Lynda Chin

117.2k total citations · 15 hit papers
160 papers, 29.4k citations indexed

About

Lynda Chin is a scholar working on Molecular Biology, Oncology and Cancer Research. According to data from OpenAlex, Lynda Chin has authored 160 papers receiving a total of 29.4k indexed citations (citations by other indexed papers that have themselves been cited), including 126 papers in Molecular Biology, 47 papers in Oncology and 41 papers in Cancer Research. Recurrent topics in Lynda Chin's work include Melanoma and MAPK Pathways (29 papers), Cancer Genomics and Diagnostics (27 papers) and Cancer-related Molecular Pathways (16 papers). Lynda Chin is often cited by papers focused on Melanoma and MAPK Pathways (29 papers), Cancer Genomics and Diagnostics (27 papers) and Cancer-related Molecular Pathways (16 papers). Lynda Chin collaborates with scholars based in United States, Brazil and United Kingdom. Lynda Chin's co-authors include Ronald A. DePinho, Cameron Brennan, Levi A. Garraway, Carlos Cordon‐Cardo, Han‐Woong Lee, P. Andrew Futreal, Keith L. Ligon, Alexei Protopopov, Geoffrey J. Gottlieb and William C. Hahn and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Lynda Chin

158 papers receiving 28.9k citations

Hit Papers

Malignant astrocytic glioma: genetics, biology, and p... 1996 2026 2006 2016 2007 1996 2013 1998 2004 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lynda Chin United States 82 20.4k 9.3k 6.7k 3.9k 2.9k 160 29.4k
William C. Hahn United States 101 26.5k 1.3× 11.2k 1.2× 7.8k 1.2× 5.8k 1.5× 3.5k 1.2× 293 40.9k
Lena Claesson‐Welsh Sweden 87 22.2k 1.1× 6.9k 0.7× 5.8k 0.9× 1.7k 0.4× 4.8k 1.7× 256 32.3k
Alan D. D’Andrea United States 98 25.3k 1.2× 11.2k 1.2× 6.7k 1.0× 1.7k 0.5× 2.9k 1.0× 313 32.7k
Mary W. Brooks United States 24 13.1k 0.6× 10.7k 1.2× 4.7k 0.7× 2.3k 0.6× 2.0k 0.7× 28 21.2k
Martine F. Roussel United States 83 19.4k 1.0× 12.4k 1.3× 3.3k 0.5× 1.4k 0.4× 2.9k 1.0× 242 27.9k
Julian Downward United Kingdom 101 30.1k 1.5× 11.4k 1.2× 4.9k 0.7× 1.6k 0.4× 5.9k 2.1× 292 41.7k
Thomas Ried United States 84 17.7k 0.9× 7.3k 0.8× 6.2k 0.9× 1.3k 0.3× 2.3k 0.8× 378 27.8k
Ruggero De Maria Italy 72 13.1k 0.6× 9.1k 1.0× 6.1k 0.9× 1.1k 0.3× 2.2k 0.8× 257 22.8k
Robert T. Abraham United States 88 20.2k 1.0× 7.5k 0.8× 4.4k 0.7× 1.5k 0.4× 3.2k 1.1× 215 29.0k
Erik Larsson Sweden 56 21.9k 1.1× 8.3k 0.9× 9.7k 1.4× 1.3k 0.3× 2.5k 0.9× 208 34.1k

Countries citing papers authored by Lynda Chin

Since Specialization
Citations

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

Fields of papers citing papers by Lynda Chin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lynda Chin

This figure shows the co-authorship network connecting the top 25 collaborators of Lynda Chin. A scholar is included among the top collaborators of Lynda Chin 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 Lynda Chin. Lynda Chin 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.
Watson, Ian R., Li Li, Tony Gutschner, et al.. (2014). The RAC1 P29S Hotspot Mutation in Melanoma Confers Resistance to Pharmacological Inhibition of RAF. Cancer Research. 74(17). 4845–4852. 116 indexed citations
2.
Kwong, Lawrence N. & Lynda Chin. (2014). Chromosome 10, Frequently Lost in Human Melanoma, Encodes Multiple Tumor-Suppressive Functions. Cancer Research. 74(6). 1814–1821. 16 indexed citations
3.
Chew, Su Kit, Dong Lu, Lia S. Campos, et al.. (2014). Polygenic in vivovalidation of cancer mutations using transposons. Genome biology. 15(9). 455–455. 3 indexed citations
4.
Yang, Lixing, Lovelace J. Luquette, Nils Gehlenborg, et al.. (2014). Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes. Cell. 157(7). 1736–1736. 7 indexed citations
5.
Sanborn, Zack, Sofie R. Salama, Mia Grifford, et al.. (2013). Double Minute Chromosomes in Glioblastoma Multiforme Are Revealed by Precise Reconstruction of Oncogenic Amplicons. Cancer Research. 73(19). 6036–6045. 73 indexed citations
6.
Gutiérrez, Alejandro, Suzanne E. Dahlberg, Donna Neuberg, et al.. (2010). Absence of Biallelic TCR γ Deletion Predicts Early Treatment Failure in Pediatric T-Cell Acute Lymphoblastic Leukemia. Journal of Clinical Oncology. 28(24). 3816–3823. 69 indexed citations
7.
Jeon, Hye-Min, Xun Jin, Se-Yeong Oh, et al.. (2008). Inhibitor of differentiation 4 drives brain tumor-initiating cell genesis through cyclin E and notch signaling. Genes & Development. 22(15). 2028–2033. 101 indexed citations
8.
Stommel, Jayne M., Alec C. Kimmelman, Haoqiang Ying, et al.. (2007). Coactivation of Receptor Tyrosine Kinases Affects the Response of Tumor Cells to Targeted Therapies. Science. 318(5848). 287–290. 699 indexed citations breakdown →
9.
Oh, Se-Yeong, Xun Jin, Yun‐Jaie Choi, et al.. (2007). Direct Transcriptional Activation of Promyelocytic Leukemia Protein by IFN Regulatory Factor 3 Induces the p53-Dependent Growth Inhibition of Cancer Cells. Cancer Research. 67(23). 11133–11140. 38 indexed citations
10.
Martin, Eric S., Giovanni Tonon, Raktim Sinha, et al.. (2007). Common and Distinct Genomic Events in Sporadic Colorectal Cancer and Diverse Cancer Types. Cancer Research. 67(22). 10736–10743. 54 indexed citations
11.
Greshock, Joel, Bin Feng, Cristina Nogueira, et al.. (2007). A Comparison of DNA Copy Number Profiling Platforms. Cancer Research. 67(21). 10173–10180. 54 indexed citations
12.
Ji, Hongbin, Zhenxiong Wang, Samanthi A. Perera, et al.. (2007). Mutations in BRAF and KRAS Converge on Activation of the Mitogen-Activated Protein Kinase Pathway in Lung Cancer Mouse Models. Cancer Research. 67(10). 4933–4939. 137 indexed citations
13.
Rivera, Miguel N., Woo‐Jae Kim, Julie Wells, et al.. (2007). An X Chromosome Gene, WTX , Is Commonly Inactivated in Wilms Tumor. Science. 315(5812). 642–645. 225 indexed citations
14.
Liu, Fenghua, Peter J. Park, Weil Lai, et al.. (2006). A Genome-Wide Screen Reveals Functional Gene Clusters in the Cancer Genome and Identifies EphA2 as a Mitogen in Glioblastoma. Cancer Research. 66(22). 10815–10823. 94 indexed citations
15.
Maher, Elizabeth A., Cameron Brennan, Patrick Y. Wen, et al.. (2006). Marked Genomic Differences Characterize Primary and Secondary Glioblastoma Subtypes and Identify Two Distinct Molecular and Clinical Secondary Glioblastoma Entities. Cancer Research. 66(23). 11502–11513. 140 indexed citations
16.
Smolen, Gromoslaw A., Beth Muir, Gayatry Mohapatra, et al.. (2006). Frequent Met Oncogene Amplification in a Brca1/Trp53 Mouse Model of Mammary Tumorigenesis. Cancer Research. 66(7). 3452–3455. 32 indexed citations
17.
Brennan, Cameron, Yunyu Zhang, Christopher Leo, et al.. (2004). High-Resolution Global Profiling of Genomic Alterations with Long Oligonucleotide Microarray. Cancer Research. 64(14). 4744–4748. 101 indexed citations
18.
Yang, Fan, Glenn Merlino, & Lynda Chin. (2001). Genetic dissection of melanoma pathways in the mouse. Seminars in Cancer Biology. 11(3). 261–268. 17 indexed citations
19.
Muhle, Rebecca, et al.. (1997). Role for N-CoR and histone deacetylase in Sin3-mediated transcriptional repression. Nature. 387(6628). 49–55. 728 indexed citations breakdown →
20.
Rao, Govinda, Leila Alland, Peter Guida, et al.. (1996). Mouse Sin3A interacts with and can functionally substitute for the amino-terminal repression of the Myc antagonist Mxi1.. PubMed. 12(5). 1165–72. 36 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026