Borahm Kim

493 total citations
21 papers, 289 citations indexed

About

Borahm Kim is a scholar working on Hematology, Genetics and Cancer Research. According to data from OpenAlex, Borahm Kim has authored 21 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Hematology, 7 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Borahm Kim's work include Acute Myeloid Leukemia Research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Borahm Kim is often cited by papers focused on Acute Myeloid Leukemia Research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Borahm Kim collaborates with scholars based in South Korea. Borahm Kim's co-authors include Seung‐Tae Lee, Jong Rak Choi, Hoon‐Chul Kang, Se Hee Kim, Heung Dong Kim, Saeam Shin, Joon Soo Lee, Dongju Won, Yoo Hong Min and Donghwa Yang and has published in prestigious journals such as PLoS ONE, Scientific Reports and Epilepsy Research.

In The Last Decade

Borahm Kim

21 papers receiving 287 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Borahm Kim South Korea 11 89 84 83 55 42 21 289
H Jani United Kingdom 6 69 0.8× 60 0.7× 107 1.3× 43 0.8× 47 1.1× 11 372
Alessandra Franzoni Italy 11 54 0.6× 53 0.6× 166 2.0× 11 0.2× 28 0.7× 33 307
Francesca Bertola Italy 10 76 0.9× 43 0.5× 66 0.8× 12 0.2× 68 1.6× 20 291
Sara Lewis United States 7 33 0.4× 37 0.4× 79 1.0× 18 0.3× 10 0.2× 13 227
Tahir Naeem Khan Pakistan 11 23 0.3× 59 0.7× 118 1.4× 16 0.3× 47 1.1× 32 308
June Allison-Thacker United States 1 110 1.2× 35 0.4× 50 0.6× 30 0.5× 107 2.5× 2 329
Sara Bertok Slovenia 10 23 0.3× 122 1.5× 166 2.0× 18 0.3× 18 0.4× 35 354
Sonia Avila Spain 5 26 0.3× 103 1.2× 460 5.5× 28 0.5× 9 0.2× 9 579
James Garifallou United States 10 25 0.3× 20 0.2× 77 0.9× 24 0.4× 16 0.4× 15 274
Juan S. Medina-Martínez United States 7 64 0.7× 12 0.1× 99 1.2× 18 0.3× 35 0.8× 21 243

Countries citing papers authored by Borahm Kim

Since Specialization
Citations

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

Fields of papers citing papers by Borahm Kim

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Borahm Kim

This figure shows the co-authorship network connecting the top 25 collaborators of Borahm Kim. A scholar is included among the top collaborators of Borahm 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 Borahm Kim. Borahm Kim 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.
Koh, June‐Young, Borahm Kim, Younhee Park, et al.. (2021). Impact of maternal engrafted cytomegalovirus‐specific CD8+ T cells in a patient with severe combined immunodeficiency. Clinical & Translational Immunology. 10(4). e1272–e1272. 4 indexed citations
2.
Kim, Se Hee, Borahm Kim, Seung‐Tae Lee, et al.. (2020). Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern. Epilepsy Research. 163. 106323–106323. 16 indexed citations
3.
Kim, Borahm, Seung‐Tae Lee, Keon Hee Yoo, et al.. (2020). Prevalence and clinical implications of germline predisposition gene mutations in patients with acute myeloid leukemia. Scientific Reports. 10(1). 14297–14297. 24 indexed citations
4.
Won, Dongju, Se Hee Kim, Borahm Kim, et al.. (2020). Reanalysis of Genomic Sequencing Results in a Clinical Laboratory: Advantages and Limitations. Frontiers in Neurology. 11. 612–612. 9 indexed citations
5.
Na, Jihoon, Saeam Shin, Donghwa Yang, et al.. (2020). Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy. Brain and Development. 42(6). 438–448. 26 indexed citations
6.
Shin, Saeam, Seung‐Tae Lee, Junwon Lee, et al.. (2020). Serial Detection of MYD88 L265P Mutation in the Aqueous Humor of a Patient with Vitreoretinal Lymphoma for Disease Monitoring. Ocular Immunology and Inflammation. 29(3). 485–489. 9 indexed citations
7.
Kim, Hyo Jeong, Donghwa Yang, Se Hee Kim, et al.. (2020). The phenotype and treatment of SCN2A‐related developmental and epileptic encephalopathy. Epileptic Disorders. 22(5). 563–570. 13 indexed citations
8.
Kim, Borahm, Ji Eun Jang, Soo‐Jeong Kim, et al.. (2019). Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neoplasms. PLoS ONE. 14(3). e0212228–e0212228. 9 indexed citations
9.
Kim, Borahm, Dongju Won, Seung‐Tae Lee, & Jong Rak Choi. (2019). Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy. PLoS ONE. 14(6). e0217521–e0217521. 8 indexed citations
10.
Kim, Se Hee, Borahm Kim, Seung‐Tae Lee, et al.. (2019). Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development. Pediatric Neurology. 103. 27–34. 5 indexed citations
11.
Kim, Se Hee, Borahm Kim, Joon Soo Lee, et al.. (2019). Proband-Only Clinical Exome Sequencing for Neurodevelopmental Disabilities. Pediatric Neurology. 99. 47–54. 23 indexed citations
12.
13.
Kim, Borahm, Seung‐Tae Lee, June‐Won Cheong, et al.. (2019). Detection of recurrent, rare, and novel gene fusions in patients with acute leukemia using next‐generation sequencing approaches. Hematological Oncology. 38(1). 82–88. 17 indexed citations
14.
Kim, Borahm, Soo‐Jeong Kim, Seung‐Tae Lee, Yoo Hong Min, & Jong Rak Choi. (2019). FLT3 Internal Tandem Duplication in Patients With Acute Myeloid Leukemia Is Readily Detectable in a Single Next-Generation Sequencing Assay Using the Pindel Algorithm. Annals of Laboratory Medicine. 39(3). 327–329. 9 indexed citations
15.
Kim, Hyo Jeong, Donghwa Yang, Se Hee Kim, et al.. (2019). Genetic and clinical features of SCN8A developmental and epileptic encephalopathy. Epilepsy Research. 158. 106222–106222. 12 indexed citations
16.
Kim, Borahm, et al.. (2019). Clinical utility of targeted NGS panel with comprehensive bioinformatics analysis for patients with acute lymphoblastic leukemia. Leukemia & lymphoma. 60(13). 3138–3145. 6 indexed citations
17.
Kim, Borahm, et al.. (2018). Clinical Evaluation of Massively Parallel RNA Sequencing for Detecting Recurrent Gene Fusions in Hematologic Malignancies. Journal of Molecular Diagnostics. 21(1). 163–170. 29 indexed citations
18.
Kim, Borahm, et al.. (2015). Transfusion Strategy and Laboratory Update on the DEL Variant. The Korean Journal of Blood Transfusion. 26(1). 1–8. 3 indexed citations
19.
Kim, Borahm, Hyung‐Doo Park, Jong‐Won Kim, et al.. (2015). Dried Blood Spot Testing for Seven Steroids Using Liquid Chromatography-Tandem Mass Spectrometry With Reference Interval Determination in the Korean Population. Annals of Laboratory Medicine. 35(6). 578–585. 24 indexed citations
20.
Kim, Borahm, Seung‐Tae Lee, Hee‐Jin Kim, et al.. (2014). Acute Lymphoblastic Leukemia with Mature B-Cell Phenotype and t(9;11;11)(p22;q23;p11.2): A Case Study and Literature Review. Annals of Laboratory Medicine. 34(2). 166–169. 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.

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