Boram Kim

Clinical assistant professor

Samsung Medical Center

South Korea

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About

Boram Kim is a Clinical Assistant Professor at Samsung Medical Center in South Korea. His research areas include hematologic malignancies, T-cell lymphoma diagnostics, and genetic variants in pediatric myeloproliferative neoplasms. He has contributed to significant studies on somatic variants and chromosomal microarray technologies, providing insights into the clinical applicability of advanced diagnostic methods.

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Seoul National University Hospital

SOUTH KOREA

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Boram Kim

Research Interests

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Articles (20)

Flow Cytometric Assessment of TRBC1 Expression for the Diagnosis of T‐Cell Lymphoma: Clinical Utility and Pitfalls Related to T‐Cell Clones of Uncertain Significance

High-resolution Chromosomal Microarray with Diagnostic Potential for Detecting Exon-level Copy Number Variations Using Targeted and Non-targeted Approaches

Intrafamilial variability in Diamond-Blackfan anemia with a novel canonical splice-site variant in the <i>RPL11</i> gene

Genetic Variants in Pediatric Myeloproliferative Neoplasms Revealed by Next Generation Sequencing.

Assessing the clinical applicability of dimensionality reduction algorithms in flow cytometry for hematologic malignancies

TP53 Mutation Status in Myelodysplastic Neoplasm and Acute Myeloid Leukemia: Impact of Reclassification Based on the 5th WHO and International Consensus Classification Criteria: A Korean Multicenter Study

Correction to: ETV6::ABL1 fusion: from overlooked minor clone in myeloproliferative neoplasm to major player in leukemic transformation

Rare Non-Cryptic NUP98 Rearrangements Associated With Myeloid Neoplasms and Their Poor Prognostic Impact

Genetic Landscape and Clinical Manifestations of Multiple Endocrine Neoplasia Type 1 in a Korean Cohort: A Multicenter Retrospective Analysis

Recommendations for Interpretation and Reporting of Somatic Variants in Hematologic Malignancies

Prevalence and founder effect of DRC1 exon 1–4 deletion in Korean patients with primary ciliary dyskinesia

Cryptic KMT2A/MLLT10 fusion detected by next-generation sequencing in a case of pediatric acute megakaryoblastic leukemia

The Korean Genetic Diagnosis Program for Rare Disease Phase II: outcomes of a 6-year national project

Immunological Characteristics of Unvaccinated Patients with COVID-19 in the Early Pandemic Period

Coffin-Siris Syndrome: Genotype-Phenotype Clustering and Novel Variants

First Korean Case of Weaver Syndrome Along with Neuroblastoma and Genetic Confirmation of EZH2 Variant

SARS-CoV-2 shedding dynamics and transmission in immunosuppressed patients

A Novel Missense PRKAR1A Variant Causes Carney Complex

A Korean Child with Schaaf-Yang Syndrome Presented with Hearing Impairment: A Case Report

Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing

Collaborators (6)

YOON HWAN CHANG

Ee-Kyung Kim

Seung Han Shin

Sheehyun Kim

Jiwon Yun

Moon-Woo Seong

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