Hane Lee

13.1k total citations · 2 hit papers
86 papers, 5.3k citations indexed

About

Hane Lee is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Hane Lee has authored 86 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 42 papers in Genetics and 8 papers in Surgery. Recurrent topics in Hane Lee's work include Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Hane Lee is often cited by papers focused on Genomics and Rare Diseases (25 papers), Genomic variations and chromosomal abnormalities (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Hane Lee collaborates with scholars based in United States, Singapore and South Korea. Hane Lee's co-authors include Stanley F. Nelson, Zugen Chen, Thinle Chodon, Jeffrey A. Sosman, Antoni Ribas, Mi‐Kyung Lee, Richard C. Koya, Roger S. Lo, Hubing Shi and Xiangju Kong and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Hane Lee

79 papers receiving 5.2k citations

Hit Papers

Melanomas acquire resista... 2010 2026 2015 2020 2010 2012 500 1000 1.5k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation
    2010 1.6k citations Hane Lee, Stanley F. Nelson et al. profile →
  2. Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance
    2012 470 citations Hane Lee, Stanley F. Nelson et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Hane Lee 3.7k 1.3k 1.1k 640 486 86 5.3k
Sharon Shacham 4.4k 1.2× 1.4k 1.1× 380 0.3× 369 0.6× 406 0.8× 221 5.8k
Cory M. Johannessen 2.9k 0.8× 1.3k 1.0× 203 0.2× 667 1.0× 360 0.7× 28 4.2k
Matthew Mort 6.1k 1.7× 394 0.3× 3.5k 3.2× 964 1.5× 511 1.1× 79 9.1k
Isabella A. Graef 4.1k 1.1× 637 0.5× 569 0.5× 487 0.8× 294 0.6× 39 5.8k
Abdel Elkahloun 4.3k 1.2× 1.1k 0.8× 1.3k 1.2× 1.5k 2.4× 411 0.8× 114 7.1k
Ashani T. Weeraratna 3.9k 1.1× 1.8k 1.3× 405 0.4× 1.1k 1.7× 185 0.4× 114 6.6k
Hubert Hondermarck 3.2k 0.9× 1.3k 0.9× 370 0.3× 1.0k 1.6× 295 0.6× 151 6.0k
Andrea I. McClatchey 4.8k 1.3× 1.9k 1.4× 497 0.5× 672 1.1× 387 0.8× 68 8.9k
Michael Shtutman 4.3k 1.2× 1.2k 0.9× 456 0.4× 498 0.8× 346 0.7× 72 5.6k
Teresa Druck 5.1k 1.4× 1.2k 0.9× 2.8k 2.5× 626 1.0× 387 0.8× 87 6.8k

Countries citing papers authored by Hane Lee

Since Specialization
Citations

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

Fields of papers citing papers by Hane Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hane Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Hane Lee. A scholar is included among the top collaborators of Hane Lee 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 Hane Lee. Hane Lee 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
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Han, Heonjong, Go Hun Seo, Kisang Kwon, et al.. (2025). Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders. npj Genomic Medicine. 10(1). 6–6. 2 indexed citations
3.
Villafán-Bernal, José Rafael, Humberto Garcia‐Ortíz, Angélica Martínez‐Hernández, et al.. (2025). First Latin American Case of MLASA2 Caused by a Pathogenic Variant in the Anticodon-Binding Domain of YARS2. International Journal of Molecular Sciences. 26(24). 12039–12039.
4.
Raber, Irving M., Rin Khang, Ralph C. Eagle, et al.. (2025). Corneal Myofibromatous and Pterygium-Like Changes in a Family With a PDGFRB Variant. Cornea. 44(10). 1219–1228.
5.
Vela‐Amieva, Marcela, Miguel Angel Alcántara‐Ortigoza, Ariadna González‐del Angel, et al.. (2024). Concordance Between Biochemical and Molecular Diagnosis Obtained by WES in Mexican Patients with Inborn Errors of Intermediary Metabolism: Utility for Therapeutic Management. International Journal of Molecular Sciences. 25(21). 11722–11722.
6.
Song, Yongjun, et al.. (2024). A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE‐1 insertion in LDLR. Molecular Genetics & Genomic Medicine. 12(3). e2410–e2410. 1 indexed citations
7.
Ryu, Seung Woo, et al.. (2024). Identification of a complex intrachromosomal inverted insertion in the long arm of chromosome 9 as a cause of tuberous sclerosis complex in a Korean family. Molecular Genetics & Genomic Medicine. 12(3). e2330–e2330. 1 indexed citations
8.
Ngo, Kathie J., Darice Y. Wong, Jihye Kim, et al.. (2024). Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing. Neurology Genetics. 10(3). e200133–e200133. 4 indexed citations
9.
Janković, Milena, et al.. (2024). Secondary findings in 443 exome sequencing data. Annals of Human Genetics. 89(2-3). 67–76. 1 indexed citations
10.
Ryu, Seung Woo, Geu‐Ru Hong, Jung Sun Cho, et al.. (2024). High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients. Frontiers in Cardiovascular Medicine. 11.
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Loh, Abigail, Kiat Yi Tan, Hane Lee, et al.. (2023). RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis. EMBO Molecular Medicine. 15(5). e17078–e17078. 5 indexed citations
14.
Kwon, Kisang, et al.. (2023). P661: A database of high allele frequency variants from exome sequencing data of 20,455 patients enriched with Asian population. SHILAP Revista de lepidopterología. 1(1). 100726–100726.
15.
Chang, Yin‐Hsi, Eugene Yu‐Chuan Kang, Laura Liu, et al.. (2023). Maternal mosaicism in SSBP1 causing optic atrophy with retinal degeneration: implications for genetic counseling. Orphanet Journal of Rare Diseases. 18(1). 131–131.
16.
Chia, Poh Hui, Franklin L. Zhong, Shinsuke Niwa, et al.. (2018). A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. eLife. 7. 44 indexed citations
17.
Csukasi, Fabiana, Iván Durán, Tomáš Bárta, et al.. (2018). The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling. Science Translational Medicine. 10(459). 41 indexed citations
18.
Praissman, Jeremy L., Tobias Willer, M. Osman Sheikh, et al.. (2016). The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition. eLife. 5. 93 indexed citations
19.
Yoshida‐Moriguchi, Takako, Tobias Willer, Mary E. Anderson, et al.. (2013). SGK196 Is a Glycosylation-Specific O -Mannose Kinase Required for Dystroglycan Function. Science. 341(6148). 896–899. 159 indexed citations
20.
Lee, Hane, et al.. (1987). Gezinsvorming in Vlaanderen: nieuwe vormen, andere timing.. Tijdschrift voor Sociologie. 8(2-3). 1 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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