Gerald B. Call

2.2k total citations
27 papers, 1.6k citations indexed

About

Gerald B. Call is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Immunology. According to data from OpenAlex, Gerald B. Call has authored 27 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Immunology. Recurrent topics in Gerald B. Call's work include Neurobiology and Insect Physiology Research (7 papers), Developmental Biology and Gene Regulation (6 papers) and Invertebrate Immune Response Mechanisms (3 papers). Gerald B. Call is often cited by papers focused on Neurobiology and Insect Physiology Research (7 papers), Developmental Biology and Gene Regulation (6 papers) and Invertebrate Immune Response Mechanisms (3 papers). Gerald B. Call collaborates with scholars based in United States, Switzerland and Bulgaria. Gerald B. Call's co-authors include Michael W. Wolfe, Ting Xie, Xiaoqing Song, Dániel Kirilly, Allan M. Judd, Utpal Banerjee, Kathy Ngo, Dongxiao Zhu, Hong Tang and Changjiang Weng and has published in prestigious journals such as Development, Nature Methods and Scientific Reports.

In The Last Decade

Gerald B. Call

27 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gerald B. Call United States 17 869 321 276 237 175 27 1.6k
Gabriella Chieffi Baccari Italy 26 588 0.7× 367 1.1× 186 0.7× 211 0.9× 195 1.1× 101 1.8k
Hwei‐Jan Hsu Taiwan 23 831 1.0× 345 1.1× 261 0.9× 362 1.5× 93 0.5× 46 1.6k
Enrique Leo Portiansky Argentina 25 731 0.8× 237 0.7× 171 0.6× 125 0.5× 256 1.5× 132 1.9k
Susanne Fehr Germany 25 1.1k 1.3× 470 1.5× 403 1.5× 268 1.1× 146 0.8× 45 2.3k
Yun Feng China 19 1.5k 1.8× 313 1.0× 101 0.4× 304 1.3× 262 1.5× 40 2.3k
Sara Neuman Israel 11 1.5k 1.8× 288 0.9× 127 0.5× 232 1.0× 260 1.5× 18 2.2k
Ching‐Wei Luo Taiwan 18 656 0.8× 376 1.2× 158 0.6× 272 1.1× 526 3.0× 37 2.1k
Zehava Levy Israel 11 1.5k 1.7× 316 1.0× 134 0.5× 257 1.1× 320 1.8× 14 2.0k
Gustavo González United States 13 1.8k 2.0× 748 2.3× 292 1.1× 436 1.8× 314 1.8× 29 3.0k
Cezary Skobowiat Poland 23 442 0.5× 228 0.7× 318 1.2× 178 0.8× 208 1.2× 42 2.3k

Countries citing papers authored by Gerald B. Call

Since Specialization
Citations

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

Fields of papers citing papers by Gerald B. Call

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerald B. Call. 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 Gerald B. Call. The network helps show where Gerald B. Call may publish in the future.

Co-authorship network of co-authors of Gerald B. Call

This figure shows the co-authorship network connecting the top 25 collaborators of Gerald B. Call. A scholar is included among the top collaborators of Gerald B. Call 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 Gerald B. Call. Gerald B. Call 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.
Morrison, Carolyn A., et al.. (2022). The Blimp-1 transcription factor acts in non-neuronal cells to regulate terminal differentiation of the Drosophila eye. Development. 149(7). 5 indexed citations
2.
Buhlman, Lori M., et al.. (2022). Nicotine Has a Therapeutic Window of Effectiveness in a Drosophila melanogaster Model of Parkinson’s Disease. Parkinson s Disease. 2022(1). 6 indexed citations
3.
Korch, Shaleen B., et al.. (2021). An altered microbiome in a Parkinson’s disease model Drosophila melanogaster has a negative effect on development. Scientific Reports. 11(1). 23635–23635. 4 indexed citations
4.
Call, Gerald B., et al.. (2021). Genome Sequence of Lactiplantibacillus plantarum DmPark25_157, a Bacterial Strain Isolated from Drosophila melanogaster. Microbiology Resource Announcements. 10(16). 1 indexed citations
6.
VandenBrooks, John M., et al.. (2015). Impaired climbing and flight behaviour in Drosophila melanogaster following carbon dioxide anaesthesia. Scientific Reports. 5(1). 15298–15298. 61 indexed citations
7.
Call, Gerald B., et al.. (2015). Interleukin-6 inhibits adrenal androgen release from bovine adrenal zona reticularis cells by inhibiting the expression of steroidogenic proteins. Domestic Animal Endocrinology. 53. 108–123. 5 indexed citations
8.
Call, Gerald B., et al.. (2014). Computational tools for fitting the Hill equation to dose–response curves. Journal of Pharmacological and Toxicological Methods. 71. 68–76. 157 indexed citations
9.
Tea, Joy S., et al.. (2014). Dissection and Mounting of <em>Drosophila</em> Pupal Eye Discs. Journal of Visualized Experiments. e52315–e52315. 6 indexed citations
10.
Murray, Michael J., et al.. (2013). An airtight approach to the inebriometer. Fly. 7(2). 112–117. 4 indexed citations
11.
Nagaraj, Raghavendra, Edward Owusu-Ansah, Andrew Folick, et al.. (2010). Role of Lipid Metabolism in Smoothened Derepression in Hedgehog Signaling. Developmental Cell. 19(1). 54–65. 80 indexed citations
12.
Evans, Cory J., John M. Olson, Kathy Ngo, et al.. (2009). G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila. Nature Methods. 6(8). 603–605. 259 indexed citations
13.
Pan, Lei, Changjiang Weng, Gerald B. Call, et al.. (2007). Stem Cell Aging Is Controlled Both Intrinsically and Extrinsically in the Drosophila Ovary. Cell stem cell. 1(4). 458–469. 162 indexed citations
14.
Call, Gerald B. & Michael W. Wolfe. (2002). Species differences in GnRH activation of the LHβ promoter: role of Egr1 and Sp1. Molecular and Cellular Endocrinology. 189(1-2). 85–96. 23 indexed citations
15.
Call, Gerald B., et al.. (2000). Bovine Adrenal Cells Secrete Interleukin-6 and Tumor Necrosis Factor in Vitro. General and Comparative Endocrinology. 118(2). 249–261. 25 indexed citations
16.
Judd, Allan M., et al.. (2000). Possible Function of IL‐6 and TNF as Intraadrenal Factors in the Regulation of Adrenal Steroid Secretion. Annals of the New York Academy of Sciences. 917(1). 628–637. 87 indexed citations
17.
Call, Gerald B., Omar F. Husein, Andrew Adams, et al.. (2000). Stimulation by Interleukin-6 and Inhibition by Tumor Necrosis Factor of Cortisol Release from Bovine Adrenal Zona Fasciculata Cells Through Their Receptors. Endocrine. 13(3). 369–377. 34 indexed citations
18.
Call, Gerald B. & Michael W. Wolfe. (1999). Gonadotropin-Releasing Hormone Activates the Equine Luteinizing Hormone β Promoter Through a Protein Kinase C/Mitogen-Activated Protein Kinase Pathway1. Biology of Reproduction. 61(3). 715–723. 41 indexed citations
19.
Wolfe, Michael W. & Gerald B. Call. (1999). Early Growth Response Protein 1 Binds to the Luteinizing Hormone-β Promoter and Mediates Gonadotropin-Releasing Hormone-Stimulated Gene Expression. Molecular Endocrinology. 13(5). 752–763. 95 indexed citations
20.
Spangelo, Bryan L., et al.. (1995). Role of the Cytokines in the Hypothalamic-Pituitary-Adrenal and Gonadal Axes. NeuroImmunoModulation. 2(5). 299–312. 76 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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