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Cited by in F6Publishing
For: Masset H, Ding J, Dimitriadou E, Debrock S, Tšuiko O, Smits K, Peeraer K, Voet T, Zamani Esteki M, Vermeesch JR. Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing. Nucleic Acids Res 2022:gkac134. [PMID: 35212381 DOI: 10.1093/nar/gkac134] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Yang L, Xu Y, Xia J, Yan H, Ding C, Shi Q, Wu Y, Liu P, Pan J, Zeng Y, Zhang Y, Chen F, Jiang H, Xu Y, Li W, Zhou C, Gao Y. Simultaneous detection of genomic imbalance in patients receiving preimplantation genetic testing for monogenic diseases (PGT-M). Front Genet 2022;13:976131. [DOI: 10.3389/fgene.2022.976131] [Reference Citation Analysis]
2 van Dijk W, Derks K, Drüsedau M, Meekels J, Koeck R, Essers R, Dreesen J, Coonen E, de Die-Smulders C, Stevens SJC, Brunner HG, van den Wijngaard A, Paulussen ADC, Zamani Esteki M. Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing. Hum Reprod 2022:deac208. [PMID: 36149256 DOI: 10.1093/humrep/deac208] [Reference Citation Analysis]
3 Xie P, Hu X, Kong L, Mao Y, Cheng D, Kang K, Dai J, Zhao D, Zhang Y, Lu N, Wan Z, Du R, Xiong B, Zhang J, Tan Y, Lu G, Gong F, Lin G, Liang B, Du J, Hu L. A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions. Hum Reprod 2022:deac190. [PMID: 36066440 DOI: 10.1093/humrep/deac190] [Reference Citation Analysis]