Kwanghyuk Lee

2.4k total citations
39 papers, 1.0k citations indexed

About

Kwanghyuk Lee is a scholar working on Molecular Biology, Sensory Systems and Nutrition and Dietetics. According to data from OpenAlex, Kwanghyuk Lee has authored 39 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 20 papers in Sensory Systems and 8 papers in Nutrition and Dietetics. Recurrent topics in Kwanghyuk Lee's work include Hearing, Cochlea, Tinnitus, Genetics (19 papers), Biochemical Analysis and Sensing Techniques (8 papers) and Connexins and lens biology (5 papers). Kwanghyuk Lee is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (19 papers), Biochemical Analysis and Sensing Techniques (8 papers) and Connexins and lens biology (5 papers). Kwanghyuk Lee collaborates with scholars based in United States, Pakistan and Netherlands. Kwanghyuk Lee's co-authors include Suzanne M. Leal, Wasim Ahmad, Verne M. Chapman, Tatsushi Shiomi, S Natsuume-Sakai, Yosuke Harada, Yoichi Matsuda, Muhammad Ansar, Jeffrey M. Leiden and C L Chen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Kwanghyuk Lee

38 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kwanghyuk Lee United States 16 566 310 183 148 132 39 1.0k
Markus Pfister Germany 27 842 1.5× 1.1k 3.6× 102 0.6× 429 2.9× 53 0.4× 85 2.0k
Carsten M. Pusch Germany 25 818 1.4× 243 0.8× 374 2.0× 90 0.6× 63 0.5× 76 1.7k
Jason R. Willer United States 19 1.2k 2.2× 102 0.3× 507 2.8× 45 0.3× 157 1.2× 31 1.8k
Jacques Loiselet Lebanon 25 1.3k 2.4× 547 1.8× 490 2.7× 251 1.7× 362 2.7× 60 2.6k
Anne Marcuz Switzerland 17 389 0.7× 122 0.4× 97 0.5× 17 0.1× 463 3.5× 29 999
Marie‐Christine Simmler France 19 1.0k 1.8× 557 1.8× 756 4.1× 226 1.5× 94 0.7× 26 1.8k
Nick Parkinson United Kingdom 20 1.1k 2.0× 98 0.3× 190 1.0× 269 1.8× 83 0.6× 41 2.4k
Hans‐Henrik M. Dahl Australia 23 1.2k 2.0× 392 1.3× 380 2.1× 95 0.6× 78 0.6× 51 1.9k
István Sziklai Hungary 26 335 0.6× 685 2.2× 35 0.2× 465 3.1× 55 0.4× 88 1.7k
Benjamin K. August United States 19 717 1.3× 312 1.0× 138 0.8× 232 1.6× 108 0.8× 40 1.5k

Countries citing papers authored by Kwanghyuk Lee

Since Specialization
Citations

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

Fields of papers citing papers by Kwanghyuk Lee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kwanghyuk Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Kwanghyuk Lee. A scholar is included among the top collaborators of Kwanghyuk 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 Kwanghyuk Lee. Kwanghyuk 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
1.
Bourquard, Thomas, Kwanghyuk Lee, Ismael Al‐Ramahi, et al.. (2023). Functional variants identify sex-specific genes and pathways in Alzheimer’s Disease. Nature Communications. 14(1). 2765–2765. 11 indexed citations
2.
Lee, Kwanghyuk, et al.. (2023). Evolutionary Action–Machine Learning Model Identifies Candidate Genes Associated With Early‐Onset Coronary Artery Disease. Journal of the American Heart Association. 12(17). e029103–e029103. 5 indexed citations
3.
Donehower, Lawrence A., et al.. (2022). EPIMUTESTR: a nearest neighbor machine learning approach to predict cancer driver genes from the evolutionary action of coding variants. Nucleic Acids Research. 50(12). e70–e70. 7 indexed citations
4.
Lee, Kwanghyuk, Saadullah Khan, Muhammad Ansar, et al.. (2011). A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families. PubMed. 2011. 1–4. 9 indexed citations
5.
Emery, Sarah B., et al.. (2011). Autosomal Dominant Progressive Sensorineural Hearing Loss Due to a Novel Mutation in the KCNQ4 Gene. Archives of Otolaryngology - Head and Neck Surgery. 137(1). 54–54. 24 indexed citations
6.
Rehman, Atteeq U., Robert J. Morell, Kwanghyuk Lee, et al.. (2011). Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. Human Genetics. 130(6). 759–765. 34 indexed citations
7.
Lee, Kwanghyuk, Saad Ullah Khan, Abul Bashar Mir Md. Khademul Islam, et al.. (2011). Novel TMPRSS3 variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment. Clinical Genetics. 82(1). 56–63. 15 indexed citations
8.
Schraders, Margit, Kwanghyuk Lee, Jaap Oostrik, et al.. (2010). Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. The American Journal of Human Genetics. 86(2). 138–147. 50 indexed citations
9.
Basit, Sulman, Kwanghyuk Lee, Rabia Habib, et al.. (2010). DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2. Human Genetics. 129(4). 379–385. 12 indexed citations
10.
Chishti, Muhammad Salman, Attya Bhatti, Kwanghyuk Lee, et al.. (2007). Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families. Journal of Human Genetics. 53(2). 101–105. 41 indexed citations
11.
El‐Shanti, Hatem, et al.. (2006). A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan. Brain and Development. 28(6). 353–357. 6 indexed citations
12.
Ali, Ghazanfar, et al.. (2006). The mapping of DFNB62, a new locus for autosomal recessive non‐syndromic hearing impairment, to chromosome 12p13.2‐p11.23. Clinical Genetics. 69(5). 429–433. 7 indexed citations
13.
Pemberton, Trevor J., Kwanghyuk Lee, Raquel Mantuaneli Scarel‐Caminaga, et al.. (2006). A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3. Human Genetics. 120(5). 653–662. 22 indexed citations
14.
Tariq, Aamira, et al.. (2006). Localization of a novel autosomal recessive nonsyndromic hearing impairment locus DFNB65 to chromosome 20q13.2–q13.32. Journal of Molecular Medicine. 84(6). 484–490. 5 indexed citations
15.
Naeem, Muhammad, Musharraf Jelani, Kwanghyuk Lee, et al.. (2006). Ectodermal dysplasia of hair and nail type: mapping of a novel locus to chromosome 17p12-q21.2. British Journal of Dermatology. 155(6). 1184–1190. 17 indexed citations
16.
El‐Shanti, Hatem, Kwanghyuk Lee, Attya Bhatti, et al.. (2005). Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment. Journal of Molecular Medicine. 84(3). 226–231. 19 indexed citations
17.
Irshad, Saba, et al.. (2005). Localization of a novel autosomal recessive non‐syndromic hearing impairment locus DFNB55 to chromosome 4q12‐q13.2. Clinical Genetics. 68(3). 262–267. 8 indexed citations
18.
Baek, Kwang‐Hyun, Kwanghyuk Lee, Hae‐Moon Chung, et al.. (2002). The rgl-1 is a legitimate homologue of lethal giant larvae recessive oncogene in rat. International Journal of Oncology. 20(6). 1219–25. 10 indexed citations
19.
Matsuda, Yoichi, Yosuke Harada, S Natsuume-Sakai, et al.. (1992). Location of the mouse complement factor H gene (<i>cfh</i>) by FISH analysis and replication R-banding. Cytogenetic and Genome Research. 61(4). 282–285. 193 indexed citations
20.
Tjoelker, Larry W., Louise Carlson, Kwanghyuk Lee, et al.. (1990). Evolutionary conservation of antigen recognition: the chicken T-cell receptor beta chain.. Proceedings of the National Academy of Sciences. 87(20). 7856–7860. 100 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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