Tian Xu

21.2k total citations · 7 hit papers
155 papers, 17.1k citations indexed

About

Tian Xu is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Tian Xu has authored 155 papers receiving a total of 17.1k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Molecular Biology, 44 papers in Cell Biology and 21 papers in Genetics. Recurrent topics in Tian Xu's work include Hippo pathway signaling and YAP/TAZ (32 papers), Developmental Biology and Gene Regulation (23 papers) and CRISPR and Genetic Engineering (21 papers). Tian Xu is often cited by papers focused on Hippo pathway signaling and YAP/TAZ (32 papers), Developmental Biology and Gene Regulation (23 papers) and CRISPR and Genetic Engineering (21 papers). Tian Xu collaborates with scholars based in United States, China and Japan. Tian Xu's co-authors include Gerald M. Rubin, Christopher J. Potter, Spyros Artavanis‐Tsakonas, Yuan Zhuang, Min Han, Kun‐Liang Guan, Yong Li, Ken Inoki, Raymond Pagliarini and Xiaohui Wu and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Tian Xu

152 papers receiving 16.9k citations

Hit Papers

Analysis of genetic mosaics in developing and adult Droso... 1985 2026 1998 2012 1993 2003 1985 2002 2005 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tian Xu United States 54 12.8k 5.6k 2.4k 2.2k 1.9k 155 17.1k
Bruce A. Edgar United States 58 10.5k 0.8× 4.1k 0.7× 3.3k 1.4× 3.4k 1.6× 1.7k 0.9× 124 15.3k
Konrad Basler Switzerland 75 19.1k 1.5× 5.6k 1.0× 3.6k 1.5× 2.0k 0.9× 3.3k 1.7× 199 23.2k
Spyros Artavanis‐Tsakonas United States 70 18.1k 1.4× 3.2k 0.6× 3.2k 1.3× 2.0k 0.9× 2.5k 1.3× 121 22.4k
Hermann Steller United States 65 12.9k 1.0× 3.5k 0.6× 3.4k 1.4× 3.5k 1.6× 1.4k 0.8× 127 17.7k
Ben Margolis United States 67 11.8k 0.9× 5.2k 0.9× 1.4k 0.6× 1.4k 0.6× 1.9k 1.0× 116 15.9k
Masato Nakafuku Japan 59 12.9k 1.0× 3.1k 0.6× 3.0k 1.3× 839 0.4× 1.6k 0.8× 93 17.6k
Philippe Soriano United States 82 18.1k 1.4× 4.5k 0.8× 4.3k 1.8× 2.4k 1.1× 4.6k 2.4× 150 26.7k
Kensaku Mizuno Japan 66 8.0k 0.6× 6.2k 1.1× 3.1k 1.3× 2.4k 1.1× 865 0.5× 174 15.3k
Richard Treisman United Kingdom 70 19.1k 1.5× 4.2k 0.7× 1.8k 0.8× 2.8k 1.3× 3.2k 1.7× 116 25.1k
Frank B. Gertler United States 78 9.8k 0.8× 7.9k 1.4× 3.4k 1.4× 1.8k 0.8× 1.2k 0.6× 163 18.9k

Countries citing papers authored by Tian Xu

Since Specialization
Citations

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

Fields of papers citing papers by Tian Xu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tian Xu

This figure shows the co-authorship network connecting the top 25 collaborators of Tian Xu. A scholar is included among the top collaborators of Tian Xu 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 Tian Xu. Tian Xu 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.
Li, Delong, Wenting Song, Liang Liu, et al.. (2025). CRISPR Screening Reveals a Novel Role for FOXH1 in Regulating Pluripotency of Porcine Embryonic Stem Cells. Advanced Science. 12(34). e09495–e09495.
2.
Xu, Tian, et al.. (2025). Cholesterol and 24S-OHC Induce Neuronal Apoptosis and Necroptosis, but Not Ferroptosis Despite Elevated Iron Levels. Molecular Neurobiology. 62(12). 16617–16635. 1 indexed citations
3.
Xu, Tian, Shuqin Xu, Youben Fan, et al.. (2023). Genomic Profiling Reveals the Variant Landscape of Sporadic Parathyroid Adenomas in Chinese Population. The Journal of Clinical Endocrinology & Metabolism. 108(7). 1768–1775. 9 indexed citations
4.
Yang, Xiaoqiang, Wei‐Wen Cai, Yanwei Bi, et al.. (2020). Defined host factors support HBV infection in non‐hepatic 293T cells. Journal of Cellular and Molecular Medicine. 24(4). 2507–2518. 6 indexed citations
5.
Chang, Hao, Sean F. Landrette, Sheng Ding, et al.. (2019). Efficient genome-wide first-generation phenotypic screening system in mice using the piggyBac transposon. Proceedings of the National Academy of Sciences. 116(37). 18507–18516. 9 indexed citations
6.
Hu, Zhiwei, Rulong Shen, Elizabeth L. McMichael, et al.. (2018). Targeting Tissue Factor for Immunotherapy of Triple-Negative Breast Cancer Using a Second-Generation ICON. Cancer Immunology Research. 6(6). 671–684. 33 indexed citations
7.
Li, Min‐Dian, Nicholas B. Vera, Yunfan Yang, et al.. (2018). Adipocyte OGT governs diet-induced hyperphagia and obesity. Nature Communications. 9(1). 5103–5103. 53 indexed citations
8.
Cui, Jing, Yi Ding, Chen Shu, et al.. (2016). Disruption of Gpr45 causes reduced hypothalamic POMC expression and obesity. Journal of Clinical Investigation. 126(9). 3192–3206. 30 indexed citations
9.
Ma, Xianjue, et al.. (2013). Bendless modulates JNK-mediated cell death and migration in Drosophila. Cell Death and Differentiation. 21(3). 407–415. 52 indexed citations
10.
Xu, Tian, et al.. (2011). Shaping Cells and Organs in Drosophila by Opposing Roles of Fat Body-Secreted Collagen IV and Perlecan. Developmental Cell. 21(2). 245–256. 262 indexed citations
11.
Lei, Kai, Xiaochang Zhang, Xu Ding, et al.. (2009). SUN1 and SUN2 play critical but partially redundant roles in anchoring nuclei in skeletal muscle cells in mice. Proceedings of the National Academy of Sciences. 106(25). 10207–10212. 195 indexed citations
12.
Liu, Jiang, Murad Ghanim, Lei Xue, et al.. (2009). Analysis of Drosophila Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer. Science. 323(5918). 1218–1222. 98 indexed citations
13.
Dong, Yongli, Xingrong Du, Jian Ye, et al.. (2009). A Cell-Intrinsic Role for Mst1 in Regulating Thymocyte Egress. The Journal of Immunology. 183(6). 3865–3872. 89 indexed citations
14.
Wu, Ming, et al.. (2008). An innate immune response of blood cells to tumors and tissue damage in Drosophila. Disease Models & Mechanisms. 1(2-3). 144–154. 238 indexed citations
15.
Xu, Rong, Kejing Deng, Yue Wu, et al.. (2008). A large-scale functional approach to uncover human genes and pathways in Drosophila. Cell Research. 18(11). 1114–1127. 18 indexed citations
16.
Zhang, Xiaochang, Rener Xu, Xiujuan Yang, et al.. (2007). Syne-1 and Syne-2 play crucial roles in myonuclear anchorage and motor neuron innervation. Development. 134(5). 901–908. 217 indexed citations
17.
Sun, Lei, Ke Jin, Yi Liu, et al.. (2007). PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice. Nucleic Acids Research. 36(Database). D729–D734. 39 indexed citations
18.
Yu, Juehua, Daniel A. Starr, Xiaohui Wu, et al.. (2005). The KASH domain protein MSP-300 plays an essential role in nuclear anchoring during Drosophila oogenesis. Developmental Biology. 289(2). 336–345. 59 indexed citations
19.
Pagliarini, Raymond & Tian Xu. (2003). A Genetic Screen in Drosophila for Metastatic Behavior. Science. 302(5648). 1227–1231. 436 indexed citations
20.
John, Maie A.R. St. & Tian Xu. (1997). Understanding Human Cancer in a Fly?. The American Journal of Human Genetics. 61(5). 1006–1010. 27 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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