Cong Qian

8.1k total citations · 3 hit papers
62 papers, 6.3k citations indexed

About

Cong Qian is a scholar working on Obstetrics and Gynecology, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Cong Qian has authored 62 papers receiving a total of 6.3k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Obstetrics and Gynecology, 24 papers in Molecular Biology and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Cong Qian's work include Pregnancy and preeclampsia studies (26 papers), Birth, Development, and Health (17 papers) and MicroRNA in disease regulation (6 papers). Cong Qian is often cited by papers focused on Pregnancy and preeclampsia studies (26 papers), Birth, Development, and Health (17 papers) and MicroRNA in disease regulation (6 papers). Cong Qian collaborates with scholars based in United States, China and Cameroon. Cong Qian's co-authors include Richard J. Levine, S. Ananth Karumanchi, Ravi Thadhani, Benjamin Sachs, Lucinda J. England, Enrique F. Schisterman, Vikas P. Sukhatme, Roberto Romero, Chun Sing Lam and Kai Yu and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Cong Qian

59 papers receiving 6.2k citations

Hit Papers

Circulating Angiogenic Fa... 2004 2026 2011 2018 2004 2006 2020 500 1000 1.5k 2.0k 2.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Cong Qian 4.7k 3.7k 1.9k 1.1k 552 62 6.3k
Isabella Caniggia 3.7k 0.8× 2.5k 0.7× 1.5k 0.8× 1.9k 1.7× 892 1.6× 105 6.1k
Kee-Hak Lim 3.4k 0.7× 2.4k 0.7× 1.5k 0.8× 542 0.5× 290 0.5× 8 4.0k
Padma Murthi 1.8k 0.4× 1.2k 0.3× 801 0.4× 1.1k 0.9× 389 0.7× 138 3.6k
Eeva‐Marja Rutanen 987 0.2× 534 0.1× 882 0.5× 828 0.7× 268 0.5× 71 3.8k
Ronald J. Torry 1.3k 0.3× 691 0.2× 777 0.4× 761 0.7× 196 0.4× 50 2.3k
Yang Xiang 672 0.1× 1.4k 0.4× 315 0.2× 565 0.5× 258 0.5× 282 3.9k
Keiichi Isaka 704 0.2× 305 0.1× 467 0.2× 814 0.7× 575 1.0× 116 2.5k
Antonio Mollo 2.1k 0.5× 481 0.1× 334 0.2× 376 0.3× 328 0.6× 145 3.6k
Birger Åstedt 640 0.1× 310 0.1× 388 0.2× 715 0.6× 1.9k 3.5× 232 5.8k
Whitfield B. Growdon 921 0.2× 300 0.1× 126 0.1× 545 0.5× 214 0.4× 139 2.7k

Countries citing papers authored by Cong Qian

Since Specialization
Citations

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

Fields of papers citing papers by Cong Qian

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cong Qian

This figure shows the co-authorship network connecting the top 25 collaborators of Cong Qian. A scholar is included among the top collaborators of Cong Qian 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 Cong Qian. Cong Qian 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.
Hu, Yizhong, Xinchen Wu, Jin Yu, et al.. (2025). Piezo1-mediated mechanotransduction controls osteocyte maturation and dendrite development via a YAP-CCN-Src signaling axis. Nature Communications. 16(1). 10859–10859.
2.
Lang, Zhaobo, Yuxin Zhao, Cong Qian, et al.. (2025). Cancer therapy–induced cardiac metabolic reprogramming: A new frontier in cardio-oncology. International Immunopharmacology. 164. 115397–115397.
4.
Cai, Wentao, Zezhao Wang, Cong Qian, et al.. (2023). Proteome changes in Neck-arm restraint and Achilles tendon suspensions during early post-mortem aging in cattle. Livestock Science. 274. 105288–105288. 1 indexed citations
5.
Qian, Cong, et al.. (2023). Yap controls notochord formation and neural tube patterning by integrating mechanotransduction with FoxA2 and Shh expression. Science Advances. 9(24). eadf6927–eadf6927. 14 indexed citations
6.
Zhang, Qi, Qian Li, Yahui Wang, et al.. (2023). Characterization of Chromatin Accessibility in Fetal Bovine Chondrocytes. Animals. 13(11). 1875–1875. 2 indexed citations
7.
Yadav, Prem Swaroop, Shuhao Feng, Cong Qian, et al.. (2021). Stat3 loss in mesenchymal progenitors causes Job syndrome–like skeletal defects by reducing Wnt/β-catenin signaling. Proceedings of the National Academy of Sciences. 118(26). 18 indexed citations
8.
Qian, Cong, Yuchen Liu, Taifeng Zhou, et al.. (2021). A self-amplifying loop of YAP and SHH drives formation and expansion of heterotopic ossification. Science Translational Medicine. 13(599). 36 indexed citations
9.
Zhou, Taifeng, Bo Gao, Yi Fan, et al.. (2020). Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-catenin. eLife. 9. 266 indexed citations breakdown →
10.
Qian, Cong, et al.. (2020). Tri-domain proteins 27 reduce inflammation and apoptosis in HK-2 cells and protect against acute kidney injury in mice.. SHILAP Revista de lepidopterología. 24(23). 12258–12266. 6 indexed citations
11.
Jin, Yunyun, Cong Qian, Jelena Gvozdenovic‐Jeremic, et al.. (2018). Enpp1 inhibits ectopic joint calcification and maintains articular chondrocytes by repressing hedgehog signaling. Development. 145(18). 23 indexed citations
12.
Qian, Cong, Ruoshi Xu, & Yingzi Yang. (2018). Gαs signaling in skeletal development, homeostasis and diseases. Current topics in developmental biology. 133. 281–307. 26 indexed citations
13.
Qian, Cong, Hao Jia, Ping Li, et al.. (2016). p38α MAPK Regulates Lineage Commitment and OPG Synthesis of Bone Marrow Stromal Cells to Prevent Bone Loss under Physiological and Pathological Conditions. Stem Cell Reports. 6(4). 566–578. 35 indexed citations
14.
Wang, Kun, Xuan Wang, Jian Zou, et al.. (2013). miR-92b controls glioma proliferation and invasion through regulating Wnt/beta-catenin signaling via Nemo-like kinase. Neuro-Oncology. 15(5). 578–588. 98 indexed citations
15.
Qian, Cong. (2012). Study on Emotional Intelligence and Its Relationship with Coping Efficacy in Medical College Students. 1 indexed citations
16.
Levine, Richard J., Lars J. Vatten, Gary L. Horowitz, et al.. (2010). Pre-Eclampsia, Soluble Fms-Like Tyrosine Kinase 1, and the Risk of Reduced Thyroid Function: Nested Case-Control and Population Based Study. Obstetrical & Gynecological Survey. 65(4). 213–214. 7 indexed citations
17.
Qian, Cong, et al.. (2009). Circulating angiogenic factors in gestational proteinuria without hypertension. American Journal of Obstetrics and Gynecology. 200(4). 392.e1–392.e10. 36 indexed citations
18.
Young, Brett C., Richard J. Levine, Saira Salahuddin, et al.. (2009). The use of angiogenic biomarkers to differentiate non-HELLP related thrombocytopenia from HELLP syndrome. The Journal of Maternal-Fetal & Neonatal Medicine. 23(5). 1–6. 48 indexed citations
19.
Levine, Richard J., Chun Sing Lam, Cong Qian, et al.. (2007). Soluble Endoglin and Other Circulating Antiangiogenic Factors in Preeclampsia. Obstetrical & Gynecological Survey. 62(2). 82–83. 177 indexed citations
20.
Signore, Caroline, James L. Mills, Cong Qian, et al.. (2006). Circulating Angiogenic Factors and Placental Abruption. Obstetrics and Gynecology. 108(2). 338–344. 84 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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