Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (8511)
All Articles published online
|
Featured Article
|
Publishing Process of This Article
|
Dec 26, 2017 (publication date) through May 15, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Cardiology
ISSN
1949-8462
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Karunanithi Z, Vestergaard EM, Lauridsen MH. Transposition of the great arteries - a phenotype associated with 16p11.2 duplications? World J Cardiol 2017; 9(12): 848-852 [PMID: 29317992 DOI: 10.4330/wjc.v9.i12.848] |
|---|---|
| URL: | https://www.wjgnet.com/1949-8462/full/v9/i12/848.htm |
| Number | Citing Articles |
| 1 |
Alessandra Suuberg. Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2. SSRN Electronic Journal 2018; doi: 10.2139/ssrn.3185741
|
| 2 |
Majed J. Dasouki, Salma M. Wakil, Olfat Al-Harazi, Maarab Alkorashy, Nzioka P. Muiya, Editha Andres, Samya Hagos, Haya Aldusery, Nduna Dzimiri, Dilek Colak. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia. OMICS: A Journal of Integrative Biology 2020; 24(1): 16 doi: 10.1089/omi.2019.0165
|
| 3 |
Laurent Ehrlich, Siddharth K Prakash. Copy-number variation in congenital heart disease. Current Opinion in Genetics & Development 2022; 77: 101986 doi: 10.1016/j.gde.2022.101986
|
| 4 |
Mikhail Vysotskiy, Xue Zhong, Tyne W. Miller-Fleming, Dan Zhou, Nancy J. Cox, Lauren A. Weiss. Integration of genetic, transcriptomic, and clinical data provides insight into 16p11.2 and 22q11.2 CNV genes. Genome Medicine 2021; 13(1) doi: 10.1186/s13073-021-00972-1
|