Jingchun Luo

1.9k total citations
17 papers, 477 citations indexed

About

Jingchun Luo is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Jingchun Luo has authored 17 papers receiving a total of 477 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Oncology and 4 papers in Genetics. Recurrent topics in Jingchun Luo's work include Pregnancy and preeclampsia studies (3 papers), Cancer Risks and Factors (3 papers) and Fibroblast Growth Factor Research (3 papers). Jingchun Luo is often cited by papers focused on Pregnancy and preeclampsia studies (3 papers), Cancer Risks and Factors (3 papers) and Fibroblast Growth Factor Research (3 papers). Jingchun Luo collaborates with scholars based in United States, Canada and China. Jingchun Luo's co-authors include Robert C. Millikan, Jill S. Barnholtz‐Sloan, Sarah J. Nyante, Priya B. Shetty, Donal J. Brennan, Xiaowei Guan, Ethan M. Lange, Jeannette T. Bensen, Marilie D. Gammon and Jin Li and has published in prestigious journals such as Human Molecular Genetics, Carcinogenesis and Breast Cancer Research and Treatment.

In The Last Decade

Jingchun Luo

16 papers receiving 468 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jingchun Luo United States	12	138	116	114	96	88	17	477
F-J Tsai Taiwan	12	141 1.0×	81 0.7×	85 0.7×	72 0.8×	19 0.2×	21	438
Renfang Han China	14	158 1.1×	31 0.3×	230 2.0×	93 1.0×	54 0.6×	27	404
Huiyong Peng China	12	196 1.4×	33 0.3×	96 0.8×	190 2.0×	233 2.6×	26	507
Luz Agana United States	8	127 0.9×	56 0.5×	104 0.9×	79 0.8×	40 0.5×	8	393
Hoda A. Hagrass Egypt	12	129 0.9×	73 0.6×	57 0.5×	28 0.3×	84 1.0×	16	386
Tianbo Jin China	15	301 2.2×	93 0.8×	23 0.2×	76 0.8×	137 1.6×	48	522
Shirley Yan United States	11	95 0.7×	62 0.5×	38 0.3×	187 1.9×	24 0.3×	17	550
Tzu-Ting Hsu Australia	4	182 1.3×	25 0.2×	42 0.4×	68 0.7×	75 0.9×	4	468
Juling Zhou United States	11	175 1.3×	131 1.1×	45 0.4×	128 1.3×	21 0.2×	14	381

Countries citing papers authored by Jingchun Luo

Since Specialization

Citations

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

Fields of papers citing papers by Jingchun Luo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jingchun Luo

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

All Works

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17 of 17 papers shown

Bauer, Anna E., Christy L. Avery, Min Shi, et al.. (2021). Do Genetic Variants Modify the Effect of Smoking on Risk of Preeclampsia in Pregnancy?. American Journal of Perinatology. 41(1). 44–52. 1 indexed citations

Huang, Wei, Ying Wu, Jinxiu Shi, et al.. (2020). Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index. UNC Libraries. 1 indexed citations

Barnholtz‐Sloan, Jill S., Jingchun Luo, Xiaowei Guan, et al.. (2020). FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women. UNC Libraries.

Bauer, Anna E., Christy L. Avery, Min Shi, et al.. (2017). A Family Based Study of Carbon Monoxide and Nitric Oxide Signalling Genes and Preeclampsia. Paediatric and Perinatal Epidemiology. 32(1). 1–12. 2 indexed citations

Li, Jin, Jinxiu Shi, Wei Huang, et al.. (2015). Variant Near FGF5 Has Stronger Effects on Blood Pressure in Chinese With a Higher Body Mass Index. American Journal of Hypertension. 28(8). 1031–1037. 16 indexed citations

Nyante, Sarah J., Marilie D. Gammon, Jay S. Kaufman, et al.. (2014). Genetic variation in estrogen and progesterone pathway genes and breast cancer risk: an exploration of tumor subtype-specific effects. Cancer Causes & Control. 26(1). 121–131. 15 indexed citations

Millikan, Robert C., et al.. (2014). Polymorphisms in the carcinogen detoxification genes CYB5A and CYB5R3 and breast cancer risk in African American women. Cancer Causes & Control. 25(11). 1513–1521. 13 indexed citations

Harmon, Quaker E., Stephanie M. Engel, Michael C. Wu, et al.. (2014). Polymorphisms in Inflammatory Genes are Associated with Term Small for Gestational Age and Preeclampsia. American Journal of Reproductive Immunology. 71(5). 472–484. 22 indexed citations

Taylor, Nicholas, Jeannette T. Bensen, Charles Poole, et al.. (2014). Genetic variation in cell cycle regulatory geneAURKAand association with intrinsic breast cancer subtype. Molecular Carcinogenesis. 54(12). 1668–1677. 16 indexed citations

10.

Lange, Ethan M., Claudia A. Salinas, Kimberly A. Zuhlke, et al.. (2011). Early onset prostate cancer has a significant genetic component. The Prostate. 72(2). 147–156. 56 indexed citations

11.

Nyante, Sarah J., Marilie D. Gammon, Jay S. Kaufman, et al.. (2011). Common genetic variation in adiponectin, leptin, and leptin receptor and association with breast cancer subtypes. Breast Cancer Research and Treatment. 129(2). 593–606. 54 indexed citations

12.

Croteau‐Chonka, Damien C., Ying Wu, Yun Li, et al.. (2011). Population-specific coding variant underlies genome-wide association with adiponectin level. Human Molecular Genetics. 21(2). 463–471. 36 indexed citations

13.

Barnholtz‐Sloan, Jill S., Priya B. Shetty, Xiaowei Guan, et al.. (2010). FGFR2 and other loci identified in genome-wide association studies are associated with breast cancer in African-American and younger women. Carcinogenesis. 31(8). 1417–1423. 102 indexed citations

14.

Martin, Tammy M., Ge Zhang, Jingchun Luo, et al.. (2005). A locus on chromosome 9p predisposes to a specific disease manifestation, acute anterior uveitis, in ankylosing spondylitis, a genetically complex, multisystem, inflammatory disease. Arthritis & Rheumatism. 52(1). 269–274. 43 indexed citations

15.

Li, Jin, Ge Zhang, Joshua M. Akey, et al.. (2004). Lack of linkage of IL1RN genotypes with ankylosing spondylitis susceptibility. Arthritis & Rheumatism. 50(9). 3047–3048. 14 indexed citations

16.

Zhang, Ge, Jingchun Luo, J Brückel, et al.. (2004). Genetic studies in familial ankylosing spondylitis susceptibility. Arthritis & Rheumatism. 50(7). 2246–2254. 81 indexed citations

17.

Xiao, Junhua, Fang Hu, Hongyan Xu, et al.. (2000). Provincial distribution of three HIV-1 resistant polymorphisms (CCR5-Δ32, CCR2-64I, and SDF1-3′ A) in China. Science in China Series C Life Sciences. 43(1). 16–20. 5 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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