Han‐Wook Yoo

5.9k total citations
300 papers, 4.0k citations indexed

About

Han‐Wook Yoo is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Han‐Wook Yoo has authored 300 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 152 papers in Molecular Biology, 81 papers in Genetics and 52 papers in Physiology. Recurrent topics in Han‐Wook Yoo's work include Metabolism and Genetic Disorders (45 papers), Lysosomal Storage Disorders Research (39 papers) and Sexual Differentiation and Disorders (31 papers). Han‐Wook Yoo is often cited by papers focused on Metabolism and Genetic Disorders (45 papers), Lysosomal Storage Disorders Research (39 papers) and Sexual Differentiation and Disorders (31 papers). Han‐Wook Yoo collaborates with scholars based in South Korea, United States and Germany. Han‐Wook Yoo's co-authors include Gu-Hwan Kim, Jin‐Ho Choi, Beom Hee Lee, Jung Min Ko, Jae‐Min Kim, Kyung Mo Kim, Yoo‐Mi Kim, Hye Young Jin, Eul‐Ju Seo and Young‐Lim Shin and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Gastroenterology.

In The Last Decade

Han‐Wook Yoo

284 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Han‐Wook Yoo South Korea 33 1.8k 971 650 560 501 300 4.0k
Yoshiki Seino Japan 39 1.9k 1.0× 1.4k 1.5× 507 0.8× 1.3k 2.3× 474 0.9× 238 6.0k
John C. Fyfe United States 25 1.3k 0.7× 667 0.7× 373 0.6× 234 0.4× 558 1.1× 52 2.9k
Jin‐Ho Choi South Korea 28 2.1k 1.2× 614 0.6× 294 0.5× 347 0.6× 133 0.3× 210 3.8k
Barbara Villaggio Italy 39 786 0.4× 505 0.5× 584 0.9× 465 0.8× 937 1.9× 84 4.0k
Allan M. Lund Denmark 32 1.1k 0.6× 876 0.9× 1.1k 1.7× 159 0.3× 756 1.5× 171 3.3k
John L. Fowlkes United States 38 1.8k 1.0× 549 0.6× 370 0.6× 1.5k 2.6× 242 0.5× 89 4.1k
R Gitzelmann Switzerland 35 1.3k 0.7× 1.2k 1.2× 642 1.0× 405 0.7× 740 1.5× 141 3.8k
Michel Le Hir Switzerland 38 2.1k 1.1× 702 0.7× 370 0.6× 178 0.3× 437 0.9× 87 5.0k
Kathryn M. Thrailkill United States 36 1.5k 0.8× 582 0.6× 339 0.5× 1.2k 2.1× 172 0.3× 75 3.5k
Sharon J. Elliot United States 36 1.2k 0.7× 584 0.6× 357 0.5× 822 1.5× 148 0.3× 87 3.9k

Countries citing papers authored by Han‐Wook Yoo

Since Specialization
Citations

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

Fields of papers citing papers by Han‐Wook Yoo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Han‐Wook Yoo. 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 Han‐Wook Yoo. The network helps show where Han‐Wook Yoo may publish in the future.

Co-authorship network of co-authors of Han‐Wook Yoo

This figure shows the co-authorship network connecting the top 25 collaborators of Han‐Wook Yoo. A scholar is included among the top collaborators of Han‐Wook Yoo 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 Han‐Wook Yoo. Han‐Wook Yoo 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.
Hwang, Soojin, et al.. (2024). Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene. Annals of Pediatric Endocrinology & Metabolism. 29(1). 54–59. 2 indexed citations
2.
Hwang, Soojin, Ja Hye Kim, Hyery Kim, et al.. (2024). Long-term endocrine sequelae after hematopoietic stem cell transplantation in children and adolescents. Annals of Pediatric Endocrinology & Metabolism. 29(2). 109–118.
3.
Kim, Ja Hye, et al.. (2023). Clinical outcomes and genotype-phenotype correlations in patients with complete and partial androgen insensitivity syndromes. Annals of Pediatric Endocrinology & Metabolism. 28(3). 184–192. 1 indexed citations
4.
Yoo, Han‐Wook. (2023). Fabry disease: current treatment and future perspective. 20(1). 6–14. 6 indexed citations
5.
Yoo, Han‐Wook. (2023). Development of orphan drugs for rare diseases. Clinical and Experimental Pediatrics. 67(7). 315–327. 14 indexed citations
6.
Hwang, Soojin, et al.. (2022). Genotype-phenotype correlations and long-term efficacy of pamidronate therapy in patients with osteogenesis imperfecta. Annals of Pediatric Endocrinology & Metabolism. 27(1). 22–29. 5 indexed citations
7.
Oh, Seak Hee, Yu Bin Kim, Han‐Wook Yoo, et al.. (2021). Efficacy of Living Donor Liver Transplantation in Patients with Methylmalonic Acidemia. Pediatric Gastroenterology Hepatology & Nutrition. 24(3). 288–288. 4 indexed citations
8.
Yoo, Han‐Wook. (2021). Inborn Errors of Mitochondrial Fatty Acid Oxidation: Overview from a Clinical Perspective. Journal of Lipid and Atherosclerosis. 10(1). 1–1. 4 indexed citations
9.
Lee, Byong Sop, Jiyoon Jeong, Euiseok Jung, et al.. (2020). Surgical Interventions and Clinical Outcomes of Patients with Trisomy 18: a Single Center Experience. 31(3). 129–129. 1 indexed citations
10.
Kim, Jin‐Kyung, et al.. (2020). A female with typical fragile-X phenotype caused by maternal isodisomy of the entire X chromosome. Journal of Human Genetics. 65(6). 551–555. 3 indexed citations
11.
Kim, Woo-Shik, Jinho Shin, Jong Chun Park, et al.. (2019). Prevalence of Fabry Disease in Korean Men with Left Ventricular Hypertrophy. Journal of Korean Medical Science. 34(7). e63–e63. 15 indexed citations
12.
Seo, Go Hun & Han‐Wook Yoo. (2018). Growth hormone therapy in patients with Noonan syndrome. Annals of Pediatric Endocrinology & Metabolism. 23(4). 176–181. 23 indexed citations
13.
14.
Seo, Go Hun, et al.. (2018). Hepatopulmonary syndrome caused by hypothalamic obesity and nonalcoholic fatty liver disease after surgery for craniopharyngioma: a case report. Annals of Pediatric Endocrinology & Metabolism. 23(1). 51–55. 7 indexed citations
15.
Hong, Jeana, Seak Hee Oh, Han‐Wook Yoo, et al.. (2018). Complete Recovery of Oxysterol 7α-Hydroxylase Deficiency by Living Donor Transplantation in a 4-Month-Old Infant: the First Korean Case Report and Literature Review. Journal of Korean Medical Science. 33(51). e324–e324. 7 indexed citations
16.
Kang, Eungu, et al.. (2017). DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea. Journal of Korean Medical Science. 32(6). 1042–1042. 13 indexed citations
17.
Kim, Hyun Jin, Yoon-Myung Kim, Eungu Kang, et al.. (2017). Diabetes mellitus caused by secondary hemochromatosis after multiple blood transfusions in 2 patients with severe aplastic anemia. Annals of Pediatric Endocrinology & Metabolism. 22(1). 60–60. 1 indexed citations
18.
19.
Yoo, Han‐Wook, et al.. (2007). Genetic Analysis of TGFA, MTHFR, and IFR6 in Korean Patients Affected by Nonsyndromic Cleft Lip with or without Cleft Palate (CL/P). Genomics & Informatics. 5(2). 56–60. 2 indexed citations
20.
Seo, Eul‐Ju, et al.. (2006). Novel mutations in the human elastin gene (ELN) causing isolated supravalvular aortic stenosis. International Journal of Molecular Medicine. 18(2). 329–32. 12 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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