Arum Oh

440 total citations
18 papers, 247 citations indexed

About

Arum Oh is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Arum Oh has authored 18 papers receiving a total of 247 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Arum Oh's work include Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). Arum Oh is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). Arum Oh collaborates with scholars based in South Korea, United States and Germany. Arum Oh's co-authors include Beom Hee Lee, Han‐Wook Yoo, Go Hun Seo, Jin‐Ho Choi, Gu-Hwan Kim, Yoon-Myung Kim, Changwon Keum, Hajeong Lee, Jungsul Lee and Min Hyun Cho and has published in prestigious journals such as SHILAP Revista de lepidopterología, Medicine and Clinica Chimica Acta.

In The Last Decade

Arum Oh

17 papers receiving 242 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arum Oh South Korea 7 109 91 46 38 30 18 247
Weiyue Gu China 11 139 1.3× 101 1.1× 21 0.5× 47 1.2× 17 0.6× 50 317
М. С. Назаренко Russia 11 215 2.0× 56 0.6× 32 0.7× 26 0.7× 14 0.5× 88 381
Sheng Yao China 12 253 2.3× 58 0.6× 118 2.6× 15 0.4× 31 1.0× 33 434
L Kádasi Slovakia 9 207 1.9× 67 0.7× 59 1.3× 27 0.7× 17 0.6× 18 416
Katrin Handschug Germany 9 180 1.7× 56 0.6× 11 0.2× 15 0.4× 30 1.0× 10 381
Shouyue Sun China 11 257 2.4× 133 1.5× 16 0.3× 10 0.3× 19 0.6× 29 380
Nadine Kossler Germany 7 128 1.2× 28 0.3× 113 2.5× 21 0.6× 27 0.9× 8 258
P Larrodé Spain 9 82 0.8× 17 0.2× 76 1.7× 33 0.9× 32 1.1× 21 238
Francesca Clementina Radio Italy 15 194 1.8× 149 1.6× 6 0.1× 17 0.4× 20 0.7× 40 421

Countries citing papers authored by Arum Oh

Since Specialization
Citations

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

Fields of papers citing papers by Arum Oh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arum Oh

This figure shows the co-authorship network connecting the top 25 collaborators of Arum Oh. A scholar is included among the top collaborators of Arum Oh 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 Arum Oh. Arum Oh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
2.
Oh, Arum, et al.. (2021). Three pediatric patients with primary hyperparathyroidism caused by parathyroid adenoma. Annals of Pediatric Endocrinology & Metabolism. 27(2). 142–147. 4 indexed citations
3.
Park, Hee Sue, Arum Oh, Jisu Lee, et al.. (2021). A novel likely pathogenic PLCG2 variant in a patient with a recurrent skin blistering disease and B-cell lymphopenia. European Journal of Medical Genetics. 65(1). 104387–104387. 5 indexed citations
4.
Oh, Arum, et al.. (2021). Unfavorable clinical outcomes in patients with carbamoyl phosphate synthetase 1 deficiency. Clinica Chimica Acta. 526. 55–61. 6 indexed citations
5.
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
6.
Choi, Jin‐Ho, Arum Oh, Gu-Hwan Kim, et al.. (2020). Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency. Annals of Pediatric Endocrinology & Metabolism. 25(2). 97–103. 6 indexed citations
7.
Oh, Arum, et al.. (2020). Efficacy and safety of parenteral vitamin D therapy in infants and children with vitamin D deficiency caused by intestinal malabsorption. Annals of Pediatric Endocrinology & Metabolism. 25(2). 112–117. 4 indexed citations
8.
Lee, Jiwon, et al.. (2020). A Study on the Composition of Image-Based Ship-type/class Identification System. 203–206. 4 indexed citations
9.
Choi, Jin‐Ho, et al.. (2020). Functional Characteristics of Novel FGFR1 Mutations in Patients with Isolated Gonadotropin-Releasing Hormone Deficiency. Experimental and Clinical Endocrinology & Diabetes. 129(6). 457–463. 3 indexed citations
10.
Seo, Go Hun, Arum Oh, Changwon Keum, et al.. (2020). Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia. Medicine. 99(51). e23864–e23864. 8 indexed citations
11.
12.
Kang, Eungu, Yoon-Myung Kim, Go Hun Seo, et al.. (2019). Phenotype categorization of neurofibromatosis type I and correlation to NF1 mutation types. Journal of Human Genetics. 65(2). 79–89. 38 indexed citations
13.
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
14.
Kim, Yoon-Myung, Mi‐Sun Yum, Sun Hee Heo, et al.. (2019). Pharmacologic properties of high-dose ambroxol in four patients with Gaucher disease and myoclonic epilepsy. Journal of Medical Genetics. 57(2). 124–131. 36 indexed citations
15.
Seo, Go Hun, Arum Oh, Eun Na Kim, et al.. (2019). Identification of extremely rare mitochondrial disorders by whole exome sequencing. Journal of Human Genetics. 64(11). 1117–1125. 12 indexed citations
16.
Kim, Yoon-Myung, et al.. (2019). Pubertal outcomes and sex of rearing of patients with ovotesticular disorder of sex development and mixed gonadal dysgenesis. Annals of Pediatric Endocrinology & Metabolism. 24(4). 231–236. 11 indexed citations
17.
Seo, Go Hun, Arum Oh, Eun Na Kim, et al.. (2019). An ANKRD11 exonic deletion accompanied by a congenital megacolon in an infant with KBG syndrome. 16(1). 39–42. 2 indexed citations
18.
Oh, Arum, et al.. (2015). Two Pediatric Patients with Herbal Medicine-Induced Nephrotic Syndrome. SHILAP Revista de lepidopterología. 19(2). 171–175. 4 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 Weiyue Gu Breakdown of academic impact, for papers by М. С. Назаренко Breakdown of academic impact, for papers by Sheng Yao Breakdown of academic impact, for papers by L Kádasi Breakdown of academic impact, for papers by Katrin Handschug Breakdown of academic impact, for papers by Shouyue Sun Breakdown of academic impact, for papers by Nadine Kossler Breakdown of academic impact, for papers by P Larrodé Breakdown of academic impact, for papers by Francesca Clementina Radio
Rankless by CCL
2026