Byeonghyeon Lee

436 total citations
18 papers, 352 citations indexed

About

Byeonghyeon Lee is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Byeonghyeon Lee has authored 18 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Sensory Systems and 5 papers in Neurology. Recurrent topics in Byeonghyeon Lee's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), RNA regulation and disease (3 papers) and Electron Spin Resonance Studies (3 papers). Byeonghyeon Lee is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), RNA regulation and disease (3 papers) and Electron Spin Resonance Studies (3 papers). Byeonghyeon Lee collaborates with scholars based in South Korea, United States and Türkiye. Byeonghyeon Lee's co-authors include Un‐Kyung Kim, Kyu-Yup Lee, Min-A Kim, Ye‐Ri Kim, Jeong‐In Baek, Kyung‐Hee Kim, Tae-Jun Kwon, Se‐Kyung Oh, Won Jong Kim and Dongsik Park and has published in prestigious journals such as Scientific Reports, Gene and Experimental Brain Research.

In The Last Decade

Byeonghyeon Lee

15 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Byeonghyeon Lee South Korea	9	221	127	47	45	21	18	352
Tamás Horváth Hungary	12	282 1.3×	76 0.6×	13 0.3×	21 0.5×	28 1.3×	26	429
Nesrine Benkafadar United States	10	113 0.5×	166 1.3×	15 0.3×	56 1.2×	40 1.9×	15	294
Robin M. Gibson United States	9	280 1.3×	117 0.9×	10 0.2×	24 0.5×	18 0.9×	9	434
Le Xie China	12	165 0.7×	192 1.5×	12 0.3×	85 1.9×	39 1.9×	35	328
Florence François France	7	105 0.5×	221 1.7×	13 0.3×	84 1.9×	118 5.6×	11	378
H Dahl Australia	9	300 1.4×	69 0.5×	158 3.4×	19 0.4×	17 0.8×	12	459
Klemens Frei Austria	12	263 1.2×	228 1.8×	77 1.6×	86 1.9×	50 2.4×	41	516
Jingrong Lü China	9	93 0.4×	155 1.2×	6 0.1×	43 1.0×	94 4.5×	32	334
Ilona Kondratiuk Poland	9	207 0.9×	18 0.1×	38 0.8×	21 0.5×	16 0.8×	9	329

Countries citing papers authored by Byeonghyeon Lee

Since Specialization

Citations

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

Fields of papers citing papers by Byeonghyeon Lee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Byeonghyeon Lee

This figure shows the co-authorship network connecting the top 25 collaborators of Byeonghyeon Lee. A scholar is included among the top collaborators of Byeonghyeon 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 Byeonghyeon Lee. Byeonghyeon 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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18 of 18 papers shown

Lee, Byeonghyeon, Ryul Kim, Ki Wha Chung, et al.. (2025). DCTN1 -associated neurological disorder with symptoms similar to spinal bulbar muscular atrophy. Journal of Neuromuscular Diseases. 12(6). 804–813.

Kim, Ye‐Ri, Sun Hwa Jung, Byeonghyeon Lee, et al.. (2024). Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss. Biomedicine & Pharmacotherapy. 182. 117767–117767.

Kim, Ye‐Ri, Hye-Min Kim, Byeonghyeon Lee, et al.. (2023). Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS. Genes & Genomics. 45(2). 225–230. 1 indexed citations

Lee, Byeonghyeon, Min Cheol Kim, Ye‐Ri Kim, et al.. (2023). Therapeutic effect of intraperitoneal dexamethasone on noise-induced permanent threshold shift in mice model. Experimental Brain Research. 242(1). 257–265.

Seo, Min‐Soo, Byeonghyeon Lee, Kyung‐Ku Kang, et al.. (2021). Phenotype of the Aging-Dependent Spontaneous Onset of Hearing Loss in DBA/2 Mice. Veterinary Sciences. 8(3). 49–49. 3 indexed citations

Lee, Byeonghyeon, et al.. (2020). An autosomal dominant ERLIN2 mutation leads to a pure HSP phenotype distinct from the autosomal recessive ERLIN2 mutations (SPG18). Scientific Reports. 10(1). 3295–3295. 13 indexed citations

Lee, Byeonghyeon, Ye‐Ri Kim, Sung‐Ho Goh, et al.. (2019). Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss. Human Mutation. 40(8). 1172–1180. 13 indexed citations

Kim, Min-A, Hye-Min Kim, Ye‐Ri Kim, et al.. (2019). Targeted Gene Delivery into the Mammalian Inner Ear Using Synthetic Serotypes of Adeno-Associated Virus Vectors. Molecular Therapy — Methods & Clinical Development. 13. 197–204. 24 indexed citations

Lee, Byeonghyeon, Bo Young Chun, Eun Hye Oh, et al.. (2019). A family with a mild form of congenital nystagmus and optic disc coloboma caused by a novel PAX6 mutation. Gene. 705. 177–180. 5 indexed citations

10.

Lee, Byeonghyeon, Jeong‐In Baek, Min-A Kim, et al.. (2018). Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of Hearing. Molecular Neurobiology. 55(8). 6518–6532. 8 indexed citations

11.

Kim, Min-A, Dongsik Park, Byeonghyeon Lee, et al.. (2018). Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy. Nanomedicine Nanotechnology Biology and Medicine. 14(7). 2095–2102. 77 indexed citations

12.

Kim, Kyung‐Hee, Byeonghyeon Lee, Ye‐Ri Kim, et al.. (2018). Evaluating protective and therapeutic effects of alpha-lipoic acid on cisplatin-induced ototoxicity. Cell Death and Disease. 9(8). 827–827. 56 indexed citations

13.

Kim, Ye‐Ri, Jeong‐In Baek, Sung Hwan Kim, et al.. (2018). Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiency. Redox Biology. 20. 544–555. 53 indexed citations

14.

Park, Hong-Joon, Byeonghyeon Lee, Tae-Jun Kwon, et al.. (2017). Identification of a novel splicing mutation within SLC17A8 in a Korean family with hearing loss by whole-exome sequencing. Gene. 627. 233–238. 12 indexed citations

15.

Lee, Byeonghyeon, Mehmet Buğrahan Düz, Asuman Koparır, et al.. (2015). Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome. Gene. 576(2). 776–781. 5 indexed citations

16.

Kim, Min-A, Hyun-Ju Cho, Byeonghyeon Lee, et al.. (2015). Methionine Sulfoxide Reductase B3-Targeted In Utero Gene Therapy Rescues Hearing Function in a Mouse Model of Congenital Sensorineural Hearing Loss. Antioxidants and Redox Signaling. 24(11). 590–602. 67 indexed citations

17.

Park, Moo Kyun, Jong Dae Lee, Byeonghyeon Lee, et al.. (2014). A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome. International Journal of Pediatric Otorhinolaryngology. 78(11). 1996–1999. 4 indexed citations

18.

Kwon, Tae-Jun, Se‐Kyung Oh, Ye‐Ri Kim, et al.. (2014). Methionine Sulfoxide Reductase A, B1 and B2 Are Likely to Be Involved in the Protection against Oxidative Stress in the Inner Ear. Cells Tissues Organs. 199(4). 294–300. 11 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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