Murim Choi, Ph.D.
Affiliations: | 2001-2006 | Duke University, Durham, NC | |
| 2013- | Seoul National University, Seoul, South Korea |
Area:
Developmental Biology, Craniofacial, Neurobiology, Mouse, ZebrafishWebsite:
https://www.snugenomics.com/peopleGoogle:
"Murim Choi"Bio:
https://scholar.google.com/citations?user=eg5nmmAAAAAJ&hl=en
Mean distance: 6.87 | S | N | B | C | P |
Cross-listing: danioTree
Parents
Sign in to add mentor| 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) | |
Children
Sign in to add trainee| Sangmoon Lee | grad student | 2013-2018 | Seoul National University (GenetiTree) |
| Yongjin Yoo | grad student | 2013-2018 | Seoul National Univerity |
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Publications
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| Kiryluk K, Sanchez-Rodriguez E, Zhou XJ, et al. (2023) Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy. Nature Genetics |
| Park S, Lee H, Lee J, et al. (2022) RNA-seq profiling of tubulointerstitial tissue reveals a potential therapeutic role of dual anti-phosphatase 1 in glomerulonephritis. Journal of Cellular and Molecular Medicine |
| Yoo Y, Park SY, Jo EB, et al. (2021) Overexpression of Replication-Dependent Histone Signifies a Subset of Dedifferentiated Liposarcoma with Increased Aggressiveness. Cancers. 13 |
| Lee S, Shin CH, Lee J, et al. (2021) Somatic uniparental disomy mitigates the most damaging EFL1 allele combination in Shwachman-Diamond syndrome. Blood |
| Kour S, Rajan DS, Fortuna TR, et al. (2021) Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder. Nature Communications. 12: 2558 |
| Kim JS, Jeon H, Lee H, et al. (2021) Biallelic novel mutations of the COL27A1 gene in a patient with Steel syndrome. Human Genome Variation. 8: 17 |
| 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 |
| Chung HL, Wangler MF, Marcogliese PC, et al. (2020) Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron |
| Lee JS, Yoo T, Lee M, et al. (2020) Genetic heterogeneity in Leigh syndrome: Highlighting treatable and novel genetic causes. Clinical Genetics |