# Murim Choi

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/murim-choi/

## Facts

| Field | Value |
| --- | --- |
| Citations | 31,731 |
| Field | Genomics and Rare Diseases |
| h-index | 65 |
| i10-index | 148 |
| Last Known Institution | Seoul National University |
| OpenAlex ID | https://openalex.org/A5001348492 |
| ORCID iD | https://orcid.org/0000-0002-9195-1455 |
| Works | 323 |

## Researcher papers

Showing 12 of 15.

- [Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism](https://scholariq.org/papers/multiple-recurrent-de-novo-cnvs-including-duplications-of-the-7q11-23-williams/)
- [Co-occurring Genomic Alterations Define Major Subsets of <i>KRAS</i> -Mutant Lung Adenocarcinoma with Distinct Biology, Immune Profiles, and Therapeutic Vulnerabilities](https://scholariq.org/papers/co-occurring-genomic-alterations-define-major-subsets-of-i-kras-i-mutant-lung/)
- [Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i>](https://scholariq.org/papers/genomic-analysis-of-non-i-nf2-i-meningiomas-reveals-mutations-in-i-traf7-i-i/)
- [Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities](https://scholariq.org/papers/mutations-in-kelch-like-3-and-cullin-3-cause-hypertension-and-electrolyte/)
- [Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens](https://scholariq.org/papers/discovery-of-new-risk-loci-for-iga-nephropathy-implicates-genes-involved-in/)
- [Genome-wide association study identifies susceptibility loci for IgA nephropathy](https://scholariq.org/papers/genome-wide-association-study-identifies-susceptibility-loci-for-iga-nephropathy/)
- [Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism](https://scholariq.org/papers/somatic-and-germline-cacna1d-calcium-channel-mutations-in-aldosterone-producing/)
- [Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations](https://scholariq.org/papers/whole-exome-sequencing-identifies-recessive-wdr62-mutations-in-severe-brain/)
- [Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome](https://scholariq.org/papers/recessive-mutations-in-dgke-cause-atypical-hemolytic-uremic-syndrome/)
- [Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis](https://scholariq.org/papers/geographic-differences-in-genetic-susceptibility-to-iga-nephropathy-gwas/)
- [Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism](https://scholariq.org/papers/recurrent-gain-of-function-mutation-in-calcium-channel-cacna1h-causes-early/)
- [ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption](https://scholariq.org/papers/adck4-mutations-promote-steroid-resistant-nephrotic-syndrome-through-coq10/)

## Researcher topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [RNA modifications and cancer](https://scholariq.org/topics/rna-modifications-and-cancer/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Cancer Genomics and Diagnostics](https://scholariq.org/topics/cancer-genomics-and-diagnostics/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

## Researcher university

- [Seoul National University](https://scholariq.org/institutions/seoul-national-university/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.