Fuli Yu
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 17
- Genetic Associations and Epidemiology 9
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 4
- Evolution and Genetic Dynamics 3
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- Genomics and Phylogenetic Studies 4
- Gene expression and cancer classification 3
- Co-authors
- Richard A. Gibbs (17 shared papers)Jin Yu (7 shared papers)Cristian Coarfa (6 shared papers)Aleksandar Milosavljevic (6 shared papers)Donna M. Muzny (10 shared papers)Eric Boerwinkle (9 shared papers)Sameer Paithankar (3 shared papers)Uday S. Evani (4 shared papers)
- Journals
- BMC Genomics (6 papers)BMC Bioinformatics (4 papers)PLoS ONE (3 papers)Blood (3 papers)Human Mutation (3 papers)
- Partner nations
- United StatesChinaTaiwan
In The Last Decade
Fuli Yu
40 papers receiving 1.5k citations
Fuli Yu's Hit Papers
Peers
Comparison fields: 5 of 111
- Genetics 632
- Pediatrics, Perinatology and Child Health 232
- Cancer Research 133
- Hematology 98
- Molecular Biology 571
Countries citing papers authored by Fuli Yu
This map shows the geographic impact of Fuli Yu'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 Fuli Yu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fuli Yu more than expected).
Fields of papers citing papers by Fuli Yu
This network shows the impact of papers produced by Fuli Yu. 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 Fuli Yu. The network helps show where Fuli Yu may publish in the future.
Co-authors
The 25 scholars most cited alongside Fuli Yu, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes Hit paper breakdown → | 2019 | 168 |
| 2 | 2012 | 161 | |
| 3 | 2009 | 126 | |
| 4 | 2014 | 112 | |
| 5 | 2013 | 91 | |
| 6 | 2018 | 78 | |
| 7 | 2013 | 65 | |
| 8 | 2018 | 59 | |
| 9 | 2010 | 56 | |
| 10 | 2015 | 54 | |
| 11 | 2007 | 50 | |
| 12 | 2011 | 40 | |
| 13 | 2005 | 40 | |
| 14 | 2012 | 39 | |
| 15 | 2010 | 37 | |
| 16 | 2012 | 29 | |
| 17 | 2017 | 29 | |
| 18 | 2022 | 29 | |
| 19 | 2017 | 28 | |
| 20 | 2011 | 27 |
About Fuli Yu
Fuli Yu is a scholar working on Genetics, Molecular Biology, Hematology, Immunology and Computer Networks and Communications, having authored 41 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Platelet Disorders and Treatments (4 papers), Genomics and Phylogenetic Studies (4 papers), Gene expression and cancer classification (3 papers), Blood groups and transfusion (3 papers) and Evolution and Genetic Dynamics (3 papers). The work is most often cited by research in Genetics (632 citations), Pediatrics, Perinatology and Child Health (232 citations), Cancer Research (133 citations), Hematology (98 citations) and Molecular Biology (571 citations). Fuli Yu has collaborated with scholars based in United States, China and Taiwan. Frequent co-authors include Richard A. Gibbs, Jin Yu, Cristian Coarfa, Aleksandar Milosavljevic, Donna M. Muzny, Eric Boerwinkle, Sameer Paithankar, Uday S. Evani, Danny Challis and Andrew R. Jackson. Their work appears in journals such as BMC Genomics, BMC Bioinformatics, PLoS ONE, Blood and Human Mutation.
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.