Man Jin Kim

1.0k total citations
76 papers, 489 citations indexed

About

Man Jin Kim is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Man Jin Kim has authored 76 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 29 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Man Jin Kim's work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Man Jin Kim is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Man Jin Kim collaborates with scholars based in South Korea, Ethiopia and United States. Man Jin Kim's co-authors include Moon‐Woo Seong, Sung Sup Park, Sung Im Cho, Jong‐Hee Chae, Hyukmin Lee, Soo Hyun Seo, Kwangsic Joo, Min Seok Kim, Soo Yeon Kim and Kyu Hyung Park and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Emerging infectious diseases.

In The Last Decade

Man Jin Kim

67 papers receiving 481 citations

Peers

Man Jin Kim

GENET

SURGE

Soo Hyun Seo South Korea

I R Cohen Israel

Farhad Salari Iran

Anshika Srivastava India

Maria Margherita De Santi Italy

Emily M. L. Chastain United States

Jude Samulski United States

Saori Sakaue Japan

Derek Pappas United States

Sachiko Kubo Japan

Soo Hyun Seo South Korea

Man Jin Kim

241 ×1.1

81 ×0.6

GENET

44 ×0.8

85 ×1.7

SURGE

81 ×1.7

Citations per year, relative to Man Jin Kim Man Jin Kim (= 1×) peers Soo Hyun Seo

Countries citing papers authored by Man Jin Kim

Since Specialization

Citations

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

Fields of papers citing papers by Man Jin Kim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Man Jin Kim. 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 Man Jin Kim. The network helps show where Man Jin Kim may publish in the future.

Co-authorship network of co-authors of Man Jin Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Man Jin Kim. A scholar is included among the top collaborators of Man Jin Kim 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 Man Jin Kim. Man Jin Kim 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

Ahn, Jong Hyeon, Jihoon G. Yoon, Seungbok Lee, et al.. (2024). Implementing genomic medicine in clinical practice for adults with undiagnosed rare diseases. npj Genomic Medicine. 9(1). 63–63. 1 indexed citations

Kim, Man Jin, Sheehyun Kim, Seungbok Lee, et al.. (2023). Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia. Journal of Human Genetics. 68(6). 369–374. 6 indexed citations

Kim, Soo Yeon, Seungbok Lee, Jihoon G. Yoon, et al.. (2023). Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort. Frontiers in Neurology. 14. 1218706–1218706. 2 indexed citations

Yoon, Jihoon G., Man Jin Kim, Yong Jin Kwon, & Jong‐Hee Chae. (2023). Clinical applications of next-generation sequencing in the diagnosis of genetic disorders in Korea: a narrative review. Journal of Korean Medical Association. 66(10). 613–623.

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

Yoon, Jihoon G., Seungbok Lee, Sheehyun Kim, et al.. (2023). Expansion of clinico-genetic spectrum of PRDX3 disease: a literature review with two additional cases. Brain Communications. 5(5). fcad233–fcad233. 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, Soo Yeon Kim, Jin Sook Lee, et al.. (2022). Rapid Targeted Sequencing Using Dried Blood Spot Samples for Patients With Suspected Actionable Genetic Diseases. Annals of Laboratory Medicine. 43(3). 280–289. 8 indexed citations

10.

Shin, Choong Ho, et al.. (2022). Case Report and Review of Literature: Autosomal Recessive Hypophosphatemic Rickets Type 2 Caused by a Pathogenic Variant in ENPP1 Gene. Frontiers in Endocrinology. 13. 911672–911672. 10 indexed citations

11.

Kim, Soo Yeon, Hyunook Kang, Man Jin Kim, et al.. (2022). Fatal systemic disorder caused by biallelic variants in FARSA. Orphanet Journal of Rare Diseases. 17(1). 306–306. 4 indexed citations

12.

Kim, Young‐Gon, Hong Yeul Lee, Nakwon Kwak, et al.. (2021). Determination of Clinical Characteristics of Mycobacterium kansasii-Derived Species by Reanalysis of Isolates Formerly Reported as M. kansasii. Annals of Laboratory Medicine. 41(5). 463–468. 3 indexed citations

13.

Lee, Seunghyun, Saebeom Hur, Dong In Suh, et al.. (2021). Transcatheter Dynamic Contrast-Enhanced MR Lymphangiography for Nontraumatic Lymphatic Disorders: Technical Feasibility and Imaging Findings. Journal of Vascular and Interventional Radiology. 32(12). 1654–1660.e2. 3 indexed citations

14.

Moon, Jin Soo, et al.. (2020). Hereditary Fructose Intolerance Diagnosed in Adulthood. Gut and Liver. 15(1). 142–145. 8 indexed citations

15.

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

16.

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

17.

Yoo, Dallah, Ji-Hyun Choi, Man Jin Kim, et al.. (2020). Young-Onset Parkinson’s Disease with Impulse Control Disorder Due to Novel Variants of F-Box Only Protein 7. Journal of Movement Disorders. 13(3). 225–228. 6 indexed citations

18.

Lee, Jin Sook, Man Jin Kim, Soo Yeon Kim, et al.. (2019). Clinical and genetic characteristics of Korean patients with IARS2-related disorders. 16(2). 55–61. 5 indexed citations

19.

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

20.

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

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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