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For: Turkmen AS, Lin S. Detecting X-linked common and rare variant effects in family-based sequencing studies. Genet Epidemiol 2021;45:36-45. [PMID: 32864779 DOI: 10.1002/gepi.22352] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 Li MK, Yuan YX, Zhu B, Wang KW, Fung WK, Zhou JY. Gene-Based Methods for Estimating the Degree of the Skewness of X Chromosome Inactivation. Genes (Basel) 2022;13. [PMID: 35627212 DOI: 10.3390/genes13050827] [Reference Citation Analysis]
2 Berg EL, Silverman JL. Animal models of autism. The Neuroscience of Autism 2022. [DOI: 10.1016/b978-0-12-816393-1.00010-5] [Reference Citation Analysis]
3 Koch AA, Rampersaud E. Determining the Genetic Component of a Disease. Genetic Analysis of Complex Diseases 2021. [DOI: 10.1002/9781119104100.ch3] [Reference Citation Analysis]