Peng‐Chieh Chen

6.0k total citations
25 papers, 633 citations indexed

About

Peng‐Chieh Chen is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cell Biology. According to data from OpenAlex, Peng‐Chieh Chen has authored 25 papers receiving a total of 633 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Pathology and Forensic Medicine and 8 papers in Cell Biology. Recurrent topics in Peng‐Chieh Chen's work include Skin and Cellular Biology Research (4 papers), Genetic factors in colorectal cancer (4 papers) and Autoimmune Bullous Skin Diseases (3 papers). Peng‐Chieh Chen is often cited by papers focused on Skin and Cellular Biology Research (4 papers), Genetic factors in colorectal cancer (4 papers) and Autoimmune Bullous Skin Diseases (3 papers). Peng‐Chieh Chen collaborates with scholars based in Taiwan, United States and United Kingdom. Peng‐Chieh Chen's co-authors include Roderick T. Bronson, Steven M. Lipkin, Amy E. Roberts, Benjamin G. Neel, Yuan Tao, Raju Kucherlapati, Kan Yang, Eric S. Martin, Kenneth E. Hung and Larissa Georgeon Richard and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Peng‐Chieh Chen

25 papers receiving 624 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peng‐Chieh Chen Taiwan 11 443 176 157 142 129 25 633
Clare M. Adams United States 16 641 1.4× 122 0.7× 244 1.6× 102 0.7× 225 1.7× 26 858
Huaizeng Chen China 16 514 1.2× 75 0.4× 280 1.8× 144 1.0× 165 1.3× 44 788
Sabine Franke Germany 11 281 0.6× 100 0.6× 139 0.9× 102 0.7× 146 1.1× 24 557
Sébastien de Feraudy United States 13 277 0.6× 106 0.6× 174 1.1× 76 0.5× 113 0.9× 32 655
Emmanuel Tubacher France 8 465 1.0× 111 0.6× 95 0.6× 73 0.5× 170 1.3× 11 708
Mandy Boer Netherlands 9 338 0.8× 80 0.5× 173 1.1× 61 0.4× 76 0.6× 10 471
Antònia Obrador‐Hevia Spain 15 440 1.0× 123 0.7× 214 1.4× 57 0.4× 141 1.1× 25 676
Sangok Kim South Korea 9 390 0.9× 175 1.0× 153 1.0× 111 0.8× 211 1.6× 15 652
Susan Morgan United Kingdom 10 236 0.5× 87 0.5× 187 1.2× 114 0.8× 55 0.4× 18 445

Countries citing papers authored by Peng‐Chieh Chen

Since Specialization
Citations

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

Fields of papers citing papers by Peng‐Chieh Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peng‐Chieh Chen. 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 Peng‐Chieh Chen. The network helps show where Peng‐Chieh Chen may publish in the future.

Co-authorship network of co-authors of Peng‐Chieh Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Peng‐Chieh Chen. A scholar is included among the top collaborators of Peng‐Chieh Chen 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 Peng‐Chieh Chen. Peng‐Chieh Chen 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.
Chou, Yen‐Yin, Pao‐Lin Kuo, Hui‐Pin Hsiao, et al.. (2024). Syndromic ciliopathy: a taiwanese single-center study. BMC Medical Genomics. 17(1). 106–106. 1 indexed citations
2.
Lin, Yu‐Chen, Alexandros Onoufriadis, Hans I‐Chen Harn, et al.. (2024). Dominant dystrophic epidermolysis bullosa is associated with glycolytically active GATA3+ T helper 2 cells which may contribute to pruritus in lesional skin. British Journal of Dermatology. 191(2). 252–260. 4 indexed citations
3.
Hwang, Daw‐Yang, Chao‐Chun Yang, Siao Muk Cheng, et al.. (2024). Profibrotic Subsets of SPP1+ Macrophages and POSTN+ Fibroblasts Contribute to Fibrotic Scarring in Acne Keloidalis. Journal of Investigative Dermatology. 144(7). 1491–1504.e10. 14 indexed citations
4.
Chiang, Po‐Min, Yung‐Yeh Su, Yu‐Ting Yu, et al.. (2024). Cytoplasmic Lipid Droplets Predict Worse Prognosis in Diffuse Large B-Cell Lymphoma. The American Journal of Surgical Pathology. 48(11). 1425–1438. 1 indexed citations
5.
Tsai, Meng‐Che, et al.. (2023). Whole-Exome Sequencing Identified Rare Genetic Variants Associated with Undervirilized Genitalia in Taiwanese Pediatric Patients. Biomedicines. 11(2). 242–242. 1 indexed citations
6.
Chen, Peng‐Chieh, Hsin‐Yu Huang, Jingyu Wang, et al.. (2022). Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients. Orphanet Journal of Rare Diseases. 17(1). 451–451. 4 indexed citations
7.
Ding, Li-Yun, Chien‐Hung Yu, Hsin‐Yi Wu, et al.. (2022). RNA bisulfite sequencing reveals NSUN2-mediated suppression of epithelial differentiation in pancreatic cancer. Oncogene. 41(22). 3162–3176. 42 indexed citations
8.
Hou, Peng, Ken Natsuga, Hsin‐Yu Huang, et al.. (2021). Complexity of Transcriptional and Translational Interference of Laminin-332 Subunits in Junctional Epidermolysis Bullosa with LAMB3 Mutations. Acta Dermato Venereologica. 101(8). adv00522–adv00522. 1 indexed citations
9.
Tsai, Meng‐Che, et al.. (2021). New Structural and Single Nucleotide Mutations in Type I and Type II Collagens in Taiwanese Children With Type I and Type II Collagenopathies. Frontiers in Genetics. 12. 594285–594285. 1 indexed citations
10.
Liao, Yi-Chu, Tzu‐Yi Chan, Chun‐Hsin Wu, et al.. (2021). NOX2-Deficient Neutrophils Facilitate Joint Inflammation Through Higher Pro-Inflammatory and Weakened Immune Checkpoint Activities. Frontiers in Immunology. 12. 743030–743030. 14 indexed citations
11.
12.
Chen, Peng‐Chieh, Peng Hou, Hsin‐Yu Huang, et al.. (2020). Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex. Acta Dermato Venereologica. 100(15). adv00242–adv00242. 6 indexed citations
13.
Chen, Peng‐Chieh, et al.. (2020). FGF primes angioblast formation by inducing ETV2 and LMO2 via FGFR1/BRAF/MEK/ERK. Cellular and Molecular Life Sciences. 78(5). 2199–2212. 3 indexed citations
14.
Chen, Jiann-Shiuh, et al.. (2018). A novel pathogenic mutation on Interleukin-7 receptor leading to severe combined immunodeficiency identified with newborn screening and whole exome sequencing. Journal of Microbiology Immunology and Infection. 53(1). 99–105. 12 indexed citations
15.
16.
Roper, Jatin, Michael P. Richardson, Larissa Georgeon Richard, et al.. (2011). The Dual PI3K/mTOR Inhibitor NVP-BEZ235 Induces Tumor Regression in a Genetically Engineered Mouse Model of PIK3CA Wild-Type Colorectal Cancer. PLoS ONE. 6(9). e25132–e25132. 106 indexed citations
17.
Chen, Peng‐Chieh, Mari Kuraguchi, Yuxun Wang, et al.. (2008). Novel Roles for MLH3 Deficiency and TLE6-Like Amplification in DNA Mismatch Repair-Deficient Gastrointestinal Tumorigenesis and Progression. PLoS Genetics. 4(6). e1000092–e1000092. 29 indexed citations
18.
Chen, Peng‐Chieh, Sandra Dudley, Diana Dizon, et al.. (2005). Contributions by MutL Homologues Mlh3 and Pms2 to DNA Mismatch Repair and Tumor Suppression in the Mouse. Cancer Research. 65(19). 8662–8670. 77 indexed citations
19.
Frank, Steven A., Peng‐Chieh Chen, & Steven M. Lipkin. (2005). Kinetics of cancer: a method to test hypotheses of genetic causation. BMC Cancer. 5(1). 163–163. 3 indexed citations
20.
Lipkin, Steven M., Laura S. Rozek, Gad Rennert, et al.. (2004). The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. Nature Genetics. 36(7). 694–699. 72 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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