Identification of genetic variants associated with clinical features of sickle cell disease-Reference-Cited by-同舟云学术

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Identification of genetic variants associated with clinical features of sickle cell disease

Published:2024-08-29 Issue:1 Volume:14 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Tsukahara Katharine,Chang Xiao,Mentch Frank,Smith-Whitley Kim,Bhandari Anita,Norris Cindy,Glessner Joseph T.,Hakonarson Hakon

Funder

National Institutes of Health

The Children’s Hospital of Philadelphia

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41598-024-70922-5.pdf

Reference42 articles.

1. Piel, F. B., Steinberg, M. H. & Rees, D. C. Sickle cell disease. N. Engl. J. Med. 376, 1561–1573. https://doi.org/10.1056/NEJMra1510865 (2017).

2. Dampier, C. et al. Health-related quality of life in children with sickle cell disease: A report from the Comprehensive Sickle Cell Centers Clinical Trial Consortium. Pediatr. Blood Cancer 55, 485–494. https://doi.org/10.1002/pbc.22497 (2010).

3. Jain, S., Bakshi, N. & Krishnamurti, L. Acute chest syndrome in children with sickle cell disease. Pediatr. Allergy Immunol. Pulmonol. 30, 191–201. https://doi.org/10.1089/ped.2017.0814 (2017).

4. Castro, O. et al. The acute chest syndrome in sickle cell disease: Incidence and risk factors: The cooperative study of sickle cell disease. Blood 84, 643–649 (1994).

5. Kato, G. J. et al. Sickle cell disease. Nat. Rev. Dis. Primers 4, 18010. https://doi.org/10.1038/nrdp.2018.10 (2018).

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