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 Canada. Hane Lee's co-authors include Stanley F. Nelson, Zugen Chen, Xiangju Kong, Richard C. Koya, Antoni Ribas, Thinle Chodon, Hubing Shi, Mi‐Kyung Lee, Jeffrey A. Sosman and Roger S. Lo 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

align trajectories

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.

Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation

2010 1.6k citations Ramin Nazarian, Hubing Shi et al. Nature profile →
Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance

2012 470 citations Hubing Shi, Xiangju Kong et al. profile →

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	First Latin American Case of MLASA2 Caused by a Pathogenic Variant in the Anticodon-Binding Domain of YARS2 2025 ·International Journal of Molecular Sciences ·José Rafael Villafán-Bernal, (unknown), Humberto Garcia‐Ortíz, Angélica Martínez‐Hernández, Cecilia Contreras-Cubas, (unknown), Hane Lee, Go Hun Seo, Alessandra Carnevale, Francisco Barajas‐Olmos, Lorena Orozco	0
2	In vivo consequences of varying degrees of OTOA alteration elucidated using knock-in mouse models and pseudogene contamination-free long-read sequencing 2025 ·Genes & Diseases ·(unknown), Bong Jik Kim, Chung Lee, Go Hun Seo, Hane Lee, Jin Hee Han, (unknown), (unknown), Byung Yoon Choi, (unknown)	0
3	Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders 2025 ·npj Genomic Medicine ·Heonjong Han, Go Hun Seo, (unknown), Kisang Kwon, Seung Woo Ryu, Rin Khang, Eugene Lee, Jihye Kim, Yongjun Song, (unknown), (unknown), Dongwook Kim, (unknown), SoHyun Lee, (unknown), Jungsul Lee, Hane Lee	2
4	Corneal Myofibromatous and Pterygium-Like Changes in a Family With a PDGFRB Variant 2025 ·Cornea ·Irving M. Raber, (unknown), Rin Khang, (unknown), Ralph C. Eagle, Go Hun Seo, Hane Lee, Tatyana Milman	0
5	Concordance Between Biochemical and Molecular Diagnosis Obtained by WES in Mexican Patients with Inborn Errors of Intermediary Metabolism: Utility for Therapeutic Management 2024 ·International Journal of Molecular Sciences ·Marcela Vela‐Amieva, Miguel Angel Alcántara‐Ortigoza, Ariadna González‐del Angel, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Isabel Ibarra‐González, Seung Woo Ryu, Hane Lee, Cynthia Fernández‐Lainez	0
6	A case report of an Egyptian family with familial hypercholesterolemia and an exonic LINE‐1 insertion in LDLR 2024 ·Molecular Genetics & Genomic Medicine ·Yongjun Song, (unknown), (unknown), Go Hun Seo, Hane Lee	1
7	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 2024 ·Molecular Genetics & Genomic Medicine ·Seung Woo Ryu, (unknown), Dongwook Kim, (unknown), (unknown), (unknown), Hane Lee, Go Hun Seo, Beom Hee Lee	1
8	Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing 2024 ·Neurology Genetics ·(unknown), Kathie J. Ngo, (unknown), Darice Y. Wong, Jihye Kim, Yongjun Song, (unknown), (unknown), Rin Khang, Seung Woo Ryu, Eugene Lee, (unknown), Hane Lee, Clara Lajonchere, Brent L. Fogel	4
9	Secondary findings in 443 exome sequencing data 2024 ·Annals of Human Genetics ·(unknown), (unknown), Milena Janković, (unknown), (unknown), (unknown), (unknown), (unknown), Hane Lee, Stojan Perić	1
10	High prevalence of ALPK3 premature terminating variants in Korean hypertrophic cardiomyopathy patients 2024 ·Frontiers in Cardiovascular Medicine ·Seung Woo Ryu, (unknown), Geu‐Ru Hong, Jung Sun Cho, (unknown), Hyungseop Kim, Jeong Yoon Jang, Sun Hwa Lee, (unknown), Jae Yeong Cho, Ji Hee Kim, Kyung‐Hee Kim, Jang Won Son, (unknown), Go Hun Seo, Hane Lee	0
11	Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature 2023 ·BMC Medical Genomics ·(unknown), Yongjun Song, Hane Lee, (unknown), (unknown), (unknown), Mohammad Amin Tabatabaiefar	5
12	A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review 2023 ·Molecular Genetics & Genomic Medicine ·(unknown), Yongjun Song, Hane Lee, (unknown), (unknown), Mohammad Amin Tabatabaiefar	4
13	RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis 2023 ·EMBO Molecular Medicine ·(unknown), (unknown), Abigail Loh, Kiat Yi Tan, Hane Lee, (unknown), Stanley F. Nelson, Engin Özkan, Hülya Kayserili, Nathalie Escande‐Beillard, Bruno Reversade	5
14	A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability 2018 ·eLife ·Poh Hui Chia, Franklin L. Zhong, Shinsuke Niwa, Carine Bonnard, Kagistia Hana Utami, Ruizhu Zeng, Hane Lee, Ascia Eskin, Stanley F. Nelson, William Xie, (unknown), Mohammad El-Khateeb, Mohammad Shboul, Mahmoud A. Pouladi, Mohammed Al‐Raqad, Bruno Reversade	44
15	The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling 2018 ·Science Translational Medicine ·Fabiana Csukasi, Iván Durán, (unknown), Tomáš Bárta, Iva Gudernová, Lukáš Trantı́rek, Jorge Martı́n, Caroline Y. Kuo, Jeremy D. Woods, Hane Lee, Daniel H. Cohn, Pavel Krejčı́, Deborah Krakow	41
16	Kcnd2 Mutation Associated with Autism and Epilepsy Impairs Inactivation Gating in Kv4.2 K+ Channels 2014 ·Biophysical Journal ·Meng‐Chin Lin, Hane Lee, Harley I. Kornblum, Stanley F. Nelson, Diane M. Papazian	1
17	SGK196 Is a Glycosylation-Specific O -Mannose Kinase Required for Dystroglycan Function 2013 ·Science ·Takako Yoshida‐Moriguchi, Tobias Willer, Mary E. Anderson, David Venzke, Tamieka Whyte, Francesco Muntoni, Hane Lee, Stanley F. Nelson, Liping Yu, Kevin P. Campbell	159
18	Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation breakdown → 2010 ·Nature ·Ramin Nazarian, Hubing Shi, Qi Wang, Xiangju Kong, Richard C. Koya, Hane Lee, Zugen Chen, Mi‐Kyung Lee, Narsis Attar, Hooman Sazegar, Thinle Chodon, Stanley F. Nelson, Grant A. McArthur, Jeffrey A. Sosman, Antoni Ribas, Roger S. Lo	1614
19	Accuracy of phenotyping of autistic children based on internet implemented parent report 2010 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Hane Lee, Alison R. Marvin, Tamara Watson, Judith Piggot, J. Kiely Law, Paul A. Law, John N. Constantino, Stanley F. Nelson	145
20	Gezinsvorming in Vlaanderen: nieuwe vormen, andere timing. 1987 ·Tijdschrift voor Sociologie ·Hane Lee, (unknown), (unknown), Ronny Lesthaeghe	1

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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