Murim Choi, Ph.D.

2001-2006 Duke University, Durham, NC 
 2013- Seoul National University, Seoul, South Korea 
Developmental Biology, Craniofacial, Neurobiology, Mouse, Zebrafish
"Murim Choi"

Mean distance: 6.87


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John A. Klingensmith grad student 2006 Duke
 (On the multiple roles of BMP signaling during mammalian heart development.)
Richard P. Lifton post-doc 2007-2013 Yale (GenetiTree)


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Sangmoon Lee grad student 2013-2018 Seoul National University (GenetiTree)
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Yoo T, Joo SK, Kim HJ, et al. (2021) Disease-specific eQTL screening reveals an anti-fibrotic effect of AGXT2 in non-alcoholic fatty liver disease. Journal of Hepatology
Kang JH, Lee SH, Lee J, et al. (2021) The mutation of BCOR is highly recurrent and oncogenic in mature T-cell lymphoma. Bmc Cancer. 21: 82
Seo J, Byun MS, Yi D, et al. (2020) Genetic associations of in vivo pathology influence Alzheimer's disease susceptibility. Alzheimer's Research & Therapy. 12: 156
Kim SH, Ahn S, Suh KJ, et al. (2020) Identifying germline APOBEC3B deletion and immune phenotype in Korean patients with operable breast cancer. Breast Cancer Research and Treatment
Seo J, Lee CR, Paeng JC, et al. (2020) Biallelic mutations in ABCB1 display recurrent reversible encephalopathy. Annals of Clinical and Translational Neurology
Han JY, Kim SY, Cheon JE, et al. (2020) A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel Mutations. Journal of Clinical Neurology (Seoul, Korea). 16: 338-340
Lee JS, Yoo T, Lee M, et al. (2020) Genetic heterogeneity in Leigh syndrome: Highlighting treatable and novel genetic causes. Clinical Genetics
Lee Y, Park S, Lee JS, et al. (2020) Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population. Scientific Reports. 10: 1413
Seidel E, Walenda G, Messerschmidt C, et al. (2020) Generation and characterization of a mitotane-resistant adrenocortical cell line. Endocrine Connections
Kim H, Lee JS, Lee Y, et al. (2019) Diagnostic Challenges Associated with GLUT1 Deficiency: Phenotypic Variabilities and Evolving Clinical Features. Yonsei Medical Journal. 60: 1209-1215
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