Xiao–Ning Chen
Impact in
-
- Genetic Neurodegenerative Diseases
- Developmental Neuroscience top 5%
Papers in
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- Congenital heart defects research 6
- Genomics and Chromatin Dynamics 5
- RNA Research and Splicing 5
- RNA and protein synthesis mechanisms 3
- Genetics 17
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Julie R. Korenberg (31 shared papers)Tamilla Nechiporuk (1 shared paper)Suzana Gispert (1 shared paper)Sidney Starkman (1 shared paper)Susan Pearlman (1 shared paper)Georg Auburger (1 shared paper)Stefan-M. Pulst (1 shared paper)Alex Nechiporuk (1 shared paper)
- Journals
- Genomics (12 papers)Genetics in Medicine (4 papers)Biochemical and Biophysical Research Communications (3 papers)Nature Genetics (2 papers)Genome Research (2 papers)
- Partner nations
- United StatesCanadaFrance
In The Last Decade
Xiao–Ning Chen
32 papers receiving 2.2k citations
Xiao–Ning Chen's Hit Papers
Peers
Comparison fields: 5 of 103
- Cellular and Molecular Neuroscience 920
- Developmental Neuroscience 125
- Molecular Biology 1.7k
- Neurology 361
- Genetics 181
Countries citing papers authored by Xiao–Ning Chen
This map shows the geographic impact of Xiao–Ning Chen'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 Xiao–Ning Chen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Xiao–Ning Chen more than expected).
Fields of papers citing papers by Xiao–Ning Chen
This network shows the impact of papers produced by Xiao–Ning Chen. 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 Xiao–Ning Chen. The network helps show where Xiao–Ning Chen may publish in the future.
Co-authors
The 25 scholars most cited alongside Xiao–Ning Chen, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 Hit paper breakdown → | 1996 | 901 |
| 2 | 1992 | 210 | |
| 3 | 2001 | 126 | |
| 4 | 1995 | 110 | |
| 5 | 1997 | 104 | |
| 6 | 2003 | 88 | |
| 7 | 1999 | 65 | |
| 8 | 1999 | 58 | |
| 9 | 2006 | 56 | |
| 10 | 1995 | 49 | |
| 11 | 1994 | 42 | |
| 12 | 2002 | 41 | |
| 13 | 1995 | 41 | |
| 14 | 1996 | 38 | |
| 15 | 1997 | 33 | |
| 16 | 1997 | 32 | |
| 17 | 1994 | 31 | |
| 18 | 1996 | 31 | |
| 19 | 1994 | 29 | |
| 20 | 1999 | 27 |
About Xiao–Ning Chen
Xiao–Ning Chen is a scholar working on Molecular Biology, Genetics, Plant Science, Oncology and Rheumatology, having authored 32 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (6 papers), Congenital heart defects research (6 papers), Genomics and Chromatin Dynamics (5 papers), RNA Research and Splicing (5 papers), RNA and protein synthesis mechanisms (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Williams Syndrome Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (920 citations), Developmental Neuroscience (125 citations), Molecular Biology (1.7k citations), Neurology (361 citations) and Genetics (181 citations). Xiao–Ning Chen has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Julie R. Korenberg, Tamilla Nechiporuk, Suzana Gispert, Sidney Starkman, Susan Pearlman, Georg Auburger, Stefan-M. Pulst, Alex Nechiporuk, Guy A. Rouleau and Pieter DeJong. Their work appears in journals such as Genomics, Genetics in Medicine, Biochemical and Biophysical Research Communications, Nature Genetics and Genome Research.
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.