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Cited by in F6Publishing
For: . Next-Generation Sequencing to Diagnose Suspected Genetic Disorders. N Engl J Med 2019;380:200-1. [DOI: 10.1056/nejmc1814955] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Li X, Peng B, Hou C, Li J, Zeng Y, Wu W, Liao Y, Tian Y, Chen WX. Novel compound heterozygous TARS2 variants in a Chinese family with mitochondrial encephalomyopathy: a case report. BMC Med Genet 2020;21:217. [PMID: 33153448 DOI: 10.1186/s12881-020-01149-0] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Kim WJ, Shin HL, Kim BS, Kim HJ, Ryoo HM. RUNX2-modifying enzymes: therapeutic targets for bone diseases. Exp Mol Med 2020;52:1178-84. [PMID: 32788656 DOI: 10.1038/s12276-020-0471-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
3 Zhao Y, Fang X, Fan Y, Sun Y, He L, Xu M, Xu G, Li Y, Huang Y, Yu Y, Geng H. Integration of exome sequencing and metabolic evaluation for the diagnosis of children with urolithiasis. World J Urol 2021;39:2759-65. [PMID: 32936332 DOI: 10.1007/s00345-020-03449-9] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Lv JJ, Su W, Chen XY, Yu Y, Xu X, Xu CD, Deng X, Huang JB, Wang XQ, Xiao Y. Autosomal recessive 333 base pair interleukin 10 receptor alpha subunit deletion in very early-onset inflammatory bowel disease. World J Gastroenterol 2021; 27(44): 7705-7715 [PMID: 34908808 DOI: 10.3748/wjg.v27.i44.7705] [Reference Citation Analysis]