Murim Choi

30.9k citations

112 papers · 5.9k indexed · 2 hit papers · h-index 35

Impact in

Endocrinology, Diabetes and Metabolism top 1%
- Hormonal Regulation and Hypertension
Genetics top 1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 38
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 5
Aging 2

Co-authors: Richard P. Lifton Carol Nelson‐Williams Ute I. Scholl Shrikant Mane John Klingensmith Anita Farhi Weizhen Ji Tobias Carling
Journals: Proceedings of the National Academy of Sciences (5 papers)Experimental & Molecular Medicine (4 papers)Brain and Development (3 papers)Nature Genetics (3 papers)Molecules and Cells (2 papers)
Partner nations: South Korea United States Puerto Rico

In The Last Decade

Murim Choi

107 papers receiving 5.8k citations

Hit Papers

align trajectories log scale

K ⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension 2011 · 679 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2011 Science
2009 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Murim Choi

Since Specialization

Citations

This map shows the geographic impact of Murim Choi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Murim Choi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Murim Choi more than expected).

Fields of papers citing papers by Murim Choi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Murim Choi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Murim Choi. The network helps show where Murim Choi may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Murim Choi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Murim Choi Line = papers co-authored together Murim Choi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Role of expression quantitative trait loci (eQTL) in understanding genetic mechanisms underlying common complex diseases Molecules and Cells ·Devie Siauw Meiline, Murim Choi, Ashutosh Tiwari	2025	0
2	Inhibiting EZH2 complements steroid effects in Duchenne muscular dystrophy Science Advances ·Ghosh Ajoy, Rongzhang Xie, D Metcalf, On Profinite Quandles Alexander W. Byard, 敦本庄, Qing-Wei Wang, F.C Schüller, Dayoung Ko, Jae‐Kyung Won, Anna Cho, Inkyung Jung, Chul‐Hwan Lee, Jeongbin Park, Hyun‐Young Kim, Jong‐Hee Chae, Murim Choi	2025	0
3	Normalization of network activity in an epilepsy model with a constitutively active GABBR2 variant Brain ·Michał Stawarski, Daniel Ulrich, Abdeslem Ettaouil, Jochen Schwenk, Phil Davignon, 攻雄橋本, Kazumi Tsureishi, Mehdi Tafti, Yoon Jeon, Ho Lee, Je Kyung Seong, Murim Choi, Robert Lütjens, Martin Gassmann, Bernd Fakler, Tania Rinaldi Barkat, Bernhard Bettler	2025	0
4	Increased inflammatory signature in myeloid cells of non-small cell lung cancer patients with high clonal hematopoiesis burden eLife ·Katherine Muise, Pedro Garcia Abilleira de Castro, Hichem Zouater, Yeon Jeong Kim, Woong‐Yang Park, Se‐Hoon Lee, Murim Choi	2024	5
5	Biallelic novel mutations of the COL27A1 gene in a patient with Steel syndrome Human Genome Variation ·U Craemer, И. В. Кубланов, Hyeran Lee, Jung Min Ko, Yonghwan Kim, Murim Choi, Gen Nishimura, Gerald L. Gibson, Tae‐Joon Cho	2021	1
6	Genetic heterogeneity in Leigh syndrome: Highlighting treatable and novel genetic causes Clinical Genetics ·Jin Sook Lee, Taekyeong Yoo, Moses Lee, Youngha Lee, Luke Nugent, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Murim Choi, Jong‐Hee Chae	2020	54
7	Identifying germline APOBEC3B deletion and immune phenotype in Korean patients with operable breast cancer Breast Cancer Research and Treatment ·Se Hyun Kim, Soomin Ahn, Koung Jin Suh, Yu Jung Kim, So Yeon Park, Eunyoung Kang, Eun‐Kyu Kim, In Ah Kim, Sumin Chae, Murim Choi, Jee Hyun Kim	2020	2
8	IL23-Producing Human Lung Cancer Cells Promote Tumor Growth via Conversion of Innate Lymphoid Cell 1 (ILC1) into ILC3 Clinical Cancer Research ·Jaemoon Koh, Hye Young Kim, Youngha Lee, In Kyu Park, Chang Hyun Kang, Young Tae Kim, Ji-Eun Kim, Murim Choi, Won‐Woo Lee, Yoon Kyung Jeon, Doo Hyun Chung	2019	57
9	Clinical and genetic characteristics of Korean patients with IARS2-related disorders Jin Sook Lee, Man Jin Kim, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Murim Choi, Moon‐Woo Seong, Jong‐Hee Chae	2019	5
10	Diagnostic Challenges Associated with GLUT1 Deficiency: Phenotypic Variabilities and Evolving Clinical Features Yonsei Medical Journal ·Hyuna Kim, Jin Sook Lee, Youngha Lee, Soo Yeon Kim, Byung Chan Lim, Ki Joong Kim, Murim Choi, Jong‐Hee Chae	2019	21
11	A family with NKX2.5 gene mutations presenting as familial atrial septal defect and atrioventricular block: A case report Youn Young Choi, D JONES, Gi Beom Kim, Mi Kyoung Song, Sang Yoon Lee, Eun Jung Bae, Murim Choi, Young‐Sook Kim	2018	1
12	Isolated polycystic liver disease genes define effectors of polycystin-1 function Journal of Clinical Investigation ·Whitney Besse, Ke Dong, Jungmin Choi, Sohan Punia, Sorin V. Fedeles, Murim Choi, Anna‐Rachel Gallagher, Emily Huang, Ashima Gulati, James Knight, Shrikant Mane, Esa Tahvanainen, Pia Tahvanainen, Simone Sanna‐Cherchi, Richard P. Lifton, Terry Watnick, York Pei, Vicente E. Torres, Stefan Somlo	2017	123
13	Identification of Somatic Mutations in Parathyroid Tumors Using Whole-Exome Sequencing The Journal of Clinical Endocrinology & Metabolism ·M. Kyle Cromer, Lee F. Starker, Murim Choi, Robert Udelsman, Carol Nelson‐Williams, Richard P. Lifton, Tobias Carling	2012	107
14	K ⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension Science ·Murim Choi, Ute I. Scholl, Peng Yue, Peyman Björklund, Bixiao Zhao, Carol Nelson‐Williams, Weizhen Ji, Yoonsang Cho, Aniruddh P. Patel, Clara J. Men, Elias Lolis, Max Wisgerhof, David S. Geller, Shrikant Mane, Per Hellman, Gunnar Westin, Göran Åkerström, Wen‐Hui Wang, Tobias Carling, Richard P. Lifton Hit paper breakdown →	2011	679
15	Mitotic Recombination in Patients with Ichthyosis Causes Reversion of Dominant Mutations in KRT10 Science ·Keith A. Choate, Yin Lu, Jing Zhou, Murim Choi, Peter M. Elias, Anita Farhi, Carol Nelson‐Williams, Debra Crumrine, Mary L. Williams, Amy J. Nopper, Alanna F. Bree, Leonard M. Milstone, Richard P. Lifton	2010	116
16	Genetic diagnosis by whole exome capture and massively parallel DNA sequencing Proceedings of the National Academy of Sciences ·Murim Choi, Ute I. Scholl, Weizhen Ji, Meister Katharina, Irina R. Tikhonova, Paul Zumbo, Ahmet Nayır, Ayşı̇n Bakkaloğlu, Seza Özen, Sami A. Sanjad, Carol Nelson‐Williams, Anita Farhi, Shrikant Mane, Richard P. Lifton Hit paper breakdown →	2009	885
17	Morphogenesis of the trachea and esophagus: current players and new roles for noggin and Bmps Differentiation ·Jianwen Que, Murim Choi, Joshua W. Ziel, John Klingensmith, Brigid L.M. Hogan	2006	181
18	BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium Development ·Rolf W. Stottmann, Murim Choi, Yuji Mishina, Erik N. Meyers, John Klingensmith	2004	138
19	Multiple Activities of Oleate-Activated Phospholipase D Exist in Rat Brain Microsomes Solubilized by Decanoyl N-Methylglucamide Bulletin of the Korean Chemical Society ·Oleksandra Shalina, Д.В. Сорокин, Murim Choi	1998	1
20	PURIFICATION AND CHARACTERIZATION OF THE RECOMBINANT ARABIDOPSIS THALIANA ACETOLACTATE SYNTHASE Bulletin of the Korean Chemical Society ·Kyungae Jo, Sungyoul Hong, Murim Choi, Soo‐Ik Chang, Y. Choi, R. D	1997	2

About Murim Choi

Murim Choi is a scholar working on Genetics, Aging, Molecular Biology, Nephrology and Cell Biology, having authored 112 papers that have together received 5.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers), RNA modifications and cancer (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), Ion channel regulation and function (6 papers), Congenital heart defects research (6 papers), Liver Disease Diagnosis and Treatment (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.0k citations), Genetics (1.5k citations), Molecular Biology (3.2k citations), Nephrology (259 citations) and Cancer Research (493 citations). Murim Choi has collaborated with scholars based in South Korea, United States and Puerto Rico. Frequent co-authors include Richard P. Lifton, Carol Nelson‐Williams, Ute I. Scholl, Shrikant Mane, John Klingensmith, Anita Farhi, Weizhen Ji, Tobias Carling, Irina R. Tikhonova and Ayşı̇n Bakkaloğlu. Their work appears in journals such as Proceedings of the National Academy of Sciences, Experimental & Molecular Medicine, Brain and Development, Nature Genetics and Molecules and Cells.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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