Heasoo Koo

1.2k total citations
54 papers, 875 citations indexed

About

Heasoo Koo is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Epidemiology. According to data from OpenAlex, Heasoo Koo has authored 54 papers receiving a total of 875 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Cellular and Molecular Neuroscience, 15 papers in Molecular Biology and 10 papers in Epidemiology. Recurrent topics in Heasoo Koo's work include Hereditary Neurological Disorders (19 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurological diseases and metabolism (6 papers). Heasoo Koo is often cited by papers focused on Hereditary Neurological Disorders (19 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurological diseases and metabolism (6 papers). Heasoo Koo collaborates with scholars based in South Korea, United States and Russia. Heasoo Koo's co-authors include Ki Wha Chung, Byung‐Ok Choi, Jeong Hyun Yoo, Young Bin Hong, Young Se Hyun, Herbert L. DuPont, Robert L. Atmar, Flor M. Muñoz, Alun Cameron and Mary K. Estes and has published in prestigious journals such as Neurology, Clinical Infectious Diseases and PLoS Genetics.

In The Last Decade

Heasoo Koo

52 papers receiving 864 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heasoo Koo South Korea 18 316 291 143 122 120 54 875
Kunihiko Asakura Japan 16 257 0.8× 226 0.8× 53 0.4× 364 3.0× 130 1.1× 38 1.2k
Claus Meier Switzerland 15 316 1.0× 225 0.8× 51 0.4× 233 1.9× 123 1.0× 27 844
Kenji Matsumuro Japan 12 185 0.6× 264 0.9× 51 0.4× 182 1.5× 222 1.9× 23 1.1k
Linda L. Kusner United States 23 388 1.2× 104 0.4× 204 1.4× 729 6.0× 58 0.5× 51 1.3k
Makoto Kunishige Japan 17 447 1.4× 192 0.7× 31 0.2× 286 2.3× 61 0.5× 38 820
Arnaud Lacour France 17 250 0.8× 170 0.6× 29 0.2× 319 2.6× 75 0.6× 31 857
Ana Lía Taratuto Argentina 19 402 1.3× 189 0.6× 22 0.2× 226 1.9× 34 0.3× 42 1.1k
Pedro M. Rodríguez Cruz United Kingdom 18 313 1.0× 119 0.4× 107 0.7× 609 5.0× 20 0.2× 41 1.0k
Chiara Passarelli Italy 17 540 1.7× 80 0.3× 131 0.9× 51 0.4× 18 0.1× 32 856
Samantha L. Bailey United States 8 274 0.9× 83 0.3× 36 0.3× 64 0.5× 426 3.5× 9 1.6k

Countries citing papers authored by Heasoo Koo

Since Specialization
Citations

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

Fields of papers citing papers by Heasoo Koo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heasoo Koo

This figure shows the co-authorship network connecting the top 25 collaborators of Heasoo Koo. A scholar is included among the top collaborators of Heasoo Koo 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 Heasoo Koo. Heasoo Koo 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.
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
2.
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
3.
Choi, Yu‐Ri, Young Bin Hong, Sung‐Chul Jung, et al.. (2015). A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy. BMC Neurology. 15(1). 179–179. 17 indexed citations
4.
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
5.
Nakhro, Khriezhanuo, Ye Jin Kim, Jeong Hyun Yoo, et al.. (2013). A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot–Marie–Tooth disease type 2L. Neuromuscular Disorders. 23(8). 656–663. 34 indexed citations
6.
Kim, Ye Jin, Jeong Hyun Yoo, Young Bin Hong, et al.. (2013). A novel MYH7 mutation with prominent paraspinal and proximal muscle involvement. Neuromuscular Disorders. 23(7). 580–586. 14 indexed citations
7.
Kim, Hyeon Jin, Young Bin Hong, Yu‐Ri Choi, et al.. (2013). Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease. Orphanet Journal of Rare Diseases. 8(1). 104–104. 29 indexed citations
8.
Song, Eun Mi, Kyoung Eun Lee, Jung Youn Jo, et al.. (2011). An Adrenocorticotropic Hormone-secreting Malignant Pancreatic Neuroendocrine Tumor. The Korean Journal of Internal Medicine. 80(2). 238–242. 2 indexed citations
9.
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
10.
Kim, Hyun Sook, Ki Wha Chung, Sun Young Cho, et al.. (2010). Myotonic dystrophy type I combined with X-linked dominant Charcot–Marie–Tooth neuropathy. Neurogenetics. 11(4). 425–433. 11 indexed citations
11.
Lee, Sun Wha, et al.. (2009). Isolated Heterotopic Pancreas in Ileoileal Intussusception. Journal of Ultrasound in Medicine. 28(4). 545–548. 10 indexed citations
12.
Koo, Heasoo, et al.. (2007). Drug-Drug Interaction between Itraconazole and Efavirenz in a Patient with AIDS and Disseminated Histoplasmosis. Clinical Infectious Diseases. 45(6). e77–e79. 24 indexed citations
13.
Lee, Minjin, et al.. (2006). Prognostic value of p16INK4a and p14ARF gene hypermethylation in human colon cancer. Pathology - Research and Practice. 202(6). 415–424. 48 indexed citations
14.
Chung, Ki Wha, et al.. (2005). Two missense mutations of EGR2 R359W and GJB1 V136A in a Charcot–Marie–Tooth disease family. Neurogenetics. 6(3). 159–163. 27 indexed citations
15.
Chang, Seung H., et al.. (2004). The Radioprotective Effect and Mechanism of Captopril on Radiation Induced-Heart Damage in Rats. 22(1). 40–54. 3 indexed citations
16.
Koo, Heasoo, et al.. (2003). 방광암 선별 및 추적검사시 신선뇨침사 Cytospin Wright 염색 세포검사의 유용성 검토. The Korean Journal of Laboratory Medicine. 23(3). 164–169. 1 indexed citations
17.
Suh, Yeon‐Lim, Heasoo Koo, Tai Seung Kim, et al.. (2002). Tumors of the Central Nervous System in Korea A Multicenter Study of 3221 Cases.. Journal of Neuro-Oncology. 56(3). 251–259. 47 indexed citations
18.
Koo, Heasoo & Bernard Choi. (2001). Expression of glial cell line‐derived neurotrophic factor (GDNF) in the developing human fetal brain. International Journal of Developmental Neuroscience. 19(6). 549–558. 23 indexed citations
19.
Koo, Heasoo, et al.. (2000). Middle mediastinal lesions: imaging findings and pathologic correlation. European Journal of Radiology. 35(1). 30–38. 7 indexed citations
20.
Koo, Heasoo & Uros Roessmann. (1988). Astrocyte Response to Perinatal Liver Disease, Hyperammonemia, and Hyperbilirubinemia. Pediatric Pathology. 8(3). 301–311. 3 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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