Léonard Rabinow

1.2k total citations
34 papers, 918 citations indexed

About

Léonard Rabinow is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Immunology. According to data from OpenAlex, Léonard Rabinow has authored 34 papers receiving a total of 918 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 11 papers in Immunology. Recurrent topics in Léonard Rabinow's work include Neurobiology and Insect Physiology Research (11 papers), Invertebrate Immune Response Mechanisms (10 papers) and RNA Research and Splicing (8 papers). Léonard Rabinow is often cited by papers focused on Neurobiology and Insect Physiology Research (11 papers), Invertebrate Immune Response Mechanisms (10 papers) and RNA Research and Splicing (8 papers). Léonard Rabinow collaborates with scholars based in United States, France and Slovakia. Léonard Rabinow's co-authors include James A. Birchler, Cheng Du, Róbert Farkas, Anh Tuan Nguyen‐Huynh, Yun Bai, Kun Hee Lee, William J. Dickinson, Mark A. Horn, William Mattox and Brigitte Dauwalder and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and The EMBO Journal.

In The Last Decade

Léonard Rabinow

34 papers receiving 905 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Léonard Rabinow United States 18 732 198 151 134 109 34 918
Stanley Tiong Canada 14 597 0.8× 143 0.7× 180 1.2× 104 0.8× 115 1.1× 24 707
Brian A. Mozer United States 13 1.1k 1.4× 157 0.8× 225 1.5× 130 1.0× 157 1.4× 15 1.2k
Andrew Lambertsson Sweden 18 1.2k 1.6× 202 1.0× 164 1.1× 181 1.4× 194 1.8× 42 1.4k
А. Н. Краснов Russia 19 1.1k 1.5× 161 0.8× 159 1.1× 182 1.4× 56 0.5× 72 1.3k
Antony W. Shermoen United States 13 988 1.3× 273 1.4× 206 1.4× 96 0.7× 139 1.3× 14 1.1k
Fabrizio Rossi Spain 15 628 0.9× 289 1.5× 131 0.9× 75 0.6× 208 1.9× 22 796
Sheryl T. Smith United States 17 1.3k 1.8× 267 1.3× 242 1.6× 110 0.8× 71 0.7× 24 1.5k
David L. Cribbs France 18 1.2k 1.6× 192 1.0× 346 2.3× 231 1.7× 145 1.3× 34 1.3k
Orbán Komonyi Hungary 15 576 0.8× 118 0.6× 79 0.5× 101 0.8× 103 0.9× 24 711

Countries citing papers authored by Léonard Rabinow

Since Specialization
Citations

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

Fields of papers citing papers by Léonard Rabinow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Léonard Rabinow

This figure shows the co-authorship network connecting the top 25 collaborators of Léonard Rabinow. A scholar is included among the top collaborators of Léonard Rabinow 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 Léonard Rabinow. Léonard Rabinow 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.
Hu, Yanhui, Richelle Sopko, Verena Chung, et al.. (2018). iProteinDB: An Integrative Database of Drosophila Post-translational Modifications. G3 Genes Genomes Genetics. 9(1). 1–11. 23 indexed citations
2.
Tang, Hong-Wen, Yanhui Hu, Chiao‐Lin Chen, et al.. (2018). The TORC1-Regulated CPA Complex Rewires an RNA Processing Network to Drive Autophagy and Metabolic Reprogramming. Cell Metabolism. 27(5). 1040–1054.e8. 62 indexed citations
3.
Zhao, Yunpo, Claudia Cocco, Séverine Domenichini, Marie‐Laure Samson, & Léonard Rabinow. (2015). The IMD innate immunity pathway of Drosophila influences somatic sex determination via regulation of the Doa locus. Developmental Biology. 407(2). 224–231. 5 indexed citations
4.
Durand, Marjorie, et al.. (2014). Negative regulation of MAP kinase signaling in Drosophila by Ptp61F/PTP1B. Molecular Genetics and Genomics. 289(5). 795–806. 10 indexed citations
5.
Fan, Yujie, et al.. (2014). Multifunctional RNA Processing Protein SRm160 Induces Apoptosis and Regulates Eye and Genital Development in Drosophila. Genetics. 197(4). 1251–1265. 8 indexed citations
6.
Rabinow, Léonard, et al.. (2013). Transcriptomic Analysis of Sexual Differentiation in Somatic Tissues of <b><i>Drosophila melanogaster:</i></b> Successes and Caveats. Sexual Development. 8(1-3). 113–126. 3 indexed citations
7.
Rabinow, Léonard & Marie‐Laure Samson. (2010). The role of the Drosophila LAMMER protein kinase DOA in somatic sex determination. Journal of Genetics. 89(3). 271–277. 14 indexed citations
8.
Wu, Chia‐Lun, et al.. (2009). Organization of F-Actin via Concerted Regulation of Kette by PTP61F and dAbl. Molecular and Cellular Biology. 29(13). 3623–3632. 9 indexed citations
9.
Fan, Yujie, Michael Schlierf, Ana Cuervo, et al.. (2009). Drosophila Translational Elongation Factor-1γ Is Modified in Response to DOA Kinase Activity and Is Essential for Cellular Viability. Genetics. 184(1). 141–154. 15 indexed citations
10.
Kpebe, Arlette & Léonard Rabinow. (2008). Alternative promoter usage generates multiple evolutionarily conserved isoforms of Drosophila DOA kinase. genesis. 46(3). 132–143. 14 indexed citations
11.
Rabinow, Léonard. (2002). The Proliferation ofDrosophilain Cancer Research: A System for the Functional Characterization of Tumor Suppressors and Oncogenes. Cancer Investigation. 20(4). 531–556. 2 indexed citations
12.
13.
Talmadge, Catherine B., et al.. (1998). Chromosomal mapping of three human LAMMER protein-kinase-encoding genes. Human Genetics. 103(4). 523–524. 5 indexed citations
14.
Du, Cheng, M.Elaine McGuffin, Brigitte Dauwalder, Léonard Rabinow, & William Mattox. (1998). Protein Phosphorylation Plays an Essential Role in the Regulation of Alternative Splicing and Sex Determination in Drosophila. Molecular Cell. 2(6). 741–750. 96 indexed citations
15.
Lee, Kun Hee, Cheng Du, Mark A. Horn, & Léonard Rabinow. (1996). Activity and Autophosphorylation of LAMMER Protein Kinases. Journal of Biological Chemistry. 271(44). 27299–27303. 74 indexed citations
16.
Birchler, James A., Utpal Bhadra, Léonard Rabinow, R Linsk, & Anh Tuan Nguyen‐Huynh. (1994). Weakener of white (Wow), a gene that modifies the expression of the white eye color locus and that suppresses position effect variegation in Drosophila melanogaster.. Genetics. 137(4). 1057–1070. 31 indexed citations
17.
Rabinow, Léonard, Su L. Chiang, & James A. Birchler. (1993). Mutations at the Darkener of apricot locus modulate transcript levels of copia and copia-induced mutations in Drosophila melanogaster.. Genetics. 134(4). 1175–1185. 32 indexed citations
18.
Rabinow, Léonard, Anh Tuan Nguyen‐Huynh, & James A. Birchler. (1991). A trans-acting regulatory gene that inversely affects the expression of the white, brown and scarlet loci in Drosophila.. Genetics. 129(2). 463–480. 63 indexed citations
19.
Rabinow, Léonard & James A. Birchler. (1990). Interactions among modifiers of retrotransposon-induced alleles of thewhitelocus ofDrosophila melanogaster. Genetics Research. 55(3). 141–151. 7 indexed citations
20.
Rabinow, Léonard & James A. Birchler. (1990). Interactions of vestigial and scabrous with the Notch locus of Drosophila melanogaster.. Genetics. 125(1). 41–50. 26 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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