Robert L. Glaser

3.3k total citations · 2 hit papers
28 papers, 2.7k citations indexed

About

Robert L. Glaser is a scholar working on Molecular Biology, Immunology and Insect Science. According to data from OpenAlex, Robert L. Glaser has authored 28 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 6 papers in Immunology and 5 papers in Insect Science. Recurrent topics in Robert L. Glaser's work include Genomics and Chromatin Dynamics (8 papers), Heat shock proteins research (7 papers) and Invertebrate Immune Response Mechanisms (6 papers). Robert L. Glaser is often cited by papers focused on Genomics and Chromatin Dynamics (8 papers), Heat shock proteins research (7 papers) and Invertebrate Immune Response Mechanisms (6 papers). Robert L. Glaser collaborates with scholars based in United States, Russia and Argentina. Robert L. Glaser's co-authors include John T. Lis, Mariana F. Wolfner, Michael P. Washburn, John R. Yates, Laurence Florens, Jerry L. Workman, T Kusch, Susan M. Abmayr, Selene K. Swanson and Jeffrey A. Simon and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Robert L. Glaser

28 papers receiving 2.6k citations

Hit Papers

Nucleosome organization in the Drosophila genome 2004 2026 2011 2018 2008 2004 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert L. Glaser United States 21 2.1k 471 446 300 275 28 2.7k
Andor Udvardy Hungary 30 2.6k 1.2× 369 0.8× 202 0.5× 83 0.3× 453 1.6× 83 3.0k
Barry M. Honda Canada 25 2.5k 1.2× 919 2.0× 104 0.2× 90 0.3× 386 1.4× 51 2.9k
Hitoshi Ueda Japan 28 1.9k 0.9× 287 0.6× 368 0.8× 79 0.3× 1.1k 3.9× 53 2.8k
David I. Bryson United States 8 3.1k 1.5× 427 0.9× 182 0.4× 110 0.4× 808 2.9× 10 3.2k
Ved V. Topkar United States 11 4.2k 2.0× 443 0.9× 290 0.7× 227 0.8× 904 3.3× 15 4.3k
Celeste A. Berg United States 24 1.1k 0.5× 277 0.6× 174 0.4× 95 0.3× 299 1.1× 37 1.5k
G. Devauchelle France 25 980 0.5× 393 0.8× 396 0.9× 111 0.4× 237 0.9× 94 1.7k
N. E. Crook United Kingdom 19 1.7k 0.8× 447 0.9× 840 1.9× 62 0.2× 201 0.7× 37 2.2k
Heidi Scholze Germany 6 1.8k 0.9× 871 1.8× 131 0.3× 83 0.3× 429 1.6× 6 2.3k
Michael T. Marr United States 25 2.6k 1.2× 236 0.5× 135 0.3× 60 0.2× 949 3.5× 41 3.2k

Countries citing papers authored by Robert L. Glaser

Since Specialization
Citations

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

Fields of papers citing papers by Robert L. Glaser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert L. Glaser. 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 Robert L. Glaser. The network helps show where Robert L. Glaser may publish in the future.

Co-authorship network of co-authors of Robert L. Glaser

This figure shows the co-authorship network connecting the top 25 collaborators of Robert L. Glaser. A scholar is included among the top collaborators of Robert L. Glaser 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 Robert L. Glaser. Robert L. Glaser 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.
Gao, Xin, Wanqing Shao, Hua Li, et al.. (2019). A Role for FACT in RNA Polymerase II Promoter-Proximal Pausing. Cell Reports. 27(13). 3770–3779.e7. 44 indexed citations
2.
Micieli, María Victoria & Robert L. Glaser. (2014). Somatic <I>Wolbachia</I> (Rickettsiales: Rickettsiaceae) Levels in <I>Culex quinquefasciatus</I> and <I>Culex pipiens</I> (Diptera: Culicidae) and Resistance to West Nile Virus Infection. Journal of Medical Entomology. 51(1). 189–199. 38 indexed citations
3.
Thomas, Colin, Elena Kotova, Mark Andrake, et al.. (2014). Kinase-Mediated Changes in Nucleosome Conformation Trigger Chromatin Decondensation via Poly(ADP-Ribosyl)ation. Molecular Cell. 53(5). 831–842. 36 indexed citations
4.
Etten, Jamie Van, John A. Kohler, Nicole Hansen, et al.. (2008). The Drosophila protein palmitoylome: Characterizing palmitoyl-thioesterases and DHHC palmitoyl-transferases. Fly. 2(4). 198–214. 45 indexed citations
5.
Ciota, Alexander T., et al.. (2008). West Nile virus infection of Drosophila melanogaster induces a protective RNAi response. Virology. 377(1). 197–206. 90 indexed citations
6.
Mavrich, Travis N., Cizhong Jiang, Ilya Ioshikhes, et al.. (2008). Nucleosome organization in the Drosophila genome. Nature. 453(7193). 358–362. 559 indexed citations breakdown →
7.
Andreyeva, Evgeniya N., Т. Д. Колесникова, E. S. Belyaeva, Robert L. Glaser, & И. Ф. Жимулев. (2008). Local DNA underreplication correlates with accumulation of phosphorylated H2Av in the Drosophila melanogaster polytene chromosomes. Chromosome Research. 16(6). 851–862. 32 indexed citations
8.
Kusch, T, Laurence Florens, Selene K. Swanson, et al.. (2004). Acetylation by Tip60 Is Required for Selective Histone Variant Exchange at DNA Lesions. Science. 306(5704). 2084–2087. 539 indexed citations breakdown →
9.
Glaser, Robert L., et al.. (2003). Characterization of Drosophila palmitoyl-protein thioesterase 1. Gene. 312. 271–279. 15 indexed citations
10.
Glaser, Robert L., et al.. (2000). Replication of Heterochromatin and Structure of Polytene Chromosomes. Molecular and Cellular Biology. 20(17). 6308–6316. 58 indexed citations
11.
Mazzeo, Maria Fiorella, et al.. (2000). Histone H2A.Z Is Widely but Nonrandomly Distributed in Chromosomes of Drosophila melanogaster. Journal of Biological Chemistry. 275(30). 23267–23272. 114 indexed citations
12.
Glaser, Robert L., et al.. (1999). Paternal origin of FGFR2 mutations in sporadic cases of Crouzon and Pfeiffer syndromes.. The American Journal of Human Genetics. 65. 3 indexed citations
13.
Glaser, Robert L., et al.. (1998). Quantitative hybridization to genomic DNA fractionated by pulsed-field gel electrophoresis. Nucleic Acids Research. 26(20). 4787–4789. 10 indexed citations
14.
Glaser, Robert L., et al.. (1997). The Structure of Heterochromatic DNA Is Altered in Polyploid Cells of Drosophila melanogaster. Molecular and Cellular Biology. 17(3). 1254–1263. 12 indexed citations
15.
Glaser, Robert L. & Allan C. Spradling. (1994). Unusual properties of genomic DNA molecules spanning the euchromatic – heterochromatic junction of a Drosophila minichromosome. Nucleic Acids Research. 22(23). 5068–5075. 21 indexed citations
16.
17.
Glaser, Robert L., Gary H. Karpen, & Allan C. Spradling. (1992). Replication forks are not found in a Drosophila minichromosome demonstrating a gradient of polytenization. Chromosoma. 102(1). 15–19. 27 indexed citations
18.
Glaser, Robert L., Graham H. Thomas, Esther Siegfried, Sarah C. R. Elgin, & John T. Lis. (1990). Optimal heat-induced expression of the Drosophila hsp26 gene requires a promoter sequence containing (CT) · (GA) repeats. Journal of Molecular Biology. 211(4). 751–761. 76 indexed citations
19.
Glaser, Robert L. & John T. Lis. (1990). Multiple, compensatory regulatory elements specify spermatocyte-specific expression of the Drosophila melanogaster hsp26 gene.. Molecular and Cellular Biology. 10(1). 131–137. 55 indexed citations
20.
Glaser, Robert L., Mariana F. Wolfner, & John T. Lis. (1986). Spatial and temporal pattern of hsp26 expression during normal development.. The EMBO Journal. 5(4). 747–754. 175 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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