Wei V. Chen

5.8k total citations · 1 hit paper
15 papers, 791 citations indexed

About

Wei V. Chen is a scholar working on Molecular Biology, Cell Biology and Oncology. According to data from OpenAlex, Wei V. Chen has authored 15 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Cell Biology and 4 papers in Oncology. Recurrent topics in Wei V. Chen's work include melanin and skin pigmentation (4 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Cutaneous Melanoma Detection and Management (3 papers). Wei V. Chen is often cited by papers focused on melanin and skin pigmentation (4 papers), Chronic Lymphocytic Leukemia Research (3 papers) and Cutaneous Melanoma Detection and Management (3 papers). Wei V. Chen collaborates with scholars based in United States, United Kingdom and France. Wei V. Chen's co-authors include Peter K. Gregersen, Christopher I. Amos, Lynn Petukhova, David A. Norris, Maria Hordinsky, Vera H. Price, Hyunmi Kim, Colin A.B. Jahoda, Ralf Paus and Katja C. Meyer and has published in prestigious journals such as Nature, International Journal of Cancer and Journal of Investigative Dermatology.

In The Last Decade

Wei V. Chen

15 papers receiving 776 citations

Hit Papers

Genome-wide association study in alopecia areata implicat... 2010 2026 2015 2020 2010 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wei V. Chen United States 11 385 257 250 200 156 15 791
Jonghyeob Lee United States 10 86 0.2× 110 0.4× 351 1.4× 68 0.3× 115 0.7× 11 699
Charles H. W. Horne United Kingdom 12 54 0.1× 60 0.2× 201 0.8× 58 0.3× 52 0.3× 24 613
Silvia Majore Italy 16 85 0.2× 16 0.1× 427 1.7× 59 0.3× 26 0.2× 48 808
Kuniko Inoue Japan 13 15 0.0× 56 0.2× 210 0.8× 93 0.5× 37 0.2× 21 393
Mari Higashiyama Japan 13 11 0.0× 94 0.4× 91 0.4× 149 0.7× 68 0.4× 35 481
Tatiana M. Grzeszkiewicz United States 7 20 0.1× 28 0.1× 600 2.4× 112 0.6× 41 0.3× 8 704
David Grote Canada 9 128 0.3× 15 0.1× 693 2.8× 39 0.2× 30 0.2× 12 856
Andrew Thomas United States 9 320 0.8× 11 0.0× 200 0.8× 41 0.2× 102 0.7× 14 645
Hyun‐Tae Shin South Korea 13 24 0.1× 87 0.3× 168 0.7× 20 0.1× 20 0.1× 37 506
D W Pennington United States 7 14 0.0× 67 0.3× 213 0.9× 117 0.6× 26 0.2× 10 420

Countries citing papers authored by Wei V. Chen

Since Specialization
Citations

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

Fields of papers citing papers by Wei V. Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wei V. 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 Wei V. Chen. The network helps show where Wei V. Chen may publish in the future.

Co-authorship network of co-authors of Wei V. Chen

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

All Works

15 of 15 papers shown
1.
Vaysse, Amaury, Shenying Fang, Myriam Brossard, et al.. (2016). A comprehensive genome‐wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants. International Journal of Cancer. 139(9). 2012–2020. 9 indexed citations
2.
Wei, Chongjuan, Bo Peng, Younghun Han, et al.. (2015). Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers. Familial Cancer. 14(2). 297–306. 27 indexed citations
3.
Brossard, Myriam, Shenying Fang, Amaury Vaysse, et al.. (2015). Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma risk. International Journal of Cancer. 137(8). 1901–1909. 12 indexed citations
4.
Yin, Jieyun, Hongliang Liu, Zhensheng Liu, et al.. (2014). Genetic Variants in Fanconi Anemia Pathway Genes BRCA2 and FANCA Predict Melanoma Survival. Journal of Investigative Dermatology. 135(2). 542–550. 29 indexed citations
5.
Liu, Hongliang, Li‐E Wang, Zhensheng Liu, et al.. (2013). Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk. Carcinogenesis. 34(4). 885–892. 10 indexed citations
6.
Chen, Jinyun, Mala Pande, Chongjuan Wei, et al.. (2012). Cell cycle–related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients. Carcinogenesis. 34(2). 299–306. 9 indexed citations
8.
Pande, Mala, Margaret R. Spitz, Xifeng Wu, et al.. (2011). Novel genetic variants in the chromosome 5p15.33 region associate with lung cancer risk. Carcinogenesis. 32(10). 1493–1499. 53 indexed citations
9.
Petukhova, Lynn, Madeleine Duvic, Maria Hordinsky, et al.. (2010). Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. Nature. 466(7302). 113–117. 538 indexed citations breakdown →
10.
Wu, Chih‐Chieh, Sanjay Shete, Wei V. Chen, et al.. (2009). Detection of disease-associated deletions in case–control studies using SNP genotypes with application to rheumatoid arthritis. Human Genetics. 126(2). 303–315. 8 indexed citations
11.
Chen, Wei V., Christopher I. Amos, Carol J. Etzel, Sanjay Shete, & Peter K. Gregersen. (2007). Comparison of genome-wide single-nucleotide polymorphism linkage analyses in Caucasian and Hispanic NARAC families. BMC Proceedings. 1(S1). S97–S97. 3 indexed citations
12.
Etzel, Carol J., Wei V. Chen, Damini Jawaheer, et al.. (2006). Genome-wide meta-analysis for rheumatoid arthritis. Human Genetics. 119(6). 634–641. 29 indexed citations
13.
Criswell, Lindsey A., Wei V. Chen, Damini Jawaheer, et al.. (2006). Dissecting the heterogeneity of rheumatoid arthritis through linkage analysis of quantitative traits. Arthritis & Rheumatism. 56(1). 58–68. 15 indexed citations
14.
Derom, Cathérine, Damini Jawaheer, Wei V. Chen, et al.. (2005). Genome-wide linkage scan for spontaneous DZ twinning. European Journal of Human Genetics. 14(1). 117–122. 15 indexed citations
15.
Chen, Wei V., J. Fielding Hejtmancik, Joram Piatigorsky, & Melinda K. Duncan. (2001). The mouse βB1-crystallin promoter: strict regulation of lens fiber cell specificity. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1519(1-2). 30–38. 15 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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