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For: Masih S, Moirangthem A, Phadke SR. Homozygous Missense Variation in PNPLA8 Causes Prenatal-Onset Severe Neurodegeneration. Mol Syndromol 2021;12:174-8. [PMID: 34177434 DOI: 10.1159/000513524] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Wu S, Chen X, Huang F, Lin M, Chen P, Wan H, Gao F, Zheng T, Zheng X. Transcriptomic Analysis of Long Noncoding RNA and mRNA Expression Profiles in the Amygdala of Rats with Bone Cancer Pain-Depression Comorbidity. Life (Basel) 2021;11:834. [PMID: 34440578 DOI: 10.3390/life11080834] [Reference Citation Analysis]
2 Abitbol M, Jagannathan V, Laurent N, Noblet E, Dutil GF, Troupel T, de Dufaure de Citres C, Gache V, Blot S, Escriou C, Leeb T. A PNPLA8 frameshift variant in Australian shepherd dogs with hereditary ataxia. Anim Genet 2022. [PMID: 35864734 DOI: 10.1111/age.13245] [Reference Citation Analysis]
3 Masih S, Moirangthem A, Shambhavi A, Rai A, Mandal K, Saxena D, Nilay M, Agrawal N, Srivastava S, Sait H, Phadke SR. Deciphering the molecular landscape of microcephaly in 87 Indian families by exome sequencing. Eur J Med Genet 2022;:104520. [PMID: 35568357 DOI: 10.1016/j.ejmg.2022.104520] [Reference Citation Analysis]