Deborah J. Andrew

5.8k total citations · 1 hit paper
81 papers, 4.5k citations indexed

About

Deborah J. Andrew is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Deborah J. Andrew has authored 81 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Molecular Biology, 29 papers in Cell Biology and 26 papers in Cellular and Molecular Neuroscience. Recurrent topics in Deborah J. Andrew's work include Developmental Biology and Gene Regulation (36 papers), Neurobiology and Insect Physiology Research (26 papers) and Invertebrate Immune Response Mechanisms (18 papers). Deborah J. Andrew is often cited by papers focused on Developmental Biology and Gene Regulation (36 papers), Neurobiology and Insect Physiology Research (26 papers) and Invertebrate Immune Response Mechanisms (18 papers). Deborah J. Andrew collaborates with scholars based in United States, Canada and United Kingdom. Deborah J. Andrew's co-authors include Monn Monn Myat, Purnima Bhanot, Daniel D. Isaac, Jennifer P. Macke, Roel Nusse, Marcel R.M. van den Brink, Yanshu Wang, Jeremy Nathans, Andrew J. Ewald and Elliott W. Abrams and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Deborah J. Andrew

79 papers receiving 4.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A new member of the frizzled family from Drosophila functions as a Wingless receptor

1996 1.2k citations Deborah J. Andrew et al. profile →

Peers

Deborah J. Andrew

CMN

GENET

IMMUN

Alan M. Michelson United States

Jean‐Paul Vincent United Kingdom

Jessica E. Treisman United States

Ilaria Rebay United States

Mary K. Baylies United States

Susan M. Abmayr United States

Enrique Amaya United Kingdom

Jordi Casanova Spain

Talila Volk Israel

Andreas Wodarz Germany

Alan M. Michelson United States

Deborah J. Andrew

3.9k ×1.1

933 ×0.7

846 ×0.9

CMN

851 ×1.2

GENET

705 ×1.2

IMMUN

Citations per year, relative to Deborah J. Andrew Deborah J. Andrew (= 1×) peers Alan M. Michelson

Countries citing papers authored by Deborah J. Andrew

Since Specialization

Citations

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

Fields of papers citing papers by Deborah J. Andrew

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah J. Andrew. 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 Deborah J. Andrew. The network helps show where Deborah J. Andrew may publish in the future.

Co-authorship network of co-authors of Deborah J. Andrew

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah J. Andrew. A scholar is included among the top collaborators of Deborah J. Andrew 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 Deborah J. Andrew. Deborah J. Andrew is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Cahan, Patrick, et al.. (2025). CrebA regulation of secretory capacity: genome-wide transcription profiling coupled with in vivo DNA binding studies. Genetics. 231(4).

Kim, Ji Hoon, et al.. (2025). Arc controls organ architecture through modulation of Crb and MyoII. The Journal of Cell Biology. 224(9). 1 indexed citations

Kim, Ji Hoon, et al.. (2025). The Drosophila larval salivary gland, a simple and elegant model system to understand secretory organ development and function. Current Opinion in Insect Science. 73. 101435–101435.

Loganathan, Rajprasad, Ji Hoon Kim, Michael B. Wells, et al.. (2022). Ribbon boosts ribosomal protein gene expression to coordinate organ form and function. The Journal of Cell Biology. 221(4). 6 indexed citations

Pascini, Tales Vicari, Wei Huang, Juliana M. Sá, et al.. (2022). Transgenic Anopheles mosquitoes expressing human PAI-1 impair malaria transmission. Nature Communications. 13(1). 2949–2949. 13 indexed citations

Cheng, Yim Ling, et al.. (2021). Isoform-specific roles of the Drosophila filamin-type protein Jitterbug (Jbug) during development. Genetics. 219(2). 3 indexed citations

Wells, Michael B., Rebecca Fox, Joslynn S. Lee, et al.. (2020). Creb A increases secretory capacity through direct transcriptional regulation of the secretory machinery, a subset of secretory cargo, and other key regulators. Traffic. 21(9). 560–577. 16 indexed citations

Andrew, Deborah J., et al.. (2016). Drosophila FoxL1 non-autonomously coordinates organ placement during embryonic development. Developmental Biology. 419(2). 273–284. 6 indexed citations

Maruyama, Rika, et al.. (2011). Genome-Wide Analysis Reveals a Major Role in Cell Fate Maintenance and an Unexpected Role in Endoreduplication for the Drosophila FoxA Gene Fork Head. PLoS ONE. 6(6). e20901–e20901. 19 indexed citations

10.

Andrew, Deborah J. & Andrew J. Ewald. (2009). Morphogenesis of epithelial tubes: Insights into tube formation, elongation, and elaboration. Developmental Biology. 341(1). 34–55. 256 indexed citations

11.

Kerman, Bilal E., et al.. (2008). Ribbon modulates apical membrane during tube elongation through Crumbs and Moesin. Developmental Biology. 320(1). 278–288. 57 indexed citations

12.

Andrew, Deborah J. & Bruce S. Baker. (2008). Expression of the Drosophila secreted cuticle protein 73 (dsc73) requires shavenbaby. Developmental Dynamics. 237(4). 1198–1206. 18 indexed citations

13.

Abrams, Elliott W., et al.. (2006). Fork head and Sage maintain a uniform and patent salivary gland lumen through regulation of two downstream target genes,PH4αSG1andPH4αSG2. Development. 133(18). 3517–3527. 51 indexed citations

14.

Myat, Monn Monn, et al.. (2005). A molecular link between FGF and Dpp signaling in branch-specific migration of the Drosophila trachea. Developmental Biology. 281(1). 38–52. 28 indexed citations

15.

Haberman, Adam, Daniel D. Isaac, & Deborah J. Andrew. (2003). Specification of cell fates within the salivary gland primordium. Developmental Biology. 258(2). 443–453. 41 indexed citations

16.

Bradley, Pamela L., Monn Monn Myat, Christy Comeaux, & Deborah J. Andrew. (2003). Posterior migration of the salivary gland requires an intact visceral mesoderm and integrin function. Developmental Biology. 257(2). 249–262. 64 indexed citations

17.

Myat, Monn Monn & Deborah J. Andrew. (2002). Epithelial Tube Morphology Is Determined by the Polarized Growth and Delivery of Apical Membrane. Cell. 111(6). 879–891. 108 indexed citations

18.

Myat, Monn Monn, et al.. (2001). pasilla, the Drosophila Homologue of the Human Nova-1 and Nova-2 Proteins, Is Required for Normal Secretion in the Salivary Gland. Developmental Biology. 239(2). 309–322. 36 indexed citations

19.

Andrew, Deborah J., et al.. (2000). Salivary gland development in Drosophila melanogaster. Mechanisms of Development. 92(1). 5–17. 77 indexed citations

20.

Andrew, Deborah J.. (1998). Regulation and Formation of the Drosophila Salivary Glands^a,. Annals of the New York Academy of Sciences. 842(1). 55–69. 9 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