Louis C. Doré

6.3k total citations · 2 hit papers
26 papers, 3.5k citations indexed

About

Louis C. Doré is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Louis C. Doré has authored 26 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 4 papers in Genetics and 4 papers in Hematology. Recurrent topics in Louis C. Doré's work include RNA modifications and cancer (11 papers), Epigenetics and DNA Methylation (7 papers) and RNA and protein synthesis mechanisms (5 papers). Louis C. Doré is often cited by papers focused on RNA modifications and cancer (11 papers), Epigenetics and DNA Methylation (7 papers) and RNA and protein synthesis mechanisms (5 papers). Louis C. Doré collaborates with scholars based in United States, Israel and Switzerland. Louis C. Doré's co-authors include Chuan He, John D. Crispino, Guanqun Zheng, Mitchell J. Weiss, Dali Han, Kai Chen, Guan‐Zheng Luo, Timothy M. Chlon, Oz Solomon and Sigrid Nachtergaele and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Louis C. Doré

25 papers receiving 3.5k citations

Hit Papers

The dynamic N1-methyladen... 2016 2026 2019 2022 2016 2017 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
Louis C. Doré United States 19 3.0k 1.1k 376 273 261 26 3.5k
Camila O. dos Santos United States 20 2.2k 0.7× 1.4k 1.3× 231 0.6× 213 0.8× 19 0.1× 42 3.0k
Jörg Bungert United States 29 2.0k 0.7× 244 0.2× 176 0.5× 278 1.0× 33 0.1× 66 2.3k
Adam S. Sperling United States 22 1.3k 0.4× 191 0.2× 724 1.9× 214 0.8× 46 0.2× 73 2.1k
Fatih Kocabaş Türkiye 16 1.4k 0.4× 430 0.4× 631 1.7× 205 0.8× 22 0.1× 55 2.1k
Richard P. Koche United States 35 3.9k 1.3× 589 0.5× 840 2.2× 243 0.9× 13 0.0× 97 4.7k
Ania Wilczynska United Kingdom 26 2.0k 0.7× 602 0.6× 159 0.4× 166 0.6× 9 0.0× 44 2.6k
Yoshihiro Takihara Japan 27 1.6k 0.5× 138 0.1× 301 0.8× 119 0.4× 30 0.1× 88 2.2k
Eric Wang United States 22 3.2k 1.0× 320 0.3× 1.0k 2.8× 150 0.5× 16 0.1× 36 3.8k
Dolores Martínez Spain 16 1.7k 0.6× 580 0.5× 61 0.2× 94 0.3× 25 0.1× 22 2.7k
Loretta Cerruti Australia 21 1.1k 0.4× 152 0.1× 156 0.4× 268 1.0× 36 0.1× 28 1.8k

Countries citing papers authored by Louis C. Doré

Since Specialization
Citations

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

Fields of papers citing papers by Louis C. Doré

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Louis C. Doré. 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 Louis C. Doré. The network helps show where Louis C. Doré may publish in the future.

Co-authorship network of co-authors of Louis C. Doré

This figure shows the co-authorship network connecting the top 25 collaborators of Louis C. Doré. A scholar is included among the top collaborators of Louis C. Doré 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 Louis C. Doré. Louis C. Doré 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.
Yoon, Ki‐Jun, Francisca Rojas, Caroline Vissers, et al.. (2017). Temporal Control of Mammalian Cortical Neurogenesis by m6A Methylation. Cell. 171(4). 877–889.e17. 551 indexed citations breakdown →
2.
Johansen, Jostein, Jan Magnus Aronsen, Cathrine Broberg Vågbø, et al.. (2017). Genome-wide profiling of DNA 5-hydroxymethylcytosine during rat Sertoli cell maturation. Cell Discovery. 3(1). 17013–17013. 8 indexed citations
3.
Verma, Nipun, Heng Pan, Louis C. Doré, et al.. (2017). TET proteins safeguard bivalent promoters from de novo methylation in human embryonic stem cells. Nature Genetics. 50(1). 83–95. 145 indexed citations
4.
Dominissini, Dan, Sigrid Nachtergaele, Sharon Moshitch-Moshkovitz, et al.. (2016). The dynamic N1-methyladenosine methylome in eukaryotic messenger RNA. Nature. 530(7591). 441–446. 766 indexed citations breakdown →
5.
Fu, Ye, Guan‐Zheng Luo, Kai Chen, et al.. (2015). N6-Methyldeoxyadenosine Marks Active Transcription Start Sites in Chlamydomonas. Cell. 161(4). 879–892. 380 indexed citations
7.
Luo, Guan‐Zheng, Alice MacQueen, Guanqun Zheng, et al.. (2014). Unique features of the m6A methylome in Arabidopsis thaliana. Nature Communications. 5(1). 5630–5630. 371 indexed citations
8.
Doré, Louis C., Timothy M. Chlon, Christopher D. Brown, Kevin P. White, & John D. Crispino. (2012). Chromatin occupancy analysis reveals genome-wide GATA factor switching during hematopoiesis. Blood. 119(16). 3724–3733. 87 indexed citations
9.
Chlon, Timothy M., Louis C. Doré, & John D. Crispino. (2012). Cofactor-Mediated Restriction of GATA-1 Chromatin Occupancy Coordinates Lineage-Specific Gene Expression. Molecular Cell. 47(4). 608–621. 55 indexed citations
10.
Yu, Duonan, Camila O. dos Santos, Guowei Zhao, et al.. (2010). miR-451 protects against erythroid oxidant stress by repressing 14-3-3ζ. Genes & Development. 24(15). 1620–1633. 189 indexed citations
11.
Huang, Zan, Louis C. Doré, Zhe Li, et al.. (2009). GATA-2 Reinforces Megakaryocyte Development in the Absence of GATA-1. Molecular and Cellular Biology. 29(18). 5168–5180. 82 indexed citations
12.
Maeda, Takahiro, Keisuke Ito, Taha Merghoub, et al.. (2009). LRF Is an Essential Downstream Target of GATA1 in Erythroid Development and Regulates BIM-Dependent Apoptosis. Developmental Cell. 17(4). 527–540. 92 indexed citations
13.
Santos, Camila O. dos, Louis C. Doré, Suresh G. Shelat, et al.. (2008). An Iron Responsive Element-like Stem-Loop Regulates α-Hemoglobin-stabilizing Protein mRNA. Journal of Biological Chemistry. 283(40). 26956–26964. 48 indexed citations
14.
Cheng, Yong, David King, Louis C. Doré, et al.. (2008). Transcriptional enhancement by GATA1-occupied DNA segments is strongly associated with evolutionary constraint on the binding site motif. Genome Research. 18(12). 1896–1905. 27 indexed citations
15.
Santos, Camila O. dos, Duonan Yu, Julio Amigo, et al.. (2008). The microRNA144/451 Locus Enhances Nuclear FOXO3a Activity to Protect Erythroid Cells against Oxidant Stress. Blood. 112(11). 277–277. 2 indexed citations
16.
Yu, Xiang, Yi Kong, Louis C. Doré, et al.. (2007). An erythroid chaperone that facilitates folding of α-globin subunits for hemoglobin synthesis. Journal of Clinical Investigation. 117(7). 1856–1865. 84 indexed citations
17.
Wang, Hao, Ying Zhang, Yong Cheng, et al.. (2006). Experimental validation of predicted mammalian erythroid cis-regulatory modules. Genome Research. 16(12). 1480–1492. 47 indexed citations
18.
Munugalavadla, Veerendra, et al.. (2005). Repression of c-Kit and Its Downstream Substrates by GATA-1 Inhibits Cell Proliferation during Erythroid Maturation. Molecular and Cellular Biology. 25(15). 6747–6759. 88 indexed citations
19.
Doré, Louis C., et al.. (1986). Comparison of the acute hemodynamic effects of ibopamine and dopamine in chronic congestive heart failure.. PubMed. 36(2A). 355–9. 7 indexed citations
20.
Doré, Louis C., et al.. (1981). [Pharmacologic cardioversion with intravenous amiodarone].. PubMed. 26(6). 553–8. 1 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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