Lin Ye

1.2k total citations
27 papers, 828 citations indexed

About

Lin Ye is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Lin Ye has authored 27 papers receiving a total of 828 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Lin Ye's work include CRISPR and Genetic Engineering (16 papers), Pluripotent Stem Cells Research (10 papers) and DNA Repair Mechanisms (5 papers). Lin Ye is often cited by papers focused on CRISPR and Genetic Engineering (16 papers), Pluripotent Stem Cells Research (10 papers) and DNA Repair Mechanisms (5 papers). Lin Ye collaborates with scholars based in United States, Japan and China. Lin Ye's co-authors include Yuet Wai Kan, Judy C. Chang, Jingwei Yu, Ashley I. Beyer, Marcus O. Muench, Zhongxia Qi, Chin Jia Lin, Xiaofang Sun, Fernando Teque and Jay A. Levy and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and SHILAP Revista de lepidopterología.

In The Last Decade

Lin Ye

27 papers receiving 806 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lin Ye United States 11 738 161 85 78 68 27 828
David A. Shivak United States 9 856 1.2× 508 3.2× 61 0.7× 20 0.3× 40 0.6× 10 1.0k
M. Kyle Cromer United States 11 992 1.3× 443 2.8× 23 0.3× 48 0.6× 46 0.7× 17 1.2k
Christine S. Lai Australia 6 973 1.3× 238 1.5× 133 1.6× 69 0.9× 20 0.3× 19 1.1k
Johannes Kuehle Germany 17 756 1.0× 403 2.5× 39 0.5× 45 0.6× 41 0.6× 22 1.0k
Yi-Li Min United States 11 1.3k 1.7× 368 2.3× 32 0.4× 116 1.5× 53 0.8× 11 1.4k
Carsten T. Charlesworth United States 7 854 1.2× 357 2.2× 15 0.2× 29 0.4× 44 0.6× 10 938
Seok‐Jin Heo United States 13 942 1.3× 193 1.2× 203 2.4× 19 0.2× 113 1.7× 19 1.1k
Namritha Ravinder United States 7 950 1.3× 242 1.5× 29 0.3× 26 0.3× 21 0.3× 11 1.0k
Wenqin Ying China 16 1.2k 1.6× 384 2.4× 21 0.2× 21 0.3× 28 0.4× 17 1.3k
Timothy Davis United States 12 768 1.0× 320 2.0× 25 0.3× 18 0.2× 69 1.0× 17 1.1k

Countries citing papers authored by Lin Ye

Since Specialization
Citations

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

Fields of papers citing papers by Lin Ye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lin Ye

This figure shows the co-authorship network connecting the top 25 collaborators of Lin Ye. A scholar is included among the top collaborators of Lin Ye 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 Lin Ye. Lin Ye 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.
2.
Nishino, Tomohiro, Sanjeev S. Ranade, Angelo Pelonero, et al.. (2023). Single-cell multimodal analyses reveal epigenomic and transcriptomic basis for birth defects in maternal diabetes. Nature Cardiovascular Research. 2(12). 1190–1203. 5 indexed citations
3.
Ye, Lin, Isadora Asunis, Maria Franca Marongiu, et al.. (2020). Induction of therapeutic levels of HbF in genome‐edited primary β039‐thalassaemia haematopoietic stem and progenitor cells. British Journal of Haematology. 192(2). 395–404. 13 indexed citations
4.
Stone, Nicole R., Casey A. Gifford, Reuben Thomas, et al.. (2019). Context-Specific Transcription Factor Functions Regulate Epigenomic and Transcriptional Dynamics during Cardiac Reprogramming. Cell stem cell. 25(1). 87–102.e9. 94 indexed citations
5.
Tan, Yuting, Lin Ye, Fei Xie, et al.. (2018). Respecifying human iPSC-derived blood cells into highly engraftable hematopoietic stem and progenitor cells with a single factor. Proceedings of the National Academy of Sciences. 115(9). 2180–2185. 56 indexed citations
6.
Xie, Fei, Kerui Gong, Mingliang Zhang, et al.. (2016). Reversible Immortalization Enables Seamless Transdifferentiation of Primary Fibroblasts into Other Lineage Cells. Stem Cells and Development. 25(16). 1243–1248. 6 indexed citations
7.
Ye, Lin, Jiaming Wang, Ashley I. Beyer, et al.. (2014). Seamless modification of wild-type induced pluripotent stem cells to the natural CCR5Δ32 mutation confers resistance to HIV infection. Proceedings of the National Academy of Sciences. 111(26). 9591–9596. 247 indexed citations
8.
Wang, Ji, Vera Huang, Lin Ye, et al.. (2014). Identification of Small Activating RNAs that Enhance Endogenous OCT4 Expression in Human Mesenchymal Stem Cells. Stem Cells and Development. 24(3). 345–353. 14 indexed citations
9.
Ye, Lin, Marcus O. Muench, Noemi Fusaki, et al.. (2013). Blood Cell-Derived Induced Pluripotent Stem Cells Free of Reprogramming Factors Generated by Sendai Viral Vectors. Stem Cells Translational Medicine. 2(8). 558–566. 54 indexed citations
10.
Ye, Lin, Judy C. Chang, Chin Jia Lin, et al.. (2010). Generation of induced pluripotent stem cells using site-specific integration with phage integrase. Proceedings of the National Academy of Sciences. 107(45). 19467–19472. 36 indexed citations
11.
Ye, Lin, Judy C. Chang, Chin Jia Lin, et al.. (2009). Induced pluripotent stem cells offer new approach to therapy in thalassemia and sickle cell anemia and option in prenatal diagnosis in genetic diseases. Proceedings of the National Academy of Sciences. 106(24). 9826–9830. 155 indexed citations
12.
Ye, Lin, Rosalie Maurisse, Jennifer Schwarz, et al.. (2009). Sequence-Specific Correction of Genomic Hypoxanthine-Guanine Phosphoribosyl Transferase Mutations in Lymphoblasts by Small Fragment Homologous Replacement. Oligonucleotides. 20(1). 7–16. 7 indexed citations
13.
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
14.
Nakura, Jun, Lin Ye, Asako Takahashi-Fujii, et al.. (1996). Two dinucleotide repeat polymorphisms at the D8S1444 and D8S1445 loci. The Japanese Journal of Human Genetics. 41(2). 261–263. 2 indexed citations
15.
Mitsuda, Noriaki, Jun Nakura, Lin Ye, Tetsuro Miki, & Toshio Ogihara. (1996). Dinucleotide repeat polymorphism at the D8S1223 locus. The Japanese Journal of Human Genetics. 41(2). 265–266. 2 indexed citations
16.
Nakura, Jun, Tetsuro Miki, Lin Ye, et al.. (1996). Narrowing the Position of the Werner Syndrome Locus by Homozygosity Analysis—Extension of Homozygosity Analysis. Genomics. 36(1). 130–141. 6 indexed citations
17.
Ye, Lin, Jun Nakura, Noriaki Mitsuda, et al.. (1996). Two dinucleotide repeat polymorphisms at the D8S1218 and D8S1219 loci. The Japanese Journal of Human Genetics. 41(2). 257–259. 1 indexed citations
18.
Ye, Lin, Jun Nakura, Kouzin Kamino, et al.. (1994). Dinucleotide repeat polymorphism at the D8S1055. The Japanese Journal of Human Genetics. 39(4). 441–443. 3 indexed citations
19.
Nakura, Jun, Tetsuro Miki, Keiko Nagano, et al.. (1993). Close Linkage of the Gene for Werner’s Syndrome to ANK1 and D8S87 on the Short Arm of Chromosome 8. Gerontology. 39(1). 11–15. 6 indexed citations
20.
Kamino, Kouzin, Jun Nakura, Lin Ye, et al.. (1993). Population variation in the dinucleotide repeat polymorphism at the D8S360 locus. Human Molecular Genetics. 2(10). 1751–1751. 8 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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