1. Pettigrew, Kerry A, Frinton, Emily, Nudel, Ron, Newbury, Dianne F, Paracchini, Silvia. 2016. Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes. In Journal of neurodevelopmental disorders, 8, 24. doi:10.1186/s11689-016-9157-6. https://pubmed.ncbi.nlm.nih.gov/27307794/
2. Andres, Erin M, Earnest, Kathleen Kelsey, Smith, Shelley D, Rice, Mabel L, Raza, Muhammad Hashim. 2020. Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment. In Journal of speech, language, and hearing research : JSLHR, 63, 4046-4061. doi:10.1044/2020_JSLHR-20-00102. https://pubmed.ncbi.nlm.nih.gov/33186502/
3. Moriano-Gutierrez, A, Colomer-Revuelta, J, Sanjuan, J, Carot-Sierra, J M. . [Environmental and genetic variables related with alterations in language acquisition in early childhood]. In Revista de neurologia, 64, 31-37. doi:. https://pubmed.ncbi.nlm.nih.gov/28000910/
4. Thomson, Emma, Rappsilber, Juri, Tollervey, David. 2007. Nop9 is an RNA binding protein present in pre-40S ribosomes and required for 18S rRNA synthesis in yeast. In RNA (New York, N.Y.), 13, 2165-74. doi:. https://pubmed.ncbi.nlm.nih.gov/17956976/
5. Thomas, Tina, Litwin, Griffin, Francis, David J, Grigorenko, Elena L. 2023. Exploring Genetic and Neural Risk of Specific Reading Disability within a Nuclear Twin Family Case Study: A Translational Clinical Application. In Journal of personalized medicine, 13, . doi:10.3390/jpm13010156. https://pubmed.ncbi.nlm.nih.gov/36675818/
6. Nudel, R, Simpson, N H, Baird, G, Fisher, S E, Newbury, D F. 2014. Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. In Genes, brain, and behavior, 13, 418-29. doi:10.1111/gbb.12127. https://pubmed.ncbi.nlm.nih.gov/24571439/
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