Young Se Hyun

1.1k total citations
35 papers, 656 citations indexed

About

Young Se Hyun is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Young Se Hyun has authored 35 papers receiving a total of 656 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Cellular and Molecular Neuroscience, 17 papers in Molecular Biology and 10 papers in Genetics. Recurrent topics in Young Se Hyun's work include Hereditary Neurological Disorders (17 papers), Genetic Neurodegenerative Diseases (11 papers) and Neurological diseases and metabolism (8 papers). Young Se Hyun is often cited by papers focused on Hereditary Neurological Disorders (17 papers), Genetic Neurodegenerative Diseases (11 papers) and Neurological diseases and metabolism (8 papers). Young Se Hyun collaborates with scholars based in South Korea, United States and Taiwan. Young Se Hyun's co-authors include Ki Wha Chung, Byung‐Ok Choi, Young Bin Hong, Heasoo Koo, Byung‐Ok Choi, Soo Hyun Nam, Sung‐Chul Jung, Geon Kwak, Jeong Hyun Yoo and Kyoung‐Gyu Choi and has published in prestigious journals such as PLoS Genetics, American Journal of Botany and Cells.

In The Last Decade

Young Se Hyun

35 papers receiving 635 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Young Se Hyun South Korea 16 321 312 140 138 91 35 656
Diego Lorenzetti United States 12 516 1.6× 512 1.6× 161 1.1× 104 0.8× 63 0.7× 12 805
Chiaki Ohtaka‐Maruyama Japan 16 495 1.5× 181 0.6× 159 1.1× 42 0.3× 106 1.2× 27 797
Minyeop Nahm South Korea 14 393 1.2× 246 0.8× 49 0.3× 94 0.7× 282 3.1× 34 704
Catherine M. Drerup United States 12 400 1.2× 179 0.6× 54 0.4× 48 0.3× 215 2.4× 22 642
Wen‐Wen Lin China 12 299 0.9× 81 0.3× 69 0.5× 57 0.4× 51 0.6× 25 531
Saskia Biskup Germany 17 771 2.4× 264 0.8× 358 2.6× 49 0.4× 99 1.1× 37 1.1k
Rossella Di Giaimo Italy 15 436 1.4× 111 0.4× 156 1.1× 68 0.5× 153 1.7× 34 848
Νικόλαος Γιαγτζόγλου United States 16 568 1.8× 232 0.7× 80 0.6× 70 0.5× 154 1.7× 23 815
Shinichi Katada Japan 9 383 1.2× 311 1.0× 62 0.4× 43 0.3× 58 0.6× 19 701
Inga Ebermann Germany 15 845 2.6× 134 0.4× 232 1.7× 162 1.2× 144 1.6× 19 1.1k

Countries citing papers authored by Young Se Hyun

Since Specialization
Citations

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

Fields of papers citing papers by Young Se Hyun

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Young Se Hyun. 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 Young Se Hyun. The network helps show where Young Se Hyun may publish in the future.

Co-authorship network of co-authors of Young Se Hyun

This figure shows the co-authorship network connecting the top 25 collaborators of Young Se Hyun. A scholar is included among the top collaborators of Young Se Hyun 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 Young Se Hyun. Young Se Hyun 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.
Hyun, Young Se, In Young Choi, Jeong Hee Kim, et al.. (2023). Peripheral Neuron-Organoid Interaction Induces Colonic Epithelial Differentiation via Non-Synaptic Substance P Secretion. International Journal of Stem Cells. 16(3). 269–280. 5 indexed citations
2.
Kim, Jeong Hee, Young Se Hyun, Su Haeng Sung, et al.. (2023). Enhancing Viability of Human Embryonic Stem Cells during Cryopreservation via RGD-REP-Mediated Activation of FAK/AKT/FoxO3a Signaling Pathway. Tissue Engineering and Regenerative Medicine. 20(7). 1133–1143. 2 indexed citations
3.
4.
Mi, Ruifa, Barbara Kern, In Young Choi, et al.. (2019). Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder. Nature Biomedical Engineering. 3(7). 571–582. 23 indexed citations
5.
6.
Hong, Young Bin, JungHee Kang, Ji Hyun Kim, et al.. (2016). DGAT2Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease. Human Mutation. 37(5). 473–480. 40 indexed citations
7.
Wou, Karen, Young Se Hyun, David Chitayat, et al.. (2016). Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol. European Journal of Medical Genetics. 59(8). 417–424. 28 indexed citations
8.
Hyun, Young Se, et al.. (2016). Complete mitochondrial genome of the Pacific cod, Gadus macrocephalus (Gadiformes, Gadidae). Mitochondrial DNA Part B. 1(1). 829–830. 1 indexed citations
9.
Hong, Young Bin, Young Se Hyun, Geon Kwak, et al.. (2016). A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy. PLoS Genetics. 12(2). e1005829–e1005829. 40 indexed citations
10.
Hyun, Young Se, Soo Hyun Nam, Heasoo Koo, et al.. (2015). Novel Compound Heterozygous NonsensePRXMutations in a Korean Dejerine-Sottas Neuropathy Family. Journal of Clinical Neurology. 11(1). 92–92. 8 indexed citations
11.
Hong, Young Bin, Hyung Jun Park, Young Se Hyun, et al.. (2014). A family with axonal sensorimotor polyneuropathy with TUBB3 mutation. Molecular Medicine Reports. 11(4). 2729–2734. 14 indexed citations
12.
Park, Ji Hye, et al.. (2013). Population genetics of insertion–deletion polymorphisms in South Koreans using Investigator DIPplex kit. Forensic Science International Genetics. 8(1). 80–83. 38 indexed citations
13.
Lee, Hye Jin, Do‐Hyun Lee, Dae Hyun Kim, et al.. (2013). Characterization of 20 microsatellite loci by multiplex PCR in swimming crab, Portunus trituberculatus. Genes & Genomics. 35(1). 77–85. 22 indexed citations
14.
Choi, Byung‐Ok, Soo Kyung Koo, Mi‐Hyun Park, et al.. (2012). Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth Disease. Human Mutation. 33(11). 1610–1615. 83 indexed citations
15.
Hyun, Young Se, Joonki Kim, & Ki Wha Chung. (2012). Development of polymorphic microsatellite markers for Cymbidium goeringii (Orchidaceae). American Journal of Botany. 99(5). e193–8. 8 indexed citations
16.
Choi, Byung‐Ok, Young Se Hyun, Heasoo Koo, et al.. (2011). A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14. Human Mutation. 32(6). 669–677. 41 indexed citations
17.
Chung, Ki Wha, et al.. (2011). Two recessive intermediate Charcot‐Marie‐Tooth patients with GDAP1 mutations. Journal of the Peripheral Nervous System. 16(2). 143–146. 12 indexed citations
18.
Choi, Byung‐Ok, et al.. (2010). Inheritance of Charcot–Marie–Tooth disease 1A with rare nonrecurrent genomic rearrangement. Neurogenetics. 12(1). 51–58. 11 indexed citations
19.
Choi, Byung‐Ok, et al.. (2010). Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases. Experimental & Molecular Medicine. 42(6). 446–446. 20 indexed citations
20.
Min, Gi‐Sik, et al.. (2009). Phylogenetic analysis of mitochondrial DNA control region in the swimming crab,portunus trituberculatus. Animal Cells and Systems. 13(3). 305–314. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Diego Lorenzetti Breakdown of academic impact, for papers by Chiaki Ohtaka‐Maruyama Breakdown of academic impact, for papers by Minyeop Nahm Breakdown of academic impact, for papers by Catherine M. Drerup Breakdown of academic impact, for papers by Wen‐Wen Lin Breakdown of academic impact, for papers by Saskia Biskup Breakdown of academic impact, for papers by Rossella Di Giaimo Breakdown of academic impact, for papers by Νικόλαος Γιαγτζόγλου Breakdown of academic impact, for papers by Shinichi Katada Breakdown of academic impact, for papers by Inga Ebermann
Rankless by CCL
2026