1. Dastidar, Sumitava, Majumdar, Debanjana, Tipanee, Jaitip, Chuah, Marinee K, VandenDriessche, Thierry. 2021. Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytes. In Molecular therapy : the journal of the American Society of Gene Therapy, 30, 75-91. doi:10.1016/j.ymthe.2021.08.004. https://pubmed.ncbi.nlm.nih.gov/34371182/
2. Matsson, Hans, Huss, Mikael, Persson, Helena, Peyrard-Janvid, Myriam, Kere, Juha. 2015. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia. In Journal of human genetics, 60, 399-401. doi:10.1038/jhg.2015.37. https://pubmed.ncbi.nlm.nih.gov/25877001/
3. Melville, Scott A, Buros, Jacqueline, Parrado, Antonio R, Saykin, Andrew J, Farrer, Lindsay A. 2012. Multiple loci influencing hippocampal degeneration identified by genome scan. In Annals of neurology, 72, 65-75. doi:10.1002/ana.23644. https://pubmed.ncbi.nlm.nih.gov/22745009/
4. Calì, Francesco, Di Blasi, Francesco Domenico, Avola, Emanuela, Saccone, Salvatore, Buono, Serafino. 2023. Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. In Medicina (Kaunas, Lithuania), 59, . doi:10.3390/medicina59081503. https://pubmed.ncbi.nlm.nih.gov/37629793/