Victor Hatini

1.6k total citations
25 papers, 1.2k citations indexed

About

Victor Hatini is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Victor Hatini has authored 25 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Cell Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Victor Hatini's work include Developmental Biology and Gene Regulation (13 papers), Cellular Mechanics and Interactions (8 papers) and Hippo pathway signaling and YAP/TAZ (7 papers). Victor Hatini is often cited by papers focused on Developmental Biology and Gene Regulation (13 papers), Cellular Mechanics and Interactions (8 papers) and Hippo pathway signaling and YAP/TAZ (7 papers). Victor Hatini collaborates with scholars based in United States, Israel and Germany. Victor Hatini's co-authors include Sung‐Oh Huh, Eseng Lai, Stephen DiNardo, Vittor Cândido Soares, Doris Herzlinger, Edmund Lai, Riva C. Marcus, Suzanne C. Li, Ryan B. Green and Judith A. Lengyel and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and The Journal of Cell Biology.

In The Last Decade

Victor Hatini

25 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Victor Hatini United States 16 1.0k 270 236 210 173 25 1.2k
Nini Guo United States 9 1.3k 1.3× 377 1.4× 249 1.1× 410 2.0× 182 1.1× 9 2.0k
Anne Seawright United Kingdom 18 1.6k 1.5× 111 0.4× 580 2.5× 145 0.7× 99 0.6× 22 1.9k
Christine Laclef France 16 1.5k 1.4× 138 0.5× 599 2.5× 84 0.4× 144 0.8× 22 1.8k
Adrian W. Moore Japan 20 1.5k 1.4× 416 1.5× 376 1.6× 675 3.2× 168 1.0× 45 2.2k
Ralf Spörle Germany 14 967 0.9× 83 0.3× 292 1.2× 78 0.4× 64 0.4× 18 1.2k
Alana Auden Australia 15 1.0k 1.0× 261 1.0× 255 1.1× 74 0.4× 57 0.3× 24 1.4k
Kris Vleminckx Belgium 24 1.4k 1.4× 252 0.9× 291 1.2× 126 0.6× 87 0.5× 58 1.8k
Haley O. Tucker United States 24 839 0.8× 123 0.5× 195 0.8× 137 0.7× 52 0.3× 55 1.3k
Jessica Sullivan-Brown United States 8 653 0.6× 328 1.2× 250 1.1× 63 0.3× 59 0.3× 13 897
Jill A. McMahon United States 6 2.4k 2.3× 182 0.7× 619 2.6× 214 1.0× 169 1.0× 6 2.5k

Countries citing papers authored by Victor Hatini

Since Specialization
Citations

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

Fields of papers citing papers by Victor Hatini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Victor Hatini

This figure shows the co-authorship network connecting the top 25 collaborators of Victor Hatini. A scholar is included among the top collaborators of Victor Hatini 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 Victor Hatini. Victor Hatini 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.
Hatini, Victor, et al.. (2024). Pten, PI3K, and PtdIns(3,4,5)P3 dynamics control pulsatile actin branching in Drosophila retina morphogenesis. Developmental Cell. 59(12). 1593–1608.e6. 4 indexed citations
2.
Hatini, Victor, et al.. (2023). Medioapical contractile pulses coordinated between cells regulate Drosophila eye morphogenesis. The Journal of Cell Biology. 223(2). 3 indexed citations
3.
Treisman, Jessica E., et al.. (2022). Sidekick dynamically rebalances contractile and protrusive forces to control tissue morphogenesis. The Journal of Cell Biology. 221(5). 15 indexed citations
4.
Letizia, Annalisa, Danqing He, Julien Colombelli, et al.. (2019). Sidekick Is a Key Component of Tricellular Adherens Junctions that Acts to Resolve Cell Rearrangements. Developmental Cell. 50(3). 313–326.e5. 54 indexed citations
5.
Signore, Steven J. Del, Rodrigo Cilla, & Victor Hatini. (2018). The WAVE Regulatory Complex and Branched F-Actin Counterbalance Contractile Force to Control Cell Shape and Packing in the Drosophila Eye. Developmental Cell. 44(4). 471–483.e4. 27 indexed citations
6.
Cilla, Rodrigo, et al.. (2015). Segmentation and Tracking of Adherens Junctions in 3D for the Analysis of Epithelial Tissue Morphogenesis. PLoS Computational Biology. 11(4). e1004124–e1004124. 18 indexed citations
7.
Hatini, Victor, et al.. (2015). RhoGAP68F controls transport of adhesion proteins in Rab4 endosomes to modulate epithelial morphogenesis of Drosophila leg discs. Developmental Biology. 399(2). 283–295. 12 indexed citations
8.
Hatini, Victor, et al.. (2013). Essential roles for stat92E in expanding and patterning the proximodistal axis of the Drosophila wing imaginal disc. Developmental Biology. 378(1). 38–50. 13 indexed citations
9.
Signore, Steven J. Del, Teru HAYASHI, & Victor Hatini. (2012). odd-skipped genes and lines organize the notum anterior–posterior axis using autonomous and non-autonomous mechanisms. Mechanisms of Development. 129(5-8). 147–161. 10 indexed citations
10.
Hatini, Victor, et al.. (2010). Systematic expression and loss-of-function analysis defines spatially restricted requirements for Drosophila RhoGEFs and RhoGAPs in leg morphogenesis. Mechanisms of Development. 128(1-2). 5–17. 24 indexed citations
11.
12.
Nusinow, David P., et al.. (2008). Reciprocal roles for bowl and lines in specifying the peripodial epithelium and the disc proper of the Drosophila wing primordium. Development. 135(18). 3031–3041. 16 indexed citations
13.
Hatini, Victor & Stephen DiNardo. (2001). Distinct Signals Generate Repeating Striped Pattern in the Embryonic Parasegment. Molecular Cell. 7(1). 151–160. 32 indexed citations
14.
Hatini, Victor & Stephen DiNardo. (2001). Divide and conquer: pattern formation in Drosophila embryonic epidermis. Trends in Genetics. 17(10). 574–579. 74 indexed citations
15.
Hatini, Victor, et al.. (2000). Tissue- and stage-specific modulation of Wingless signaling by the segment polarity gene lines. Genes & Development. 14(11). 1364–1376. 39 indexed citations
16.
Huh, Sung‐Oh, Victor Hatini, Riva C. Marcus, Suzanne C. Li, & Eseng Lai. (1999). Dorsal–Ventral Patterning Defects in the Eye of BF-1-Deficient Mice Associated with a Restricted Loss of shh Expression. Developmental Biology. 211(1). 53–63. 99 indexed citations
17.
Hatini, Victor, et al.. (1999). Dynamics of placodal lineage development revealed by targeted transgene expression. Developmental Dynamics. 215(4). 332–343. 45 indexed citations
18.
19.
Hatini, Victor, Sung‐Oh Huh, Doris Herzlinger, Vittor Cândido Soares, & Edmund Lai. (1996). Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged Helix transcription factor BF-2.. Genes & Development. 10(12). 1467–1478. 385 indexed citations
20.
Hatini, Victor, et al.. (1994). Expression of winged helix genes, BF‐1 and BF‐2, define adjacent domains within the developing forebrain and retina. Journal of Neurobiology. 25(10). 1293–1309. 182 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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