A census of mammalian imprinting.

By I. Morison, Joshua P. Ramsay, Hamish G. Spencer. Trends in Genetics, 2005

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Genomic basis for RNA alterations in cancer (2020, methodology): “All ASE events that were identified were further filtered to keep only genes that have not been identified as imprinted 26 .”
Lost Sex in the Reptiles: Constraints and Correlations (2009, background): “Mammals have the constraint of genomic imprinting, where epigenetic modification of approximately 100 genes occurs differentially in either the sperm or the egg in a parent-of-origin manner (reviewed by Morison et al. 2005; Platonov 2005; Hore et al. 2007).”
Non-coding RNA. (2006, background): “A large number of ncRNAs are specifically expressed from either the paternal or maternal allele at imprinted loci, and some are associated with human diseases, such as the Prader–Willi and Angelman syndromes (39).”
Environmental epigenomics and disease susceptibility (2007, background): “In addition, numerous linkage studies of other complex disorders such as bipolar disorder, Silver–Russell syndrome, Tourette syndrome and schizophrenia show a parent-of-origin inheritance preferenc”
Computational and experimental identification of novel human imprinted genes. (2007, background): “Indeed, experimental identification of human imprinted genes to date has been slow: The untranslated mRNA H19 was the first gene shown to be imprinted in human (Zhang and Tycko 1992), and since its discovery in 1992, only ∼40 additional human imprinted genes have been identified (Morison et al. 2005”