Key Publications

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Laurent A, et al. ZFPIP/Zfp462 is maternally required for proper early Xenopus laevis development. 2009. PMID: 19111535. https://pubmed.ncbi.nlm.nih.gov/19111535/

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Massé J, et al. Involvement of ZFPIP/Zfp462 in chromatin integrity and survival of P19 pluripotent cells. 2010. PMID: 20219459. https://pubmed.ncbi.nlm.nih.gov/20219459/

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Massé J, et al. ZFPIP/Zfp462 is involved in P19 cell pluripotency and in their neuronal fate. 2011. PMID: 21570965. https://pubmed.ncbi.nlm.nih.gov/21570965/

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Wang W, et al. Zfp462 deficiency causes anxiety-like behaviors with excessive self-grooming in mice. 2017. PMID: 27621227. https://pubmed.ncbi.nlm.nih.gov/27621227/

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Weiss K, Terhal PA, Cohen L, et al. Haploinsufficiency of ZNF462 is associated with craniofacial anomalies, corpus callosum dysgenesis, ptosis, and developmental delay.  2017;101(2):246-255. PMID: 28513610. https://pubmed.ncbi.nlm.nih.gov/28513610/

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Kruszka P, et al. Phenotype delineation of ZNF462 related syndrome. 2019. PMID: 31361404. https://pubmed.ncbi.nlm.nih.gov/31361404/

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Yelagandula R, et al. ZFP462 safeguards neural lineage specification by targeting G9A/GLP-mediated heterochromatin to silence enhancers. 2023. PMID: 36604593. https://pubmed.ncbi.nlm.nih.gov/36604593/

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McConkey H, et al. DNA methylation episignature identifies Weiss-Kruszka syndrome and provides a novel diagnostic biomarker. 2026. (PMID pending/publication details forthcoming.)