Sung Im Cho

1.4k total citations
57 papers, 786 citations indexed

About

Sung Im Cho is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sung Im Cho has authored 57 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 19 papers in Genetics and 9 papers in Genetics. Recurrent topics in Sung Im Cho's work include Cancer Genomics and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (4 papers). Sung Im Cho is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genomics and Rare Diseases (4 papers). Sung Im Cho collaborates with scholars based in South Korea, Ethiopia and United States. Sung Im Cho's co-authors include Sung Sup Park, Moon‐Woo Seong, Hyunwoong Park, Eun Hwa Choi, Mi Seon Han, Sue Shin, Namhee Kim, Kim J, Taek Soo Kim and Soo Hyun Seo and has published in prestigious journals such as Clinical Infectious Diseases, International Journal of Molecular Sciences and Journal of Clinical Microbiology.

In The Last Decade

Sung Im Cho

53 papers receiving 771 citations

Peers

Sung Im Cho

GENET

EPIDE

GENET

Diana Castaño Colombia

Fabian Hauck Germany

Kevin S. Cashman United States

Anatoly V. Rubtsov United States

Jean L. Scholz United States

J. Jeremiah Bell United States

Ryo Shinnakasu Japan

Michael G. Strainic United States

Nike Julia Kräutler Switzerland

Denise Bonney United Kingdom

Diana Castaño Colombia

Sung Im Cho

322 ×1.1

123 ×0.5

180 ×1.4

GENET

124 ×1.2

EPIDE

58 ×0.8

GENET

Citations per year, relative to Sung Im Cho Sung Im Cho (= 1×) peers Diana Castaño

Countries citing papers authored by Sung Im Cho

Since Specialization

Citations

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

Fields of papers citing papers by Sung Im Cho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sung Im Cho. 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 Sung Im Cho. The network helps show where Sung Im Cho may publish in the future.

Co-authorship network of co-authors of Sung Im Cho

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

All Works

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20 of 20 papers shown

Cho, Sung Im, et al.. (2024). Utility of Next-Generation Sequencing-Based Chimerism Analysis for Early Relapse Prediction following Allogenic Hematopoietic Cell Transplantation. International Journal of Molecular Sciences. 25(5). 2811–2811. 1 indexed citations

Kim, Boram, Seung Hun Lee, Chang Ho Ahn, et al.. (2024). Genetic Landscape and Clinical Manifestations of Multiple Endocrine Neoplasia Type 1 in a Korean Cohort: A Multicenter Retrospective Analysis. Endocrinology and Metabolism. 39(6). 956–964. 1 indexed citations

Kim, Man Jin, Boram Kim, Jee‐Soo Lee, et al.. (2023). The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project. European Journal of Human Genetics. 31(10). 1147–1153. 3 indexed citations

Lee, Sungyoung, Sung‐Soo Yoon, Youngil Koh, et al.. (2023). ITDetect: a method to detect internal tandem duplication of FMS-like tyrosine kinase (FLT3) from next-generation sequencing data with high sensitivity and clinical application. BMC Bioinformatics. 24(1). 62–62. 1 indexed citations

Kim, Man Jin, Sungyoung Lee, Hongseok Yun, et al.. (2021). Consistent count region–copy number variation (CCR-CNV): an expandable and robust tool for clinical diagnosis of copy number variation at the exon level using next-generation sequencing data. Genetics in Medicine. 24(3). 663–672. 5 indexed citations

Cho, Sung Im, et al.. (2021). Molecular basis and diagnosis of thalassemia. Blood Research. 56(S1). S39–S43. 34 indexed citations

Kim, Boram, Sung Im Cho, Man Jin Kim, et al.. (2021). Clinical Utility of Methylation-Specific Multiplex Ligation-Dependent Probe Amplification for the Diagnosis of Prader–Willi Syndrome and Angelman Syndrome. Annals of Laboratory Medicine. 42(1). 79–88. 1 indexed citations

Seo, Soo Hyun, Albino Bacolla, Dallah Yoo, et al.. (2020). Replication‐Based Rearrangements Are a Common Mechanism for SNCA Duplication in Parkinson's Disease. Movement Disorders. 35(5). 868–876. 10 indexed citations

Kim, Young‐Gon, Man Jin Kim, Hyukmin Lee, et al.. (2020). SnackVar. Journal of Molecular Diagnostics. 23(2). 140–148. 9 indexed citations

10.

Lee, Hyukmin, Mi‐Hye Yoon, Man Jin Kim, et al.. (2019). Evaluation of the new Abbott Real-Time EBV assay: fully automated quantification of EBV in whole blood by targeting BLLF1. Diagnostic Microbiology and Infectious Disease. 94(2). 135–139. 3 indexed citations

11.

Lee, Joon Kee, Moon‐Woo Seong, Jong‐Il Kim, et al.. (2019). Comparative genomics of Mycoplasma pneumoniae isolated from children with pneumonia: South Korea, 2010–2016. BMC Genomics. 20(1). 910–910. 10 indexed citations

12.

Seo, Soo Hyun, Man Jin Kim, Sung Wook Park, et al.. (2016). Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR). Investigative Ophthalmology & Visual Science. 57(15). 6902–6902. 11 indexed citations

13.

Kim, So Yeon, Sun Jae Park, Ran‐hui Cha, et al.. (2016). Viral RNA in Blood as Indicator of Severe Outcome in Middle East Respiratory Syndrome Coronavirus Infection. Emerging infectious diseases. 22(10). 1813–1816. 30 indexed citations

14.

Park, Hyunwoong, Sung Im Cho, Tae‐Joon Cho, et al.. (2014). Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene. European Journal of Medical Genetics. 58(3). 175–179. 9 indexed citations

15.

Seong, Moon‐Woo, Hyun‐Ah Kim, Il Yong Chung, et al.. (2014). A multi-institutional study on the association between BRCA1/BRCA2 mutational status and triple-negative breast cancer in familial breast cancer patients. Breast Cancer Research and Treatment. 146(1). 63–69. 12 indexed citations

16.

Seong, Moon‐Woo, Soo Hyun Seo, Young Suk Yu, et al.. (2014). Diagnostic Application of an Extensive Gene Panel for Leber Congenital Amaurosis with Severe Genetic Heterogeneity. Journal of Molecular Diagnostics. 17(1). 100–105. 16 indexed citations

17.

Kang, Hyoung Jin, et al.. (2012). A Case Report of a Male Patient With Hb Hammersmith [β42(CD1)Phe→Ser, TTT>TCT]. Hemoglobin. 36(2). 161–165. 6 indexed citations

18.

Kim, So Yeon, et al.. (2012). A novel double mutation in cis in MFN2 causes Charcot–Marie–Tooth neuropathy type 2A. Neurogenetics. 13(3). 275–280. 15 indexed citations

19.

Kwon, Hye Won, Sang Yoon Lee, Bo Sang Kwon, et al.. (2012). Long QT Syndrome and Dilated Cardiomyopathy with SCN5A p.R1193Q Polymorphism: Cardioverter‐Defibrillator Implantation at 27 Months. Pacing and Clinical Electrophysiology. 35(8). e243–6. 16 indexed citations

20.

Kang, Seong‐Ho, Sung Im Cho, Jong‐Hee Chae, et al.. (2009). False Homozygous Deletions of SMN1 Exon 7 Using Dra I PCR-RFLP Caused by a Novel Mutation in Spinal Muscular Atrophy. Genetic Testing and Molecular Biomarkers. 13(4). 511–513. 14 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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