1. Mäkitie, Riikka E, Hackl, Matthias, Weigl, Moritz, Grillari, Johannes, Mäkitie, Outi. 2020. Unique, Gender-Dependent Serum microRNA Profile in PLS3 Gene-Related Osteoporosis. In Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 35, 1962-1973. doi:10.1002/jbmr.4097. https://pubmed.ncbi.nlm.nih.gov/32453450/
2. Szkandera, Joanna, Winder, Thomas, Stotz, Michael, Gerger, Armin, Absenger, Gudrun. 2013. A common gene variant in PLS3 predicts colon cancer recurrence in women. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 34, 2183-8. doi:10.1007/s13277-013-0754-7. https://pubmed.ncbi.nlm.nih.gov/23549633/
3. Petit, Florence, Longoni, Mauro, Wells, Julie, Donahoe, Patricia K, High, Frances A. 2023. PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects. In American journal of human genetics, 110, 1787-1803. doi:10.1016/j.ajhg.2023.09.002. https://pubmed.ncbi.nlm.nih.gov/37751738/
4. Kämpe, A J, Costantini, A, Mäkitie, R E, Jiao, H, Mäkitie, O. 2017. PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants. In Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 28, 3023-3032. doi:10.1007/s00198-017-4150-9. https://pubmed.ncbi.nlm.nih.gov/28748388/