1. Brock, Pamela, Sevigny, Myriam, Liyanarachchi, Sandya, Ollila, Saara, Nieminen, Taina T. 2024. PDPR Gene Variants Predisposing to Papillary Thyroid Cancer. In Thyroid : official journal of the American Thyroid Association, 34, 575-582. doi:10.1089/thy.2023.0560. https://pubmed.ncbi.nlm.nih.gov/38062777/
2. Alazami, Anas M, Patel, Nisha, Shamseldin, Hanan E, Monies, Dorota M, Alkuraya, Fowzan S. 2014. Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families. In Cell reports, 10, 148-61. doi:10.1016/j.celrep.2014.12.015. https://pubmed.ncbi.nlm.nih.gov/25558065/
3. Bruno, Lucia Pia, Doddato, Gabriella, Valentino, Floriana, Renieri, Alessandra, Ariani, Francesca. 2021. New Candidates for Autism/Intellectual Disability Identified by Whole-Exome Sequencing. In International journal of molecular sciences, 22, . doi:10.3390/ijms222413439. https://pubmed.ncbi.nlm.nih.gov/34948243/
4. Chen, Lei, Abel, Haley J, Das, Indraniel, Stitziel, Nathan O, Hall, Ira M. . Association of structural variation with cardiometabolic traits in Finns. In American journal of human genetics, 108, 583-596. doi:10.1016/j.ajhg.2021.03.008. https://pubmed.ncbi.nlm.nih.gov/33798444/
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