
13.
Payer, Bernhard, Jeannie T. Lee, & Satoshi H. Namekawa. (2011). X-inactivation and X-reactivation: epigenetic hallmarks of mammalian reproduction and pluripotent stem cells. Human Genetics. 130(2). 265–280. 48 indexed citations
14.
Namekawa, Satoshi H., Bernhard Payer, Khanh D. Huynh, Rudolf Jaenisch, & Jeannie T. Lee. (2010). Two-Step Imprinted X Inactivation: Repeat versus Genic Silencing in the Mouse. Molecular and Cellular Biology. 30(13). 3187–3205. 98 indexed citations
15.
Ohinata, Yasuhide, Yoshiyuki Seki, Bernhard Payer, et al.. (2006). Germline Recruitment in Mice: A Genetic Program for Epigenetic Reprogramming. PubMed. 143–174. 8 indexed citations
16.
Saitou, Mitinori, Bernhard Payer, Dónal O’Carroll, Yasuhide Ohinata, & M. Azim Surani. (2005). Blimp1 and the Emergence of the Germ Line during Development in the Mouse. Cell Cycle. 4(12). 1736–1740. 56 indexed citations
17.
Ohinata, Yasuhide, Bernhard Payer, Dónal O’Carroll, et al.. (2005). Blimp1 is a critical determinant of the germ cell lineage in mice. Nature. 436(7048). 207–213. 789 indexed citations breakdown →
18.
Surani, M. Azim, Katia Ancelin, Petra Hájková, et al.. (2004). Mechanism of Mouse Germ Cell Specification: A Genetic Program Regulating Epigenetic Reprogramming. Cold Spring Harbor Symposia on Quantitative Biology. 69(0). 1–10. 33 indexed citations
19.
Payer, Bernhard, Mitinori Saitou, Sheila C. Barton, et al.. (2003). stella Is a Maternal Effect Gene Required for Normal Early Development in Mice. Current Biology. 13(23). 2110–2117. 299 indexed citations
20.
Das, Tilak, Bernhard Payer, Michel Cayouette, & William A. Harris. (2003). In Vivo Time-Lapse Imaging of Cell Divisions during Neurogenesis in the Developing Zebrafish Retina. Neuron. 37(4). 597–609. 165 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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