Xiao–Ning Chen

4.2k total citations · 1 hit paper
32 papers, 2.3k citations indexed

About

Xiao–Ning Chen is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Xiao–Ning Chen has authored 32 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Plant Science. Recurrent topics in Xiao–Ning Chen's work include Genomic variations and chromosomal abnormalities (14 papers), Congenital heart defects research (6 papers) and Chromosomal and Genetic Variations (6 papers). Xiao–Ning Chen is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Congenital heart defects research (6 papers) and Chromosomal and Genetic Variations (6 papers). Xiao–Ning Chen collaborates with scholars based in United States, Canada and France. Xiao–Ning Chen's co-authors include Julie R. Korenberg, Astrid Lunkes, Stefan-M. Pulst, Tamilla Nechiporuk, Íscia Lopes‐Cendes, Susan Pearlman, Sidney Starkman, Guy A. Rouleau, Georg Auburger and Suzana Gispert and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Biochemical and Biophysical Research Communications.

In The Last Decade

Xiao–Ning Chen

32 papers receiving 2.2k citations

Hit Papers

Moderate expansion of a normally biallelic trinucleotide ... 1996 2026 2006 2016 1996 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
    1996 901 citations Xiao–Ning Chen, Julie R. Korenberg et al. Nature Genetics profile →

Peers

Xiao–Ning Chen
Pascale Saugier-Véber France
Susan Kenwrick United Kingdom
Klaus Wagner Austria
Jennifer C. Moore United States
Tayfun Özçelık Türkiye
Carol Hicks United States
Ranhui Duan China
Vinodh Narayanan United States
Györgyi Szebenyi United States
Medha Gautam United States
Pascale Saugier-Véber France
Xiao–Ning Chen
Citations per year, relative to Xiao–Ning Chen Xiao–Ning Chen (= 1×) peers Pascale Saugier-Véber

Countries citing papers authored by Xiao–Ning Chen

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Xiao–Ning Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Xiao–Ning Chen. A scholar is included among the top collaborators of Xiao–Ning Chen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Xiao–Ning Chen. Xiao–Ning Chen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Chen, Xiao–Ning, Debra L. Mills, Albert M. Galaburda, et al.. (2009). William's syndrome: gene expression is related to parental origin and regional coordinate control. Journal of Human Genetics. 54(4). 193–198. 22 indexed citations
2.
Chen, Xiao–Ning, Laura Flores‐Sarnat, Gillian M. Barlow, et al.. (2006). Deletion of chromosome 21 disturbs human brain morphogenesis. Genetics in Medicine. 8(1). 1–7. 56 indexed citations
3.
Chen, Xiao–Ning & Julie R. Korenberg. (2003). BAC Resource for Molecular Cytogenetics. Molecular Cytogenetics. 204. 391–402. 4 indexed citations
4.
Barlow, Gillian M., Xiao–Ning Chen, Gary E. Lyons, et al.. (2001). Down syndrome congenital heart disease: A narrowed region and a candidate gene. Genetics in Medicine. 3(2). 91–101. 126 indexed citations
5.
Tuck‐Müller, Cathy M., Barbara K. Goodman, Shibo Li, et al.. (2001). Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel. Genetics in Medicine. 3(2). 126–131. 4 indexed citations
6.
Henegariu, Octavian, Sevilhan Artan, John M. Greally, et al.. (2001). Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies. Laboratory Investigation. 81(4). 483–491. 23 indexed citations
7.
Henegariu, Octavian, et al.. (2001). A triple color FISH technique for mouse chromosome identification. Mammalian Genome. 12(6). 462–465. 10 indexed citations
8.
Cargile, Colyn B., Iain McIntosh, Mark V. Clough, et al.. (2000). Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12). American Journal of Medical Genetics. 92(5). 328–335. 4 indexed citations
9.
Knauf, Jeffrey A., Rossella Elisei, Daria Mochly‐Rosen, et al.. (1999). Involvement of Protein Kinase Cε (PKCε) in Thyroid Cell Death. Journal of Biological Chemistry. 274(33). 23414–23425. 65 indexed citations
10.
Kilpatrick, Michael W., Caroline N. Dealy, Robert A. Kosher, et al.. (1999). A Novel Human Gene Encoding an F-box/WD40 Containing Protein Maps in the SHFM3 Critical Region on 10q24. Biochemical and Biophysical Research Communications. 261(1). 64–70. 27 indexed citations
11.
Zhang, Xiuqing, Huanming Yang, Morten J. Corydon, et al.. (1999). Localization of a Human Nucleoporin 155 Gene (NUP155) to the 5p13 Region and Cloning of Its cDNA. Genomics. 57(1). 144–151. 20 indexed citations
12.
DiDonato, Christine J., Xiao–Ning Chen, David Noya, et al.. (1997). Cloning, Characterization, and Copy Number of the Murine Survival Motor Neuron Gene: Homolog of the Spinal Muscular Atrophy-Determining Gene. Genome Research. 7(4). 339–352. 104 indexed citations
13.
Hubert, René, Steve Mitchell, Xiao–Ning Chen, et al.. (1997). BAC and PAC Contigs Covering 3.5 Mb of the Down Syndrome Congenital Heart Disease Region between D21S55 and MX1 on Chromosome 21. Genomics. 41(2). 218–226. 33 indexed citations
14.
Grover, Judy, Xiao–Ning Chen, Julie R. Korenberg, Anneliese D. Recklies, & Peter J. Roughley. (1996). The Gene Organization, Chromosome Location, and Expression of a 55-kDa Matrix Protein (PRELP) of Human Articular Cartilage. Genomics. 38(2). 109–117. 38 indexed citations
15.
Lane, Robert P., Xiao–Ning Chen, Kazuhiro Yamakawa, et al.. (1996). Characterization of a Highly Conserved Human Homolog to the Chicken Neural Cell Surface Protein Bravo/Nr-CAM That Maps to Chromosome Band 7q31. Genomics. 35(3). 456–465. 31 indexed citations
16.
Petrini, John H.J., et al.. (1995). Isolation and Characterization of the Human MRE11 Homologue. Genomics. 29(1). 80–86. 110 indexed citations
17.
Yamakawa, Kazuhiro, Steve Mitchell, René Hubert, et al.. (1995). Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3. Human Molecular Genetics. 4(4). 709–716. 49 indexed citations
18.
19.
SZTROLOVICS, Robert, Xiao–Ning Chen, Judy Grover, Peter J. Roughley, & Julie R. Korenberg. (1994). Localization of the Human Fibromodulin Gene (FMOD) to Chromosome 1q32 and Completion of the cDNA Sequence. Genomics. 23(3). 715–717. 29 indexed citations
20.
Wilkie, Thomas M., Debra J. Gilbert, A. Olsen, et al.. (1992). Evolution of the mammalian G protein α subunit multigene family. Nature Genetics. 1(2). 85–91. 210 indexed citations

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.

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