Hong-Joon Park

704 total citations
28 papers, 553 citations indexed

About

Hong-Joon Park is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Hong-Joon Park has authored 28 papers receiving a total of 553 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Sensory Systems, 15 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Hong-Joon Park's work include Hearing, Cochlea, Tinnitus, Genetics (22 papers), Ear Surgery and Otitis Media (8 papers) and Vestibular and auditory disorders (8 papers). Hong-Joon Park is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (22 papers), Ear Surgery and Otitis Media (8 papers) and Vestibular and auditory disorders (8 papers). Hong-Joon Park collaborates with scholars based in South Korea, United States and Netherlands. Hong-Joon Park's co-authors include Un‐Kyung Kim, Kyu-Yup Lee, Jeong‐In Baek, Seung‐Chul Lee, Jae Young Choi, Robert J. Wenthold, Jinwoong Bok, Kyu Yup Lee, Young Ho Yang and Hyun-Ju Cho and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and Gene.

In The Last Decade

Hong-Joon Park

28 papers receiving 543 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hong-Joon Park South Korea 16 374 303 143 104 85 28 553
PJ Willems Greece 5 271 0.7× 356 1.2× 124 0.9× 47 0.5× 63 0.7× 8 590
Zippora Brownstein Israel 14 327 0.9× 363 1.2× 125 0.9× 139 1.3× 90 1.1× 25 620
James W. Askew United States 6 485 1.3× 434 1.4× 141 1.0× 56 0.5× 96 1.1× 11 593
Parna Chattaraj United States 10 266 0.7× 230 0.8× 253 1.8× 105 1.0× 41 0.5× 14 469
L. Zelante Italy 10 367 1.0× 316 1.0× 142 1.0× 66 0.6× 92 1.1× 13 793
Ersan Kalay Türkiye 13 228 0.6× 316 1.0× 106 0.7× 52 0.5× 32 0.4× 24 527
Alvaro Gallego‐Martinez Spain 14 389 1.0× 128 0.4× 456 3.2× 89 0.9× 43 0.5× 28 562
Xue Gao China 13 301 0.8× 223 0.7× 133 0.9× 100 1.0× 45 0.5× 50 428
Min Young Kim South Korea 13 240 0.6× 182 0.6× 99 0.7× 78 0.8× 72 0.8× 31 379
Lingling Neng United States 13 402 1.1× 192 0.6× 363 2.5× 34 0.3× 54 0.6× 20 645

Countries citing papers authored by Hong-Joon Park

Since Specialization
Citations

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

Fields of papers citing papers by Hong-Joon Park

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hong-Joon Park. 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 Hong-Joon Park. The network helps show where Hong-Joon Park may publish in the future.

Co-authorship network of co-authors of Hong-Joon Park

This figure shows the co-authorship network connecting the top 25 collaborators of Hong-Joon Park. A scholar is included among the top collaborators of Hong-Joon Park 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 Hong-Joon Park. Hong-Joon Park 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.
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
2.
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
3.
Kim, Sung Huhn, et al.. (2016). Surgical and Audiologic Comparison Between Sophono and Bone-Anchored Hearing Aids Implantation. Clinical and Experimental Otorhinolaryngology. 9(1). 21–26. 14 indexed citations
4.
Kim, Min-A, Ye‐Ri Kim, Hyun-Ju Cho, et al.. (2014). Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss. PLoS ONE. 9(4). e95646–e95646. 20 indexed citations
5.
Park, Hong-Joon, et al.. (2014). Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing. BMC Medical Genetics. 15(1). 46–46. 24 indexed citations
6.
Park, Hong-Joon, et al.. (2013). Limitations of hearing screening in newborns with PDS mutations. International Journal of Pediatric Otorhinolaryngology. 77(5). 833–837. 20 indexed citations
7.
Park, Hong-Joon, et al.. (2013). Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. BMC Medical Genetics. 14(1). 72–72. 34 indexed citations
8.
Choi, Jae Young, Hong-Joon Park, Jong Dae Lee, et al.. (2012). Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation. PLoS ONE. 7(8). e42463–e42463. 22 indexed citations
9.
Park, Hong-Joon, et al.. (2011). Identification and functional characterization of novel compound heterozygotic mutations in the TECTA gene. Gene. 492(1). 239–243. 5 indexed citations
10.
Choi, Soo‐Young, Kyu Yup Lee, Hyun Jin Kim, et al.. (2011). Functional Evaluation of GJB2 Variants in Nonsyndromic Hearing Loss. Molecular Medicine. 17(5-6). 550–556. 29 indexed citations
11.
Park, Hong-Joon, et al.. (2010). A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss. Biochemical and Biophysical Research Communications. 396(3). 626–630. 24 indexed citations
12.
Baek, Jeong‐In, Hong-Joon Park, Kyungjoon Park, et al.. (2010). Pathogenic effects of a novel mutation (c.664_681del) in KCNQ4 channels associated with auditory pathology. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(4). 536–543. 20 indexed citations
13.
Park, Hong-Joon, Hyun-Ju Cho, Jeong‐In Baek, et al.. (2009). Evidence for a founder mutation causing DFNA5 hearing loss in East Asians. Journal of Human Genetics. 55(1). 59–62. 44 indexed citations
14.
Choi, Soo‐Young, Hong-Joon Park, Kyu Yup Lee, et al.. (2009). Different functional consequences of two missense mutations in theGJB2gene associated with non-syndromic hearing loss. Human Mutation. 30(7). E716–E727. 21 indexed citations
15.
Park, Hong-Joon, et al.. (2009). HiRes with Fidelity 120 benefit in native speakers of Korean. Cochlear Implants International. 10(sup1). 85–88. 6 indexed citations
16.
Han, Sung‐Hee, et al.. (2008). Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population. Journal of Human Genetics. 53(11-12). 1022–1028. 59 indexed citations
17.
Madeo, Anne C., Shannon Pryor, Carmen C. Brewer, et al.. (2006). Pendred Syndrome. Seminars in Hearing. 27(3). 160–170. 4 indexed citations
18.
Park, Kwang Joo, et al.. (2001). Immunohistochemical study on proliferative activity of experimental cholesteatoma. European Archives of Oto-Rhino-Laryngology. 258(3). 101–105. 14 indexed citations
19.
Park, Hong-Joon, et al.. (1997). Expression of the nicotinic acetylcholine receptor subunit, α9, in the guinea pig cochlea. Hearing Research. 112(1-2). 95–105. 38 indexed citations
20.
Park, Hong-Joon, et al.. (1995). Redistribution of Facial Nerve Motor Neurons after Recovery from Nerve Crushing Injury in the Gerbil. Acta Oto-Laryngologica. 115(2). 273–275. 13 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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