Chia‐Cheng Hung
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Hemoglobinopathies and Related Disorders
- Connective tissue disorders research
Papers in
-
- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 4
- Genetics 12
- Neurogenetic and Muscular Disorders Research 6
- Hemoglobinopathies and Related Disorders 5
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Yi‐Ning Su (36 shared papers)Chien‐Nan Lee (23 shared papers)Wu‐Shiun Hsieh (11 shared papers)Win-Li Lin (10 shared papers)Po‐Nien Tsao (7 shared papers)Chih‐Ping Chen (10 shared papers)Wen‐Fang Cheng (9 shared papers)Shin‐Yu Lin (8 shared papers)
- Journals
- Electrophoresis (4 papers)Human Mutation (3 papers)Clinical Chemistry (2 papers)Prenatal Diagnosis (2 papers)Clinical Biochemistry (2 papers)
- Partner nations
- TaiwanUnited StatesGermany
In The Last Decade
Chia‐Cheng Hung
38 papers receiving 779 citations
Peers
Comparison fields: 5 of 66
- Sensory Systems 103
- Genetics 157
- Hematology 78
- Pediatrics, Perinatology and Child Health 114
- Endocrine and Autonomic Systems 39
Countries citing papers authored by Chia‐Cheng Hung
This map shows the geographic impact of Chia‐Cheng Hung'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 Chia‐Cheng Hung with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chia‐Cheng Hung more than expected).
Fields of papers citing papers by Chia‐Cheng Hung
This network shows the impact of papers produced by Chia‐Cheng Hung. 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 Chia‐Cheng Hung. The network helps show where Chia‐Cheng Hung may publish in the future.
Co-authors
The 25 scholars most cited alongside Chia‐Cheng Hung, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 64 | |
| 2 | 2006 | 57 | |
| 3 | 2005 | 53 | |
| 4 | 2011 | 46 | |
| 5 | Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma. | 2015 | 42 |
| 6 | 2011 | 36 | |
| 7 | 2003 | 32 | |
| 8 | 2018 | 31 | |
| 9 | 2007 | 27 | |
| 10 | 2009 | 26 | |
| 11 | 2019 | 25 | |
| 12 | 2011 | 23 | |
| 13 | 2005 | 22 | |
| 14 | 2007 | 22 | |
| 15 | 2011 | 22 | |
| 16 | 2005 | 21 | |
| 17 | 2005 | 20 | |
| 18 | 2013 | 19 | |
| 19 | 2009 | 19 | |
| 20 | 2007 | 18 |
About Chia‐Cheng Hung
Chia‐Cheng Hung is a scholar working on Molecular Biology, Genetics, Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 38 papers that have together received 795 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (6 papers), Hemoglobinopathies and Related Disorders (5 papers), Epigenetics and DNA Methylation (4 papers), Prenatal Screening and Diagnostics (4 papers), RNA modifications and cancer (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Blood groups and transfusion (3 papers) and Genetic Neurodegenerative Diseases (3 papers). The work is most often cited by research in Sensory Systems (103 citations), Genetics (157 citations), Hematology (78 citations), Pediatrics, Perinatology and Child Health (114 citations) and Endocrine and Autonomic Systems (39 citations). Chia‐Cheng Hung has collaborated with scholars based in Taiwan, United States and Germany. Frequent co-authors include Yi‐Ning Su, Chien‐Nan Lee, Wu‐Shiun Hsieh, Win-Li Lin, Po‐Nien Tsao, Chih‐Ping Chen, Wen‐Fang Cheng, Shin‐Yu Lin, Shu‐Chin Chien and Chen‐Chi Wu. Their work appears in journals such as Electrophoresis, Human Mutation, Clinical Chemistry, Prenatal Diagnosis and Clinical Biochemistry.
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.