Murim Choi
Impact in
-
- Hormonal Regulation and Hypertension
- Genetics top 1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
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- Mitochondrial Function and Pathology 7
- RNA modifications and cancer 7
- Congenital heart defects research 6
- Ion channel regulation and function 6
- Single-cell and spatial transcriptomics 4
- Genetics 31
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 5
- Co-authors
- Richard P. Lifton (23 shared papers)Carol Nelson‐Williams (10 shared papers)Ute I. Scholl (6 shared papers)Shrikant Mane (9 shared papers)John Klingensmith (6 shared papers)Anita Farhi (3 shared papers)Weizhen Ji (2 shared papers)Tobias Carling (6 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (6 papers)Experimental & Molecular Medicine (4 papers)Nature Genetics (3 papers)Brain and Development (3 papers)Human Molecular Genetics (2 papers)
- Partner nations
- South KoreaUnited StatesPuerto Rico
In The Last Decade
Murim Choi
111 papers receiving 6.1k citations
Murim Choi's Hit Papers
Peers
Comparison fields: 5 of 132
- Endocrinology, Diabetes and Metabolism 974
- Genetics 1.3k
- Molecular Biology 3.0k
- Nephrology 246
- Cancer Research 426
Countries citing papers authored by Murim Choi
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
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-authors
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.
All Works
Showing the 20 most-cited of 115 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic diagnosis by whole exome capture and massively parallel DNA sequencing Hit paper breakdown → | 2009 | 892 |
| 2 | K + Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension Hit paper breakdown → | 2011 | 694 |
| 3 | 2014 | 362 | |
| 4 | 2009 | 358 | |
| 5 | 2015 | 268 | |
| 6 | 2011 | 188 | |
| 7 | 2006 | 183 | |
| 8 | 2014 | 178 | |
| 9 | 2021 | 150 | |
| 10 | 2013 | 144 | |
| 11 | 2004 | 138 | |
| 12 | 2017 | 126 | |
| 13 | 2010 | 117 | |
| 14 | 2012 | 108 | |
| 15 | 2014 | 106 | |
| 16 | 2017 | 91 | |
| 17 | 2014 | 89 | |
| 18 | 2014 | 82 | |
| 19 | 2012 | 64 | |
| 20 | 2019 | 57 |
About Murim Choi
Murim Choi is a scholar working on Molecular Biology, Genetics, Surgery, Epidemiology and Physiology, having authored 115 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (8 papers), Mitochondrial Function and Pathology (7 papers), RNA modifications and cancer (7 papers), Congenital heart defects research (6 papers), Ion channel regulation and function (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Single-cell and spatial transcriptomics (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (974 citations), Genetics (1.3k citations), Molecular Biology (3.0k citations), Nephrology (246 citations) and Cancer Research (426 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, Paul Zumbo and Sami A. Sanjad. Their work appears in journals such as Proceedings of the National Academy of Sciences, Experimental & Molecular Medicine, Nature Genetics, Brain and Development and Human Molecular Genetics.
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.