Hane Lee

13.4k citations

170 papers · 10.1k · 3 hit papers · h-index 50

Impact in

Genetics top 0.5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Molecular Biology top 1%
- Melanoma and MAPK Pathways
- Mitochondrial Function and Pathology

Papers in

Genetics 82
- Genomics and Rare Diseases 49
- Genetics and Neurodevelopmental Disorders 32
- Genomic variations and chromosomal abnormalities 23
Molecular Biology 82
- Mitochondrial Function and Pathology 11
- RNA and protein synthesis mechanisms 10
- RNA modifications and cancer 9
- RNA Research and Splicing 9
- RNA regulation and disease 9

Co-authors: Stanley F. Nelson (46 shared papers)Zugen Chen (5 shared papers)Mi‐Kyung Lee (2 shared papers)Antoni Ribas (2 shared papers)Hubing Shi (2 shared papers)Thinle Chodon (2 shared papers)Roger S. Lo (2 shared papers)Richard Chikara Koya (2 shared papers)
Journals: The American Journal of Human Genetics (23 papers)Genetics in Medicine (14 papers)Human Molecular Genetics (7 papers)Human Mutation (6 papers)Nature Genetics (5 papers)
Partner nations: United States United Kingdom Singapore

In The Last Decade

Hane Lee

158 papers receiving 9.8k citations

Hane Lee's Hit Papers

align trajectories log scale

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders 2014 · 780 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2014 JAMA
2012 Nature Communications
2010 Nature

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-authors

The 25 scholars most cited alongside Hane Lee, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hane Lee Line = papers co-authored together Hane Lee links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 170 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation Nature ·Ramin Nazarian, Hubing Shi, Qi Wang, Xiangju Kong, Richard Chikara Koya, Hane Lee, Zugen Chen, Mi‐Kyung Lee Hit paper breakdown →	2010	1808
2	Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders JAMA ·Hane Lee, Joshua L. Deignan, Naghmeh Dorrani, Samuel P. Strom, Sibel Kantarci, Fabiola Quintero‐Rivera, Kingshuk Das, Traci L. Toy Hit paper breakdown →	2014	780
3	Melanoma whole-exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance Nature Communications ·Hubing Shi, Gatien Moriceau, Xiangju Kong, Mi‐Kyung Lee, Hane Lee, Richard Chikara Koya, Charles Ng, Thinle Chodon Hit paper breakdown →	2012	539
4	Cold Urticaria, Immunodeficiency, and Autoimmunity Related to PLCG2 Deletions New England Journal of Medicine ·Michael J. Ombrello, Elaine F. Remmers, Guangping Sun, Alexandra Freeman, Shrimati Datta, Parizad Torabi‐Parizi, Naeha Subramanian, Tom D. Bunney	2012	317
5	Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV Bioinformatics ·J. Fah Sathirapongsasuti, Hane Lee, Basil A. J. Horst, Georg Brunner, Alistair J. Cochran, Scott W. Binder, John D. Quackenbush, Stanley F. Nelson	2011	313
6	U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line PLoS Genetics ·Michael James Clark, Nils Homer, Brian D. O’Connor, Zugen Chen, Ascia Eskin, Hane Lee, Barry Merriman, Stanley F. Nelson	2010	234
7	ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Nature Genetics ·Tobias Willer, Hane Lee, Mark Lommel, Takako Yoshida‐Moriguchi, Daniel Beltrán Valero de Bernabé, David P. Venzke, Sebahattin Çirak, Harry Schachter	2012	201
8	Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia JAMA Neurology ·Brent L. Fogel, Hane Lee, Joshua L. Deignan, Samuel P. Strom, Sibel Kantarci, Xizhe Wang, Fabiola Quintero‐Rivera, Eric J. N. Vilain	2014	196
9	Mutations in PYCR1 cause cutis laxa with progeroid features Nature Genetics ·Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou, Björn Fischer‐Zirnsak, Serene C. Chng, Yun Li, Mohammad Shboul, Puay-Yoke Tham	2009	190
10	Identification of EpCAM as the Gene for Congenital Tufting Enteropathy Gastroenterology ·Mamata Sivagnanam, James L. Mueller, Hane Lee, Zugen Chen, Stanley F. Nelson, Dan Turner, Stanley Howard Zlotkin, Paul B. Pencharz	2008	180
11	SGK196 Is a Glycosylation-Specific O -Mannose Kinase Required for Dystroglycan Function Science ·Takako Yoshida‐Moriguchi, Tobias Willer, Mary E. Anderson, David P. Venzke, Tamieka Whyte, Francesco Muntoni, Hane Lee, Stanley F. Nelson	2013	178
12	Diagnostic utility of transcriptome sequencing for rare Mendelian diseases Genetics in Medicine ·Hane Lee, Alden Huang, Lee-kai Wang, Amanda J. Yoon, Genecee Renteria, Ascia Eskin, Rebecca H. Signer, Naghmeh Dorrani	2019	163
13	Exome Sequencing for the Diagnosis of 46,XY Disorders of Sex Development The Journal of Clinical Endocrinology & Metabolism ·Ruth M. Baxter, Valerie A. Arboleda, Hane Lee, Hayk Barseghyan, Margaret P Adam, Patricia Y. Fechner, Renee Bargman, Catherine E. Keegan	2014	162
14	MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome The American Journal of Human Genetics ·Julia Wang, Rami Al‐Ouran, Yanhui Hu, Seon‐Young Kim, Ying‐Wooi Wan, Michael F. Wangler, Shinya Yamamoto, Hsiao‐Tuan Chao	2017	162
15	Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome Nature Genetics ·Valerie A. Arboleda, Hane Lee, Rahul Parnaik, Alice A. Fleming, Abhik K. Banerjee, Bruno Ferraz‐de‐Souza, Emmanuèle C. Délot, Imilce A. Rodriguez‐Fernandez	2012	153
16	Accuracy of phenotyping of autistic children based on internet implemented parent report 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 Nicholas Constantino, Stanley F. Nelson	2010	152
17	The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease The American Journal of Human Genetics ·Rachel Badovinac Ramoni, John Joseph Mulvihill, David R. Adams, Patrick Allard, Euan Angus Ashley, Jonathan Adam Bernstein, William Allen Gahl, Rizwan Hamid	2017	133
18	Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance Human Molecular Genetics ·Frank J. Kaiser, Morad Ansari, Diana Braunholz, María Concepción Gil‐Rodríguez, Christophe Decroos, Jonathan J. Wilde, Christopher T. Fincher, Maninder Kaur	2014	128
19	Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1 Nature Genetics ·David R. Goudie, Mariella D’Alessandro, Barry Merriman, Hane Lee, Ildikó Szeverényi, Stuart Avery, Brian D. O’Connor, Stanley F. Nelson	2011	122
20	De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay The American Journal of Human Genetics ·Valerie A. Arboleda, Hane Lee, Naghmeh Dorrani, Neda Zadeh, Mary J H Willis, Colleen Macmurdo, Melanie A. Manning, Andrea C. Kwan	2015	119

About Hane Lee

Hane Lee is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Cell Biology and Neurology, having authored 170 papers that have together received 10.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (49 papers), Genetics and Neurodevelopmental Disorders (32 papers), Genomic variations and chromosomal abnormalities (23 papers), Mitochondrial Function and Pathology (11 papers), RNA and protein synthesis mechanisms (10 papers), RNA modifications and cancer (9 papers), RNA Research and Splicing (9 papers) and RNA regulation and disease (9 papers). The work is most often cited by research in Genetics (3.1k citations), Molecular Biology (5.8k citations), Cancer Research (880 citations), Oncology (1.4k citations) and Cell Biology (752 citations). Hane Lee has collaborated with scholars based in United States, United Kingdom and Singapore. Frequent co-authors include Stanley F. Nelson, Zugen Chen, Mi‐Kyung Lee, Antoni Ribas, Hubing Shi, Thinle Chodon, Roger S. Lo, Richard Chikara Koya, Xiangju Kong and Jeffrey Alan Sosman. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Human Molecular Genetics, Human Mutation and Nature Genetics.

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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Hane Lee's Hit Papers

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