Heon Yung Gee

10.6k total citations · 1 hit paper
108 papers, 3.0k citations indexed

About

Heon Yung Gee is a scholar working on Molecular Biology, Sensory Systems and Cell Biology. According to data from OpenAlex, Heon Yung Gee has authored 108 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 27 papers in Sensory Systems and 18 papers in Cell Biology. Recurrent topics in Heon Yung Gee's work include Hearing, Cochlea, Tinnitus, Genetics (25 papers), Cellular transport and secretion (11 papers) and Vestibular and auditory disorders (10 papers). Heon Yung Gee is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (25 papers), Cellular transport and secretion (11 papers) and Vestibular and auditory disorders (10 papers). Heon Yung Gee collaborates with scholars based in South Korea, United States and United Kingdom. Heon Yung Gee's co-authors include Min Goo Lee, Bor Luen Tang, Shin Hye Noh, Jiyoon Kim, Friedhelm Hildebrandt, Kyung Hwan Kim, Jae Young Choi, Jinsei Jung, John Hoon Rim and Eunjoon Kim and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Heon Yung Gee

100 papers receiving 2.9k 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.

Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

2012 535 citations Heon Yung Gee, Min Goo Lee et al. profile →

Peers

Heon Yung Gee

GENET

NEPHR

Annick Raas‐Rothschild Israel

Helen Christian United Kingdom

Bruce A. Hamilton United States

Lingzhi Fan China

Boris V. Skryabin Germany

Arif B. Ekici Germany

Isabella A. Graef United States

J Engel United States

Maria Lindahl Finland

Annick Raas‐Rothschild Israel

Heon Yung Gee

1.7k ×1.1

898 ×1.3

GENET

781 ×1.7

129 ×0.3

NEPHR

71 ×0.2

Citations per year, relative to Heon Yung Gee Heon Yung Gee (= 1×) peers Annick Raas‐Rothschild

Countries citing papers authored by Heon Yung Gee

Since Specialization

Citations

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

Fields of papers citing papers by Heon Yung Gee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heon Yung Gee. 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 Heon Yung Gee. The network helps show where Heon Yung Gee may publish in the future.

Co-authorship network of co-authors of Heon Yung Gee

This figure shows the co-authorship network connecting the top 25 collaborators of Heon Yung Gee. A scholar is included among the top collaborators of Heon Yung Gee 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 Heon Yung Gee. Heon Yung Gee 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

Kim, Se Jin, Ho Lee, Kyu Min Kim, et al.. (2025). Biallelic variants of SEMA3F are associated with nonsyndromic hearing loss. PubMed. 48(3). 100190–100190. 1 indexed citations

Choi, Hojun, Seung‐Bin Yoon, Hye‐Jung Kim, et al.. (2025). Single-cell analysis of the decidua unveils the mechanism of anti-inflammatory exosomes for chorioamnionitis in nonhuman primates. Science Advances. 11(27). eadp0467–eadp0467.

Gee, Heon Yung, et al.. (2024). Common genetic etiologies of sensorineural hearing loss in Koreans. Genomics & Informatics. 22(1). 27–27. 3 indexed citations

Jung, Jinsei, Sun Young Joo, John Hoon Rim, et al.. (2024). MYH1 deficiency disrupts outer hair cell electromotility, resulting in hearing loss. Experimental & Molecular Medicine. 56(11). 2423–2435. 2 indexed citations

Gee, Heon Yung, et al.. (2024). High level of gamma-glutamyltransferase is a possible risk factor for psoriasis: A nationwide population-based cohort study. Indian Journal of Dermatology Venereology and Leprology. 91(1). 23–30. 2 indexed citations

Lee, Seok Jae, Hui Jiang, Dong Hyun Jo, et al.. (2024). Genotype–Phenotype Correlations in 83 Korean X-linked Retinoschisis Patients. Ophthalmology Retina. 9(3). 288–298.

Won, Dongju, et al.. (2024). Natural History of Auditory Function in Patients with Alport Syndrome: A Case Series Study. Journal of Clinical Medicine. 13(22). 6639–6639. 1 indexed citations

Han, Kyungdo, et al.. (2023). Increased Risk of Renal Malignancy in Patients with Moderate to Severe Atopic Dermatitis. Cancers. 15(20). 5007–5007. 1 indexed citations

Kang, Minjin, Mee Hyun Song, Sun Young Joo, et al.. (2023). Novel Variant in CEP250 Causes Protein Mislocalization and Leads to Nonsyndromic Autosomal Recessive Type of Progressive Hearing Loss. Cells. 12(18). 2328–2328. 5 indexed citations

10.

Jung, Jinsei, et al.. (2023). Genetic Characteristics and Audiological Performance After Cochlear Implantation in Patients With Incomplete Partition Type III. Clinical and Experimental Otorhinolaryngology. 16(4). 403–406. 1 indexed citations

11.

Yu, Seyoung, John Hoon Rim, Hye‐Youn Kim, et al.. (2023). Disease modeling of ADAMTS9-related nephropathy using kidney organoids reveals its roles in tubular cells and podocytes. Frontiers in Medicine. 10. 1089159–1089159. 6 indexed citations

12.

Park, Jun Yong, et al.. (2023). Lactobacillus plantarum ameliorates NASH-related inflammation by upregulating l-arginine production. Experimental & Molecular Medicine. 55(11). 2332–2345. 28 indexed citations

13.

Kim, Kyung Won, Dankyu Yoon, Haerin Jang, et al.. (2021). Genome‐wide association study identifies TNFSF15 associated with childhood asthma. Allergy. 77(1). 218–229. 15 indexed citations

14.

Widmeier, Eugen, Seyoung Yu, Anish Nag, et al.. (2020). ADCK4 Deficiency Destabilizes the Coenzyme Q Complex, Which Is Rescued by 2,4-Dihydroxybenzoic Acid Treatment. Journal of the American Society of Nephrology. 31(6). 1191–1211. 44 indexed citations

15.

Kim, Jiyoon, Hyeyon Kim, Shin Hye Noh, et al.. (2020). Grasp55−/− mice display impaired fat absorption and resistance to high-fat diet-induced obesity. Nature Communications. 11(1). 1418–1418. 19 indexed citations

16.

Rim, John Hoon, Joon Suk Lee, Jinsei Jung, et al.. (2019). Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency. Scientific Reports. 9(1). 4583–4583. 13 indexed citations

17.

Jung, Jinsei, Joon Suk Lee, John Hoon Rim, et al.. (2019). Rare KCNQ4 variants found in public databases underlie impaired channel activity that may contribute to hearing impairment. Experimental & Molecular Medicine. 51(8). 1–12. 24 indexed citations

18.

Kim, Jiyoon, Heon Yung Gee, & Min Goo Lee. (2018). Unconventional protein secretion – new insights into the pathogenesis and therapeutic targets of human diseases. Journal of Cell Science. 131(12). 80 indexed citations

19.

Jung, Jinsei, John Hoon Rim, Joon Suk Lee, et al.. (2018). A recurrent mutation in KCNQ4 in Korean families with nonsyndromic hearing loss and rescue of the channel activity by KCNQ activators. Human Mutation. 40(3). 335–346. 15 indexed citations

20.

Lee, Jiwon M., Jae‐Won Shin, Sol Kim, et al.. (2018). Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neuroendocrine Tumors (ROHHADNET) Syndrome: A Systematic Review. BioMed Research International. 2018. 1–17. 38 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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