Changwon Keum

565 total citations
23 papers, 321 citations indexed

About

Changwon Keum is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Changwon Keum has authored 23 papers receiving a total of 321 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Changwon Keum's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Changwon Keum is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Syndromes and Imprinting (2 papers). Changwon Keum collaborates with scholars based in South Korea, United States and United Kingdom. Changwon Keum's co-authors include Sang Youl Rhee, Jeong‐Taek Woo, Hyung Jin Choi, Sang Ouk Chin, Beom Hee Lee, Go Hun Seo, In Hee Choi, Yoon Jeon Kim, Arum Oh and Hajeong Lee and has published in prestigious journals such as Scientific Reports, Medicine and BMC Genomics.

In The Last Decade

Changwon Keum

23 papers receiving 314 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Changwon Keum South Korea 9 128 109 76 53 26 23 321
Karen Fieggen South Africa 13 146 1.1× 125 1.1× 29 0.4× 50 0.9× 13 0.5× 42 390
Lydia Choi United States 10 146 1.1× 36 0.3× 28 0.4× 69 1.3× 53 2.0× 21 430
Melissa Martyn Australia 14 111 0.9× 415 3.8× 43 0.6× 100 1.9× 8 0.3× 40 647
Laura Bryson United States 3 237 1.9× 70 0.6× 40 0.5× 41 0.8× 13 0.5× 4 408
Catherine Delva France 11 68 0.5× 114 1.0× 17 0.2× 126 2.4× 41 1.6× 21 412
James M. Wilkins United States 9 152 1.2× 62 0.6× 49 0.6× 54 1.0× 15 0.6× 26 481
Ebony Bookman United States 8 49 0.4× 154 1.4× 34 0.4× 149 2.8× 64 2.5× 10 324
Juliann M. Savatt United States 10 82 0.6× 219 2.0× 34 0.4× 28 0.5× 12 0.5× 20 320
Karen E. Wain United States 14 120 0.9× 378 3.5× 34 0.4× 53 1.0× 10 0.4× 28 567
Patricia Vega Argentina 11 83 0.6× 200 1.8× 28 0.4× 53 1.0× 32 1.2× 18 413

Countries citing papers authored by Changwon Keum

Since Specialization
Citations

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

Fields of papers citing papers by Changwon Keum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Changwon Keum

This figure shows the co-authorship network connecting the top 25 collaborators of Changwon Keum. A scholar is included among the top collaborators of Changwon Keum 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 Changwon Keum. Changwon Keum 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.
2.
Jung, Jiwon, Joo Hoon Lee, Go Hun Seo, et al.. (2023). Genetic diagnosis of kidney disease by whole exome sequencing and its clinical application. Clinical Genetics. 104(3). 298–312. 2 indexed citations
3.
Yoon, Ju Young, et al.. (2022). The first case of novel variants of the FSHR mutation causing primary amenorrhea in 2 siblings in Korea. Annals of Pediatric Endocrinology & Metabolism. 28(1). 54–60. 3 indexed citations
4.
Choi, Jungmin, Soojin Hwang, Go Hun Seo, et al.. (2022). KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature. Molecular Genetics & Genomic Medicine. 11(4). e2127–e2127. 8 indexed citations
5.
Seo, Go Hun, Gu-Hwan Kim, Changwon Keum, et al.. (2021). Phenotypic and molecular spectra of patients with switch/sucrose nonfermenting complex-related intellectual disability disorders in Korea. BMC Medical Genomics. 14(1). 254–254. 5 indexed citations
6.
Kim, So Young, Seungmin Lee, Go Hun Seo, et al.. (2021). Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneity. Scientific Reports. 11(1). 19476–19476. 2 indexed citations
7.
Jung, Jiwon, Joo Hoon Lee, Young Seo Park, et al.. (2021). Ultra-rare renal diseases diagnosed with whole-exome sequencing: Utility in diagnosis and management. BMC Medical Genomics. 14(1). 177–177. 7 indexed citations
8.
Kim, Yoon Jeon, Young‐Hee Yoon, Eul‐Ju Seo, et al.. (2021). Diverse Genetic Landscape of Suspected Retinitis Pigmentosa in a Large Korean Cohort. Genes. 12(5). 675–675. 15 indexed citations
9.
Seo, Go Hun, Tae Ho Kim, In Hee Choi, et al.. (2020). Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE. Clinical Genetics. 98(6). 562–570. 92 indexed citations
10.
11.
Seo, Go Hun, Gu-Hwan Kim, In Hee Choi, et al.. (2020). Clinical and molecular spectra of BRAF-associated RASopathy. Journal of Human Genetics. 66(4). 389–399. 13 indexed citations
12.
Seo, Go Hun, Changwon Keum, Sun Hee Heo, et al.. (2020). Diagnosis of metachromatic leukodystrophy in a patient with regression and Phelan-McDermid syndrome. Brain and Development. 42(5). 414–417. 5 indexed citations
13.
Song, Joon Seon, Seak Hee Oh, Yoon Jeon Kim, et al.. (2020). Clinical characteristics and disease progression of retinitis pigmentosa associated with PDE6B mutations in Korean patients. Scientific Reports. 10(1). 19540–19540. 11 indexed citations
14.
Oh, Seung Hwan, Changwon Keum, Minyoung Her, et al.. (2020). A Novel Missense Mutation (L44V) of PAX2 Associated with Adult-Onset End-Stage Renal Disease and No Syndromic Features.. PubMed. 50(5). 687–690. 1 indexed citations
15.
Oh, Seung Hwan, et al.. (2020). First Korean Case of Coffin-Siris Syndrome with a Novel Frameshift ARID1B Mutation.. PubMed. 50(1). 140–145. 3 indexed citations
16.
Oh, Seung Hwan, et al.. (2020). Effects of long-term growth hormone therapy in a girl with Floating-Harbor syndrome. Annals of Pediatric Endocrinology & Metabolism. 25(2). 126–131. 6 indexed citations
17.
Kang, Eungu, Taeho Kim, Arum Oh, et al.. (2019). Lysinuric protein intolerance with homozygous SLC7A7 mutation caused by maternal uniparental isodisomy of chromosome 14. Journal of Human Genetics. 64(11). 1137–1140. 5 indexed citations
18.
Keum, Changwon, et al.. (2017). Effects of climatic variables on weight loss: a global analysis. Scientific Reports. 7(1). 40708–40708. 9 indexed citations
19.
Chin, Sang Ouk, et al.. (2016). Successful weight reduction and maintenance by using a smartphone application in those with overweight and obesity. Scientific Reports. 6(1). 34563–34563. 99 indexed citations
20.
Keum, Changwon, et al.. (2009). Improving gene expression similarity measurement using pathway-based analytic dimension. BMC Genomics. 10(S3). S15–S15. 5 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 Karen Fieggen Breakdown of academic impact, for papers by Lydia Choi Breakdown of academic impact, for papers by Melissa Martyn Breakdown of academic impact, for papers by Laura Bryson Breakdown of academic impact, for papers by Catherine Delva Breakdown of academic impact, for papers by James M. Wilkins Breakdown of academic impact, for papers by Ebony Bookman Breakdown of academic impact, for papers by Juliann M. Savatt Breakdown of academic impact, for papers by Karen E. Wain Breakdown of academic impact, for papers by Patricia Vega
Rankless by CCL
2026