Yi‐Ning Su
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
- Hemoglobinopathies and Related Disorders
Papers in
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- Prenatal Screening and Diagnostics 53
- Genetics 51
- Genomic variations and chromosomal abnormalities 16
- Connective tissue disorders research 14
- Genomics and Rare Diseases 11
- Neurogenetic and Muscular Disorders Research 7
- Genetic Syndromes and Imprinting 7
- Hemoglobinopathies and Related Disorders 6
- Co-authors
- Chien‐Nan Lee (50 shared papers)Wu‐Shiun Hsieh (33 shared papers)Chih‐Ping Chen (67 shared papers)Chia‐Cheng Hung (38 shared papers)Wen‐Fang Cheng (25 shared papers)Pau‐Chung Chen (15 shared papers)Wayseen Wang (55 shared papers)Chi‐An Chen (19 shared papers)
- Journals
- Prenatal Diagnosis (7 papers)Taiwanese Journal of Obstetrics and Gynecology (56 papers)Human Mutation (4 papers)Electrophoresis (4 papers)The Journal of Pediatrics (4 papers)
- Partner nations
- TaiwanUnited StatesUnited Kingdom
In The Last Decade
Yi‐Ning Su
181 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 121
- Pediatrics, Perinatology and Child Health 603
- Genetics 210
- Sensory Systems 119
- Genetics 495
- Endocrine and Autonomic Systems 79
Countries citing papers authored by Yi‐Ning Su
This map shows the geographic impact of Yi‐Ning Su'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 Yi‐Ning Su with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Yi‐Ning Su more than expected).
Fields of papers citing papers by Yi‐Ning Su
This network shows the impact of papers produced by Yi‐Ning Su. 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 Yi‐Ning Su. The network helps show where Yi‐Ning Su may publish in the future.
Co-authors
The 25 scholars most cited alongside Yi‐Ning Su, 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 181 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 115 | |
| 2 | Nationwide singleton birth weight percentiles by gestational age in Taiwan, 1998-2002. | 2006 | 108 |
| 3 | 2003 | 76 | |
| 4 | 2016 | 70 | |
| 5 | 2007 | 67 | |
| 6 | 2009 | 64 | |
| 7 | 2006 | 61 | |
| 8 | 2005 | 56 | |
| 9 | 2004 | 55 | |
| 10 | 2007 | 55 | |
| 11 | Targeted next-generation sequencing of cancer genes identified frequent TP53 and ATRX mutations in leiomyosarcoma. | 2015 | 53 |
| 12 | 2013 | 49 | |
| 13 | Serum mesothelin in epithelial ovarian carcinoma: a new screening marker and prognostic factor. | 2007 | 43 |
| 14 | 2007 | 43 | |
| 15 | 2005 | 42 | |
| 16 | 2011 | 42 | |
| 17 | 2012 | 42 | |
| 18 | 2005 | 39 | |
| 19 | 2009 | 34 | |
| 20 | 2018 | 34 |
About Yi‐Ning Su
Yi‐Ning Su is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Genetics, Endocrine and Autonomic Systems and Developmental Biology, having authored 181 papers that have together received 3.2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (53 papers), Genomic variations and chromosomal abnormalities (16 papers), Connective tissue disorders research (14 papers), Genomics and Rare Diseases (11 papers), Neurogenetic and Muscular Disorders Research (7 papers), Genetic Syndromes and Imprinting (7 papers), Neuroscience of respiration and sleep (6 papers) and Hemoglobinopathies and Related Disorders (6 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (603 citations), Genetics (210 citations), Sensory Systems (119 citations), Genetics (495 citations) and Endocrine and Autonomic Systems (79 citations). Yi‐Ning Su has collaborated with scholars based in Taiwan, United States and United Kingdom. Frequent co-authors include Chien‐Nan Lee, Wu‐Shiun Hsieh, Chih‐Ping Chen, Chia‐Cheng Hung, Wen‐Fang Cheng, Pau‐Chung Chen, Wayseen Wang, Chi‐An Chen, Schu‐Rern Chern and Fon‐Jou Hsieh. Their work appears in journals such as Prenatal Diagnosis, Taiwanese Journal of Obstetrics and Gynecology, Human Mutation, Electrophoresis and The Journal of Pediatrics.
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.