Murim Choi

Associate Professor

Seoul National University

South Korea

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About

Dr. Murim Choi is an Associate Professor at Seoul National University, South Korea. His research focuses on genetic and nongenetic factors influencing skin traits, as well as the genetic mechanisms underlying complex diseases and metabolic dysfunctions. He has contributed to significant studies, including work on single-cell eQTL mapping in immune cells related to lung cancer and the genetic landscape of various neurological and inflammatory conditions.

Articles (14)

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2025

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2024

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2023

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2021

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2021

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2021

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2020

Collaborators (14)

Sangmoon Lee

University of California, San Diego

UNITED STATES

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Yongjin Yoo

Assistant Professor

Korea University

SOUTH KOREA

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Hyun Woo Lee

SOUTH KOREA

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Kon Chu

Professor

Seoul National University Hospital

SOUTH KOREA

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Soon-Tae Lee

Professor

Seoul National University Hospital

SOUTH KOREA

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Deog Kyeom Kim

SOUTH KOREA

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Soo Heon Kwak

Seoul National University Hospital

SOUTH KOREA

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Hyungtai Sim

Seoul National University

SOUTH KOREA

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Vincent Cantagrel

Université Paris Cité

FRANCE

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Goh Eun Chung

SOUTH KOREA

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Bo Kyung Koo

Associate Professor

Seoul National University Hospital

SOUTH KOREA

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Jinsoo Seo

Assistant Professor

Daegu Gyeongbuk Institute of Science and Technology

SOUTH KOREA

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Won Kim

SOUTH KOREA

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Dong Hyeon Lee

Assistant Professor

Seoul National University Hospital

SOUTH KOREA

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Murim Choi

Research Interests

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About

Articles (14)

Comprehensive Profiling of Genetic and Nongenetic Factors that Influence Skin Traits in Asian Women from 4 Countries

Role of expression quantitative trait loci (eQTL) in understanding genetic mechanisms underlying common complex diseases

Single‐cell‐eQTL mapping in circulating immune cells reveals genetic regulation of response‐associated networks in lung cancer immunotherapy

Single-cell eQTL analysis identifies genetic variation underlying metabolic dysfunction-associated steatohepatitis

Autosomal dominant HK1-related neurodevelopmental disorder with visual defects and brain anomalies (NEDVIBA): An emerging mitochondrial disorder

Increased inflammatory signature in myeloid cells of non-small cell lung cancer patients with high clonal hematopoiesis burden

Increased inflammatory signature in myeloid cells of non-small cell lung cancer patients with high clonal hematopoiesis burden

Polygenic Landscape of Cryptogenic New‐Onset Refractory Status Epilepticus: A Comprehensive Whole‐Genome Sequencing Study

Latrophilin-2 Deletion in Cardiomyocyte Disrupts Cell Junction, Leading to D-CMP

Impact of Evolutionary Changes in Nonalcoholic Fatty Liver Disease on Lung Function Decline

A logical network-based drug-screening platform for Alzheimer’s disease representing pathological features of human brain organoids

Overexpression of Replication-Dependent Histone Signifies a Subset of Dedifferentiated Liposarcoma with Increased Aggressiveness

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder

A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations

Collaborators (14)

Sangmoon Lee

Yongjin Yoo

Hyun Woo Lee

Kon Chu

Soon-Tae Lee

Deog Kyeom Kim

Soo Heon Kwak

Hyungtai Sim

Vincent Cantagrel

Goh Eun Chung

Bo Kyung Koo

Jinsoo Seo

Won Kim

Dong Hyeon Lee

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