Sung‐Hae Kang
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 5
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- Congenital heart defects research 5
- Epigenetics and DNA Methylation 3
- Co-authors
- Sau Wai Cheung (18 shared papers)Chad A. Shaw (11 shared papers)Ankita Patel (15 shared papers)James R. Lupski (10 shared papers)Arthur L. Beaudet (6 shared papers)Paweł Stankiewicz (8 shared papers)Weimin Bi (6 shared papers)Amber N. Pursley (7 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)PLoS Genetics (3 papers)Prenatal Diagnosis (2 papers)Journal of Clinical Oncology (1 paper)Molecular Cell (1 paper)
- Partner nations
- United StatesPolandFrance
In The Last Decade
Sung‐Hae Kang
30 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 72
- Genetics 763
- Pediatrics, Perinatology and Child Health 282
- Molecular Biology 628
- Urology 47
- Genetics 66
Countries citing papers authored by Sung‐Hae Kang
This map shows the geographic impact of Sung‐Hae Kang'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 Sung‐Hae Kang with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sung‐Hae Kang more than expected).
Fields of papers citing papers by Sung‐Hae Kang
This network shows the impact of papers produced by Sung‐Hae Kang. 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 Sung‐Hae Kang. The network helps show where Sung‐Hae Kang may publish in the future.
Co-authors
The 25 scholars most cited alongside Sung‐Hae Kang, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 156 | |
| 2 | 2015 | 152 | |
| 3 | 2009 | 133 | |
| 4 | 2010 | 108 | |
| 5 | 2009 | 103 | |
| 6 | 2010 | 81 | |
| 7 | 2013 | 78 | |
| 8 | 2008 | 65 | |
| 9 | 2012 | 64 | |
| 10 | 2009 | 56 | |
| 11 | 2011 | 46 | |
| 12 | 2007 | 45 | |
| 13 | 2014 | 42 | |
| 14 | 2014 | 35 | |
| 15 | 2015 | 35 | |
| 16 | 2010 | 29 | |
| 17 | 2010 | 25 | |
| 18 | 2011 | 24 | |
| 19 | 2007 | 20 | |
| 20 | 2008 | 19 |
About Sung‐Hae Kang
Sung‐Hae Kang is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Pathology and Forensic Medicine, having authored 30 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (5 papers), Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (5 papers), Cancer Genomics and Diagnostics (3 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Genetics (763 citations), Pediatrics, Perinatology and Child Health (282 citations), Molecular Biology (628 citations), Urology (47 citations) and Genetics (66 citations). Sung‐Hae Kang has collaborated with scholars based in United States, Poland and France. Frequent co-authors include Sau Wai Cheung, Chad A. Shaw, Ankita Patel, James R. Lupski, Arthur L. Beaudet, Paweł Stankiewicz, Weimin Bi, Amber N. Pursley, Carlos A. Bacino and A. Craig Chinault. Their work appears in journals such as European Journal of Human Genetics, PLoS Genetics, Prenatal Diagnosis, Journal of Clinical Oncology and Molecular Cell.
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.