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For: Hu X, Guo R, Guo J, Qi Z, Li W, Hao C. Parallel Tests of Whole Exome Sequencing and Copy Number Variant Sequencing Increase the Diagnosis Yields of Rare Pediatric Disorders. Front Genet 2020;11:473. [PMID: 32595695 DOI: 10.3389/fgene.2020.00473] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Liu R, Huang Y, Li C, Wang P, Wang Y, Zhang L. A novel nonsense mutation in PPP2R5D is associated with neurodevelopmental disorders and shows incomplete penetrance in a Chinese pedigree. Clinical Neurology and Neurosurgery 2022. [DOI: 10.1016/j.clineuro.2022.107524] [Reference Citation Analysis]
2 Liu Y, Hao C, Li K, Hu X, Gao H, Zeng J, Guo R, Liu J, Guo J, Li Z, Qi Z, Jia X, Li W, Qian S. Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of China. Front Genet 2021;12:677699. [PMID: 34539730 DOI: 10.3389/fgene.2021.677699] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Arteche-López A, Álvarez-Mora MI, Sánchez Calvin MT, Lezana Rosales JM, Palma Milla C, Gómez Rodríguez MJ, Gomez Manjón I, Blázquez A, Juarez Rufián A, Ramos Gómez P, Sierra Tomillo O, Hidalgo Mayoral I, Pérez de la Fuente R, Posada Rodríguez IJ, González Granado LI, Martin MA, Quesada-Espinosa JF, Moreno-García M. Biallelic variants in genes previously associated with dominant inheritance: CACNA1A, RET and SLC20A2. Eur J Hum Genet 2021. [PMID: 34267336 DOI: 10.1038/s41431-021-00919-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Hao C, Guo R, Liu J, Hu X, Guo J, Yao Y, Zhao Z, Qi Z, Yin J, Chen L, Wang H, Xu B, Li W. Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study. Hum Mutat 2021;42:891-900. [PMID: 33942430 DOI: 10.1002/humu.24216] [Reference Citation Analysis]